Papers associated with bmp4 (and gsc)Search for bmp4 morpholinos using Textpresso
Results 1 - 10 of 109 results
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|Lineage commitment of embryonic cells involves MEK1-dependent clearance of pluripotency regulator Ventx2.
Scerbo P, Marchal L, Kodjabachian L.
Elife. August 17, 2017; 6
|Activation of a T-box-Otx2-Gsc gene network independent of TBP and TBP-related factors.
Gazdag E, Jacobi UG, van Kruijsbergen I, Weeks DL, Veenstra GJ.
Development. April 15, 2016; 143 (8): 1340-50.
|Specification of anteroposterior axis by combinatorial signaling during Xenopus development.
Carron C, Shi DL.
Wiley Interdiscip Rev Dev Biol. March 1, 2016; 5 (2): 150-68.
|Differential requirement of bone morphogenetic protein receptors Ia (ALK3) and Ib (ALK6) in early embryonic patterning and neural crest development.
Schille C, Heller J, Schambony A.
BMC Dev Biol. January 19, 2016; 16 1.
|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.
|Insulin-like factor regulates neural induction through an IGF1 receptor-independent mechanism.
Haramoto Y, Takahashi S, Oshima T, Onuma Y, Ito Y, Asashima M.
Sci Rep. September 21, 2015; 5 11603.
|Temporally coordinated signals progressively pattern the anteroposterior and dorsoventral body axes.
Tuazon FB, Mullins MC.
Semin Cell Dev Biol. June 1, 2015; 42 118-33.
|Notum is required for neural and head induction via Wnt deacylation, oxidation, and inactivation.
Zhang X, Cheong SM, Amado NG, Reis AH, MacDonald BT, Zebisch M, Jones EY, Abreu JG, He X.
Dev Cell. March 23, 2015; 32 (6): 719-30.
|Direct regulation of siamois by VegT is required for axis formation in Xenopus embryo.
Li HY, El Yakoubi W, Shi DL.
Int J Dev Biol. January 1, 2015; 59 (10-12): 443-51.
|Fezf2 promotes neuronal differentiation through localised activation of Wnt/β-catenin signalling during forebrain development.
Zhang S, Li J, Lea R, 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.
|Occupancy of tissue-specific cis-regulatory modules by Otx2 and TLE/Groucho for embryonic head specification.
Yasuoka Y, Suzuki Y, Takahashi S, Someya H, Sudou N, Haramoto Y, Cho KW, Asashima M, Sugano S, Taira M.
Nat Commun. July 8, 2014; 5 4322.
|Inference of the Xenopus tropicalis embryonic regulatory network and spatial gene expression patterns.
Zheng Z, Christley S, Chiu WT, Blitz IL, Xie X, Cho KW, Nie Q.
BMC Syst Biol. January 8, 2014; 8 3.
|A genome-wide survey of maternal and embryonic transcripts during Xenopus tropicalis development.
Paranjpe SS, Jacobi UG, van Heeringen SJ, Veenstra GJ.
BMC Genomics. May 28, 2013; 14 762.
|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.
|Eps15R is required for bone morphogenetic protein signalling and differentially compartmentalizes with Smad proteins.
Callery EM, Park CY, Xu X, Zhu H, Smith JC, Thomsen GH.
Open Biol. April 1, 2012; 2 (4): 120060.
|Transcriptional activation by Oct4 is sufficient for the maintenance and induction of pluripotency.
Hammachi F, Morrison GM, Sharov AA, Livigni A, Narayan S, Papapetrou EP, O'Malley J, Kaji K, Ko MS, Ptashne M, Brickman JM.
Cell Rep. February 23, 2012; 1 (2): 99-109.
|mNanog possesses dorsal mesoderm-inducing ability by modulating both BMP and Activin/nodal signaling in Xenopus ectodermal cells.
Miyazaki A, Ishii K, Yamashita S, Nejigane S, Matsukawa S, Ito Y, Onuma Y, Asashima M, Michiue T.
PLoS One. January 1, 2012; 7 (10): e46630.
|Novel functions of Noggin proteins: inhibition of Activin/Nodal and Wnt signaling.
Bayramov AV, Eroshkin FM, Martynova NY, Ermakova GV, Solovieva EA, Zaraisky AG.
Development. December 1, 2011; 138 (24): 5345-56.
|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.