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Summary Expression Gene Literature (271) GO Terms (23) Nucleotides (66) Proteins (34) Interactants (904) Wiki
XB--482367

Papers associated with sia1 (and morpholino)

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Identification of microRNAs and microRNA targets in Xenopus gastrulae: The role of miR-26 in the regulation of Smad1., Liu C, Lou CH, Shah V, Ritter R, Talley J, Soibam B, Benham A, Zhu H, Perez E, Shieh YE, Gunaratne PH, Sater AK., Dev Biol. January 1, 2016; 409 (1): 26-38.                


NF2/Merlin is required for the axial pattern formation in the Xenopus laevis embryo., Zhu X, Min Z, Tan R, Tao Q, Tao Q., Mech Dev. November 1, 2015; 138 Pt 3 305-12.                


JmjC Domain-containing Protein 6 (Jmjd6) Derepresses the Transcriptional Repressor Transcription Factor 7-like 1 (Tcf7l1) and Is Required for Body Axis Patterning during Xenopus Embryogenesis., Zhang X, Gao Y, Lu L, Zhang Z, Zhang Z, Gan S, Xu L, Lei A, Cao Y, Cao Y., J Biol Chem. August 14, 2015; 290 (33): 20273-83.                      


Kdm2a/b Lysine Demethylases Regulate Canonical Wnt Signaling by Modulating the Stability of Nuclear β-Catenin., Lu L, Gao Y, Zhang Z, Cao Q, Zhang X, Zou J, Cao Y., Dev Cell. June 22, 2015; 33 (6): 660-74.                                  


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.                                  


Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development., Zhang S, Li J, Lea R, Vleminckx K, Vleminckx K, Amaya E., Development. December 1, 2014; 141 (24): 4794-805.                            


The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling., Iwasaki Y, Thomsen GH., Development. October 1, 2014; 141 (19): 3740-51.                                          


The PDZ domain protein Mcc is a novel effector of non-canonical Wnt signaling during convergence and extension in zebrafish., Young T, Poobalan Y, Tan EK, Tao S, Ong S, Wehner P, Schwenty-Lara J, Lim CY, Sadasivam A, Lovatt M, Wang ST, Ali Y, Borchers A, Sampath K, Dunn NR., Development. September 1, 2014; 141 (18): 3505-16.        


Polarized Wnt signaling regulates ectodermal cell fate in Xenopus., Huang YL, Niehrs C., Dev Cell. April 28, 2014; 29 (2): 250-7.                  


PTK7 modulates Wnt signaling activity via LRP6., Bin-Nun N, Lichtig H, Malyarova A, Levy M, Elias S, Frank D., Development. January 1, 2014; 141 (2): 410-21.              


Loss of Xenopus cadherin-11 leads to increased Wnt/β-catenin signaling and up-regulation of target genes c-myc and cyclin D1 in neural crest., Koehler A, Schlupf J, Schneider M, Kraft B, Winter C, Kashef J., Dev Biol. November 1, 2013; 383 (1): 132-45.                        


Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus., Lim CY, Reversade B, Knowles BB, Solter D., Development. February 1, 2013; 140 (4): 853-60.                                              


IQGAP1 functions as a modulator of dishevelled nuclear localization in Wnt signaling., Goto T, Sato A, Shimizu M, Adachi S, Satoh K, Iemura S, Natsume T, Shibuya H., PLoS One. January 1, 2013; 8 (4): e60865.              


Klf4 is required for germ-layer differentiation and body axis patterning during Xenopus embryogenesis., Cao Q, Zhang X, Lu L, Yang L, Gao J, Gao Y, Ma H, Cao Y., Development. November 1, 2012; 139 (21): 3950-61.                  


Subfunctionalization and neofunctionalization of vertebrate Lef/Tcf transcription factors., Klingel S, Morath I, Strietz J, Menzel K, Holstein TW, Gradl D., Dev Biol. August 1, 2012; 368 (1): 44-53.              


A developmental requirement for HIRA-dependent H3.3 deposition revealed at gastrulation in Xenopus., Szenker E, Lacoste N, Almouzni G., Cell Rep. June 28, 2012; 1 (6): 730-40.                                      


Down''s-syndrome-related kinase Dyrk1A modulates the p120-catenin-Kaiso trajectory of the Wnt signaling pathway., Hong JY, Park JI, Lee M, Muñoz WA, Miller RK, Ji H, Gu D, Ezan J, Sokol SY, McCrea PD., J Cell Sci. February 1, 2012; 125 (Pt 3): 561-9.                


Xenopus Zic3 controls notochord and organizer development through suppression of the Wnt/β-catenin signaling pathway., Fujimi TJ, Hatayama M, Aruga J., Dev Biol. January 15, 2012; 361 (2): 220-31.                          


Serotonin signaling is required for Wnt-dependent GRP specification and leftward flow in Xenopus., Beyer T, Danilchik M, Thumberger T, Vick P, Tisler M, Schneider I, Bogusch S, Andre P, Ulmer B, Walentek P, Niesler B, Blum M, Schweickert A., Curr Biol. January 10, 2012; 22 (1): 33-9.                


Ventx factors function as Nanog-like guardians of developmental potential in Xenopus., Scerbo P, Girardot F, Vivien C, Markov GV, Luxardi G, Demeneix B, Kodjabachian L, Coen L., PLoS One. January 1, 2012; 7 (5): e36855.              


The dual regulator Sufu integrates Hedgehog and Wnt signals in the early Xenopus embryo., Min TH, Kriebel M, Hou S, Pera EM., Dev Biol. October 1, 2011; 358 (1): 262-76.                            


The functions of maternal Dishevelled 2 and 3 in the early Xenopus embryo., Tadjuidje E, Cha SW, Louza M, Wylie C, Heasman J., Dev Dyn. July 1, 2011; 240 (7): 1727-36.          


Siamois and Twin are redundant and essential in formation of the Spemann organizer., Bae S, Reid CD, Kessler DS., Dev Biol. April 15, 2011; 352 (2): 367-81.                    


A gene regulatory network controlling hhex transcription in the anterior endoderm of the organizer., Rankin SA, Rankin SA, Kormish J, Kofron M, Jegga A, Zorn AM., Dev Biol. March 15, 2011; 351 (2): 297-310.                            


Use of fully modified 2''-O-methyl antisense oligos for loss-of-function studies in vertebrate embryos., Schneider PN, Olthoff JT, Matthews AJ, Houston DW., Genesis. March 1, 2011; 49 (3): 117-23.        


Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone., Gee ST, Milgram SL, Kramer KL, Conlon FL, Moody SA., PLoS One. January 1, 2011; 6 (6): e20309.                  


beta-Catenin primes organizer gene expression by recruiting a histone H3 arginine 8 methyltransferase, Prmt2., Blythe SA, Cha SW, Tadjuidje E, Heasman J, Klein PS., Dev Cell. August 17, 2010; 19 (2): 220-31.      


Bone morphogenetic protein 15 (BMP15) acts as a BMP and Wnt inhibitor during early embryogenesis., Di Pasquale E, Brivanlou AH., J Biol Chem. September 18, 2009; 284 (38): 26127-36.                        


The non-methylated DNA-binding function of Kaiso is not required in early Xenopus laevis development., Ruzov A, Savitskaya E, Hackett JA, Reddington JP, Prokhortchouk A, Madej MJ, Chekanov N, Li M, Dunican DS, Prokhortchouk E, Pennings S, Meehan RR., Development. March 1, 2009; 136 (5): 729-38.            


Modulation of the beta-catenin signaling pathway by the dishevelled-associated protein Hipk1., Louie SH, Yang XY, Conrad WH, Muster J, Angers S, Moon RT, Cheyette BN., PLoS One. January 1, 2009; 4 (2): e4310.                    


Regulation of TGF-(beta) signalling by N-acetylgalactosaminyltransferase-like 1., Herr P, Korniychuk G, Yamamoto Y, Grubisic K, Oelgeschläger M., Development. May 1, 2008; 135 (10): 1813-22.                    


Lrig3 regulates neural crest formation in Xenopus by modulating Fgf and Wnt signaling pathways., Zhao H, Tanegashima K, Ro H, Dawid IB., Development. April 1, 2008; 135 (7): 1283-93.                            


Expression of Siamois and Twin in the blastula Chordin/Noggin signaling center is required for brain formation in Xenopus laevis embryos., Ishibashi H, Matsumura N, Hanafusa H, Matsumoto K, De Robertis EM, Kuroda H., Mech Dev. January 1, 2008; 125 (1-2): 58-66.              


Jun NH2-terminal kinase (JNK) prevents nuclear beta-catenin accumulation and regulates axis formation in Xenopus embryos., Liao G, Tao Q, Tao Q, Kofron M, Chen JS, Schloemer A, Davis RJ, Hsieh JC, Wylie C, Heasman J, Kuan CY., Proc Natl Acad Sci U S A. October 31, 2006; 103 (44): 16313-8.                    


NARF, an nemo-like kinase (NLK)-associated ring finger protein regulates the ubiquitylation and degradation of T cell factor/lymphoid enhancer factor (TCF/LEF)., Yamada M, Ohnishi J, Ohkawara B, Iemura S, Satoh K, Hyodo-Miura J, Kawachi K, Natsume T, Shibuya H., J Biol Chem. July 28, 2006; 281 (30): 20749-20760.                    


SOX7 and SOX18 are essential for cardiogenesis in Xenopus., Zhang C, Basta T, Klymkowsky MW., Dev Dyn. December 1, 2005; 234 (4): 878-91.                    


Antagonistic interaction between IGF and Wnt/JNK signaling in convergent extension in Xenopus embryo., Carron C, Bourdelas A, Li HY, Boucaut JC, Shi DL., Mech Dev. November 1, 2005; 122 (11): 1234-47.                


Kaiso/p120-catenin and TCF/beta-catenin complexes coordinately regulate canonical Wnt gene targets., Park JI, Kim SW, Lyons JP, Ji H, Nguyen TT, Cho K, Barton MC, Deroo T, Vleminckx K, Vleminckx K, Moon RT, McCrea PD., Dev Cell. June 1, 2005; 8 (6): 843-54.            


XIC is required for Siamois activity and dorsoanterior development., Snider L, Tapscott SJ., Mol Cell Biol. June 1, 2005; 25 (12): 5061-72.


Depletion of three BMP antagonists from Spemann''s organizer leads to a catastrophic loss of dorsal structures., Khokha MK, Yeh J, Grammer TC, Harland RM., Dev Cell. March 1, 2005; 8 (3): 401-11.                          


Olfactory and lens placode formation is controlled by the hedgehog-interacting protein (Xhip) in Xenopus., Cornesse Y, Pieler T, Hollemann T., Dev Biol. January 15, 2005; 277 (2): 296-315.                          


Negative regulation of Smad2 by PIASy is required for proper Xenopus mesoderm formation., Daniels M, Shimizu K, Zorn AM, Ohnuma S., Development. November 1, 2004; 131 (22): 5613-26.                                


The involvement of Frodo in TCF-dependent signaling and neural tissue development., Hikasa H, Sokol SY., Development. October 1, 2004; 131 (19): 4725-34.      


Neural induction in Xenopus: requirement for ectodermal and endomesodermal signals via Chordin, Noggin, beta-Catenin, and Cerberus., Kuroda H, Wessely O, De Robertis EM., PLoS Biol. May 1, 2004; 2 (5): E92.                


The initiation of Hox gene expression in Xenopus laevis is controlled by Brachyury and BMP-4., Wacker SA, McNulty CL, Durston AJ., Dev Biol. February 1, 2004; 266 (1): 123-37.                  


PP2A:B56epsilon is required for Wnt/beta-catenin signaling during embryonic development., Yang J, Wu J, Tan C, Klein PS., Development. December 1, 2003; 130 (23): 5569-78.            


Wise, a context-dependent activator and inhibitor of Wnt signalling., Itasaki N, Jones CM, Mercurio S, Rowe A, Domingos PM, Smith JC, Krumlauf R., Development. September 1, 2003; 130 (18): 4295-305.                


PKC delta is essential for Dishevelled function in a noncanonical Wnt pathway that regulates Xenopus convergent extension movements., Kinoshita N, Iioka H, Miyakoshi A, Ueno N., Genes Dev. July 1, 2003; 17 (13): 1663-76.                    


Flamingo, a cadherin-type receptor involved in the Drosophila planar polarity pathway, can block signaling via the canonical wnt pathway in Xenopus laevis., Morgan R, El-Kadi AM, Theokli C., Int J Dev Biol. May 1, 2003; 47 (4): 245-52.              


The IGF pathway regulates head formation by inhibiting Wnt signaling in Xenopus., Richard-Parpaillon L, Héligon C, Chesnel F, Boujard D, Philpott A., Dev Biol. April 15, 2002; 244 (2): 407-17.                    

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