Papers associated with cell part (and smad1)

Limit to papers also referencing gene:
Show all cell part papers

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest

Sort Oldest To Newest

	R-Spondin 2 governs Xenopus left-right body axis formation by establishing an FGF signaling gradient., Lee H, Lee H., Nat Commun. February 2, 2024; 15 (1): 1003.
	ZSWIM4 regulates embryonic patterning and BMP signaling by promoting nuclear Smad1 degradation., Wang C., EMBO Rep. February 1, 2024; 25 (2): 646-671.
	ADAM11 a novel regulator of Wnt and BMP4 signaling in neural crest and cancer., Pandey A., Front Cell Dev Biol. January 1, 2023; 11 1271178.
	The homeodomain transcription factor Ventx2 regulates respiratory progenitor cell number and differentiation timing during Xenopus lung development., Rankin SA, Rankin SA., Dev Growth Differ. September 1, 2022; 64 (7): 347-361.
	BMP signaling is enhanced intracellularly by FHL3 controlling WNT-dependent spatiotemporal emergence of the neural crest., Alkobtawi M., Cell Rep. June 22, 2021; 35 (12): 109289.
	R-spondins are BMP receptor antagonists in Xenopus early embryonic development., Lee H, Lee H., Nat Commun. November 4, 2020; 11 (1): 5570.
	Foxd4l1.1 negatively regulates transcription of neural repressor ventx1.1 during neuroectoderm formation in Xenopus embryos., Kumar S, Kumar S., Sci Rep. October 8, 2020; 10 (1): 16780.
	Maternal pluripotency factors initiate extensive chromatin remodelling to predefine first response to inductive signals., Gentsch GE., Nat Commun. September 19, 2019; 10 (1): 4269.
	PAWS1 controls Wnt signalling through association with casein kinase 1α., Bozatzi P., EMBO Rep. April 1, 2018; 19 (4):
	Wbp2nl has a developmental role in establishing neural and non-neural ectodermal fates., Marchak A., Dev Biol. September 1, 2017; 429 (1): 213-224.
	Noggin4 is a long-range inhibitor of Wnt8 signalling that regulates head development in Xenopus laevis., Eroshkin FM., Sci Rep. January 22, 2016; 6 23049.
	Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S., Development. December 1, 2014; 141 (24): 4794-805.
	Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A., Dev Biol. August 15, 2014; 392 (2): 358-67.
	USP15 targets ALK3/BMPR1A for deubiquitylation to enhance bone morphogenetic protein signalling., Herhaus L., Open Biol. May 1, 2014; 4 (5): 140065.
	Cubilin, a high affinity receptor for fibroblast growth factor 8, is required for cell survival in the developing vertebrate head., Cases O., J Biol Chem. June 7, 2013; 288 (23): 16655-16670.
	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.
	TAK1 promotes BMP4/Smad1 signaling via inhibition of erk MAPK: a new link in the FGF/BMP regulatory network., Liu C., Differentiation. April 1, 2012; 83 (4): 210-9.
	Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins., Callery EM., Open Biol. April 1, 2012; 2 (4): 120060.
	KDEL tagging: a method for generating dominant-negative inhibitors of the secretion of TGF-beta superfamily proteins., Matsukawa S., Int J Dev Biol. January 1, 2012; 56 (5): 351-6.
	Bmp indicator mice reveal dynamic regulation of transcriptional response., Javier AL., PLoS One. January 1, 2012; 7 (9): e42566.
	Neuronatin promotes neural lineage in ESCs via Ca(2+) signaling., Lin HH., Stem Cells. November 1, 2010; 28 (11): 1950-60.
	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.
	Identification of a novel negative regulator of activin/nodal signaling in mesendodermal formation of Xenopus embryos., Cheong SM., J Biol Chem. June 19, 2009; 284 (25): 17052-60.
	FGF-activated calcium channels control neural gene expression in Xenopus., Lee KW., Biochim Biophys Acta. June 1, 2009; 1793 (6): 1033-40.
	TGF-beta signaling is required for multiple processes during Xenopus tail regeneration., Ho DM., Dev Biol. March 1, 2008; 315 (1): 203-16.
	Integrating patterning signals: Wnt/GSK3 regulates the duration of the BMP/Smad1 signal., Fuentealba LC., Cell. November 30, 2007; 131 (5): 980-93.
	Interpretation of BMP signaling in early Xenopus development., Simeoni I., Dev Biol. August 1, 2007; 308 (1): 82-92.
	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.
	Unique players in the BMP pathway: small C-terminal domain phosphatases dephosphorylate Smad1 to attenuate BMP signaling., Knockaert M., Proc Natl Acad Sci U S A. August 8, 2006; 103 (32): 11940-5.
	Plx1 is the 3F3/2 kinase responsible for targeting spindle checkpoint proteins to kinetochores., Wong OK., J Cell Biol. August 29, 2005; 170 (5): 709-19.
	Germ-layer specification and control of cell growth by Ectodermin, a Smad4 ubiquitin ligase., Dupont S., Cell. April 8, 2005; 121 (1): 87-99.
	A new role for BMP5 during limb development acting through the synergic activation of Smad and MAPK pathways., Zuzarte-Luís V., Dev Biol. August 1, 2004; 272 (1): 39-52.
	[The role of Smads and related transcription factors in the signal transduction of bone morphogenetic protein inducing bone formation]., Xu XL., Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. September 1, 2003; 17 (5): 359-62.
	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.
	TGF-beta signalling pathways in early Xenopus development., Hill CS., Curr Opin Genet Dev. October 1, 2001; 11 (5): 533-40.
	Regulation of Smad degradation and activity by Smurf2, an E3 ubiquitin ligase., Zhang Y, Zhang Y., Proc Natl Acad Sci U S A. January 30, 2001; 98 (3): 974-9.
	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.
	Functional analysis of human Smad1: role of the amino-terminal domain., Xu RH., Biochem Biophys Res Commun. May 10, 1999; 258 (2): 366-73.
	Spindle checkpoint protein Xmad1 recruits Xmad2 to unattached kinetochores., Chen RH., J Cell Biol. October 19, 1998; 143 (2): 283-95.
	Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth factor-beta receptors., Souchelnytskyi S., J Biol Chem. September 25, 1998; 273 (39): 25364-70.
	Smad6 functions as an intracellular antagonist of some TGF-beta family members during Xenopus embryogenesis., Nakayama T., Genes Cells. June 1, 1998; 3 (6): 387-94.
	Xenopus Smad8 acts downstream of BMP-4 to modulate its activity during vertebrate embryonic patterning., Nakayama T., Development. March 1, 1998; 125 (5): 857-67.
	Smad6 inhibits BMP/Smad1 signaling by specifically competing with the Smad4 tumor suppressor., Hata A., Genes Dev. January 15, 1998; 12 (2): 186-97.
	Dual role of the Smad4/DPC4 tumor suppressor in TGFbeta-inducible transcriptional complexes., Liu F., Genes Dev. December 1, 1997; 11 (23): 3157-67.
	Concentration-dependent patterning of the Xenopus ectoderm by BMP4 and its signal transducer Smad1., Wilson PA., Development. August 1, 1997; 124 (16): 3177-84.
	Partnership between DPC4 and SMAD proteins in TGF-beta signalling pathways., Lagna G., Nature. October 31, 1996; 383 (6603): 832-6.
	A human Mad protein acting as a BMP-regulated transcriptional activator., Liu F., Nature. June 13, 1996; 381 (6583): 620-3.
	Xenopus Mad proteins transduce distinct subsets of signals for the TGF beta superfamily., Graff JM., Cell. May 17, 1996; 85 (4): 479-87.

???pagination.result.page??? 1