Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Gene Literature (467) GO Terms (27) Nucleotides (241) Proteins (41) Interactants (2118) Wiki
XB--1017497

Papers associated with myod1 (and OMIM)

Search for myod1 morpholinos using Textpresso

Limit to papers also referencing gene:
Show all myod1 papers

Results 1 - 5 of 5 results

Page(s): 1

Sort Newest To Oldest Sort Oldest To Newest

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.          


Current status and future prospect of FSHD region gene 1., Hansda AK, Tiwari A, Dixit M., J Biosci. June 1, 2017; 42 (2): 345-353.


Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA, Woolf AS, Stuart HM, Thuret R, McKenzie EA, Newman WG, Hilton EN., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.                


Paraxial T-box genes, Tbx6 and Tbx1, are required for cranial chondrogenesis and myogenesis., Tazumi S, Yabe S, Uchiyama H., Dev Biol. October 15, 2010; 346 (2): 170-80.                                


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.            

Page(s): 1

Xenbase: The Xenopus Model Organism Knowledgebase.
Version: 4.14.0
Major funding for Xenbase is provided by grant P41 HD064556