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Items: 16

1.
FILAMENTOUS FLOWER controls lateral organ development by acting as both an activator and a repressor
Oliver Bonaccorso, Joanne E Lee, Libby Puah, Charles P Scutt, John F Golz
BMC Plant Biol. 2012; 12: 176. Published online 2012 Oct 1. doi: 10.1186/1471-2229-12-176
PMCID:
PMC3520853
AbstractArticlePDF–1.9M
2.
A novel allele of FILAMENTOUS FLOWER reveals new insights on the link between inflorescence and floral meristem organization and flower morphogenesis
Nitsan Lugassi, Naomi Nakayama, Rachel Bochnik, Moriyah Zik
BMC Plant Biol. 2010; 10: 131. Published online 2010 Jun 28. doi: 10.1186/1471-2229-10-131
PMCID:
PMC3017777
AbstractArticlePDF–2.7M
3.
FILAMENTOUS FLOWER, a meristem and organ identity gene of Arabidopsis, encodes a protein with a zinc finger and HMG-related domains
Shinichiro Sawa, Keiro Watanabe, Koji Goto, Eiko Kanaya, Eugene Hayato Morita, Kiyotaka Okada
Genes Dev. 1999 May 1; 13(9): 1079–1088. doi: 10.1101/gad.13.9.1079
PMCID:
PMC316944
AbstractArticlePDF–2.7M
4.
FILAMENTOUS FLOWER controls the formation and development of arabidopsis inflorescences and floral meristems.
S Sawa, T Ito, Y Shimura, K Okada
Plant Cell. 1999 Jan; 11(1): 69–86. doi: 10.1105/tpc.11.1.69
PMCID:
PMC144087
SummaryPDF–1.9M
5.
A novel Filamentous Flower mutant suppresses brevipedicellus developmental defects and modulates glucosinolate and auxin levels
Scott J. Douglas, Baohua Li, Daniel J. Kliebenstein, Eiji Nambara, C. Daniel Riggs
PLoS One. 2017; 12(5): e0177045. Published online 2017 May 11. doi: 10.1371/journal.pone.0177045
PMCID:
PMC5426679
AbstractArticlePDF–56M
6.
FILAMENTOUS FLOWER Is a Direct Target of JAZ3 and Modulates Responses to Jasmonate
Marta Boter, John F. Golz, Selena Giménez-Ibañez, Gemma Fernandez-Barbero, José M. Franco-Zorrilla, Roberto Solano
Plant Cell. 2015 Nov; 27(11): 3160–3174. Published online 2015 Nov 3. doi: 10.1105/tpc.15.00220
PMCID:
PMC4682293
AbstractArticlePDF–1.1M
7.
Control of Arabidopsis Leaf Morphogenesis Through Regulation of the YABBY and KNOX Families of Transcription Factors
Chan Man Ha, Ji Hyung Jun, Jennifer C. Fletcher
Genetics. 2010 Sep; 186(1): 197–206. doi: 10.1534/genetics.110.118703
PMCID:
PMC2940287
AbstractArticlePDF–5.4M
8.
Signals Derived from YABBY Gene Activities in Organ Primordia Regulate Growth and Partitioning of Arabidopsis Shoot Apical Meristems
Alexander Goldshmidt, John Paul Alvarez, John L. Bowman, Yuval Eshed
Plant Cell. 2008 May; 20(5): 1217–1230. doi: 10.1105/tpc.107.057877
PMCID:
PMC2438466
AbstractArticlePDF–2.2M
9.
AINTEGUMENTA Contributes to Organ Polarity and Regulates Growth of Lateral Organs in Combination with YABBY Genes
Staci Nole-Wilson, Beth A. Krizek
Plant Physiol. 2006 Jul; 141(3): 977–987. doi: 10.1104/pp.106.076604
PMCID:
PMC1489906
AbstractArticlePDF–529K
10.
Quantitative expression analysis of selected transcription factors in pavement, basal and trichome cells of mature leaves from Arabidopsis thaliana
Martin Schliep, Berit Ebert, Ulrike Simon-Rosin, Daniela Zoeller, Joachim Fisahn
Protoplasma. 2010; 241(1): 29–36. Published online 2010 Jan 26. doi: 10.1007/s00709-009-0099-7
PMCID:
PMC2856857
AbstractArticlePDF–243K
11.
Organ Polarity in Arabidopsis. NOZZLE Physically Interacts with Members of the YABBY Family
Patrick Sieber, Michael Petrascheck, Alcide Barberis, Kay Schneitz
Plant Physiol. 2004 Aug; 135(4): 2172–2185. doi: 10.1104/pp.104.040154
PMCID:
PMC520788
AbstractArticlePDF–992K
12.
YABBYs and the Transcriptional Corepressors LEUNIG and LEUNIG_HOMOLOG Maintain Leaf Polarity and Meristem Activity in Arabidopsis
Melissa I. Stahle, Janine Kuehlich, Lindsay Staron, Albrecht G. von Arnim, John F. Golz
Plant Cell. 2009 Oct; 21(10): 3105–3118. doi: 10.1105/tpc.109.070458
PMCID:
PMC2782291
AbstractArticlePDF–2.5M
13.
A PXY-Mediated Transcriptional Network Integrates Signaling Mechanisms to Control Vascular Development in Arabidopsis
Margot E. Smit, Shauni R. McGregor, Heng Sun, Catherine Gough, Anne-Maarit Bågman, Cara L. Soyars, Johannes T. Kroon, Allison Gaudinier, Clara J. Williams, Xiyan Yang, Zachary L. Nimchuk, Dolf Weijers, Simon R. Turner, Siobhán M. Brady, J. Peter Etchells
Plant Cell. 2020 Feb; 32(2): 319–335. Published online 2019 Dec 5. doi: 10.1105/tpc.19.00562
PMCID:
PMC7008486
AbstractArticlePDF–3.0M
14.
MAPK target networks in Arabidopsis thaliana revealed using functional protein microarrays
Sorina C. Popescu, George V. Popescu, Shawn Bachan, Zimei Zhang, Mark Gerstein, Michael Snyder, Savithramma P. Dinesh-Kumar
Genes Dev. 2009 Jan 1; 23(1): 80–92. doi: 10.1101/gad.1740009
PMCID:
PMC2632172
AbstractArticlePDF–2.5M
15.
CrY2H-seq: a massively-multiplexed assay for deep coverage interactome mapping
Shelly A. Wanamaker, Renee M. Garza, Andrew MacWilliams, Joseph R. Nery, Anna Bartlett, Rosa Castanon, Adeline Goubil, Joseph Feeney, Ronan O’Malley, Shao-shan Carol Huang, Zhuzhu Z. Zhang, Mary Galli, Joseph R. Ecker
Nat Methods. Author manuscript; available in PMC 2017 Dec 26.
Published in final edited form as: Nat Methods. 2017 Aug; 14(8): 819–825. Published online 2017 Jun 26. doi: 10.1038/nmeth.4343
Correction in:
Nat Methods. 2023 Jan 23
PMCID:
PMC5564216
AbstractArticlePDF–1.3M
16.
Evidence for Network Evolution in an Arabidopsis Interactome Map
Arabidopsis Interactome Mapping Consortium
Science. Author manuscript; available in PMC 2012 Jan 29.
Published in final edited form as: Science. 2011 Jul 29; 333(6042): 601–607. doi: 10.1126/science.1203877
PMCID:
PMC3170756
AbstractArticlePDF–2.0M

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