Table of Contents

Plant Physiology: 104 (2)
Feb 1994

A

  1. Abadia, A.

    1. Chlorophyll Fluorescence as a Possible Tool for Salinity Tolerance Screening in Barley (Hordeum vulgare L.)
      R. Belkhodja, F. Morales, A. Abadia, J. Gomez-Aparisi, J. Abadia
      Plant Physiol. Feb 1994, 104 (2) 667-673; DOI: https://doi.org/10.1104/pp.104.2.667

  2. Abadia, J.

    1. Chlorophyll Fluorescence as a Possible Tool for Salinity Tolerance Screening in Barley (Hordeum vulgare L.)
      R. Belkhodja, F. Morales, A. Abadia, J. Gomez-Aparisi, J. Abadia
      Plant Physiol. Feb 1994, 104 (2) 667-673; DOI: https://doi.org/10.1104/pp.104.2.667

  3. Al-Bashir, M.

    1. Following Suberization in Potato Wound Periderm by Histochemical and Solid-State 13C Nuclear Magnetic Resonance Methods
      R. E. Stark, W. Sohn, R. A. Pacchiano Jr, M. Al-Bashir, J. R. Garbow
      Plant Physiol. Feb 1994, 104 (2) 527-533; DOI: https://doi.org/10.1104/pp.104.2.527

  4. Albersheim, P.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

  5. Allan, D. L.

    1. Phosphorus Stress-Induced Proteoid Roots Show Altered Metabolism in Lupinus albus
      J. F. Johnson, D. L. Allan, C. P. Vance
      Plant Physiol. Feb 1994, 104 (2) 657-665; DOI: https://doi.org/10.1104/pp.104.2.657

  6. An, H.

    1. ESI3, a Stress-Induced Gene from Lophopyrum elongatum
      P. J. Gulick, W. Shen, H. An
      Plant Physiol. Feb 1994, 104 (2) 799-800; DOI: https://doi.org/10.1104/pp.104.2.799

  7. Anderson, S. L.

    1. Genetic Manipulation of the Cyanobacterium Synechocystis sp. PCC 6803 (Development of Strains Lacking Photosystem I for the Analysis of Mutations in Photosystem II)
      L. B. Smart, N. R. Bowlby, S. L. Anderson, I. Sithole, L. McIntosh
      Plant Physiol. Feb 1994, 104 (2) 349-354; DOI: https://doi.org/10.1104/pp.104.2.349

  8. Ashworth, E. N.

    1. Response of Xylem Ray Parenchyma Cells of Red Osier Dogwood (Cornus sericea L.) to Freezing Stress (Microscopic Evidence of Protoplasm Contraction)
      Z. Ristic, E. N. Ashworth
      Plant Physiol. Feb 1994, 104 (2) 737-746; DOI: https://doi.org/10.1104/pp.104.2.737

B

  1. Badger, M. R.

    1. A Mutant Isolated from the Cyanobacterium Synechococcus PCC7942 Is Unable to Adapt to Low Inorganic Carbon Conditions
      J. W. Yu, G. D. Price, M. R. Badger
      Plant Physiol. Feb 1994, 104 (2) 605-611; DOI: https://doi.org/10.1104/pp.104.2.605

  2. Bahk, J. D.

    1. Isolation and Characterization of Three Soybean Extensin cDNAs
      J. C. Hong, Y. H. Cheong, R. T. Nagao, J. D. Bahk, M. J. Cho, J. L. Key
      Plant Physiol. Feb 1994, 104 (2) 793-796; DOI: https://doi.org/10.1104/pp.104.2.793

  3. Barber, M. S.

    1. Elicitor-Induced Cinnamyl Alcohol Dehydrogenase Activity in Lignifying Wheat (Triticum aestivum L.) Leaves
      H. J. Mitchell, J. L. Hall, M. S. Barber
      Plant Physiol. Feb 1994, 104 (2) 551-556; DOI: https://doi.org/10.1104/pp.104.2.551

  4. Basel, L. E.

    1. Modulation of Fusicoccin-Binding Protein Activity in Mung Bean (Vigna radiata L.) Hypocotyls by Tissue Maturation and by Fusicoccin
      L. E. Basel, A. T. Zukowski, R. E. Cleland
      Plant Physiol. Feb 1994, 104 (2) 691-697; DOI: https://doi.org/10.1104/pp.104.2.691

  5. Becana, M.

    1. Cloning and Sequence Analysis of a cDNA Encoding Ferric Leghemoglobin Reductase from Soybean Nodules
      L. Ji, M. Becana, G. Sarath, R. V. Klucas
      Plant Physiol. Feb 1994, 104 (2) 453-459; DOI: https://doi.org/10.1104/pp.104.2.453

  6. Bednarek, S. Y.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  7. Belkhodja, R.

    1. Chlorophyll Fluorescence as a Possible Tool for Salinity Tolerance Screening in Barley (Hordeum vulgare L.)
      R. Belkhodja, F. Morales, A. Abadia, J. Gomez-Aparisi, J. Abadia
      Plant Physiol. Feb 1994, 104 (2) 667-673; DOI: https://doi.org/10.1104/pp.104.2.667

  8. Bogorad, L.

    1. Evidence That [sigma] Factors Are Components of Chloroplast RNA Polymerase
      R. F. Troxler, F. Zhang, J. Hu, L. Bogorad
      Plant Physiol. Feb 1994, 104 (2) 753-759; DOI: https://doi.org/10.1104/pp.104.2.753

  9. Bowlby, N. R.

    1. Genetic Manipulation of the Cyanobacterium Synechocystis sp. PCC 6803 (Development of Strains Lacking Photosystem I for the Analysis of Mutations in Photosystem II)
      L. B. Smart, N. R. Bowlby, S. L. Anderson, I. Sithole, L. McIntosh
      Plant Physiol. Feb 1994, 104 (2) 349-354; DOI: https://doi.org/10.1104/pp.104.2.349

  10. Bradford, K. J.

    1. Development of Desiccation Tolerance during Embryogenesis in Rice (Oryza sativa) and Wild Rice (Zizania palustris) (Dehydrin Expression, Abscisic Acid Content, and Sucrose Accumulation)
      D. W. Still, D. A. Kovach, K. J. Bradford
      Plant Physiol. Feb 1994, 104 (2) 431-438; DOI: https://doi.org/10.1104/pp.104.2.431
    2. Cell-Wall Autohydrolysis in Isolated Endosperms of Lettuce (Lactuca sativa L.)
      S. Dutta, K. J. Bradford, D. J. Nevins
      Plant Physiol. Feb 1994, 104 (2) 623-628; DOI: https://doi.org/10.1104/pp.104.2.623

  11. Brenner, M.

    1. A Role for Cytokinins in De-Etiolation in Arabidopsis (det Mutants Have an Altered Response to Cytokinins)
      J. Chory, D. Reinecke, S. Sim, T. Washburn, M. Brenner
      Plant Physiol. Feb 1994, 104 (2) 339-347; DOI: https://doi.org/10.1104/pp.104.2.339

  12. Brenner, M. L.

    1. Temporal and Spatial Expression Pattern of Sucrose Synthase during Tomato Fruit Development
      F. Wang, A. G. Smith, M. L. Brenner
      Plant Physiol. Feb 1994, 104 (2) 535-540; DOI: https://doi.org/10.1104/pp.104.2.535

  13. Brush, R. A.

    1. Characterization and Quantification of Intrinsic Ice Nucleators in Winter Rye (Secale cereale) Leaves
      R. A. Brush, M. Griffith, A. Mlynarz
      Plant Physiol. Feb 1994, 104 (2) 725-735; DOI: https://doi.org/10.1104/pp.104.2.725

  14. Bucheli, E.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

C

  1. Caldwell, C. R.

    1. Modification of the Cellular Heat Sensitivity of Cucumber by Growth under Supplemental Ultraviolet-B Radiation
      C. R. Caldwell
      Plant Physiol. Feb 1994, 104 (2) 395-399; DOI: https://doi.org/10.1104/pp.104.2.395

  2. Carrasco, J. L.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  3. Cheong, Y. H.

    1. Isolation and Characterization of Three Soybean Extensin cDNAs
      J. C. Hong, Y. H. Cheong, R. T. Nagao, J. D. Bahk, M. J. Cho, J. L. Key
      Plant Physiol. Feb 1994, 104 (2) 793-796; DOI: https://doi.org/10.1104/pp.104.2.793

  4. Chino, M.

    1. Expression of a Soybean (Glycine max [L.] Merr.) Seed Storage Protein Gene in Transgenic Arabidopsis thaliana and Its Response to Nutritional Stress and to Abscisic Acid Mutations
      S. Naito, M. Y. Hirai, M. Chino, Y. Komeda
      Plant Physiol. Feb 1994, 104 (2) 497-503; DOI: https://doi.org/10.1104/pp.104.2.497

  5. Chitnis, P. R.

    1. Synechocystis PCC 6803 Contains a Single Gene for the [beta] Subunit of Tryptophan Synthase with Strong Homology to the trpB Genes of Arabidopsis and Maize (Zea mays L.)
      G. P. Zhao, R. L. Somerville, P. R. Chitnis
      Plant Physiol. Feb 1994, 104 (2) 461-466; DOI: https://doi.org/10.1104/pp.104.2.461

  6. Cho, M. J.

    1. Isolation and Characterization of Three Soybean Extensin cDNAs
      J. C. Hong, Y. H. Cheong, R. T. Nagao, J. D. Bahk, M. J. Cho, J. L. Key
      Plant Physiol. Feb 1994, 104 (2) 793-796; DOI: https://doi.org/10.1104/pp.104.2.793

  7. Chory, J.

    1. A Role for Cytokinins in De-Etiolation in Arabidopsis (det Mutants Have an Altered Response to Cytokinins)
      J. Chory, D. Reinecke, S. Sim, T. Washburn, M. Brenner
      Plant Physiol. Feb 1994, 104 (2) 339-347; DOI: https://doi.org/10.1104/pp.104.2.339
    2. The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A
      T. Shinomura, A. Nagatani, J. Chory, M. Furuya
      Plant Physiol. Feb 1994, 104 (2) 363-371; DOI: https://doi.org/10.1104/pp.104.2.363

  8. Chueca, A.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  9. Cleland, R. E.

    1. Modulation of Fusicoccin-Binding Protein Activity in Mung Bean (Vigna radiata L.) Hypocotyls by Tissue Maturation and by Fusicoccin
      L. E. Basel, A. T. Zukowski, R. E. Cleland
      Plant Physiol. Feb 1994, 104 (2) 691-697; DOI: https://doi.org/10.1104/pp.104.2.691

  10. Clouse, S. D.

    1. Investigation of Gene Expression, Growth Kinetics, and Wall Extensibility during Brassinosteroid-Regulated Stem Elongation
      D. M. Zurek, D. L. Rayle, T. C. McMorris, S. D. Clouse
      Plant Physiol. Feb 1994, 104 (2) 505-513; DOI: https://doi.org/10.1104/pp.104.2.505

  11. Cooper, J. B.

    1. 3,4-Dehydroproline Inhibits Cell Wall Assembly and Cell Division in Tobacco Protoplasts
      J. B. Cooper, J. E. Heuser, J. E. Varner
      Plant Physiol. Feb 1994, 104 (2) 747-752; DOI: https://doi.org/10.1104/pp.104.2.747

  12. Cossins, E. A.

    1. Folate Metabolism in Datura innoxia (In Vivo and in Vitro Folylpolyglutamate Synthesis in Wild-Type and Methotrexate-Resistant Cells)
      K. Wu, E. A. Cossins, J. King
      Plant Physiol. Feb 1994, 104 (2) 373-380; DOI: https://doi.org/10.1104/pp.104.2.373

  13. Crofts, A. R.

    1. Mutants of Chloroplast Coupling Factor Reduction in Arabidopsis
      H. Gabrys, D. M. Kramer, A. R. Crofts, D. R. Ort
      Plant Physiol. Feb 1994, 104 (2) 769-776; DOI: https://doi.org/10.1104/pp.104.2.769

  14. Crotty, C. M.

    1. Quenching of Chlorophyll a Fluorescence in Response to Na+-Dependent HCO3- Transport-Mediated Accumulation of Inorganic Carbon in the Cyanobacterium Synechococcus UTEX 625
      C. M. Crotty, P. N. Tyrrell, G. S. Espie
      Plant Physiol. Feb 1994, 104 (2) 785-791; DOI: https://doi.org/10.1104/pp.104.2.785

D

  1. Darvill, A. G.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

  2. Davies, W. J.

    1. How Do Chemical Signals Work in Plants that Grow in Drying Soil?
      W. J. Davies, F. Tardieu, C. L. Trejo
      Plant Physiol. Feb 1994, 104 (2) 309-314; DOI: https://doi.org/10.1104/pp.104.2.309

  3. DeWald, D. B.

    1. Sucrose Modulation of Soybean Vsp Gene Expression Is Inhibited by Auxin
      D. B. DeWald, A. Sadka, J. E. Mullet
      Plant Physiol. Feb 1994, 104 (2) 439-444; DOI: https://doi.org/10.1104/pp.104.2.439

  4. Diez, J.

    1. Occurrence of Only One Form of Glutamine Synthetase in the Green Alga Monoraphidium braunii
      J. M. Garcia-Fernandez, A. Lopez-Ruiz, F. Toribio, J. M. Roldan, J. Diez
      Plant Physiol. Feb 1994, 104 (2) 425-430; DOI: https://doi.org/10.1104/pp.104.2.425

  5. Douce, R.

    1. Purification and Kinetic Properties of Serine Acetyltransferase Free of O-Acetylserine(thiol)lyase from Spinach Chloroplasts
      M. L. Ruffet, M. Droux, R. Douce
      Plant Physiol. Feb 1994, 104 (2) 597-604; DOI: https://doi.org/10.1104/pp.104.2.597

  6. Droux, M.

    1. Purification and Kinetic Properties of Serine Acetyltransferase Free of O-Acetylserine(thiol)lyase from Spinach Chloroplasts
      M. L. Ruffet, M. Droux, R. Douce
      Plant Physiol. Feb 1994, 104 (2) 597-604; DOI: https://doi.org/10.1104/pp.104.2.597

  7. Dunning, N.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

  8. Dutta, S.

    1. Cell-Wall Autohydrolysis in Isolated Endosperms of Lettuce (Lactuca sativa L.)
      S. Dutta, K. J. Bradford, D. J. Nevins
      Plant Physiol. Feb 1994, 104 (2) 623-628; DOI: https://doi.org/10.1104/pp.104.2.623

E

  1. Elkind, Y.

    1. A Vesicular Arbuscular Mycorrhizal Fungus (Glomus intraradix) Induces a Defense Response in Alfalfa Roots
      H. Volpin, Y. Elkind, Y. Okon, Y. Kapulnik
      Plant Physiol. Feb 1994, 104 (2) 683-689; DOI: https://doi.org/10.1104/pp.104.2.683

  2. Espie, G. S.

    1. Quenching of Chlorophyll a Fluorescence in Response to Na+-Dependent HCO3- Transport-Mediated Accumulation of Inorganic Carbon in the Cyanobacterium Synechococcus UTEX 625
      C. M. Crotty, P. N. Tyrrell, G. S. Espie
      Plant Physiol. Feb 1994, 104 (2) 785-791; DOI: https://doi.org/10.1104/pp.104.2.785

F

  1. Falbel, T. G.

    1. Characterization of a Family of Chlorophyll-Deficient Wheat (Triticum) and Barley (Hordeum vulgare) Mutants with Defects in the Magnesium-Insertion Step of Chlorophyll Biosynthesis
      T. G. Falbel, L. A. Staehelin
      Plant Physiol. Feb 1994, 104 (2) 639-648; DOI: https://doi.org/10.1104/pp.104.2.639

  2. Farnden, KJF.

    1. Cloning and Characterization of a cDNA Encoding Aspartate Aminotransferase-P1 from Lupinus angustifolius Root Tips
      C. S. Winefield, B. D. Reddington, W. T. Jones, PHS. Reynolds, KJF. Farnden
      Plant Physiol. Feb 1994, 104 (2) 417-423; DOI: https://doi.org/10.1104/pp.104.2.417

  3. Fawley, M. W.

    1. A cDNA Clone Encoding a Light-Harvesting Protein from Mantoniella squamata
      S. Jiao, M. W. Fawley
      Plant Physiol. Feb 1994, 104 (2) 797-798; DOI: https://doi.org/10.1104/pp.104.2.797

  4. Fonolla, J.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  5. Furuya, M.

    1. The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A
      T. Shinomura, A. Nagatani, J. Chory, M. Furuya
      Plant Physiol. Feb 1994, 104 (2) 363-371; DOI: https://doi.org/10.1104/pp.104.2.363

G

  1. Gabrys, H.

    1. Mutants of Chloroplast Coupling Factor Reduction in Arabidopsis
      H. Gabrys, D. M. Kramer, A. R. Crofts, D. R. Ort
      Plant Physiol. Feb 1994, 104 (2) 769-776; DOI: https://doi.org/10.1104/pp.104.2.769

  2. Gallwitz, D.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  3. Garbow, J. R.

    1. Following Suberization in Potato Wound Periderm by Histochemical and Solid-State 13C Nuclear Magnetic Resonance Methods
      R. E. Stark, W. Sohn, R. A. Pacchiano Jr, M. Al-Bashir, J. R. Garbow
      Plant Physiol. Feb 1994, 104 (2) 527-533; DOI: https://doi.org/10.1104/pp.104.2.527

  4. Garcia-Fernandez, J. M.

    1. Occurrence of Only One Form of Glutamine Synthetase in the Green Alga Monoraphidium braunii
      J. M. Garcia-Fernandez, A. Lopez-Ruiz, F. Toribio, J. M. Roldan, J. Diez
      Plant Physiol. Feb 1994, 104 (2) 425-430; DOI: https://doi.org/10.1104/pp.104.2.425

  5. Gauthier, D. A.

    1. Inorganic Phosphate (Pi) Enhancement of Dark Respiration in the Pi-Limited Green Alga Selenastrum minutum (Interactions between H+/Pi Cotransport, the Plasmalemma H+-ATPase, and Dark Respiratory Carbon Flow)
      D. A. Gauthier, D. H. Turpin
      Plant Physiol. Feb 1994, 104 (2) 629-637; DOI: https://doi.org/10.1104/pp.104.2.629

  6. Gebhardt, C.

    1. Transcripts Accumulating during Cold Storage of Potato (Solanum tuberosum L.) Tubers Are Sequence Related to Stress-Responsive Genes
      J. van Berkel, F. Salamini, C. Gebhardt
      Plant Physiol. Feb 1994, 104 (2) 445-452; DOI: https://doi.org/10.1104/pp.104.2.445

  7. Gil, P.

    1. Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis
      P. Gil, Y. Liu, V. Orbovic, E. Verkamp, K. L. Poff, P. J. Green
      Plant Physiol. Feb 1994, 104 (2) 777-784; DOI: https://doi.org/10.1104/pp.104.2.777

  8. Giraudat, J.

    1. Drought Rhizogenesis in Arabidopsis thaliana (Differential Responses of Hormonal Mutants)
      N. Vartanian, L. Marcotte, J. Giraudat
      Plant Physiol. Feb 1994, 104 (2) 761-767; DOI: https://doi.org/10.1104/pp.104.2.761

  9. Goldstein, G.

    1. Water Relations and Low-Temperature Acclimation for Cactus Species Varying in Freezing Tolerance
      G. Goldstein, P. S. Nobel
      Plant Physiol. Feb 1994, 104 (2) 675-681; DOI: https://doi.org/10.1104/pp.104.2.675

  10. Gombos, Z.

    1. The Unsaturation of Membrane Lipids Stabilizes Photosynthesis against Heat Stress
      Z. Gombos, H. Wada, E. Hideg, N. Murata
      Plant Physiol. Feb 1994, 104 (2) 563-567; DOI: https://doi.org/10.1104/pp.104.2.563

  11. Gomez-Aparisi, J.

    1. Chlorophyll Fluorescence as a Possible Tool for Salinity Tolerance Screening in Barley (Hordeum vulgare L.)
      R. Belkhodja, F. Morales, A. Abadia, J. Gomez-Aparisi, J. Abadia
      Plant Physiol. Feb 1994, 104 (2) 667-673; DOI: https://doi.org/10.1104/pp.104.2.667

  12. Grabowski, R.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  13. Green, P. J.

    1. Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis
      P. Gil, Y. Liu, V. Orbovic, E. Verkamp, K. L. Poff, P. J. Green
      Plant Physiol. Feb 1994, 104 (2) 777-784; DOI: https://doi.org/10.1104/pp.104.2.777

  14. Griffin, K. L.

    1. Direct and Indirect Effects of Atmospheric Carbon Dioxide Enrichment on Leaf Respiration of Glycine max (L.) Merr
      R. B. Thomas, K. L. Griffin
      Plant Physiol. Feb 1994, 104 (2) 355-361; DOI: https://doi.org/10.1104/pp.104.2.355

  15. Griffith, M.

    1. Characterization and Quantification of Intrinsic Ice Nucleators in Winter Rye (Secale cereale) Leaves
      R. A. Brush, M. Griffith, A. Mlynarz
      Plant Physiol. Feb 1994, 104 (2) 725-735; DOI: https://doi.org/10.1104/pp.104.2.725

  16. Grusak, M. A.

    1. Iron Transport to Developing Ovules of Pisum sativum (I. Seed Import Characteristics and Phloem Iron-Loading Capacity of Source Regions)
      M. A. Grusak
      Plant Physiol. Feb 1994, 104 (2) 649-655; DOI: https://doi.org/10.1104/pp.104.2.649

  17. Gu, Y. Q.

    1. Two Classes of Proteins and mRNAs in Lilium longiflorum L. Identified by Human Vitronectin Probes
      C. S. Wang, L. L. Walling, Y. Q. Gu, C. F. Ware, E. M. Lord
      Plant Physiol. Feb 1994, 104 (2) 711-717; DOI: https://doi.org/10.1104/pp.104.2.711

  18. Gulick, P. J.

    1. ESI3, a Stress-Induced Gene from Lophopyrum elongatum
      P. J. Gulick, W. Shen, H. An
      Plant Physiol. Feb 1994, 104 (2) 799-800; DOI: https://doi.org/10.1104/pp.104.2.799

  19. Guy, R. D.

    1. A Model of the Regulation of Nitrogenase Electron Allocation in Legume Nodules (II. Comparison of Empirical and Theoretical Studies in Soybean)
      A. H. Moloney, R. D. Guy, D. B. Layzell
      Plant Physiol. Feb 1994, 104 (2) 541-550; DOI: https://doi.org/10.1104/pp.104.2.541

H

  1. Hahn, M. G.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

  2. Halevy, A. H.

    1. Chromoplast Biogenesis in Cucumis sativus Corollas (Rapid Effect of Gibberellin A3 on the Accumulation of a Chromoplast-Specific Carotenoid-Associated Protein)
      A. Vainstein, A. H. Halevy, I. Smirra, M. Vishnevetsky
      Plant Physiol. Feb 1994, 104 (2) 321-326; DOI: https://doi.org/10.1104/pp.104.2.321

  3. Hall, J. L.

    1. Elicitor-Induced Cinnamyl Alcohol Dehydrogenase Activity in Lignifying Wheat (Triticum aestivum L.) Leaves
      H. J. Mitchell, J. L. Hall, M. S. Barber
      Plant Physiol. Feb 1994, 104 (2) 551-556; DOI: https://doi.org/10.1104/pp.104.2.551

  4. Harada, H.

    1. Root-Inducing Region of Mikimopine Type Ri Plasmid pRi1724
      S. Kiyokawa, K. Kobayashi, Y. Kikuchi, H. Kamada, H. Harada
      Plant Physiol. Feb 1994, 104 (2) 801-802; DOI: https://doi.org/10.1104/pp.104.2.801

  5. Harris-Haller, L.

    1. An Auxin-Inducible Proteinase Inhibitor Gene from Tomato
      R. J. Young, C. F. Scheuring, L. Harris-Haller, B. H. Taylor
      Plant Physiol. Feb 1994, 104 (2) 811-812; DOI: https://doi.org/10.1104/pp.104.2.811

  6. Hengst, L.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  7. Hermoso, R.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  8. Heuser, J. E.

    1. 3,4-Dehydroproline Inhibits Cell Wall Assembly and Cell Division in Tobacco Protoplasts
      J. B. Cooper, J. E. Heuser, J. E. Varner
      Plant Physiol. Feb 1994, 104 (2) 747-752; DOI: https://doi.org/10.1104/pp.104.2.747

  9. Hideg, E.

    1. The Unsaturation of Membrane Lipids Stabilizes Photosynthesis against Heat Stress
      Z. Gombos, H. Wada, E. Hideg, N. Murata
      Plant Physiol. Feb 1994, 104 (2) 563-567; DOI: https://doi.org/10.1104/pp.104.2.563

  10. Hirai, M. Y.

    1. Expression of a Soybean (Glycine max [L.] Merr.) Seed Storage Protein Gene in Transgenic Arabidopsis thaliana and Its Response to Nutritional Stress and to Abscisic Acid Mutations
      S. Naito, M. Y. Hirai, M. Chino, Y. Komeda
      Plant Physiol. Feb 1994, 104 (2) 497-503; DOI: https://doi.org/10.1104/pp.104.2.497

  11. Hirano, H.

    1. Nucleotide Sequence of a Soybean (Glycine max L. Merr.) Ubiquitin Gene
      B. S. Xia, R. N. Waterhouse, Y. Watanabe, H. Kajiwara, S. Komatsu, H. Hirano
      Plant Physiol. Feb 1994, 104 (2) 805-806; DOI: https://doi.org/10.1104/pp.104.2.805

  12. Hoffmann-Benning, S.

    1. Cuticle Biosynthesis in Rapidly Growing Internodes of Deepwater Rice
      S. Hoffmann-Benning, H. Kende
      Plant Physiol. Feb 1994, 104 (2) 719-723; DOI: https://doi.org/10.1104/pp.104.2.719

  13. Hong, J. C.

    1. Isolation and Characterization of Three Soybean Extensin cDNAs
      J. C. Hong, Y. H. Cheong, R. T. Nagao, J. D. Bahk, M. J. Cho, J. L. Key
      Plant Physiol. Feb 1994, 104 (2) 793-796; DOI: https://doi.org/10.1104/pp.104.2.793

  14. Hooks, M. A.

    1. Nucleotide Availability in Maize (Zea mays L.) Root Tips (Estimation of Free and Protein-Bound Nucleotides Using 31P-Nuclear Magnetic Resonance and a Novel Protein-Ligand-Binding Assay)
      M. A. Hooks, G. C. Shearer, JKM. Roberts
      Plant Physiol. Feb 1994, 104 (2) 581-589; DOI: https://doi.org/10.1104/pp.104.2.581

  15. Hu, J.

    1. Evidence That [sigma] Factors Are Components of Chloroplast RNA Polymerase
      R. F. Troxler, F. Zhang, J. Hu, L. Bogorad
      Plant Physiol. Feb 1994, 104 (2) 753-759; DOI: https://doi.org/10.1104/pp.104.2.753

  16. Hurkman, W. J.

    1. Nucleotide Sequence of a Transcript Encoding a Germin-Like Protein That Is Present in Salt-Stressed Barley (Hordeum vulgare L.) Roots
      W. J. Hurkman, B. G. Lane, C. K. Tanaka
      Plant Physiol. Feb 1994, 104 (2) 803-804; DOI: https://doi.org/10.1104/pp.104.2.803

I

  1. Iiyama, K.

    1. Covalent Cross-Links in the Cell Wall
      K. Iiyama, TBT. Lam, B. A. Stone
      Plant Physiol. Feb 1994, 104 (2) 315-320; DOI: https://doi.org/10.1104/pp.104.2.315

J

  1. Jean-Jacques, I.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  2. Ji, L.

    1. Cloning and Sequence Analysis of a cDNA Encoding Ferric Leghemoglobin Reductase from Soybean Nodules
      L. Ji, M. Becana, G. Sarath, R. V. Klucas
      Plant Physiol. Feb 1994, 104 (2) 453-459; DOI: https://doi.org/10.1104/pp.104.2.453

  3. Jiao, S.

    1. A cDNA Clone Encoding a Light-Harvesting Protein from Mantoniella squamata
      S. Jiao, M. W. Fawley
      Plant Physiol. Feb 1994, 104 (2) 797-798; DOI: https://doi.org/10.1104/pp.104.2.797

  4. Johnson, J. F.

    1. Phosphorus Stress-Induced Proteoid Roots Show Altered Metabolism in Lupinus albus
      J. F. Johnson, D. L. Allan, C. P. Vance
      Plant Physiol. Feb 1994, 104 (2) 657-665; DOI: https://doi.org/10.1104/pp.104.2.657

  5. Jones, W. T.

    1. Cloning and Characterization of a cDNA Encoding Aspartate Aminotransferase-P1 from Lupinus angustifolius Root Tips
      C. S. Winefield, B. D. Reddington, W. T. Jones, PHS. Reynolds, KJF. Farnden
      Plant Physiol. Feb 1994, 104 (2) 417-423; DOI: https://doi.org/10.1104/pp.104.2.417

  6. Junkermann, W.

    1. Inhibition of Apoplastic and Symplastic Peroxidase Activity from Norway Spruce by the Photooxidant Hydroxymethyl Hydroperoxide
      A. Polle, W. Junkermann
      Plant Physiol. Feb 1994, 104 (2) 617-621; DOI: https://doi.org/10.1104/pp.104.2.617

K

  1. Kajiwara, H.

    1. Nucleotide Sequence of a Soybean (Glycine max L. Merr.) Ubiquitin Gene
      B. S. Xia, R. N. Waterhouse, Y. Watanabe, H. Kajiwara, S. Komatsu, H. Hirano
      Plant Physiol. Feb 1994, 104 (2) 805-806; DOI: https://doi.org/10.1104/pp.104.2.805

  2. Kamada, H.

    1. Root-Inducing Region of Mikimopine Type Ri Plasmid pRi1724
      S. Kiyokawa, K. Kobayashi, Y. Kikuchi, H. Kamada, H. Harada
      Plant Physiol. Feb 1994, 104 (2) 801-802; DOI: https://doi.org/10.1104/pp.104.2.801

  3. Kapulnik, Y.

    1. A Vesicular Arbuscular Mycorrhizal Fungus (Glomus intraradix) Induces a Defense Response in Alfalfa Roots
      H. Volpin, Y. Elkind, Y. Okon, Y. Kapulnik
      Plant Physiol. Feb 1994, 104 (2) 683-689; DOI: https://doi.org/10.1104/pp.104.2.683

  4. Kemmerer, E. C.

    1. Comparative Study of Cellulases Associated with Adventitious Root Initiation, Apical Buds, and Leaf, Flower, and Pod Abscission Zones in Soybean
      E. C. Kemmerer, M. L. Tucker
      Plant Physiol. Feb 1994, 104 (2) 557-562; DOI: https://doi.org/10.1104/pp.104.2.557

  5. Kende, H.

    1. Cuticle Biosynthesis in Rapidly Growing Internodes of Deepwater Rice
      S. Hoffmann-Benning, H. Kende
      Plant Physiol. Feb 1994, 104 (2) 719-723; DOI: https://doi.org/10.1104/pp.104.2.719

  6. Kenefick, D. G.

    1. Nucleotide Sequence of a cDNA Encoding an Elongation Factor (EF-1[infinity symbol]) from Barley Primary Leaf
      F. Sutton, D. G. Kenefick
      Plant Physiol. Feb 1994, 104 (2) 807; DOI: https://doi.org/10.1104/pp.104.2.807

  7. Key, J. L.

    1. Isolation and Characterization of Three Soybean Extensin cDNAs
      J. C. Hong, Y. H. Cheong, R. T. Nagao, J. D. Bahk, M. J. Cho, J. L. Key
      Plant Physiol. Feb 1994, 104 (2) 793-796; DOI: https://doi.org/10.1104/pp.104.2.793

  8. Kikuchi, Y.

    1. Root-Inducing Region of Mikimopine Type Ri Plasmid pRi1724
      S. Kiyokawa, K. Kobayashi, Y. Kikuchi, H. Kamada, H. Harada
      Plant Physiol. Feb 1994, 104 (2) 801-802; DOI: https://doi.org/10.1104/pp.104.2.801

  9. King, J.

    1. Folate Metabolism in Datura innoxia (In Vivo and in Vitro Folylpolyglutamate Synthesis in Wild-Type and Methotrexate-Resistant Cells)
      K. Wu, E. A. Cossins, J. King
      Plant Physiol. Feb 1994, 104 (2) 373-380; DOI: https://doi.org/10.1104/pp.104.2.373

  10. Kishinevsky, B. D.

    1. A Peanut Nodule Lectin in Infected Cells and in Vacuoles and the Extracellular Matrix of Nodule Parenchyma
      K. A. VandenBosch, L. R. Rodgers, D. J. Sherrier, B. D. Kishinevsky
      Plant Physiol. Feb 1994, 104 (2) 327-337; DOI: https://doi.org/10.1104/pp.104.2.327

  11. Kiyokawa, S.

    1. Root-Inducing Region of Mikimopine Type Ri Plasmid pRi1724
      S. Kiyokawa, K. Kobayashi, Y. Kikuchi, H. Kamada, H. Harada
      Plant Physiol. Feb 1994, 104 (2) 801-802; DOI: https://doi.org/10.1104/pp.104.2.801

  12. Kline, K.

    1. Oligomerization and the Affinity of Maize Phosphoenolpyruvate Carboxylase for Its Substrate
      R. T. Wedding, C. E. O'Brien, K. Kline
      Plant Physiol. Feb 1994, 104 (2) 613-616; DOI: https://doi.org/10.1104/pp.104.2.613

  13. Klucas, R. V.

    1. Cloning and Sequence Analysis of a cDNA Encoding Ferric Leghemoglobin Reductase from Soybean Nodules
      L. Ji, M. Becana, G. Sarath, R. V. Klucas
      Plant Physiol. Feb 1994, 104 (2) 453-459; DOI: https://doi.org/10.1104/pp.104.2.453

  14. Kobayashi, K.

    1. Root-Inducing Region of Mikimopine Type Ri Plasmid pRi1724
      S. Kiyokawa, K. Kobayashi, Y. Kikuchi, H. Kamada, H. Harada
      Plant Physiol. Feb 1994, 104 (2) 801-802; DOI: https://doi.org/10.1104/pp.104.2.801

  15. Kolloffel, C.

    1. Carbohydrate Status of Tulip Bulbs during Cold-Induced Flower Stalk Elongation and Flowering
      H. Lambrechts, F. Rook, C. Kolloffel
      Plant Physiol. Feb 1994, 104 (2) 515-520; DOI: https://doi.org/10.1104/pp.104.2.515

  16. Komatsu, S.

    1. Nucleotide Sequence of a Soybean (Glycine max L. Merr.) Ubiquitin Gene
      B. S. Xia, R. N. Waterhouse, Y. Watanabe, H. Kajiwara, S. Komatsu, H. Hirano
      Plant Physiol. Feb 1994, 104 (2) 805-806; DOI: https://doi.org/10.1104/pp.104.2.805

  17. Komeda, Y.

    1. Expression of a Soybean (Glycine max [L.] Merr.) Seed Storage Protein Gene in Transgenic Arabidopsis thaliana and Its Response to Nutritional Stress and to Abscisic Acid Mutations
      S. Naito, M. Y. Hirai, M. Chino, Y. Komeda
      Plant Physiol. Feb 1994, 104 (2) 497-503; DOI: https://doi.org/10.1104/pp.104.2.497

  18. Kovach, D. A.

    1. Development of Desiccation Tolerance during Embryogenesis in Rice (Oryza sativa) and Wild Rice (Zizania palustris) (Dehydrin Expression, Abscisic Acid Content, and Sucrose Accumulation)
      D. W. Still, D. A. Kovach, K. J. Bradford
      Plant Physiol. Feb 1994, 104 (2) 431-438; DOI: https://doi.org/10.1104/pp.104.2.431

  19. Kramer, D. M.

    1. Mutants of Chloroplast Coupling Factor Reduction in Arabidopsis
      H. Gabrys, D. M. Kramer, A. R. Crofts, D. R. Ort
      Plant Physiol. Feb 1994, 104 (2) 769-776; DOI: https://doi.org/10.1104/pp.104.2.769

  20. Kreis, M.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  21. Kremer, D. F.

    1. Photosynthetic Acclimation to Elevated CO2 Occurs in Transformed Tobacco with Decreased Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Content
      R. C. Sicher, D. F. Kremer, S. R. Rodermel
      Plant Physiol. Feb 1994, 104 (2) 409-415; DOI: https://doi.org/10.1104/pp.104.2.409

  22. Krivitzky, M.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

L

  1. Lam, TBT.

    1. Covalent Cross-Links in the Cell Wall
      K. Iiyama, TBT. Lam, B. A. Stone
      Plant Physiol. Feb 1994, 104 (2) 315-320; DOI: https://doi.org/10.1104/pp.104.2.315

  2. Lambrechts, H.

    1. Carbohydrate Status of Tulip Bulbs during Cold-Induced Flower Stalk Elongation and Flowering
      H. Lambrechts, F. Rook, C. Kolloffel
      Plant Physiol. Feb 1994, 104 (2) 515-520; DOI: https://doi.org/10.1104/pp.104.2.515

  3. Lane, B. G.

    1. Nucleotide Sequence of a Transcript Encoding a Germin-Like Protein That Is Present in Salt-Stressed Barley (Hordeum vulgare L.) Roots
      W. J. Hurkman, B. G. Lane, C. K. Tanaka
      Plant Physiol. Feb 1994, 104 (2) 803-804; DOI: https://doi.org/10.1104/pp.104.2.803

  4. Layzell, D. B.

    1. A Model of the Regulation of Nitrogenase Electron Allocation in Legume Nodules (II. Comparison of Empirical and Theoretical Studies in Soybean)
      A. H. Moloney, R. D. Guy, D. B. Layzell
      Plant Physiol. Feb 1994, 104 (2) 541-550; DOI: https://doi.org/10.1104/pp.104.2.541

  5. Lazaro, J. J.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  6. Lecharny, A.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  7. Liu, Y.

    1. Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis
      P. Gil, Y. Liu, V. Orbovic, E. Verkamp, K. L. Poff, P. J. Green
      Plant Physiol. Feb 1994, 104 (2) 777-784; DOI: https://doi.org/10.1104/pp.104.2.777

  8. Lopez-Gorge, J.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  9. Lopez-Ruiz, A.

    1. Occurrence of Only One Form of Glutamine Synthetase in the Green Alga Monoraphidium braunii
      J. M. Garcia-Fernandez, A. Lopez-Ruiz, F. Toribio, J. M. Roldan, J. Diez
      Plant Physiol. Feb 1994, 104 (2) 425-430; DOI: https://doi.org/10.1104/pp.104.2.425

  10. Lord, E. M.

    1. Two Classes of Proteins and mRNAs in Lilium longiflorum L. Identified by Human Vitronectin Probes
      C. S. Wang, L. L. Walling, Y. Q. Gu, C. F. Ware, E. M. Lord
      Plant Physiol. Feb 1994, 104 (2) 711-717; DOI: https://doi.org/10.1104/pp.104.2.711

M

  1. Marcotte, L.

    1. Drought Rhizogenesis in Arabidopsis thaliana (Differential Responses of Hormonal Mutants)
      N. Vartanian, L. Marcotte, J. Giraudat
      Plant Physiol. Feb 1994, 104 (2) 761-767; DOI: https://doi.org/10.1104/pp.104.2.761

  2. McIntosh, L.

    1. Genetic Manipulation of the Cyanobacterium Synechocystis sp. PCC 6803 (Development of Strains Lacking Photosystem I for the Analysis of Mutations in Photosystem II)
      L. B. Smart, N. R. Bowlby, S. L. Anderson, I. Sithole, L. McIntosh
      Plant Physiol. Feb 1994, 104 (2) 349-354; DOI: https://doi.org/10.1104/pp.104.2.349

  3. McMorris, T. C.

    1. Investigation of Gene Expression, Growth Kinetics, and Wall Extensibility during Brassinosteroid-Regulated Stem Elongation
      D. M. Zurek, D. L. Rayle, T. C. McMorris, S. D. Clouse
      Plant Physiol. Feb 1994, 104 (2) 505-513; DOI: https://doi.org/10.1104/pp.104.2.505

  4. Meinzer, F. C.

    1. Carbon Isotope Discrimination, Gas Exchange, and Growth of Sugarcane Cultivars under Salinity
      F. C. Meinzer, Z. Plaut, N. Z. Saliendra
      Plant Physiol. Feb 1994, 104 (2) 521-526; DOI: https://doi.org/10.1104/pp.104.2.521

  5. Mitchell, H. J.

    1. Elicitor-Induced Cinnamyl Alcohol Dehydrogenase Activity in Lignifying Wheat (Triticum aestivum L.) Leaves
      H. J. Mitchell, J. L. Hall, M. S. Barber
      Plant Physiol. Feb 1994, 104 (2) 551-556; DOI: https://doi.org/10.1104/pp.104.2.551

  6. Mitsuhashi, W.

    1. Development of Endopeptidase Activities in Maize (Zea mays L.) Endosperms
      W. Mitsuhashi, A. Oaks
      Plant Physiol. Feb 1994, 104 (2) 401-407; DOI: https://doi.org/10.1104/pp.104.2.401

  7. Mlynarz, A.

    1. Characterization and Quantification of Intrinsic Ice Nucleators in Winter Rye (Secale cereale) Leaves
      R. A. Brush, M. Griffith, A. Mlynarz
      Plant Physiol. Feb 1994, 104 (2) 725-735; DOI: https://doi.org/10.1104/pp.104.2.725

  8. Moloney, A. H.

    1. A Model of the Regulation of Nitrogenase Electron Allocation in Legume Nodules (II. Comparison of Empirical and Theoretical Studies in Soybean)
      A. H. Moloney, R. D. Guy, D. B. Layzell
      Plant Physiol. Feb 1994, 104 (2) 541-550; DOI: https://doi.org/10.1104/pp.104.2.541

  9. Morales, F.

    1. Chlorophyll Fluorescence as a Possible Tool for Salinity Tolerance Screening in Barley (Hordeum vulgare L.)
      R. Belkhodja, F. Morales, A. Abadia, J. Gomez-Aparisi, J. Abadia
      Plant Physiol. Feb 1994, 104 (2) 667-673; DOI: https://doi.org/10.1104/pp.104.2.667

  10. Mtili, N. E.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  11. Mullet, J. E.

    1. Sucrose Modulation of Soybean Vsp Gene Expression Is Inhibited by Auxin
      D. B. DeWald, A. Sadka, J. E. Mullet
      Plant Physiol. Feb 1994, 104 (2) 439-444; DOI: https://doi.org/10.1104/pp.104.2.439

  12. Murata, N.

    1. The Unsaturation of Membrane Lipids Stabilizes Photosynthesis against Heat Stress
      Z. Gombos, H. Wada, E. Hideg, N. Murata
      Plant Physiol. Feb 1994, 104 (2) 563-567; DOI: https://doi.org/10.1104/pp.104.2.563

N

  1. Nagao, R. T.

    1. Isolation and Characterization of Three Soybean Extensin cDNAs
      J. C. Hong, Y. H. Cheong, R. T. Nagao, J. D. Bahk, M. J. Cho, J. L. Key
      Plant Physiol. Feb 1994, 104 (2) 793-796; DOI: https://doi.org/10.1104/pp.104.2.793

  2. Nagatani, A.

    1. The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A
      T. Shinomura, A. Nagatani, J. Chory, M. Furuya
      Plant Physiol. Feb 1994, 104 (2) 363-371; DOI: https://doi.org/10.1104/pp.104.2.363

  3. Naito, S.

    1. Expression of a Soybean (Glycine max [L.] Merr.) Seed Storage Protein Gene in Transgenic Arabidopsis thaliana and Its Response to Nutritional Stress and to Abscisic Acid Mutations
      S. Naito, M. Y. Hirai, M. Chino, Y. Komeda
      Plant Physiol. Feb 1994, 104 (2) 497-503; DOI: https://doi.org/10.1104/pp.104.2.497

  4. Nevins, D. J.

    1. Cell-Wall Autohydrolysis in Isolated Endosperms of Lettuce (Lactuca sativa L.)
      S. Dutta, K. J. Bradford, D. J. Nevins
      Plant Physiol. Feb 1994, 104 (2) 623-628; DOI: https://doi.org/10.1104/pp.104.2.623

  5. Nobel, P. S.

    1. Water Relations and Low-Temperature Acclimation for Cactus Species Varying in Freezing Tolerance
      G. Goldstein, P. S. Nobel
      Plant Physiol. Feb 1994, 104 (2) 675-681; DOI: https://doi.org/10.1104/pp.104.2.675

O

  1. O'Brien, C. E.

    1. Oligomerization and the Affinity of Maize Phosphoenolpyruvate Carboxylase for Its Substrate
      R. T. Wedding, C. E. O'Brien, K. Kline
      Plant Physiol. Feb 1994, 104 (2) 613-616; DOI: https://doi.org/10.1104/pp.104.2.613

  2. O'Neill, S. D.

    1. Dark and Circadian Regulation of mRNA Accumulation in the Short-Day Plant Pharbitis nil
      S. D. O'Neill, X. S. Zhang, C. C. Zheng
      Plant Physiol. Feb 1994, 104 (2) 569-580; DOI: https://doi.org/10.1104/pp.104.2.569

  3. Oaks, A.

    1. Development of Endopeptidase Activities in Maize (Zea mays L.) Endosperms
      W. Mitsuhashi, A. Oaks
      Plant Physiol. Feb 1994, 104 (2) 401-407; DOI: https://doi.org/10.1104/pp.104.2.401

  4. Okon, Y.

    1. A Vesicular Arbuscular Mycorrhizal Fungus (Glomus intraradix) Induces a Defense Response in Alfalfa Roots
      H. Volpin, Y. Elkind, Y. Okon, Y. Kapulnik
      Plant Physiol. Feb 1994, 104 (2) 683-689; DOI: https://doi.org/10.1104/pp.104.2.683

  5. Orbovic, V.

    1. Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis
      P. Gil, Y. Liu, V. Orbovic, E. Verkamp, K. L. Poff, P. J. Green
      Plant Physiol. Feb 1994, 104 (2) 777-784; DOI: https://doi.org/10.1104/pp.104.2.777

  6. Ort, D. R.

    1. Mutants of Chloroplast Coupling Factor Reduction in Arabidopsis
      H. Gabrys, D. M. Kramer, A. R. Crofts, D. R. Ort
      Plant Physiol. Feb 1994, 104 (2) 769-776; DOI: https://doi.org/10.1104/pp.104.2.769

P

  1. Pacchiano Jr, R. A.

    1. Following Suberization in Potato Wound Periderm by Histochemical and Solid-State 13C Nuclear Magnetic Resonance Methods
      R. E. Stark, W. Sohn, R. A. Pacchiano Jr, M. Al-Bashir, J. R. Garbow
      Plant Physiol. Feb 1994, 104 (2) 527-533; DOI: https://doi.org/10.1104/pp.104.2.527

  2. Peschke, V. M.

    1. Characterization and Expression of Transcripts Induced by Oxygen Deprivation in Maize (Zea mays L.)
      V. M. Peschke, M. M. Sachs
      Plant Physiol. Feb 1994, 104 (2) 387-394; DOI: https://doi.org/10.1104/pp.104.2.387

  3. Plaut, Z.

    1. Carbon Isotope Discrimination, Gas Exchange, and Growth of Sugarcane Cultivars under Salinity
      F. C. Meinzer, Z. Plaut, N. Z. Saliendra
      Plant Physiol. Feb 1994, 104 (2) 521-526; DOI: https://doi.org/10.1104/pp.104.2.521

  4. Poff, K. L.

    1. Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis
      P. Gil, Y. Liu, V. Orbovic, E. Verkamp, K. L. Poff, P. J. Green
      Plant Physiol. Feb 1994, 104 (2) 777-784; DOI: https://doi.org/10.1104/pp.104.2.777

  5. Polle, A.

    1. Inhibition of Apoplastic and Symplastic Peroxidase Activity from Norway Spruce by the Photooxidant Hydroxymethyl Hydroperoxide
      A. Polle, W. Junkermann
      Plant Physiol. Feb 1994, 104 (2) 617-621; DOI: https://doi.org/10.1104/pp.104.2.617

  6. Prado, F. E.

    1. Antigenic Relationships between Chloroplast and Cytosolic Fructose-1,6-Bisphosphatases
      J. Fonolla, R. Hermoso, J. L. Carrasco, A. Chueca, J. J. Lazaro, F. E. Prado, J. Lopez-Gorge
      Plant Physiol. Feb 1994, 104 (2) 381-386; DOI: https://doi.org/10.1104/pp.104.2.381

  7. Price, G. D.

    1. A Mutant Isolated from the Cyanobacterium Synechococcus PCC7942 Is Unable to Adapt to Low Inorganic Carbon Conditions
      J. W. Yu, G. D. Price, M. R. Badger
      Plant Physiol. Feb 1994, 104 (2) 605-611; DOI: https://doi.org/10.1104/pp.104.2.605

  8. Puhlmann, J.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

R

  1. Raikhel, N. V.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  2. Rayle, D. L.

    1. Investigation of Gene Expression, Growth Kinetics, and Wall Extensibility during Brassinosteroid-Regulated Stem Elongation
      D. M. Zurek, D. L. Rayle, T. C. McMorris, S. D. Clouse
      Plant Physiol. Feb 1994, 104 (2) 505-513; DOI: https://doi.org/10.1104/pp.104.2.505

  3. Reddington, B. D.

    1. Cloning and Characterization of a cDNA Encoding Aspartate Aminotransferase-P1 from Lupinus angustifolius Root Tips
      C. S. Winefield, B. D. Reddington, W. T. Jones, PHS. Reynolds, KJF. Farnden
      Plant Physiol. Feb 1994, 104 (2) 417-423; DOI: https://doi.org/10.1104/pp.104.2.417

  4. Reinecke, D.

    1. A Role for Cytokinins in De-Etiolation in Arabidopsis (det Mutants Have an Altered Response to Cytokinins)
      J. Chory, D. Reinecke, S. Sim, T. Washburn, M. Brenner
      Plant Physiol. Feb 1994, 104 (2) 339-347; DOI: https://doi.org/10.1104/pp.104.2.339

  5. Reynolds, PHS.

    1. Cloning and Characterization of a cDNA Encoding Aspartate Aminotransferase-P1 from Lupinus angustifolius Root Tips
      C. S. Winefield, B. D. Reddington, W. T. Jones, PHS. Reynolds, KJF. Farnden
      Plant Physiol. Feb 1994, 104 (2) 417-423; DOI: https://doi.org/10.1104/pp.104.2.417

  6. Reynolds, T. L.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  7. Ristic, Z.

    1. Response of Xylem Ray Parenchyma Cells of Red Osier Dogwood (Cornus sericea L.) to Freezing Stress (Microscopic Evidence of Protoplasm Contraction)
      Z. Ristic, E. N. Ashworth
      Plant Physiol. Feb 1994, 104 (2) 737-746; DOI: https://doi.org/10.1104/pp.104.2.737

  8. Roberts, JKM.

    1. Nucleotide Availability in Maize (Zea mays L.) Root Tips (Estimation of Free and Protein-Bound Nucleotides Using 31P-Nuclear Magnetic Resonance and a Novel Protein-Ligand-Binding Assay)
      M. A. Hooks, G. C. Shearer, JKM. Roberts
      Plant Physiol. Feb 1994, 104 (2) 581-589; DOI: https://doi.org/10.1104/pp.104.2.581

  9. Rodermel, S. R.

    1. Photosynthetic Acclimation to Elevated CO2 Occurs in Transformed Tobacco with Decreased Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Content
      R. C. Sicher, D. F. Kremer, S. R. Rodermel
      Plant Physiol. Feb 1994, 104 (2) 409-415; DOI: https://doi.org/10.1104/pp.104.2.409

  10. Rodgers, L. R.

    1. A Peanut Nodule Lectin in Infected Cells and in Vacuoles and the Extracellular Matrix of Nodule Parenchyma
      K. A. VandenBosch, L. R. Rodgers, D. J. Sherrier, B. D. Kishinevsky
      Plant Physiol. Feb 1994, 104 (2) 327-337; DOI: https://doi.org/10.1104/pp.104.2.327

  11. Roldan, J. M.

    1. Occurrence of Only One Form of Glutamine Synthetase in the Green Alga Monoraphidium braunii
      J. M. Garcia-Fernandez, A. Lopez-Ruiz, F. Toribio, J. M. Roldan, J. Diez
      Plant Physiol. Feb 1994, 104 (2) 425-430; DOI: https://doi.org/10.1104/pp.104.2.425

  12. Rook, F.

    1. Carbohydrate Status of Tulip Bulbs during Cold-Induced Flower Stalk Elongation and Flowering
      H. Lambrechts, F. Rook, C. Kolloffel
      Plant Physiol. Feb 1994, 104 (2) 515-520; DOI: https://doi.org/10.1104/pp.104.2.515

  13. Ruffet, M. L.

    1. Purification and Kinetic Properties of Serine Acetyltransferase Free of O-Acetylserine(thiol)lyase from Spinach Chloroplasts
      M. L. Ruffet, M. Droux, R. Douce
      Plant Physiol. Feb 1994, 104 (2) 597-604; DOI: https://doi.org/10.1104/pp.104.2.597

S

  1. Sachs, M. M.

    1. Characterization and Expression of Transcripts Induced by Oxygen Deprivation in Maize (Zea mays L.)
      V. M. Peschke, M. M. Sachs
      Plant Physiol. Feb 1994, 104 (2) 387-394; DOI: https://doi.org/10.1104/pp.104.2.387

  2. Sadka, A.

    1. Sucrose Modulation of Soybean Vsp Gene Expression Is Inhibited by Auxin
      D. B. DeWald, A. Sadka, J. E. Mullet
      Plant Physiol. Feb 1994, 104 (2) 439-444; DOI: https://doi.org/10.1104/pp.104.2.439

  3. Salamini, F.

    1. Transcripts Accumulating during Cold Storage of Potato (Solanum tuberosum L.) Tubers Are Sequence Related to Stress-Responsive Genes
      J. van Berkel, F. Salamini, C. Gebhardt
      Plant Physiol. Feb 1994, 104 (2) 445-452; DOI: https://doi.org/10.1104/pp.104.2.445

  4. Saliendra, N. Z.

    1. Carbon Isotope Discrimination, Gas Exchange, and Growth of Sugarcane Cultivars under Salinity
      F. C. Meinzer, Z. Plaut, N. Z. Saliendra
      Plant Physiol. Feb 1994, 104 (2) 521-526; DOI: https://doi.org/10.1104/pp.104.2.521

  5. Sarath, G.

    1. Cloning and Sequence Analysis of a cDNA Encoding Ferric Leghemoglobin Reductase from Soybean Nodules
      L. Ji, M. Becana, G. Sarath, R. V. Klucas
      Plant Physiol. Feb 1994, 104 (2) 453-459; DOI: https://doi.org/10.1104/pp.104.2.453

  6. Scheuring, C. F.

    1. An Auxin-Inducible Proteinase Inhibitor Gene from Tomato
      R. J. Young, C. F. Scheuring, L. Harris-Haller, B. H. Taylor
      Plant Physiol. Feb 1994, 104 (2) 811-812; DOI: https://doi.org/10.1104/pp.104.2.811

  7. Schroeder, M.

    1. A Small GTP-Binding Protein from Arabidopsis thaliana Functionally Complements the Yeast YPT6 Null Mutant
      S. Y. Bednarek, T. L. Reynolds, M. Schroeder, R. Grabowski, L. Hengst, D. Gallwitz, N. V. Raikhel
      Plant Physiol. Feb 1994, 104 (2) 591-596; DOI: https://doi.org/10.1104/pp.104.2.591

  8. Schwebel-Dugue, N.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  9. Shearer, G. C.

    1. Nucleotide Availability in Maize (Zea mays L.) Root Tips (Estimation of Free and Protein-Bound Nucleotides Using 31P-Nuclear Magnetic Resonance and a Novel Protein-Ligand-Binding Assay)
      M. A. Hooks, G. C. Shearer, JKM. Roberts
      Plant Physiol. Feb 1994, 104 (2) 581-589; DOI: https://doi.org/10.1104/pp.104.2.581

  10. Shen, W.

    1. ESI3, a Stress-Induced Gene from Lophopyrum elongatum
      P. J. Gulick, W. Shen, H. An
      Plant Physiol. Feb 1994, 104 (2) 799-800; DOI: https://doi.org/10.1104/pp.104.2.799

  11. Sherrier, D. J.

    1. A Peanut Nodule Lectin in Infected Cells and in Vacuoles and the Extracellular Matrix of Nodule Parenchyma
      K. A. VandenBosch, L. R. Rodgers, D. J. Sherrier, B. D. Kishinevsky
      Plant Physiol. Feb 1994, 104 (2) 327-337; DOI: https://doi.org/10.1104/pp.104.2.327

  12. Shinomura, T.

    1. The Induction of Seed Germination in Arabidopsis thaliana Is Regulated Principally by Phytochrome B and Secondarily by Phytochrome A
      T. Shinomura, A. Nagatani, J. Chory, M. Furuya
      Plant Physiol. Feb 1994, 104 (2) 363-371; DOI: https://doi.org/10.1104/pp.104.2.363

  13. Sicher, R. C.

    1. Photosynthetic Acclimation to Elevated CO2 Occurs in Transformed Tobacco with Decreased Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase Content
      R. C. Sicher, D. F. Kremer, S. R. Rodermel
      Plant Physiol. Feb 1994, 104 (2) 409-415; DOI: https://doi.org/10.1104/pp.104.2.409

  14. Sim, S.

    1. A Role for Cytokinins in De-Etiolation in Arabidopsis (det Mutants Have an Altered Response to Cytokinins)
      J. Chory, D. Reinecke, S. Sim, T. Washburn, M. Brenner
      Plant Physiol. Feb 1994, 104 (2) 339-347; DOI: https://doi.org/10.1104/pp.104.2.339

  15. Sithole, I.

    1. Genetic Manipulation of the Cyanobacterium Synechocystis sp. PCC 6803 (Development of Strains Lacking Photosystem I for the Analysis of Mutations in Photosystem II)
      L. B. Smart, N. R. Bowlby, S. L. Anderson, I. Sithole, L. McIntosh
      Plant Physiol. Feb 1994, 104 (2) 349-354; DOI: https://doi.org/10.1104/pp.104.2.349

  16. Smart, L. B.

    1. Genetic Manipulation of the Cyanobacterium Synechocystis sp. PCC 6803 (Development of Strains Lacking Photosystem I for the Analysis of Mutations in Photosystem II)
      L. B. Smart, N. R. Bowlby, S. L. Anderson, I. Sithole, L. McIntosh
      Plant Physiol. Feb 1994, 104 (2) 349-354; DOI: https://doi.org/10.1104/pp.104.2.349

  17. Smirra, I.

    1. Chromoplast Biogenesis in Cucumis sativus Corollas (Rapid Effect of Gibberellin A3 on the Accumulation of a Chromoplast-Specific Carotenoid-Associated Protein)
      A. Vainstein, A. H. Halevy, I. Smirra, M. Vishnevetsky
      Plant Physiol. Feb 1994, 104 (2) 321-326; DOI: https://doi.org/10.1104/pp.104.2.321

  18. Smith, A. G.

    1. Temporal and Spatial Expression Pattern of Sucrose Synthase during Tomato Fruit Development
      F. Wang, A. G. Smith, M. L. Brenner
      Plant Physiol. Feb 1994, 104 (2) 535-540; DOI: https://doi.org/10.1104/pp.104.2.535

  19. Sohn, W.

    1. Following Suberization in Potato Wound Periderm by Histochemical and Solid-State 13C Nuclear Magnetic Resonance Methods
      R. E. Stark, W. Sohn, R. A. Pacchiano Jr, M. Al-Bashir, J. R. Garbow
      Plant Physiol. Feb 1994, 104 (2) 527-533; DOI: https://doi.org/10.1104/pp.104.2.527

  20. Somerville, R. L.

    1. Synechocystis PCC 6803 Contains a Single Gene for the [beta] Subunit of Tryptophan Synthase with Strong Homology to the trpB Genes of Arabidopsis and Maize (Zea mays L.)
      G. P. Zhao, R. L. Somerville, P. R. Chitnis
      Plant Physiol. Feb 1994, 104 (2) 461-466; DOI: https://doi.org/10.1104/pp.104.2.461

  21. Staehelin, L. A.

    1. Characterization of a Family of Chlorophyll-Deficient Wheat (Triticum) and Barley (Hordeum vulgare) Mutants with Defects in the Magnesium-Insertion Step of Chlorophyll Biosynthesis
      T. G. Falbel, L. A. Staehelin
      Plant Physiol. Feb 1994, 104 (2) 639-648; DOI: https://doi.org/10.1104/pp.104.2.639

  22. Stark, R. E.

    1. Following Suberization in Potato Wound Periderm by Histochemical and Solid-State 13C Nuclear Magnetic Resonance Methods
      R. E. Stark, W. Sohn, R. A. Pacchiano Jr, M. Al-Bashir, J. R. Garbow
      Plant Physiol. Feb 1994, 104 (2) 527-533; DOI: https://doi.org/10.1104/pp.104.2.527

  23. Steponkus, P. L.

    1. A Comparison of Freezing Injury in Oat and Rye: Two Cereals at the Extremes of Freezing Tolerance
      M. S. Webb, M. Uemura, P. L. Steponkus
      Plant Physiol. Feb 1994, 104 (2) 467-478; DOI: https://doi.org/10.1104/pp.104.2.467
    2. A Contrast of the Plasma Membrane Lipid Composition of Oat and Rye Leaves in Relation to Freezing Tolerance
      M. Uemura, P. L. Steponkus
      Plant Physiol. Feb 1994, 104 (2) 479-496; DOI: https://doi.org/10.1104/pp.104.2.479

  24. Still, D. W.

    1. Development of Desiccation Tolerance during Embryogenesis in Rice (Oryza sativa) and Wild Rice (Zizania palustris) (Dehydrin Expression, Abscisic Acid Content, and Sucrose Accumulation)
      D. W. Still, D. A. Kovach, K. J. Bradford
      Plant Physiol. Feb 1994, 104 (2) 431-438; DOI: https://doi.org/10.1104/pp.104.2.431

  25. Stone, B. A.

    1. Covalent Cross-Links in the Cell Wall
      K. Iiyama, TBT. Lam, B. A. Stone
      Plant Physiol. Feb 1994, 104 (2) 315-320; DOI: https://doi.org/10.1104/pp.104.2.315

  26. Sutton, F.

    1. Nucleotide Sequence of a cDNA Encoding an Elongation Factor (EF-1[infinity symbol]) from Barley Primary Leaf
      F. Sutton, D. G. Kenefick
      Plant Physiol. Feb 1994, 104 (2) 807; DOI: https://doi.org/10.1104/pp.104.2.807

  27. Swain, M. J.

    1. Generation of Monoclonal Antibodies against Plant Cell-Wall Polysaccharides (I. Characterization of a Monoclonal Antibody to a Terminal [alpha]-(1->2)-Linked Fucosyl-Containing Epitope
      J. Puhlmann, E. Bucheli, M. J. Swain, N. Dunning, P. Albersheim, A. G. Darvill, M. G. Hahn
      Plant Physiol. Feb 1994, 104 (2) 699-710; DOI: https://doi.org/10.1104/pp.104.2.699

T

  1. Tanaka, C. K.

    1. Nucleotide Sequence of a Transcript Encoding a Germin-Like Protein That Is Present in Salt-Stressed Barley (Hordeum vulgare L.) Roots
      W. J. Hurkman, B. G. Lane, C. K. Tanaka
      Plant Physiol. Feb 1994, 104 (2) 803-804; DOI: https://doi.org/10.1104/pp.104.2.803

  2. Tardieu, F.

    1. How Do Chemical Signals Work in Plants that Grow in Drying Soil?
      W. J. Davies, F. Tardieu, C. L. Trejo
      Plant Physiol. Feb 1994, 104 (2) 309-314; DOI: https://doi.org/10.1104/pp.104.2.309

  3. Taylor, B. H.

    1. An Auxin-Inducible Proteinase Inhibitor Gene from Tomato
      R. J. Young, C. F. Scheuring, L. Harris-Haller, B. H. Taylor
      Plant Physiol. Feb 1994, 104 (2) 811-812; DOI: https://doi.org/10.1104/pp.104.2.811

  4. Thomas, M.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  5. Thomas, R. B.

    1. Direct and Indirect Effects of Atmospheric Carbon Dioxide Enrichment on Leaf Respiration of Glycine max (L.) Merr
      R. B. Thomas, K. L. Griffin
      Plant Physiol. Feb 1994, 104 (2) 355-361; DOI: https://doi.org/10.1104/pp.104.2.355

  6. Toribio, F.

    1. Occurrence of Only One Form of Glutamine Synthetase in the Green Alga Monoraphidium braunii
      J. M. Garcia-Fernandez, A. Lopez-Ruiz, F. Toribio, J. M. Roldan, J. Diez
      Plant Physiol. Feb 1994, 104 (2) 425-430; DOI: https://doi.org/10.1104/pp.104.2.425

  7. Trejo, C. L.

    1. How Do Chemical Signals Work in Plants that Grow in Drying Soil?
      W. J. Davies, F. Tardieu, C. L. Trejo
      Plant Physiol. Feb 1994, 104 (2) 309-314; DOI: https://doi.org/10.1104/pp.104.2.309

  8. Troxler, R. F.

    1. Evidence That [sigma] Factors Are Components of Chloroplast RNA Polymerase
      R. F. Troxler, F. Zhang, J. Hu, L. Bogorad
      Plant Physiol. Feb 1994, 104 (2) 753-759; DOI: https://doi.org/10.1104/pp.104.2.753

  9. Tucker, M. L.

    1. Comparative Study of Cellulases Associated with Adventitious Root Initiation, Apical Buds, and Leaf, Flower, and Pod Abscission Zones in Soybean
      E. C. Kemmerer, M. L. Tucker
      Plant Physiol. Feb 1994, 104 (2) 557-562; DOI: https://doi.org/10.1104/pp.104.2.557

  10. Turpin, D. H.

    1. Inorganic Phosphate (Pi) Enhancement of Dark Respiration in the Pi-Limited Green Alga Selenastrum minutum (Interactions between H+/Pi Cotransport, the Plasmalemma H+-ATPase, and Dark Respiratory Carbon Flow)
      D. A. Gauthier, D. H. Turpin
      Plant Physiol. Feb 1994, 104 (2) 629-637; DOI: https://doi.org/10.1104/pp.104.2.629

  11. Tyrrell, P. N.

    1. Quenching of Chlorophyll a Fluorescence in Response to Na+-Dependent HCO3- Transport-Mediated Accumulation of Inorganic Carbon in the Cyanobacterium Synechococcus UTEX 625
      C. M. Crotty, P. N. Tyrrell, G. S. Espie
      Plant Physiol. Feb 1994, 104 (2) 785-791; DOI: https://doi.org/10.1104/pp.104.2.785

U

  1. Uemura, M.

    1. A Comparison of Freezing Injury in Oat and Rye: Two Cereals at the Extremes of Freezing Tolerance
      M. S. Webb, M. Uemura, P. L. Steponkus
      Plant Physiol. Feb 1994, 104 (2) 467-478; DOI: https://doi.org/10.1104/pp.104.2.467
    2. A Contrast of the Plasma Membrane Lipid Composition of Oat and Rye Leaves in Relation to Freezing Tolerance
      M. Uemura, P. L. Steponkus
      Plant Physiol. Feb 1994, 104 (2) 479-496; DOI: https://doi.org/10.1104/pp.104.2.479

V

  1. Vainstein, A.

    1. Chromoplast Biogenesis in Cucumis sativus Corollas (Rapid Effect of Gibberellin A3 on the Accumulation of a Chromoplast-Specific Carotenoid-Associated Protein)
      A. Vainstein, A. H. Halevy, I. Smirra, M. Vishnevetsky
      Plant Physiol. Feb 1994, 104 (2) 321-326; DOI: https://doi.org/10.1104/pp.104.2.321

  2. van Berkel, J.

    1. Transcripts Accumulating during Cold Storage of Potato (Solanum tuberosum L.) Tubers Are Sequence Related to Stress-Responsive Genes
      J. van Berkel, F. Salamini, C. Gebhardt
      Plant Physiol. Feb 1994, 104 (2) 445-452; DOI: https://doi.org/10.1104/pp.104.2.445

  3. Vance, C. P.

    1. Phosphorus Stress-Induced Proteoid Roots Show Altered Metabolism in Lupinus albus
      J. F. Johnson, D. L. Allan, C. P. Vance
      Plant Physiol. Feb 1994, 104 (2) 657-665; DOI: https://doi.org/10.1104/pp.104.2.657

  4. VandenBosch, K. A.

    1. A Peanut Nodule Lectin in Infected Cells and in Vacuoles and the Extracellular Matrix of Nodule Parenchyma
      K. A. VandenBosch, L. R. Rodgers, D. J. Sherrier, B. D. Kishinevsky
      Plant Physiol. Feb 1994, 104 (2) 327-337; DOI: https://doi.org/10.1104/pp.104.2.327

  5. Varner, J. E.

    1. 3,4-Dehydroproline Inhibits Cell Wall Assembly and Cell Division in Tobacco Protoplasts
      J. B. Cooper, J. E. Heuser, J. E. Varner
      Plant Physiol. Feb 1994, 104 (2) 747-752; DOI: https://doi.org/10.1104/pp.104.2.747

  6. Vartanian, N.

    1. Drought Rhizogenesis in Arabidopsis thaliana (Differential Responses of Hormonal Mutants)
      N. Vartanian, L. Marcotte, J. Giraudat
      Plant Physiol. Feb 1994, 104 (2) 761-767; DOI: https://doi.org/10.1104/pp.104.2.761

  7. Verkamp, E.

    1. Characterization of the Auxin-Inducible SAUR-AC1 Gene for Use as a Molecular Genetic Tool in Arabidopsis
      P. Gil, Y. Liu, V. Orbovic, E. Verkamp, K. L. Poff, P. J. Green
      Plant Physiol. Feb 1994, 104 (2) 777-784; DOI: https://doi.org/10.1104/pp.104.2.777

  8. Vishnevetsky, M.

    1. Chromoplast Biogenesis in Cucumis sativus Corollas (Rapid Effect of Gibberellin A3 on the Accumulation of a Chromoplast-Specific Carotenoid-Associated Protein)
      A. Vainstein, A. H. Halevy, I. Smirra, M. Vishnevetsky
      Plant Physiol. Feb 1994, 104 (2) 321-326; DOI: https://doi.org/10.1104/pp.104.2.321

  9. Volpin, H.

    1. A Vesicular Arbuscular Mycorrhizal Fungus (Glomus intraradix) Induces a Defense Response in Alfalfa Roots
      H. Volpin, Y. Elkind, Y. Okon, Y. Kapulnik
      Plant Physiol. Feb 1994, 104 (2) 683-689; DOI: https://doi.org/10.1104/pp.104.2.683

W

  1. Wada, H.

    1. The Unsaturation of Membrane Lipids Stabilizes Photosynthesis against Heat Stress
      Z. Gombos, H. Wada, E. Hideg, N. Murata
      Plant Physiol. Feb 1994, 104 (2) 563-567; DOI: https://doi.org/10.1104/pp.104.2.563

  2. Walling, L. L.

    1. Two Classes of Proteins and mRNAs in Lilium longiflorum L. Identified by Human Vitronectin Probes
      C. S. Wang, L. L. Walling, Y. Q. Gu, C. F. Ware, E. M. Lord
      Plant Physiol. Feb 1994, 104 (2) 711-717; DOI: https://doi.org/10.1104/pp.104.2.711

  3. Wang, C. S.

    1. Two Classes of Proteins and mRNAs in Lilium longiflorum L. Identified by Human Vitronectin Probes
      C. S. Wang, L. L. Walling, Y. Q. Gu, C. F. Ware, E. M. Lord
      Plant Physiol. Feb 1994, 104 (2) 711-717; DOI: https://doi.org/10.1104/pp.104.2.711

  4. Wang, F.

    1. Temporal and Spatial Expression Pattern of Sucrose Synthase during Tomato Fruit Development
      F. Wang, A. G. Smith, M. L. Brenner
      Plant Physiol. Feb 1994, 104 (2) 535-540; DOI: https://doi.org/10.1104/pp.104.2.535

  5. Ware, C. F.

    1. Two Classes of Proteins and mRNAs in Lilium longiflorum L. Identified by Human Vitronectin Probes
      C. S. Wang, L. L. Walling, Y. Q. Gu, C. F. Ware, E. M. Lord
      Plant Physiol. Feb 1994, 104 (2) 711-717; DOI: https://doi.org/10.1104/pp.104.2.711

  6. Washburn, T.

    1. A Role for Cytokinins in De-Etiolation in Arabidopsis (det Mutants Have an Altered Response to Cytokinins)
      J. Chory, D. Reinecke, S. Sim, T. Washburn, M. Brenner
      Plant Physiol. Feb 1994, 104 (2) 339-347; DOI: https://doi.org/10.1104/pp.104.2.339

  7. Watanabe, Y.

    1. Nucleotide Sequence of a Soybean (Glycine max L. Merr.) Ubiquitin Gene
      B. S. Xia, R. N. Waterhouse, Y. Watanabe, H. Kajiwara, S. Komatsu, H. Hirano
      Plant Physiol. Feb 1994, 104 (2) 805-806; DOI: https://doi.org/10.1104/pp.104.2.805

  8. Waterhouse, R. N.

    1. Nucleotide Sequence of a Soybean (Glycine max L. Merr.) Ubiquitin Gene
      B. S. Xia, R. N. Waterhouse, Y. Watanabe, H. Kajiwara, S. Komatsu, H. Hirano
      Plant Physiol. Feb 1994, 104 (2) 805-806; DOI: https://doi.org/10.1104/pp.104.2.805

  9. Webb, M. S.

    1. A Comparison of Freezing Injury in Oat and Rye: Two Cereals at the Extremes of Freezing Tolerance
      M. S. Webb, M. Uemura, P. L. Steponkus
      Plant Physiol. Feb 1994, 104 (2) 467-478; DOI: https://doi.org/10.1104/pp.104.2.467

  10. Wedding, R. T.

    1. Oligomerization and the Affinity of Maize Phosphoenolpyruvate Carboxylase for Its Substrate
      R. T. Wedding, C. E. O'Brien, K. Kline
      Plant Physiol. Feb 1994, 104 (2) 613-616; DOI: https://doi.org/10.1104/pp.104.2.613

  11. Williams, JHH.

    1. Arabidopsis Gene and cDNA Encoding Cell-Wall Invertase
      N. Schwebel-Dugue, N. E. Mtili, M. Krivitzky, I. Jean-Jacques, JHH. Williams, M. Thomas, M. Kreis, A. Lecharny
      Plant Physiol. Feb 1994, 104 (2) 809-810; DOI: https://doi.org/10.1104/pp.104.2.809

  12. Winefield, C. S.

    1. Cloning and Characterization of a cDNA Encoding Aspartate Aminotransferase-P1 from Lupinus angustifolius Root Tips
      C. S. Winefield, B. D. Reddington, W. T. Jones, PHS. Reynolds, KJF. Farnden
      Plant Physiol. Feb 1994, 104 (2) 417-423; DOI: https://doi.org/10.1104/pp.104.2.417

  13. Wu, K.

    1. Folate Metabolism in Datura innoxia (In Vivo and in Vitro Folylpolyglutamate Synthesis in Wild-Type and Methotrexate-Resistant Cells)
      K. Wu, E. A. Cossins, J. King
      Plant Physiol. Feb 1994, 104 (2) 373-380; DOI: https://doi.org/10.1104/pp.104.2.373

X

  1. Xia, B. S.

    1. Nucleotide Sequence of a Soybean (Glycine max L. Merr.) Ubiquitin Gene
      B. S. Xia, R. N. Waterhouse, Y. Watanabe, H. Kajiwara, S. Komatsu, H. Hirano
      Plant Physiol. Feb 1994, 104 (2) 805-806; DOI: https://doi.org/10.1104/pp.104.2.805

Y

  1. Young, R. J.

    1. An Auxin-Inducible Proteinase Inhibitor Gene from Tomato
      R. J. Young, C. F. Scheuring, L. Harris-Haller, B. H. Taylor
      Plant Physiol. Feb 1994, 104 (2) 811-812; DOI: https://doi.org/10.1104/pp.104.2.811

  2. Yu, J. W.

    1. A Mutant Isolated from the Cyanobacterium Synechococcus PCC7942 Is Unable to Adapt to Low Inorganic Carbon Conditions
      J. W. Yu, G. D. Price, M. R. Badger
      Plant Physiol. Feb 1994, 104 (2) 605-611; DOI: https://doi.org/10.1104/pp.104.2.605

Z

  1. Zhang, F.

    1. Evidence That [sigma] Factors Are Components of Chloroplast RNA Polymerase
      R. F. Troxler, F. Zhang, J. Hu, L. Bogorad
      Plant Physiol. Feb 1994, 104 (2) 753-759; DOI: https://doi.org/10.1104/pp.104.2.753

  2. Zhang, X. S.

    1. Dark and Circadian Regulation of mRNA Accumulation in the Short-Day Plant Pharbitis nil
      S. D. O'Neill, X. S. Zhang, C. C. Zheng
      Plant Physiol. Feb 1994, 104 (2) 569-580; DOI: https://doi.org/10.1104/pp.104.2.569

  3. Zhao, G. P.

    1. Synechocystis PCC 6803 Contains a Single Gene for the [beta] Subunit of Tryptophan Synthase with Strong Homology to the trpB Genes of Arabidopsis and Maize (Zea mays L.)
      G. P. Zhao, R. L. Somerville, P. R. Chitnis
      Plant Physiol. Feb 1994, 104 (2) 461-466; DOI: https://doi.org/10.1104/pp.104.2.461

  4. Zheng, C. C.

    1. Dark and Circadian Regulation of mRNA Accumulation in the Short-Day Plant Pharbitis nil
      S. D. O'Neill, X. S. Zhang, C. C. Zheng
      Plant Physiol. Feb 1994, 104 (2) 569-580; DOI: https://doi.org/10.1104/pp.104.2.569

  5. Zukowski, A. T.

    1. Modulation of Fusicoccin-Binding Protein Activity in Mung Bean (Vigna radiata L.) Hypocotyls by Tissue Maturation and by Fusicoccin
      L. E. Basel, A. T. Zukowski, R. E. Cleland
      Plant Physiol. Feb 1994, 104 (2) 691-697; DOI: https://doi.org/10.1104/pp.104.2.691

  6. Zurek, D. M.

    1. Investigation of Gene Expression, Growth Kinetics, and Wall Extensibility during Brassinosteroid-Regulated Stem Elongation
      D. M. Zurek, D. L. Rayle, T. C. McMorris, S. D. Clouse
      Plant Physiol. Feb 1994, 104 (2) 505-513; DOI: https://doi.org/10.1104/pp.104.2.505
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In this issue

Plant Physiology
Vol. 104, Issue 2
Feb 1994
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