???pagination.result.count???
???pagination.result.page???
1
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome. , Ufartes R, Berger H, Till K, Salinas G, Sturm M, Altmüller J, Nürnberg P, Thiele H, Funke R, Apeshiotis N, Langen H, Wollnik B, Borchers A , Pauli S., Hum Genet. November 1, 2020; 139 (11): 1363-1379.
Modeling Bainbridge-Ropers Syndrome in Xenopus laevis Embryos. , Lichtig H, Artamonov A, Polevoy H, Reid CD, Bielas SL, Frank D ., Front Physiol. January 1, 2020; 11 75.
Studying the role of axon fasciculation during development in a computational model of the Xenopus tadpole spinal cord. , Davis O, Merrison-Hort R, Soffe SR , Borisyuk R., Sci Rep. October 19, 2017; 7 (1): 13551.
The splicing factor PQBP1 regulates mesodermal and neural development through FGF signaling. , Iwasaki Y , Thomsen GH ., Development. October 1, 2014; 141 (19): 3740-51.
Maternal xNorrin, a canonical Wnt signaling agonist and TGF-β antagonist, controls early neuroectoderm specification in Xenopus. , Xu S, Cheng F, Liang J, Wu W, Zhang J., PLoS Biol. January 1, 2012; 10 (3): e1001286.
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. , Barnett C, Yazgan O, Kuo HC, Malakar S, Thomas T, Fitzgerald A, Harbour W, Henry JJ , Krebs JE., Mech Dev. January 1, 2012; 129 (9-12): 324-38.
Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/ SIP1 and NuRD corepressor complex. , Verstappen G, van Grunsven LA, Michiels C, Van de Putte T, Souopgui J, Van Damme J, Bellefroid E , Vandekerckhove J, Huylebroeck D ., Hum Mol Genet. April 15, 2008; 17 (8): 1175-83.
Eye and neural defects associated with loss of GDF6. , Hanel ML, Hensey C., BMC Dev Biol. June 6, 2006; 6 43.
Maternal wnt11 activates the canonical wnt signaling pathway required for axis formation in Xenopus embryos. , Tao Q , Tao Q , Yokota C, Puck H, Kofron M , Birsoy B, Yan D, Asashima M , Wylie CC , Lin X, Heasman J ., Cell. March 25, 2005; 120 (6): 857-71.
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. , Stancheva I , Collins AL, Van den Veyver IB, Zoghbi H, Meehan RR ., Mol Cell. August 1, 2003; 12 (2): 425-35.