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Summary Expression Gene Literature (81) GO Terms (7) Nucleotides (77) Proteins (33) Interactants (847) Wiki
XB-GENEPAGE-481991

Papers associated with smad3

Search for smad3 morpholinos using Textpresso

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14 paper(s) referencing morpholinos

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Opposite T3 Response of ACTG1-FOS Subnetwork Differentiate Tailfin Fate in Xenopus Tadpole and Post-hatching Axolotl., Kerdivel G, Blugeon C, Fund C, Rigolet M, Sachs LM, Buisine N., Front Endocrinol (Lausanne). January 1, 2019; 10 194.              


Repression of Inappropriate Gene Expression in the Vertebrate Embryonic Ectoderm., Reich S, Weinstein DC., Genes (Basel). January 1, 2019; 10 (11):         


Coordinated regulation of the dorsal-ventral and anterior-posterior patterning of Xenopus embryos by the BTB/POZ zinc finger protein Zbtb14., Takebayashi-Suzuki K, Konishi H, Miyamoto T, Nagata T, Uchida M, Suzuki A, Suzuki A., Dev Growth Differ. April 1, 2018; 60 (3): 158-173.          


Eomesodermin-At Dawn of Cell Fate Decisions During Early Embryogenesis., Probst S, Arnold SJ., Curr Top Dev Biol. January 1, 2017; 122 93-115.


A gene regulatory program controlling early Xenopus mesendoderm formation: Network conservation and motifs., Charney RM, Paraiso KD, Blitz IL, Cho KWY., Semin Cell Dev Biol. January 1, 2017; 66 12-24.    


Aberrant regulation of Wnt signaling in hepatocellular carcinoma., Liu LJ, Xie SX, Chen YT, Xue JL, Zhang CJ, Zhu F., World J Gastroenterol. September 7, 2016; 22 (33): 7486-99.      


Monitoring Smad Activity In Vivo Using the Xenopus Model System., Montagner M, Martello G, Piccolo S., Methods Mol Biol. January 1, 2016; 1344 245-59.


FoxH1 mediates a Grg4 and Smad2 dependent transcriptional switch in Nodal signaling during Xenopus mesoderm development., Reid CD, Steiner AB, Yaklichkin S, Lu Q, Wang S, Hennessy M, Kessler DS., Dev Biol. January 1, 2016; 414 (1): 34-44.                  


Loss of expression of protein phosphatase magnesium-dependent 1A during kidney injury promotes fibrotic maladaptive repair., Samarakoon R, Rehfuss A, Khakoo NS, Falke LL, Dobberfuhl AD, Helo S, Overstreet JM, Goldschmeding R, Higgins PJ., FASEB J. January 1, 2016; 30 (10): 3308-3320.


Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling., Houtmeyers R, Tchouate Gainkam O, Glanville-Jones HA, Van den Bosch B, Chappell A, Barratt KS, Souopgui J, Tejpar S, Arkell RM., Hum Mol Genet. January 1, 2016; 25 (18): 3946-3959.


Small C-terminal Domain Phosphatase 3 Dephosphorylates the Linker Sites of Receptor-regulated Smads (R-Smads) to Ensure Transforming Growth Factor β (TGFβ)-mediated Germ Layer Induction in Xenopus Embryos., Sun G, Hu Z, Min Z, Yan X, Guan Z, Su H, Fu Y, Ma X, Chen YG, Zhang MQ, Tao Q, Wu W., J Biol Chem. July 10, 2015; 290 (28): 17239-49.                  


At new heights - endodermal lineages in development and disease., Ober EA, Grapin-Botton A., Development. June 1, 2015; 142 (11): 1912-1917.  


Genome-wide view of TGFβ/Foxh1 regulation of the early mesendoderm program., Chiu WT, Charney Le R, Blitz IL, Fish MB, Li Y, Biesinger J, Xie X, Cho KW., Development. December 1, 2014; 141 (23): 4537-47.                                  


Sox5 Is a DNA-binding cofactor for BMP R-Smads that directs target specificity during patterning of the early ectoderm., Nordin K, LaBonne C., Dev Cell. November 10, 2014; 31 (3): 374-382.                              


Developmental enhancers are marked independently of zygotic Nodal signals in Xenopus., Gupta R, Wills A, Ucar D, Baker J., Dev Biol. November 1, 2014; 395 (1): 38-49.            


Gtpbp2 is required for BMP signaling and mesoderm patterning in Xenopus embryos., Kirmizitas A, Gillis WQ, Zhu H, Thomsen GH., Dev Biol. August 15, 2014; 392 (2): 358-67.                                


Zygotic expression of Exostosin1 (Ext1) is required for BMP signaling and establishment of dorsal-ventral pattern in Xenopus., Shieh YE, Wells DE, Sater AK., Int J Dev Biol. January 1, 2014; 58 (1): 27-34.          


Activin ligands are required for the re-activation of Smad2 signalling after neurulation and vascular development in Xenopus tropicalis., Nagamori Y, Roberts S, Maciej M, Dorey K., Int J Dev Biol. January 1, 2014; 58 (10-12): 783-91.            


In vivo T-box transcription factor profiling reveals joint regulation of embryonic neuromesodermal bipotency., Gentsch GE, Owens ND, Martin SR, Piccinelli P, Faial T, Trotter MW, Gilchrist MJ, Smith JC., Cell Rep. September 26, 2013; 4 (6): 1185-96.                              


Signaling crosstalk between TGFβ and Dishevelled/Par1b., Mamidi A, Inui M, Manfrin A, Soligo S, Enzo E, Aragona M, Cordenonsi M, Wessely O, Dupont S, Piccolo S., Cell Death Differ. October 1, 2012; 19 (10): 1689-97.                    


Transient downregulation of Bmp signalling induces extra limbs in vertebrates., Christen B, Rodrigues AM, Monasterio MB, Roig CF, Izpisua Belmonte JC., Development. July 1, 2012; 139 (14): 2557-65.        


Conservation and evolutionary divergence in the activity of receptor-regulated smads., Sorrentino GM, Gillis WQ, Oomen-Hajagos J, Thomsen GH., Evodevo. January 1, 2012; 3 (1): 22.              


HEB and E2A function as SMAD/FOXH1 cofactors., Yoon SJ, Wills AE, Chuong E, Gupta R, Baker JC., Genes Dev. August 1, 2011; 25 (15): 1654-61.            


Early cardiac morphogenesis defects caused by loss of embryonic macrophage function in Xenopus., Smith SJ, Mohun TJ., Mech Dev. May 1, 2011; 128 (5-6): 303-15.                            


The function of heterodimeric AP-1 comprised of c-Jun and c-Fos in activin mediated Spemann organizer gene expression., Lee SY, Yoon J, Lee HS, Hwang YS, Cha SW, Jeong CH, Kim JI, Park JB, Lee JY, Kim S, Park MJ, Dong Z, Kim J., PLoS One. January 1, 2011; 6 (7): e21796.              


TMEPAI, a transmembrane TGF-beta-inducible protein, sequesters Smad proteins from active participation in TGF-beta signaling., Watanabe Y, Itoh S, Goto T, Ohnishi E, Inamitsu M, Itoh F, Satoh K, Wiercinska E, Yang W, Shi L, Tanaka A, Nakano N, Mommaas AM, Shibuya H, Ten Dijke P, Kato M., Mol Cell. January 15, 2010; 37 (1): 123-34.                                      


Human BAMBI cooperates with Smad7 to inhibit transforming growth factor-beta signaling., Yan X, Lin Z, Chen F, Zhao X, Chen H, Ning Y, Chen YG., J Biol Chem. October 30, 2009; 284 (44): 30097-104.


Riding shotgun: a dual role for the epidermal growth factor-Cripto/FRL-1/Cryptic protein Cripto in Nodal trafficking., Constam DB., Traffic. July 1, 2009; 10 (7): 783-91.


High-sensitivity real-time imaging of dual protein-protein interactions in living subjects using multicolor luciferases., Hida N, Awais M, Takeuchi M, Ueno N, Tashiro M, Takagi C, Singh T, Hayashi M, Ohmiya Y, Ozawa T., PLoS One. June 30, 2009; 4 (6): e5868.            


Modeling and analysis of MH1 domain of Smads and their interaction with promoter DNA sequence motif., Makkar P, Metpally RP, Sangadala S, Reddy BV., J Mol Graph Model. April 1, 2009; 27 (7): 803-12.


Nuclear export of Smad2 and Smad3 by RanBP3 facilitates termination of TGF-beta signaling., Dai F, Lin X, Chang C, Feng XH., Dev Cell. March 1, 2009; 16 (3): 345-57.


TGF-beta induces connexin43 gene expression in normal murine mammary gland epithelial cells via activation of p38 and PI3K/AKT signaling pathways., Tacheau C, Fontaine J, Loy J, Mauviel A, Verrecchia F., J Cell Physiol. December 1, 2008; 217 (3): 759-68.


Nuclear accumulation of Smad complexes occurs only after the midblastula transition in Xenopus., Saka Y, Hagemann AI, Piepenburg O, Smith JC., Development. December 1, 2007; 134 (23): 4209-18.


Erbin inhibits transforming growth factor beta signaling through a novel Smad-interacting domain., Dai F, Chang C, Lin X, Dai P, Mei L, Feng XH., Mol Cell Biol. September 1, 2007; 27 (17): 6183-94.


The MH1 domain of Smad3 interacts with Pax6 and represses autoregulation of the Pax6 P1 promoter., Grocott T, Frost V, Maillard M, Johansen T, Wheeler GN, Dawes LJ, Wormstone IM, Chantry A., Nucleic Acids Res. January 1, 2007; 35 (3): 890-901.            


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.                                    


Xenopus Dab2 is required for embryonic angiogenesis., Cheong SM, Choi SC, Han JK., BMC Dev Biol. September 29, 2006; 6 63.                  


deltaEF1 and SIP1 are differentially expressed and have overlapping activities during Xenopus embryogenesis., van Grunsven LA, Taelman V, Michiels C, Opdecamp K, Huylebroeck D, Bellefroid EJ., Dev Dyn. June 1, 2006; 235 (6): 1491-500.  


XBP1 forms a regulatory loop with BMP-4 and suppresses mesodermal and neural differentiation in Xenopus embryos., Cao Y, Cao Y, Knöchel S, Oswald F, Donow C, Zhao H, Knöchel W., Mech Dev. January 1, 2006; 123 (1): 84-96.      


The novel Smad-interacting protein Smicl regulates Chordin expression in the Xenopus embryo., Collart C, Verschueren K, Rana A, Smith JC, Huylebroeck D., Development. October 1, 2005; 132 (20): 4575-86.        


Isolation and comparative expression analysis of the Myc-regulatory proteins Mad1, Mad3, and Mnt during Xenopus development., Juergens K, Rust B, Pieler T, Henningfeld KA., Dev Dyn. August 1, 2005; 233 (4): 1554-9.                                        


Repression of bone morphogenetic protein and activin-inducible transcription by Evi-1., Alliston T, Ko TC, Cao Y, Liang YY, Feng XH, Chang C, Derynck R., J Biol Chem. June 24, 2005; 280 (25): 24227-37.


Transcriptional regulation of the TGF-beta pseudoreceptor BAMBI by TGF-beta signaling., Sekiya T, Oda T, Matsuura K, Akiyama T., Biochem Biophys Res Commun. July 30, 2004; 320 (3): 680-4.


Smad2 and Smad3 coordinately regulate craniofacial and endodermal development., Liu Y, Festing M, Thompson JC, Hester M, Rankin S, Rankin S, El-Hodiri HM, Zorn AM, Weinstein M., Dev Biol. June 15, 2004; 270 (2): 411-26.  


Molecular and functional consequences of Smad4 C-terminal missense mutations in colorectal tumour cells., De Bosscher K, Hill CS, Nicolás FJ., Biochem J. April 1, 2004; 379 (Pt 1): 209-16.


Interaction with Smad4 is indispensable for suppression of BMP signaling by c-Ski., Takeda M, Mizuide M, Oka M, Watabe T, Inoue H, Suzuki H, Fujita T, Imamura T, Miyazono K, Miyazawa K., Mol Biol Cell. March 1, 2004; 15 (3): 963-72.                


[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.


Evidence for antagonism of BMP-4 signals by MAP kinase during Xenopus axis determination and neural specification., Sater AK, El-Hodiri HM, Goswami M, Alexander TB, Al-Sheikh O, Etkin LD, Akif Uzman J., Differentiation. September 1, 2003; 71 (7): 434-44.                


Regulation of Smad signaling through a differential recruitment of coactivators and corepressors by ZEB proteins., Postigo AA, Depp JL, Taylor JJ, Kroll KL., EMBO J. May 15, 2003; 22 (10): 2453-62.


Regulation of the rat follicle-stimulating hormone beta-subunit promoter by activin., Suszko MI, Lo DJ, Suh H, Camper SA, Woodruff TK., Mol Endocrinol. March 1, 2003; 17 (3): 318-32.

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