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Summary Expression Phenotypes Gene Literature (24) GO Terms (15) Nucleotides (122) Proteins (58) Interactants (370) Wiki
XB-GENEPAGE-484685

Papers associated with smad9



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BRCA1 and ELK-1 regulate neural progenitor cell fate in the optic tectum in response to visual experience in Xenopus laevis tadpoles., Huang LC, McKeown CR, He HY, Ta AC, Cline HT., Proc Natl Acad Sci U S A. January 16, 2024; 121 (3): e2316542121.                        

BMP signalling controls the construction of vertebrate mucociliary epithelia., Cibois M, Luxardi G, Chevalier B, Thomé V, Mercey O, Zaragosi LE, Barbry P, Pasini A, Marcet B, Kodjabachian L., Development. July 1, 2015; 142 (13): 2352-63.                        

Expression of periostin during Xenopus laevis embryogenesis., Tao S, Kühl M, Kühl SJ, Kühl SJ., Dev Genes Evol. October 1, 2011; 221 (4): 247-54.

The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM, Kaltenbrun E, Callis TE, Zeng XX, Marques SR, Yelon D, Wang DZ, Conlon FL., Development. June 1, 2010; 137 (11): 1919-29.                  

Mad is required for wingless signaling in wing development and segment patterning in Drosophila., Eivers E, Fuentealba LC, Sander V, Clemens JC, Hartnett L, De Robertis EM., PLoS One. August 6, 2009; 4 (8): e6543.                    

Conditional deletion of Smad1 and Smad5 in somatic cells of male and female gonads leads to metastatic tumor development in mice., Pangas SA, Li X, Umans L, Zwijsen A, Huylebroeck D, Gutierrez C, Wang D, Martin JF, Jamin SP, Behringer RR, Robertson EJ, Matzuk MM., Mol Cell Biol. January 1, 2008; 28 (1): 248-57.

Dullard promotes degradation and dephosphorylation of BMP receptors and is required for neural induction., Satow R, Kurisaki A, Chan TC, Hamazaki TS, Asashima M., Dev Cell. December 1, 2006; 11 (6): 763-74.              

Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA, Collart C, Gilchrist MJ, Smith JC., PLoS Genet. November 17, 2006; 2 (11): e193.                                    

Dose-dependent Smad1, Smad5 and Smad8 signaling in the early mouse embryo., Arnold SJ, Maretto S, Islam A, Bikoff EK, Robertson EJ., Dev Biol. August 1, 2006; 296 (1): 104-18.

An Oct-1 binding site mediates activation of the gata2 promoter by BMP signaling., Oren T, Torregroza I, Evans T., Nucleic Acids Res. August 1, 2005; 33 (13): 4357-67.              

Smad1 and Smad8 function similarly in mammalian central nervous system development., Hester M, Thompson JC, Mills J, Liu Y, El-Hodiri HM, Weinstein M., Mol Cell Biol. June 1, 2005; 25 (11): 4683-92.

[The role of Smads and related transcription factors in the signal transduction of bone morphogenetic protein inducing bone formation]., Xu XL, Dai KR, Tang TT., Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. September 1, 2003; 17 (5): 359-62.

XMAN1, an inner nuclear membrane protein, antagonizes BMP signaling by interacting with Smad1 in Xenopus embryos., Osada S, Ohmori SY, Taira M., Development. May 1, 2003; 130 (9): 1783-94.            

Negative regulation of BMP signaling by the ski oncoprotein., Luo K., J Bone Joint Surg Am. January 1, 2003; 85-A Suppl 3 39-43.

A maternal Smad protein regulates early embryonic apoptosis in Xenopus laevis., Miyanaga Y, Torregroza I, Evans T., Mol Cell Biol. March 1, 2002; 22 (5): 1317-28.

The role of BMP signaling in outgrowth and patterning of the Xenopus tail bud., Beck CW, Whitman M, Slack JM., Dev Biol. October 15, 2001; 238 (2): 303-14.              

Mouse embryos lacking Smad1 signals display defects in extra-embryonic tissues and germ cell formation., Tremblay KD, Dunn NR, Robertson EJ., Development. September 1, 2001; 128 (18): 3609-21.

Ski represses bone morphogenic protein signaling in Xenopus and mammalian cells., Wang W, Mariani FV, Harland RM, Luo K., Proc Natl Acad Sci U S A. December 19, 2000; 97 (26): 14394-9.          

Mouse smad8 phosphorylation downstream of BMP receptors ALK-2, ALK-3, and ALK-6 induces its association with Smad4 and transcriptional activity., Kawai S, Faucheu C, Gallea S, Spinella-Jaegle S, Atfi A, Baron R, Roman SR., Biochem Biophys Res Commun. May 19, 2000; 271 (3): 682-7.

Characterization of zebrafish smad1, smad2 and smad5: the amino-terminus of smad1 and smad5 is required for specific function in the embryo., Müller F, Blader P, Rastegar S, Fischer N, Knöchel W, Strähle U., Mech Dev. October 1, 1999; 88 (1): 73-88.  

Specific activation of Smad1 signaling pathways by the BMP7 type I receptor, ALK2., Macías-Silva M, Hoodless PA, Tang SJ, Buchwald M, Wrana JL., J Biol Chem. October 2, 1998; 273 (40): 25628-36.

Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth factor-beta receptors., Souchelnytskyi S, Nakayama T, Nakao A, Morén A, Heldin CH, Christian JL, ten Dijke P., J Biol Chem. September 25, 1998; 273 (39): 25364-70.        

Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T, Snyder MA, Grewal SS, Tsuneizumi K, Tabata T, Christian JL., Development. March 1, 1998; 125 (5): 857-67.                  

Smad8 mediates the signaling of the ALK-2 [corrected] receptor serine kinase., Chen Y, Bhushan A, Vale W., Proc Natl Acad Sci U S A. November 25, 1997; 94 (24): 12938-43.          

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