Search

Your search keyword '"Estelle, Mark"' showing total 654 results
Start Over Author "Estelle, Mark"
654 results on '"Estelle, Mark"'

151. The Arabidopsis NPF3 protein is a GA transporter

Author

Tal, Iris, primary, Zhang, Yi, additional, Jørgensen, Morten Egevang, additional, Pisanty, Odelia, additional, Barbosa, Inês C. R., additional, Zourelidou, Melina, additional, Regnault, Thomas, additional, Crocoll, Christoph, additional, Erik Olsen, Carl, additional, Weinstain, Roy, additional, Schwechheimer, Claus, additional, Halkier, Barbara Ann, additional, Nour-Eldin, Hussam Hassan, additional, Estelle, Mark, additional, and Shani, Eilon, additional

Published
2016
Full Text
View/download PDF

161. Mutational studies of the Aux/IAA proteins in <italic>Physcomitrella</italic> reveal novel insights into their function.

Author

Tao, Sibo and Estelle, Mark

Subjects
*AUXIN, *PLANT growth, *HORMONE synthesis, *PHYSCOMITRELLA, *INDOLEACETIC acid, *UBIQUITIN, *GENE expression
Abstract

Summary: The plant hormone auxin regulates many aspects of plant growth and development. Auxin signaling involves hormone perception by the TRANSPORT INHIBITOR RESPONSE/AUXIN F‐BOX (TIR1/AFB)–Aux/IAA co‐receptor system, and the subsequent degradation of the Aux/IAA transcriptional repressors by the ubiquitin proteasome pathway. This leads to the activation of downstream gene expression and diverse physiological responses. Here, we investigate how the structural elements in the Aux/IAAs determine their function in Auxin perception and transcriptional repression. We took advantage of the facile genetics of the moss Physcomitrella patens to determine the activity of wild‐type and mutant PpIAA1a proteins in a Δaux/iaa null background. In this way, Aux/IAA function was characterized at the molecular and physiological levels without the interference of genetic redundancy. We identified and characterized degron variants in Aux/IAAs that affect their stability and Auxin response. We also demonstrated that neither the Aux/IAA EAR motif nor Aux/IAA oligomerization is essential for the repressive function of Aux/IAA. Our study demonstrates how key elements within the Aux/IAA proteins fine tune stability and repressor activity, as well as the long‐term developmental outcome. [ABSTRACT FROM AUTHOR]

Published
2018
Full Text
View/download PDF

162. The <italic>Arabidopsis </italic>ALF4 protein is a regulator of SCF E3 ligases.

Author

Bagchi, Rammyani, Melnyk, Charles W., Christ, Gideon, Winkler, Martin, Kirchsteiner, Kerstin, Salehin, Mohammad, Mergner, Julia, Niemeyer, Michael, Schwechheimer, Claus, Calderón Villalobos, Luz Irina A., and Estelle, Mark

Subjects
ARABIDOPSIS proteins, PLANT development, PLANT hormones, UBIQUITIN, LIGASES, PHENOTYPES
Abstract

Abstract: The cullin‐RING E3 ligases (CRLs) regulate diverse cellular processes in all eukaryotes. CRL activity is controlled by several proteins or protein complexes, including NEDD8, CAND1, and the CSN. Recently, a mammalian protein called Glomulin (GLMN) was shown to inhibit CRLs by binding to the RING BOX (RBX1) subunit and preventing binding to the ubiquitin‐conjugating enzyme. Here, we show that Arabidopsis ABERRANT LATERAL ROOT FORMATION4 (ALF4) is an ortholog of GLMN. The alf4 mutant exhibits a phenotype that suggests defects in plant hormone response. We show that ALF4 binds to RBX1 and inhibits the activity of SCFTIR1, an E3 ligase responsible for degradation of the Aux/IAA transcriptional repressors. In vivo, the alf4 mutation destabilizes the CUL1 subunit of the SCF. Reduced CUL1 levels are associated with increased levels of the Aux/IAA proteins as well as the DELLA repressors, substrate of SCFSLY1. We propose that the alf4 phenotype is partly due to increased levels of the Aux/IAA and DELLA proteins. [ABSTRACT FROM AUTHOR]

Published
2018
Full Text
View/download PDF

163. Nitric oxide regulates auxin signaling through s-nitrosylation of the Arabidopsis Transport Inhibitor Response1 auxin receptor

Author

Terrile, Maria Cecilia, Paris, Ramiro, Calderón Villalobos, Luz I. A., Iglesias, María José, Lamattina, Lorenzo, Estelle, Mark, and Casalongue, Claudia

Subjects
purl.org/becyt/ford/1 [https], Ciencias Biológicas, Arabidopsis thaliana, root growth, nitric oxide, Bioquímica y Biología Molecular, purl.org/becyt/ford/1.6 [https], auxin, TIR1 receptor, S-nitrosylation, CIENCIAS NATURALES Y EXACTAS
Abstract

Previous studies have demonstrated that auxin (indole-3-acetic acid) and nitric oxide (NO) are plant growth regulators that coordinate several plant physiological responses determining root architecture. Nonetheless, the way in which these factors interact to affect these growth and developmental processes is not well understood. The Arabidopsis thaliana F-box proteins TRANSPORT INHIBITOR RESPONSE 1/AUXIN SIGNALING F-BOX (TIR1/AFB) are auxin receptors that mediate degradation of AUXIN/INDOLE-3-ACETIC ACID (Aux/IAA) repressors to induce auxin-regulated responses. A broad spectrum of NO-mediated protein modifications are known in eukaryotic cells. Here, we provide evidence that NO donors increase auxin-dependent gene expression while NO depletion blocks Aux/IAA protein degradation. NO also enhances TIR1-Aux/IAA interaction as evidenced by pull-down and two-hybrid assays. In addition, we provide evidence for NO-mediated modulation of auxin signaling through S-nitrosylation of the TIR1 auxin receptor. S-nitrosylation of cysteine is a redox-based post-translational modification that contributes to the complexity of the cellular proteome. We show that TIR1 C140 is a critical residue for TIR1–Aux/IAA interaction and TIR1 function. These results suggest that TIR1 S-nitrosylation enhances TIR1–Aux/IAA interaction, facilitating Aux/IAA degradation and subsequently promoting activation of gene expression. Our findings underline the importance of NO in phytohormone signaling pathways. Fil: Terrile, Maria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigaciones Biológicas; Argentina. Universidad Nacional de Mar del Plata; Argentina Fil: Paris, Ramiro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigaciones Biológicas; Argentina. Universidad Nacional de Mar del Plata; Argentina Fil: Calderón Villalobos, Luz I. A.. University of California; Estados Unidos Fil: Iglesias, María José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigaciones Biológicas; Argentina. Universidad Nacional de Mar del Plata; Argentina Fil: Lamattina, Lorenzo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigaciones Biológicas; Argentina. Universidad Nacional de Mar del Plata; Argentina Fil: Estelle, Mark. University of California; Estados Unidos Fil: Casalongue, Claudia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigaciones Biológicas; Argentina. Universidad Nacional de Mar del Plata. Facultad de Ciencias Exactas y Naturales; Argentina

Published
2012

164. The compact Selaginella genome identifies changes in gene content associated with the evolution of vascular plants

Author

Banks, Jo Ann, Nishiyama, Tomoaki, Hasebe, Mitsuyasu, Bowman, John L., Gribskov, Michael, dePamphilis, Claude, Albert, Victor A., Aono, Naoki, Aoyama, Tsuyoshi, Ambrose, Barbara A., Ashton, Neil W., Axtell, Michael J., Barker, Elizabeth, Barker, Michael S., Bennetzen, Jeffrey L., Bonawitz, Nicholas D., Chapple, Clint, Cheng, Chaoyang, Correa, Luiz Gustavo Guedes, Dacre, Michael, DeBarry, Jeremy, Dreyer, Ingo, Elias, Marek, Engstrom, Eric M., Estelle, Mark, Feng, Liang, Finet, Cédric, Floyd, Sandra K., Frommer, Wolf B., Fujita, Tomomichi, Gramzow, Lydia, Gutensohn, Michael, Harholt, Jesper, Hattori, Mitsuru, Heyl, Alexander, Hirai, Tadayoshi, Hiwatashi, Yuji, Ishikawa, Masaki, Iwata, Mineko, Karol, Kenneth G., Koehler, Barbara, Kolukisaoglu, Uener, Kubo, Minoru, Kurata, Tetsuya, Lalonde, Sylvie, Li, Kejie, Li, Ying, Litt, Amy, Lyons, Eric, Manning, Gerard, Maruyama, Takeshi, Michael, Todd P., Mikami, Koji, Miyazaki, Saori, Morinaga, Shin-ichi, Murata, Takashi, Mueller-Roeber, Bernd, Nelson, David R., Obara, Mari, Oguri, Yasuko, Olmstead, Richard G., Onodera, Naoko, Petersen, Bent Larsen, Pils, Birgit, Prigge, Michael, Rensing, Stefan A., Riaño-Pachón, Diego Mauricio, Roberts, Alison W., Sato, Yoshikatsu, Scheller, Henrik Vibe, Schulz, Burkhard, Schulz, Christian, Shakirov, Eugene V., Shibagaki, Nakako, Shinohara, Naoki, Shippen, Dorothy E., Sørensen, Iben, Sotooka, Ryo, Sugimoto, Nagisa, Sugita, Mamoru, Sumikawa, Naomi, Tanurdzic, Milos, Theißen, Günter, Ulvskov, Peter, Wakazuki, Sachiko, Weng, Jing-Ke, Willats, William W.G.T., Wipf, Daniel, Wolf, Paul G., Yang, Lixing, Zimmer, Andreas D., Zhu, Qihui, Mitros, Therese, Hellsten, Uffe, Loqué, Dominique, Otillar, Robert, Salamov, Asaf, Schmutz, Jeremy, Shapiro, Harris, Lindquist, Erika, Lucas, Susan, Rokhsar, Daniel, and Grigoriev, Igor V.

Subjects
Selaginellaceae, Proteome, fungi, Chlamydomonas, Molecular Sequence Data, food and beverages, Sequence Analysis, DNA, Genes, Plant, Biological Evolution, Article, Bryopsida, Evolution, Molecular, Magnoliopsida, MicroRNAs, Gene Expression Regulation, Plant, RNA, Plant, DNA Transposable Elements, RNA Editing, Genome, Plant, Phylogeny, Plant Proteins, Repetitive Sequences, Nucleic Acid
Abstract

Vascular plants appeared ~410 million years ago, then diverged into several lineages of which only two survive: the euphyllophytes (ferns and seed plants) and the lycophytes. We report here the genome sequence of the lycophyte Selaginella moellendorffii (Selaginella), the first nonseed vascular plant genome reported. By comparing gene content in evolutionarily diverse taxa, we found that the transition from a gametophyte- to a sporophyte-dominated life cycle required far fewer new genes than the transition from a nonseed vascular to a flowering plant, whereas secondary metabolic genes expanded extensively and in parallel in the lycophyte and angiosperm lineages. Selaginella differs in posttranscriptional gene regulation, including small RNA regulation of repetitive elements, an absence of the trans-acting small interfering RNA pathway, and extensive RNA editing of organellar genes.

Published
2011

168. microRNA regulation of fruit growth

Author

José Ripoll, Juan, primary, Bailey, Lindsay J., additional, Mai, Quynh-Anh, additional, Wu, Scott L., additional, Hon, Cindy T., additional, Chapman, Elisabeth J., additional, Ditta, Gary S., additional, Estelle, Mark, additional, and Yanofsky, Martin F., additional

Published
2015
Full Text
View/download PDF

175. AXR2 Encodes a Member of the Aux/IAA Protein Family

Author

Walker, Loni M., Young, Jeff C., Sonawala, Ami, Timpte, Candace, Nagpal, Punita, Estelle, Mark, and Reed, Jason W.

Subjects
fungi, food and beverages
Abstract

The dominant gain-of-function axr2-1 mutation of Arabidopsis causes agravitropic root and shoot growth, a short hypocotyl and stem, and auxin-resistant root growth. We have cloned the AXR2 gene using a map-based approach, and find that it is the same as IAA7, a member of the IAA (indole-3-acetic acid) family of auxin-inducible genes. The axr2-1 mutation changes a single amino acid in conserved domain II of AXR2/IAA7. We isolated loss-of-function mutations in AXR2/IAA7 as intragenic suppressors of axr2-1 or in a screen for insertion mutations in IAA genes. A null mutant has a slightly longer hypocotyl than wild-type plants, indicating that AXR2/IAA7 controls development in light-grown seedlings, perhaps in concert with other gene products. Dark-grown axr2-1 mutant plants have short hypocotyls and make leaves, suggesting that activation of AXR2/IAA7 is sufficient to induce morphological responses normally elicited by light. Previously described semidominant mutations in two other Arabidopsis IAA genes cause some of the same phenotypes as axr2-1, but also cause distinct phenotypes. These results illustrate functional differences among members of the Arabidopsis IAA gene family.

Published
2000
Full Text
View/download PDF

176. Regulation of Auxin Homeostasis and Gradients in Arabidopsis Roots through the Formation of the Indole-3-Acetic Acid Catabolite 2-Oxindole-3-Acetic Acid

Author

Pěnčík, Aleš, primary, Simonovik, Biljana, additional, Petersson, Sara V., additional, Henyková, Eva, additional, Simon, Sibu, additional, Greenham, Kathleen, additional, Zhang, Yi, additional, Kowalczyk, Mariusz, additional, Estelle, Mark, additional, Zažímalová, Eva, additional, Novák, Ondřej, additional, Sandberg, Göran, additional, and Ljung, Karin, additional

Published
2013
Full Text
View/download PDF

179. FLYING SAUCER1 Is a Transmembrane RING E3 Ubiquitin Ligase That Regulates the Degree of Pectin Methylesterification in Arabidopsis Seed Mucilage

Author

Voiniciuc, Cătălin, primary, Dean, Gillian H., additional, Griffiths, Jonathan S., additional, Kirchsteiger, Kerstin, additional, Hwang, Yeen Ting, additional, Gillett, Alan, additional, Dow, Graham, additional, Western, Tamara L., additional, Estelle, Mark, additional, and Haughn, George W., additional

Published
2013
Full Text
View/download PDF

181. The Physcomitrella genome reveals evolutionary insights into the conquest of land by plants

Author

Rensing, Stefan A., Rensing, Stefan A., Lang, Daniel, Zimmer, Andreas D., Terry, Astrid, Salamov, Asaf, Shapiro, Harris, Nishiyama, Tomaoki, Perroud, Pierre-Francois, Lindquist, Erika A., Kamisugi, Yasuko, Tanahashi, Takako, Sakakibara, Keiko, Fujita, Tomomichi, Oishi, Kazuko, Shin, Tadasu, Kuroki, Yoko, Toyoda, Atsushi, Suzuki, Yutaka, Hashimoto, Shin-ichi, Yamaguchi, Kazuo, Sugano, Sumio, Kohara, Yuji, Fujiyama, Asao, Anterola, Aldwin, Aoki, Setsuyuki, Ashton, Neil, Barbazuk, W. Brad, Barker, Elizabeth, Bennetzen, Jeffrey L., Blankenship, Robert, Cho, Sung Hyun, Dutcher, Susan K., Estelle, Mark, Fawcett, Jeffrey A., Gundlach, Heidrum, Hanada, Kousuke, Melkozernov, Alexander, Murata, Takashi, Nelson, David R., Pils, Birgit, Prigge, Michael, Reiss, Bernd, Renner, Tanya, Rombauts, Stephane, Rushton, Paul J., Sanderfoot, Anton, Schween, Gabriele, Shiu, Shin-Han, Stueber, Kurt, Theodoulou, Frederica L., Tu, Hank, Peer, Yves Van de, Verrier, Paul J., Waters, Elizabeth, Wood, Andrew, Yang, Lixing, Cove, David, Cuming, Andrew C., Hasebe, Mitsayasu, Lucas, Susan, Mishler, Brent D., Reski, Ralf, Grigoriev, Igor V., Quatrano, Rakph S., Boore, Jeffrey L., Rensing, Stefan A., Rensing, Stefan A., Lang, Daniel, Zimmer, Andreas D., Terry, Astrid, Salamov, Asaf, Shapiro, Harris, Nishiyama, Tomaoki, Perroud, Pierre-Francois, Lindquist, Erika A., Kamisugi, Yasuko, Tanahashi, Takako, Sakakibara, Keiko, Fujita, Tomomichi, Oishi, Kazuko, Shin, Tadasu, Kuroki, Yoko, Toyoda, Atsushi, Suzuki, Yutaka, Hashimoto, Shin-ichi, Yamaguchi, Kazuo, Sugano, Sumio, Kohara, Yuji, Fujiyama, Asao, Anterola, Aldwin, Aoki, Setsuyuki, Ashton, Neil, Barbazuk, W. Brad, Barker, Elizabeth, Bennetzen, Jeffrey L., Blankenship, Robert, Cho, Sung Hyun, Dutcher, Susan K., Estelle, Mark, Fawcett, Jeffrey A., Gundlach, Heidrum, Hanada, Kousuke, Melkozernov, Alexander, Murata, Takashi, Nelson, David R., Pils, Birgit, Prigge, Michael, Reiss, Bernd, Renner, Tanya, Rombauts, Stephane, Rushton, Paul J., Sanderfoot, Anton, Schween, Gabriele, Shiu, Shin-Han, Stueber, Kurt, Theodoulou, Frederica L., Tu, Hank, Peer, Yves Van de, Verrier, Paul J., Waters, Elizabeth, Wood, Andrew, Yang, Lixing, Cove, David, Cuming, Andrew C., Hasebe, Mitsayasu, Lucas, Susan, Mishler, Brent D., Reski, Ralf, Grigoriev, Igor V., Quatrano, Rakph S., and Boore, Jeffrey L.

Abstract

We report the draft genome sequence of the model moss Physcomitrella patens and compare its features with those of flowering plants, from which it is separated by more than 400 million years, and unicellular aquatic algae. This comparison reveals genomic changes concomitant with the evolutionary movement to land, including a general increase in gene family complexity; loss of genes associated with aquatic environments (e.g., flagellar arms); acquisition of genes for tolerating terrestrial stresses (e.g., variation in temperature and water availability); and the development of the auxin and abscisic acid signaling pathways for coordinating multicellular growth and dehydration response. The Physcomitrella genome provides a resource for phylogenetic inferences about gene function and for experimental analysis of plant processes through this plant's unique facility for reverse genetics.

Published
2007

185. A combinatorial TIR1/AFB–Aux/IAA co-receptor system for differential sensing of auxin

Author

Calderón Villalobos, Luz Irina A, primary, Lee, Sarah, additional, De Oliveira, Cesar, additional, Ivetac, Anthony, additional, Brandt, Wolfgang, additional, Armitage, Lynne, additional, Sheard, Laura B, additional, Tan, Xu, additional, Parry, Geraint, additional, Mao, Haibin, additional, Zheng, Ning, additional, Napier, Richard, additional, Kepinski, Stefan, additional, and Estelle, Mark, additional

Published
2012
Full Text
View/download PDF

187. Root gravitropism is regulated by a transient lateral auxin gradient controlled by a tipping-point mechanism

Author

Band, Leah R., primary, Wells, Darren M., additional, Larrieu, Antoine, additional, Sun, Jianyong, additional, Middleton, Alistair M., additional, French, Andrew P., additional, Brunoud, Géraldine, additional, Sato, Ethel Mendocilla, additional, Wilson, Michael H., additional, Péret, Benjamin, additional, Oliva, Marina, additional, Swarup, Ranjan, additional, Sairanen, Ilkka, additional, Parry, Geraint, additional, Ljung, Karin, additional, Beeckman, Tom, additional, Garibaldi, Jonathan M., additional, Estelle, Mark, additional, Owen, Markus R., additional, Vissenberg, Kris, additional, Hodgman, T. Charlie, additional, Pridmore, Tony P., additional, King, John R., additional, Vernoux, Teva, additional, and Bennett, Malcolm J., additional

Published
2012
Full Text
View/download PDF

188. The Selaginella Genome Identifies Genetic Changes Associated with the Evolution of Vascular Plants

Author

Banks, Jo Ann, primary, Nishiyama, Tomoaki, additional, Hasebe, Mitsuyasu, additional, Bowman, John L., additional, Gribskov, Michael, additional, dePamphilis, Claude, additional, Albert, Victor A., additional, Aono, Naoki, additional, Aoyama, Tsuyoshi, additional, Ambrose, Barbara A., additional, Ashton, Neil W., additional, Axtell, Michael J., additional, Barker, Elizabeth, additional, Barker, Michael S., additional, Bennetzen, Jeffrey L., additional, Bonawitz, Nicholas D., additional, Chapple, Clint, additional, Cheng, Chaoyang, additional, Correa, Luiz Gustavo Guedes, additional, Dacre, Michael, additional, DeBarry, Jeremy, additional, Dreyer, Ingo, additional, Elias, Marek, additional, Engstrom, Eric M., additional, Estelle, Mark, additional, Feng, Liang, additional, Finet, Cédric, additional, Floyd, Sandra K., additional, Frommer, Wolf B., additional, Fujita, Tomomichi, additional, Gramzow, Lydia, additional, Gutensohn, Michael, additional, Harholt, Jesper, additional, Hattori, Mitsuru, additional, Heyl, Alexander, additional, Hirai, Tadayoshi, additional, Hiwatashi, Yuji, additional, Ishikawa, Masaki, additional, Iwata, Mineko, additional, Karol, Kenneth G., additional, Koehler, Barbara, additional, Kolukisaoglu, Uener, additional, Kubo, Minoru, additional, Kurata, Tetsuya, additional, Lalonde, Sylvie, additional, Li, Kejie, additional, Li, Ying, additional, Litt, Amy, additional, Lyons, Eric, additional, Manning, Gerard, additional, Maruyama, Takeshi, additional, Michael, Todd P., additional, Mikami, Koji, additional, Miyazaki, Saori, additional, Morinaga, Shin‐ichi, additional, Murata, Takashi, additional, Mueller‐Roeber, Bernd, additional, Nelson, David R., additional, Obara, Mari, additional, Oguri, Yasuko, additional, Olmstead, Richard G., additional, Onodera, Naoko, additional, Petersen, Bent Larsen, additional, Pils, Birgit, additional, Prigge, Michael, additional, Rensing, Stefan A., additional, Riaño-Pachón, Diego Mauricio, additional, Roberts, Alison W., additional, Sato, Yoshikatsu, additional, Scheller, Henrik Vibe, additional, Schulz, Burkhard, additional, Schulz, Christian, additional, Shakirov, Eugene V., additional, Shibagaki, Nakako, additional, Shinohara, Naoki, additional, Shippen, Dorothy E., additional, Sørensen, Iben, additional, Sotooka, Ryo, additional, Sugimoto, Nagisa, additional, Sugita, Mamoru, additional, Sumikawa, Naomi, additional, Tanurdzic, Milos, additional, Theißen, Günter, additional, Ulvskov, Peter, additional, Wakazuki, Sachiko, additional, Weng, Jing‐Ke, additional, Willats, William W.G.T., additional, Wipf, Daniel, additional, Wolf, Paul G., additional, Yang, Lixing, additional, Zimmer, Andreas D., additional, Zhu, Qihui, additional, Mitros, Therese, additional, Hellsten, Uffe, additional, Loqué, Dominique, additional, Otillar, Robert, additional, Salamov, Asaf, additional, Schmutz, Jeremy, additional, Shapiro, Harris, additional, Lindquist, Erika, additional, Lucas, Susan, additional, Rokhsar, Daniel, additional, and Grigoriev, Igor V., additional

Published
2011
Full Text
View/download PDF

190. The Arabidopsis D-Type Cyclin CYCD2;1 and the Inhibitor ICK2/KRP2 Modulate Auxin-Induced Lateral Root Formation

Author

Sanz, Luis, primary, Dewitte, Walter, additional, Forzani, Celine, additional, Patell, Farah, additional, Nieuwland, Jeroen, additional, Wen, Bo, additional, Quelhas, Pedro, additional, De Jager, Sarah, additional, Titmus, Craig, additional, Campilho, Aurélio, additional, Ren, Hong, additional, Estelle, Mark, additional, Wang, Hong, additional, and Murray, James A.H., additional

Published
2011
Full Text
View/download PDF

197. New auxin analogs with growth-promoting effects in intact plants reveal a chemical strategy to improve hormone delivery

Author

Savaldi-Goldstein, Sigal, primary, Baiga, Thomas J., additional, Pojer, Florence, additional, Dabi, Tsegeye, additional, Butterfield, Cristina, additional, Parry, Geraint, additional, Santner, Aaron, additional, Dharmasiri, Nihal, additional, Tao, Yi, additional, Estelle, Mark, additional, Noel, Joseph P., additional, and Chory, Joanne, additional

Published
2008
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results