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An auxin-induced polypeptide in dicotyledonous plants

https://doi.org/10.1007/bf00020538

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Auxin-induced changes in the population of translatable messenger RNA in elongating maize coleoptile sections

inferredcites →https://doi.org/10.1007/bf00410211openalex-snapshot

Auxin-regulated gene expression in intact soybean hypocotyl and excised hypocotyl sections

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Detection of antibodies specific to sodium dodecyl sulfate-treated proteins

inferredcites →https://doi.org/10.1016/0022-2836(85)90280-3openalex-snapshot

Rapid induction of specific mRNAs by auxin in pea epicotyl tissue

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Intracellular localization of heat shock proteins in Drosophila

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hsp70: Nuclear concentration during environmental stress and cytoplasmic storage during recovery

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Synthesis of human insulin gene VIII. Construction of expression vectors for fused proinsulin production in Escherichia coli

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Immunological studies on plant DNA-dependent RNA polymerases with antibodies raised against individual subunits.

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Immunological studies of yeast nuclear RNA polymerases at the subunit level.

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Regulation and in vitro translation of messenger ribonucleic acid for cellulase from auxin-treated pea epicotyls.

inferredcites →https://doi.org/10.1021/bi00286a022openalex-snapshot

Auxin-induced changes in the level of translatable ribosomal protein messenger ribonucleic acids in soybean hypocotyl

inferredcites →https://doi.org/10.1021/bi00692a011openalex-snapshot

Procedure for the rapid, large-scale purification of Escherichia coli DNA-dependent RNA polymerase involving polymin P precipitation and DNA-cellulose chromatography

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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Loss of the Sigma Activity of RNA Polymerase of Bacillus subtilis during Sporulation

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Enhancement of soybean RNA polymerase I by auxin.

inferredcites →https://doi.org/10.1073/pnas.72.5.1822openalex-snapshot

Separation of two responses to auxin by means of cytokinin inhibition.

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Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

inferredcites →https://doi.org/10.1073/pnas.79.2.418openalex-snapshot

Early auxin-regulated polyadenylylated mRNA sequences in pea stem tissue

inferredcites →https://doi.org/10.1073/pnas.79.23.7185openalex-snapshot

Isolation of cloned cDNAs to auxin-responsive poly(A) + RNAs of elongating soybean hypocotyl

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Hormonal Regulation of Cell Elongation in the Hypocotyl of Rootless Soybean: An Evaluation of the Role of DNA Synthesis

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1,3-β-d-Glucanases from Pisum sativum Seedlings

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Auxin-Induced Changes in the Population of Translatable Messenger RNA in Elongating Sections of Soybean Hypocotyl

inferredcites →https://doi.org/10.1104/pp.69.2.338openalex-snapshot

Auxin- and Ethylene-Induced Changes in the Population of Translatable Messenger RNA in Basal Sections and Intact Soybean Hypocotyl

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A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

inferredcites →https://doi.org/10.1128/mcb.5.6.1197openalex-snapshot

Rapid Induction of Selective Transcription by Auxins

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Fusicoccin: A Tool in Plant Physiology

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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The GH3 amidosynthetases family and their role in metabolic crosstalk modulation of plant signaling compounds

inferred← citeshttps://doi.org/10.1007/978-1-4684-7047-5_21openalex-snapshot

Regulation of Plant Gene Expression by Auxins

inferred← citeshttps://doi.org/10.1007/978-1-4939-0491-4_1openalex-snapshot

Auxin in Plant Growth and Stress Responses

inferred← citeshttps://doi.org/10.1007/978-3-642-74545-4_10openalex-snapshot

Auxin and Gene Expression

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The Control of Gene Expression by Auxin

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Auxin-responsive gene expression: genes, promoters and regulatory factors

inferred← citeshttps://doi.org/10.1007/bf00016498openalex-snapshot

Molecular cloning of cDNAs for auxin-induced mRNAs and developmental expression of the auxin-inducible genes

inferred← citeshttps://doi.org/10.1007/bf00040658openalex-snapshot

Auxin-induced expression of the soybean GH3 promoter in transgenic tobacco plants

inferred← citeshttps://doi.org/10.1007/bf01968942openalex-snapshot

Transgenic white clover. Studies with the auxin-responsive promoter, GH3, in root gravitropism and lateral root development

inferred← citeshttps://doi.org/10.1007/s11033-020-05477-5openalex-snapshot

Genome-wide identification, characterization analysis and expression profiling of auxin-responsive GH3 family genes in wheat (Triticum aestivum L.)

inferred← citeshttps://doi.org/10.1007/s11101-017-9510-8openalex-snapshot

Metabolism of the plant hormone jasmonate: a sentinel for tissue damage and master regulator of stress response

inferred← citeshttps://doi.org/10.1007/s11738-014-1673-yopenalex-snapshot

IAA–amido synthetase activity and GH3 expression during development of pea seedlings

inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.11.109openalex-snapshot

Local conjugation of auxin by the GH3 amido synthetases is required for normal development of roots and flowers in Arabidopsis

inferred← citeshttps://doi.org/10.1016/j.pestbp.2007.04.002openalex-snapshot

Recent developments in auxin biology and new opportunities for auxinic herbicide research

inferred← citeshttps://doi.org/10.1016/s0014-5793(97)01447-6openalex-snapshot

Isolation by differential display and characterization of a tobacco auxin‐responsive cDNA Nt‐gh3, related to GH3

inferred← citeshttps://doi.org/10.1016/s0015-3796(89)80051-4openalex-snapshot

Hormone-induced Alterations in Plant Gene Expression

inferred← citeshttps://doi.org/10.1016/s0167-7306(08)60499-8openalex-snapshot

Auxin-regulated genes and promoters

inferred← citeshttps://doi.org/10.1023/a:1015207114117openalex-snapshot

Auxin-responsive gene expression: genes, promoters and regulatory factors

inferred← citeshttps://doi.org/10.1042/bst0200097openalex-snapshot

Expression of auxin-responsive genes in soybean and transgenic tobacco

inferred← citeshttps://doi.org/10.1046/j.1365-313x.2003.01973.xopenalex-snapshot

ydk1‐D , an auxin‐responsive GH3 mutant that is involved in hypocotyl and root elongation

inferred← citeshttps://doi.org/10.1093/jxb/erv521openalex-snapshot

Hormone crosstalk in wound stress response: wound-inducible amidohydrolases can simultaneously regulate jasmonate and auxin homeostasis in Arabidopsis thaliana

inferred← citeshttps://doi.org/10.1093/jxb/erx375openalex-snapshot

Auxin signaling: a big question to be addressed by small molecules

inferred← citeshttps://doi.org/10.1100/2012/837395openalex-snapshot

Influence of Growth Regulators on Callogenesis and Somatic Embryo Development in Date Palm (Phoenix dactyliferaL.) Sahelian Cultivars

inferred← citeshttps://doi.org/10.1101/cshperspect.a040006openalex-snapshot

Casting the Net—Connecting Auxin Signaling to the Plant Genome

inferred← citeshttps://doi.org/10.1104/pp.89.1.1openalex-snapshot

Rapid Induction of Na+/H+ Exchange Activity in Barley Root Tonoplast

inferred← citeshttps://doi.org/10.1105/tpc.104.026690openalex-snapshot

Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid

inferred← citeshttps://doi.org/10.1105/tpc.3.4.419openalex-snapshot

Tissue-specific and organ-specific expression of soybean auxin-responsive transcripts GH3 and SAURs.

inferred← citeshttps://doi.org/10.1111/j.1469-8137.1995.tb04291.xopenalex-snapshot

Auxin action and auxin‐binding proteins

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2006.01677.xopenalex-snapshot

The auxin‐inducible GH3 homologue Pp‐GH3.16 is downregulated in Pinus pinaster root systems on ectomycorrhizal symbiosis establishment

inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02677.xopenalex-snapshot

Moss ( Physcomitrella patens ) GH3 proteins act in auxin homeostasis

inferred← citeshttps://doi.org/10.1111/pbr.13229openalex-snapshot

Genomic Analysis and Expression Dynamics of GH3 Genes Under Abiotic Stresses in Brassica rapa

inferred← citeshttps://doi.org/10.1186/s12870-018-1545-5openalex-snapshot

Genome-wide analysis of cotton GH3 subfamily II reveals functional divergence in fiber development, hormone response and plant architecture

inferred← citeshttps://doi.org/10.1614/ws-05-106r.1openalex-snapshot

Evaluation of auxin-responsive genes in soybean for detection of off-target plant growth regulator herbicides

inferred← citeshttps://doi.org/10.17816/ecogen12235-46openalex-snapshot

Root-specific expression of early auxin-regulated

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Genome-Wide Identification of Auxin-Responsive GH3 Gene Family in Saccharum and the Expression of ScGH3-1 in Stress Response

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GH3 Gene Family Identification in Chinese White Pear (Pyrus bretschneideri) and the Functional Analysis of PbrGH3.5 in Fe Deficiency Responses in Tomato

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Faculty Opinions recommendation of Characterization of an Arabidopsis enzyme family that conjugates amino acids to indole-3-acetic acid.

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