Year |
Citation |
Score |
2013 |
Smith H. Paul Gordon Jarvis, FRS: co-founding editor of Plant, Cell & Environment. Plant, Cell & Environment. 36: 907-8. PMID 23421651 DOI: 10.1111/Pce.12080 |
0.358 |
|
2006 |
Allen T, Ingles PJ, Praekelt U, Smith H, Whitelam GC. Phytochrome-mediated agravitropism in Arabidopsis hypocotyls requires GIL1 and confers a fitness advantage. The Plant Journal : For Cell and Molecular Biology. 46: 641-8. PMID 16640600 DOI: 10.1111/J.1365-313X.2006.02727.X |
0.44 |
|
2005 |
Newbury HJ, Smith H. Immunochemical Evidence for Phytochrome Regulation of the Specific Activity of Ascorbate Oxidase in Mustard Seedlings Febs Journal. 117: 575-580. PMID 6793360 DOI: 10.1111/J.1432-1033.1981.Tb06376.X |
0.311 |
|
2001 |
Sineshchekov V, Koppel L, Shlumukov L, Barro F, Barcelo P, Lazzeri P, Smith H. Fluorescence and photochemical properties of phytochromes in wild‐type wheat and a transgenic line overexpressing an oat phytochrome A (PHYA) gene: functional implications Plant Cell and Environment. 24: 1289-1297. DOI: 10.1046/J.1365-3040.2001.00780.X |
0.393 |
|
2000 |
Weller JL, Schreuder MEL, Smith H, Koornneef M, Kendrick RE. Physiological interactions of phytochromes A, B1 and B2 in the control of development in tomato Plant Journal. 24: 345-356. PMID 11069708 DOI: 10.1046/J.1365-313X.2000.00879.X |
0.389 |
|
2000 |
Smith H. Phytochromes and light signal perception by plants—an emerging synthesis Nature. 407: 585-591. PMID 11034200 DOI: 10.1038/35036500 |
0.437 |
|
1998 |
Hudson M, Smith H. The phytochrome B encoded by the HLG locus of Nicotiana plumbaginifolia is required for detection of photoperiod: hlg mutants show altered regulation of flowering and circadian movement The Plant Journal. 15: 281-287. DOI: 10.1046/J.1365-313X.1998.00198.X |
0.342 |
|
1997 |
Hudson M, Robson PR, Kraepiel Y, Caboche M, Smith H. Nicotiana plumbaginifolia hlg mutants have a mutation in a PHYB-type phytochrome gene: they have elongated hypocotyls in red light, but are not elongated as adult plants. The Plant Journal : For Cell and Molecular Biology. 12: 1091-101. PMID 9418050 DOI: 10.1046/J.1365-313X.1997.12051091.X |
0.392 |
|
1997 |
Smith H, Xu Y, Quail PH. Antagonistic but complementary actions of phytochromes A and B allow seedling de-etiolation. Plant Physiology. 114: 637-41. PMID 9193095 DOI: 10.1104/Pp.114.2.637 |
0.314 |
|
1997 |
Seavers GP, Smith H. The reflectance properties of plant internodes modify elongation responses to lateral far‐red radiation Plant Cell and Environment. 20: 1372-1380. DOI: 10.1046/J.1365-3040.1997.D01-37.X |
0.441 |
|
1997 |
Robson PRH, Smith H. Fundamental and biotechnological applications of phytochrome transgenes Plant Cell and Environment. 20: 831-839. DOI: 10.1046/J.1365-3040.1997.D01-106.X |
0.406 |
|
1997 |
Smith H, Whitelam GC. The shade avoidance syndrome: multiple responses mediated by multiple phytochromes Plant Cell and Environment. 20: 840-844. DOI: 10.1046/J.1365-3040.1997.D01-104.X |
0.358 |
|
1997 |
Smith H. Jeux d'ombre chez les plantes Biofutur. 1997: 49. DOI: 10.1016/S0294-3506(97)89045-X |
0.322 |
|
1996 |
Robson PR, McCormac AC, Irvine AS, Smith H. Genetic engineering of harvest index in tobacco through overexpression of a phytochrome gene. Nature Biotechnology. 14: 995-8. PMID 9631038 DOI: 10.1038/Nbt0896-995 |
0.426 |
|
1995 |
Paul W, Amiss J, Try R, Praekelt U, Scott R, Smith H. Correct processing of the kiwifruit protease actinidin in transgenic tobacco requires the presence of the C-terminal propeptide. Plant Physiology. 108: 261-8. PMID 7784505 DOI: 10.1104/Pp.108.1.261 |
0.317 |
|
1995 |
Romano CP, Robson PR, Smith H, Estelle M, Klee H. Transgene-mediated auxin overproduction in Arabidopsis: hypocotyl elongation phenotype and interactions with the hy6-1 hypocotyl elongation and axr1 auxin-resistant mutants. Plant Molecular Biology. 27: 1071-83. PMID 7766890 DOI: 10.1007/Bf00020881 |
0.449 |
|
1995 |
Gilbert IR, Seavers GP, Jarvis PG, Smith H. Photomorphogenesis and canopy dynamics. Phytochrome-mediated proximity perception accounts for the growth dynamics of canopies of Populus trichocarpa * deltoides 'Beaupre' Plant Cell and Environment. 18: 475-497. DOI: 10.1111/J.1365-3040.1995.Tb00549.X |
0.404 |
|
1995 |
Schmitt J, McCormac AC, Smith H. A test of the adaptive plasticity hypothesis using transgenic and mutant plants disabled in phytochrome-mediated elongation responses to neighbors American Naturalist. 146: 937-953. DOI: 10.1086/285832 |
0.42 |
|
1994 |
Smith H. Phytochrome transgenics: functional, ecological and biotechnological applications. Seminars in Cell Biology. 5: 315-25. PMID 7881071 DOI: 10.1006/Scel.1994.1038 |
0.398 |
|
1993 |
Robson P, Whitelam GC, Smith H. Selected Components of the Shade-Avoidance Syndrome Are Displayed in a Normal Manner in Mutants of Arabidopsis thaliana and Brassica rapa Deficient in Phytochrome B. Plant Physiology. 102: 1179-1184. PMID 12231894 DOI: 10.1104/Pp.102.4.1179 |
0.397 |
|
1993 |
Smith H, Samson G, Fork DC. Photosynthetic acclimation to shade: probing the role of phytochromes using photomorphogenic mutants of tomato Plant Cell and Environment. 16: 929-937. DOI: 10.1111/J.1365-3040.1993.Tb00516.X |
0.38 |
|
1993 |
McCORMAC AC, Smith H, Whitelam GC. Expression of Oat-phyA-cDNA in a Suspension Cell Culture of Transgenic Tobacco: A Single-Cell System for the Study of Phytochrome Function Journal of Experimental Botany. 44: 1095-1103. DOI: 10.1093/Jxb/44.7.1095 |
0.342 |
|
1993 |
McCormac AC, Wagner D, Boylan MT, Quail PH, Smith H, Whitelam GC. Photoresponses of transgenic Arabidopsis seedlings expressing introduced phytochrome B-encoding cDNAs: evidence that phytochrome A and phytochrome B have distinct photoregulatory functions The Plant Journal. 4: 19-27. DOI: 10.1046/J.1365-313X.1993.04010019.X |
0.395 |
|
1993 |
McCormac AC, Smith H, Whitelam GC. Photoregulation of germination in seed of transgenic lines of tobacco and Arabidopsis which express an introduced cDNA encoding phytochrome A or phytochrome B Planta. 191: 386-393. DOI: 10.1007/Bf00195697 |
0.382 |
|
1992 |
McCormac A, Whitelam G, Smith H. Light-grown plants of transgenic tobacco expressing an introduced oat phytochrome A gene under the control of a constitutive viral promoter exhibit persistent growth inhibition by far-red light. Planta. 188: 173-81. PMID 24178253 DOI: 10.1007/Bf00216811 |
0.484 |
|
1992 |
Smith H. The Ecological Functions Of The Phytochrome Family. Clues To A Transgenic Programme Of Crop Improvement Photochemistry and Photobiology. 56: 815-822. DOI: 10.1111/J.1751-1097.1992.Tb02238.X |
0.354 |
|
1992 |
Kerckhoffs LHJ, Kendrick RE, Whitelam GC, Smith H. Extension Growth And Anthocyanin Responses Of Photomorphogenic Tomato Mutants To Changes In The Phytochrome: Photoequilibrium During The Daily Photoperiod Photochemistry and Photobiology. 56: 611-615. DOI: 10.1111/J.1751-1097.1992.Tb02210.X |
0.412 |
|
1992 |
Smith H, Turnbull M, Kendrick RE. Light-grown plants of the cucumber long hypocotyl mutant exhibit both long-term and rapid elongation growth responses to irradiation with supplementary far-red light. Photochemistry and Photobiology. 56: 607-610. DOI: 10.1111/J.1751-1097.1992.Tb02209.X |
0.447 |
|
1992 |
Smith H, Fork DC. Direct Measurement Of Phytochrome Photoconversion Intermediates At High Photon Fluence Rates Photochemistry and Photobiology. 56: 599-606. DOI: 10.1111/J.1751-1097.1992.Tb02208.X |
0.323 |
|
1992 |
McCormac AC, Whitelam GC, Boylan MT, Quail PH, Smith H. Contrasting Responses of Etiolated and Light-Adapted Seedlings to Red: Far-Red Ratio: A Comparison of Wild Type, Mutant and Transgenic Plants has Revealed Differential Functions of Members of the Phytochrome family Journal of Plant Physiology. 140: 707-714. DOI: 10.1016/S0176-1617(11)81027-8 |
0.474 |
|
1991 |
McCormac AC, Cherry JR, Hershey HP, Vierstra RD, Smith H. Photoresponses of transgenic tobacco plants expressing an oat phytochrome gene. Planta. 185: 162-70. PMID 24186338 DOI: 10.1007/Bf00194057 |
0.471 |
|
1991 |
Whitelam GC, Smith H. Retention of Phytochrome-Mediated Shade Avoidance Responses in Phytochrome-Deficient Mutants of Arabidopsis, Cucumber and Tomato Journal of Plant Physiology. 139: 119-125. DOI: 10.1016/S0176-1617(11)80176-8 |
0.413 |
|
1990 |
Casal JJ, Whitelam GC, Smith H. Phytochrome Effects on the Relationship between Chlorophyll and Steady-State Levels of Thylakoid Polypeptides in Light-Grown Tobacco. Plant Physiology. 94: 370-4. PMID 16667711 DOI: 10.1104/Pp.94.1.370 |
0.416 |
|
1990 |
Casal JJ, Whitelam GC, Smith H. PHYTOCHROME CONTROL OF EXTRACELLULAR PEROXIDASE ACTIVITY IN MUSTARD INTERNODES: CORRELATION WITH GROWTH, and COMPARISON WITH THE EFFECT OF WOUNDING Photochemistry and Photobiology. 52: 165-172. DOI: 10.1111/J.1751-1097.1990.Tb01770.X |
0.397 |
|
1990 |
Smith H. PHYTOCHROME ACTION AT HIGH PHOTON FLUENCE RATES: RAPID EXTENSION RATE RESPONSES OF LIGHT‐GROWN MUSTARD TO VARIATIONS INFLUENCE RATE and RED: FAR‐RED RATIO* Photochemistry and Photobiology. 52: 131-142. DOI: 10.1111/J.1751-1097.1990.Tb01766.X |
0.345 |
|
1990 |
Smith H, Casal JJ, Jackson GM. Reflection signals and the perception by phytochrome of the proximity of neighbouring vegetation Plant Cell and Environment. 13: 73-78. DOI: 10.1111/J.1365-3040.1990.Tb01301.X |
0.367 |
|
1990 |
Smith H, Whitelam GC. Phytochrome, a family of photoreceptors with multiple physiological roles Plant Cell and Environment. 13: 695-707. DOI: 10.1111/J.1365-3040.1990.Tb01084.X |
0.328 |
|
1990 |
Smith H. Signal perception, differential expression within multigene families and the molecular basis of phenotypic plasticity Plant Cell and Environment. 13: 585-594. DOI: 10.1111/J.1365-3040.1990.Tb01077.X |
0.333 |
|
1989 |
Casal JJ, Smith H. The ‘end‐of‐day’ phytochrome control of internode elongation in mustard: kinetics, interaction with the previous fluence rate, and ecological implications Plant Cell and Environment. 12: 511-520. DOI: 10.1111/J.1365-3040.1989.Tb02124.X |
0.385 |
|
1989 |
Casal JJ, Smith H. The function, action and adaptive significance of phytochrome in light-grown plants Plant Cell and Environment. 12: 855-862. DOI: 10.1111/J.1365-3040.1989.Tb01966.X |
0.465 |
|
1989 |
Casal JJ, Smith H. Effects of Blue Light Pretreatments on Internode Extension Growth in Mustard Seedlings after the Transition to Darkness: Analysis of the Interaction with Phytochrome Journal of Experimental Botany. 40: 893-899. DOI: 10.1093/Jxb/40.8.893 |
0.36 |
|
1989 |
Keiller D, Smith H. Control of carbon partitioning by light quality mediated by phytochrome Plant Science. 63: 25-29. DOI: 10.1016/0168-9452(89)90097-6 |
0.465 |
|
1988 |
Smith H, Jackson GM, Whitelam GC. Photoprotection of phytochrome. Planta. 175: 471-7. PMID 24221928 DOI: 10.1007/Bf00393067 |
0.35 |
|
1988 |
Casal JJ, Smith H. Persistent effects of changes in phytochrome status on internode growth in light-grown mustard: Occurrence, kinetics and locus of perception. Planta. 175: 214-20. PMID 24221715 DOI: 10.1007/Bf00392430 |
0.4 |
|
1988 |
Viner N, Whitelam G, Smith H. Calcium and phytochrome control of leaf unrolling in dark-grown barley seedlings. Planta. 175: 209-13. PMID 24221714 DOI: 10.1007/Bf00392429 |
0.352 |
|
1988 |
Casal JJ, Smith H. The loci of perception for phytochrome control of internode growth in light-grown mustard: Promotion by low phytochrome photoequilibria in the internode is enhanced by blue light perceived by the leaves. Planta. 176: 277-82. PMID 24220784 DOI: 10.1007/Bf00392456 |
0.412 |
|
1987 |
Child R, Smith H. Phytochrome action in light-grown mustard: kinetics, fluence-rate compensation and ecological significance. Planta. 172: 219-29. PMID 24225874 DOI: 10.1007/Bf00394591 |
0.429 |
|
1987 |
Smith H, Jackson GM. Rapid phytochrome regulation of wheat seedling extension: light pretreatment extends coupling time, increases response lag, and decreases light sensitivity. Plant Physiology. 84: 1059-62. PMID 16665561 DOI: 10.1104/Pp.84.4.1059 |
0.428 |
|
1987 |
Rich TCG, Whitelam GC, Smith H. Analysis of growth rates during phototropism: modifications by separate light‐growth responses Plant Cell and Environment. 10: 303-311. DOI: 10.1111/J.1365-3040.1987.Tb01610.X |
0.369 |
|
1987 |
NAPIER RM, SMITH H. Photoreversible association of phytochrome with membranes. I. Distinguishing between two light‐induced binding responses Plant, Cell &Amp; Environment. 10: 383-389. DOI: 10.1111/1365-3040.Ep11603627 |
0.326 |
|
1986 |
Rich TCG, Smith H. Comparison of lag times in plant physiology Plant Cell and Environment. 9: 707-709. DOI: 10.1111/J.1365-3040.1986.Tb02102.X |
0.341 |
|
1985 |
Bleiss W, Smith H. Rapid suppression of extension growth in dark-grown wheat seedlings by red light. Plant Physiology. 77: 552-5. PMID 16664096 DOI: 10.1104/Pp.77.3.552 |
0.414 |
|
1985 |
Rich TCG, Whitelam GC, Smith H. PHOTOTROPISM AND AXIS EXTENSION IN LIGHT-GROWN MUSTARD (Sinapis alba L.) SEEDLINGS‡ Photochemistry and Photobiology. 42: 789-792. DOI: 10.1111/J.1751-1097.1985.Tb01649.X |
0.419 |
|
1985 |
Smith H, Hayward P. Fluence Rate Compensation Of The Perception Of Red: Far‐Red Ratio By Phytochrome In Light‐Grown Seedlings* Photochemistry and Photobiology. 42: 685-688. DOI: 10.1111/J.1751-1097.1985.Tb01631.X |
0.327 |
|
1985 |
Jenkins GI, Smith H. RED: FAR‐RED RATIO DOES NOT MODULATE THE ABUNDANCE OF TRANSCRIPTS FOR TWO MAJOR CHLOROPLAST POLYPEPTIDES IN LIGHT‐GROWN Pisum sativum TERMINAL SHOOTS* Photochemistry and Photobiology. 42: 679-684. DOI: 10.1111/J.1751-1097.1985.Tb01630.X |
0.432 |
|
1985 |
BLISS D, SMITH H. Penetration of light into soil and its role in the control of seed germination Plant, Cell & Environment. 8: 475-483. DOI: 10.1111/J.1365-3040.1985.Tb01683.X |
0.313 |
|
1984 |
Hughes JE, Morgan DC, Lambton PA, Black CR, Smith H. Photoperiodic time signals during twilight Plant Cell and Environment. 7: 269-277. DOI: 10.1111/1365-3040.Ep11589464 |
0.367 |
|
1984 |
Smith H. Botany: Plants that track the sun Nature. 308: 774. DOI: 10.1038/308774A0 |
0.354 |
|
1982 |
Watson PJ, Smith H. Integral association of phytochrome with a membranous fraction fromAvena shoots: in vivo characterization and physiological significance. Planta. 154: 128-34. PMID 24275972 DOI: 10.1007/Bf00387905 |
0.363 |
|
1982 |
Smith H. Light Quality, Photoperception, and Plant Strategy Annual Review of Plant Biology. 33: 481-518. DOI: 10.1146/Annurev.Pp.33.060182.002405 |
0.418 |
|
1982 |
Vázquez‐Yanes C, Smith H. Phytochrome Control Of Seed Germination In The Tropical Rain Forest Pioneer Trees Cecropia Obtusifolia And Piper Auritum And Its Ecological Significance New Phytologist. 92: 477-485. DOI: 10.1111/J.1469-8137.1982.Tb03405.X |
0.368 |
|
1982 |
Smith H. Light-piping by plant tissues Nature. 298: 423-424. DOI: 10.1038/298423A0 |
0.413 |
|
1981 |
Morgan DC, Child R, Smith H. Absence of fluence rate dependency of phytochrome modulation of stem extension in light-grown Sinapis alba L. Planta. 151: 497-8. PMID 24302117 DOI: 10.1007/Bf00386545 |
0.389 |
|
1981 |
Child R, Morgan DC, Smith H. Control Of Development In Chenopodium Album L. By Shadelight New Phytologist. 89: 545-555. DOI: 10.1111/J.1469-8137.1981.Tb02334.X |
0.381 |
|
1981 |
Morgan DC, Smith H. Control Of Development In Chenopodium Album L. By Shadelight: The Effect Of Light Quantity (Total Fluence Rate) And Light Quality (Red.Far‐Red Ratio) New Phytologist. 88: 239-248. DOI: 10.1111/J.1469-8137.1981.Tb01720.X |
0.415 |
|
1981 |
Smith H. Evidence that Pfr is not the active form of phytochrome in light-grown maize Nature. 293: 163-165. DOI: 10.1038/293163A0 |
0.44 |
|
1980 |
Hilton JR, Smith H. The presence of phytochrome in purified barley etioplasts and its in vitro regulation of biologically-active gibberellin levels in etioplasts. Planta. 148: 312-8. PMID 24310132 DOI: 10.1007/Bf00388117 |
0.32 |
|
1980 |
Morgan DC, O'Brien T, Smith H. Rapid photomodulation of stem extension in light-grownSinapis alba L. : Studies on kinetics, site of perception and photoreceptor. Planta. 150: 95-101. PMID 24306582 DOI: 10.1007/Bf00582351 |
0.387 |
|
1979 |
Morgan DC, Smith H. A systematic relationship between phytochrome-controlled development and species habitat, for plants grown in simulated natural radiation. Planta. 145: 253-8. PMID 24317731 DOI: 10.1007/Bf00454449 |
0.415 |
|
1979 |
Smith H. Photoperception and the regulation of plant development. Biochemical Society Transactions. 7: 1231-1236. PMID 535644 DOI: 10.1042/Bst0071231 |
0.367 |
|
1976 |
Smith H. Phytochemical Society Symposia Series, No. 11: The Chemistry and Biochemistry of Plant Proteins Biochemical Society Transactions. 4: 176-177. DOI: 10.1042/Bst0040176 |
0.341 |
|
1975 |
Smith H. To flower or not to flower Nature. 258: 462-462. DOI: 10.1038/258462A0 |
0.383 |
|
1973 |
Smith H. Ion Transport in Plants Nature. 246: 160-160. DOI: 10.1038/Newbio246160A0 |
0.311 |
|
1966 |
Smith H, Wareing PF. Apical dominance and the effect of gravity on nutrient distribution. Planta. 70: 87-94. PMID 24557931 DOI: 10.1007/BF00539912 |
0.557 |
|
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