Papers associated with whole organism (and smad10)

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	Wip1 regulates Smad4 phosphorylation and inhibits TGF-β signaling., Park DS., EMBO Rep. May 6, 2020; 21 (5): e48693.
	Fam46a regulates BMP-dependent pre-placodal ectoderm differentiation in Xenopus., Watanabe T., Development. October 26, 2018; 145 (20):
	Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome., Braun DA., Nat Genet. April 1, 2016; 48 (4): 457-65.
	Identification of p62/SQSTM1 as a component of non-canonical Wnt VANGL2-JNK signalling in breast cancer., Puvirajesinghe TM., Nat Commun. January 12, 2016; 7 10318.
	Functional analysis of Hairy genes in Xenopus neural crest initial specification and cell migration., Vega-López GA., Dev Dyn. August 1, 2015; 244 (8): 988-1013.
	Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K., Dev Cell. November 10, 2014; 31 (3): 374-382.
	The tumor suppressor Smad4/DPC4 is regulated by phosphorylations that integrate FGF, Wnt, and TGF-β signaling., Demagny H., Cell Rep. October 23, 2014; 9 (2): 688-700.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus., Young JJ., Development. April 1, 2014; 141 (8): 1683-93.
	Commitment to nutritional endoderm in Eleutherodactylus coqui involves altered nodal signaling and global transcriptional repression., Chatterjee S., J Exp Zool B Mol Dev Evol. January 1, 2014; 322 (1): 27-44.
	Signaling crosstalk between TGFβ and Dishevelled/Par1b., Mamidi A., Cell Death Differ. October 1, 2012; 19 (10): 1689-97.
	Self-regulation of the head-inducing properties of the Spemann organizer., Inui M., Proc Natl Acad Sci U S A. September 18, 2012; 109 (38): 15354-9.
	Dynamics of TGF-β signaling reveal adaptive and pulsatile behaviors reflected in the nuclear localization of transcription factor Smad4., Warmflash A., Proc Natl Acad Sci U S A. July 10, 2012; 109 (28): E1947-56.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	USP15 is a deubiquitylating enzyme for receptor-activated SMADs., Inui M., Nat Cell Biol. September 25, 2011; 13 (11): 1368-75.
	Role of BMP, FGF, calcium signaling, and Zic proteins in vertebrate neuroectodermal differentiation., Aruga J., Neurochem Res. July 1, 2011; 36 (7): 1286-92.
	SNW1 is a critical regulator of spatial BMP activity, neural plate border formation, and neural crest specification in vertebrate embryos., Wu MY., PLoS Biol. February 15, 2011; 9 (2): e1000593.
	The BMP pathway acts to directly regulate Tbx20 in the developing heart., Mandel EM., Development. June 1, 2010; 137 (11): 1919-29.
	TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y., Mol Cell. January 15, 2010; 37 (1): 123-34.
	Rab5-mediated endocytosis of activin is not required for gene activation or long-range signalling in Xenopus., Hagemann AI., Development. August 1, 2009; 136 (16): 2803-13.
	High-sensitivity real-time imaging of dual protein-protein interactions in living subjects using multicolor luciferases., Hida N., PLoS One. June 12, 2009; 4 (6): e5868.
	FAM/USP9x, a deubiquitinating enzyme essential for TGFbeta signaling, controls Smad4 monoubiquitination., Dupont S., Cell. January 9, 2009; 136 (1): 123-35.
	TGF-beta induces connexin43 gene expression in normal murine mammary gland epithelial cells via activation of p38 and PI3K/AKT signaling pathways., Tacheau C., J Cell Physiol. December 1, 2008; 217 (3): 759-68.
	A crucial role of a high mobility group protein HMGA2 in cardiogenesis., Monzen K., Nat Cell Biol. May 1, 2008; 10 (5): 567-74.
	HIF-1alpha signaling upstream of NKX2.5 is required for cardiac development in Xenopus., Nagao K., J Biol Chem. April 25, 2008; 283 (17): 11841-9.
	Dkk3 is required for TGF-beta signaling during Xenopus mesoderm induction., Pinho S., Differentiation. December 1, 2007; 75 (10): 957-67.
	XSUMO-1 is required for normal mesoderm induction and axis elongation during early Xenopus development., Yukita A., Dev Dyn. October 1, 2007; 236 (10): 2757-66.
	The MH1 domain of Smad3 interacts with Pax6 and represses autoregulation of the Pax6 P1 promoter., Grocott T., Nucleic Acids Res. January 1, 2007; 35 (3): 890-901.
	Defining synphenotype groups in Xenopus tropicalis by use of antisense morpholino oligonucleotides., Rana AA., PLoS Genet. November 17, 2006; 2 (11): e193.
	Function of the two Xenopus smad4s in early frog development., Chang C., J Biol Chem. October 13, 2006; 281 (41): 30794-803.
	Genetic screens for mutations affecting development of Xenopus tropicalis., Goda T., PLoS Genet. June 1, 2006; 2 (6): e91.
	Nucleosome regulator Xhmgb3 is required for cell proliferation of the eye and brain as a downstream target of Xenopus rax/Rx1., Terada K., Dev Biol. March 15, 2006; 291 (2): 398-412.
	GDF3, a BMP inhibitor, regulates cell fate in stem cells and early embryos., Levine AJ., Development. January 1, 2006; 133 (2): 209-16.
	XBP1 forms a regulatory loop with BMP-4 and suppresses mesodermal and neural differentiation in Xenopus embryos., Cao Y, Cao Y., Mech Dev. January 1, 2006; 123 (1): 84-96.
	The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C., Development. October 1, 2005; 132 (20): 4575-86.
	Notch signaling modulates the nuclear localization of carboxy-terminal-phosphorylated smad2 and controls the competence of ectodermal cells for activin A., Abe T., Mech Dev. May 1, 2005; 122 (5): 671-80.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	Functional specificity of the Xenopus T-domain protein Brachyury is conferred by its ability to interact with Smad1., Messenger NJ., Dev Cell. April 1, 2005; 8 (4): 599-610.
	MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1., Baldessari D., BMC Cell Biol. December 21, 2004; 5 (1): 48.
	Activin/Nodal signals mediate the ventral expression of myf-5 in Xenopus gastrula embryos., Chen Y., Biochem Biophys Res Commun. October 10, 2003; 310 (1): 121-7.
	Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activin., Suszko MI., Mol Endocrinol. March 1, 2003; 17 (3): 318-32.
	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.
	Smad10 is required for formation of the frog nervous system., LeSueur JA., Dev Cell. June 1, 2002; 2 (6): 771-83.
	A novel Xenopus Smad-interacting forkhead transcription factor (XFast-3) cooperates with XFast-1 in regulating gastrulation movements., Howell M., Development. June 1, 2002; 129 (12): 2823-34.
	Expression cloning of Xenopus Os4, an evolutionarily conserved gene, which induces mesoderm and dorsal axis., Zohn IE., Dev Biol. November 1, 2001; 239 (1): 118-31.
	Identification of two regulatory elements within the high mobility group box transcription factor XTCF-4., Pukrop T., J Biol Chem. March 23, 2001; 276 (12): 8968-78.
	Ski represses bone morphogenic protein signaling in Xenopus and mammalian cells., Wang W., Proc Natl Acad Sci U S A. December 19, 2000; 97 (26): 14394-9.
	Identification and characterization of constitutively active Smad2 mutants: evaluation of formation of Smad complex and subcellular distribution., Funaba M., Mol Endocrinol. October 1, 2000; 14 (10): 1583-91.
	Mouse smad8 phosphorylation downstream of BMP receptors ALK-2, ALK-3, and ALK-6 induces its association with Smad4 and transcriptional activity., Kawai S., Biochem Biophys Res Commun. May 19, 2000; 271 (3): 682-7.
	Cloning and characterization of zebrafish smad2, smad3 and smad4., Dick A., Gene. April 4, 2000; 246 (1-2): 69-80.

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