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Summary Anatomy Item Literature (8) Expression Attributions Wiki

Papers associated with m. intermandibularis primordium

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The emergence of Pax7-expressing muscle stem cells during vertebrate head muscle development., Nogueira JM., Front Aging Neurosci. January 1, 2015; 7 62.                                            

Myogenic waves and myogenic programs during Xenopus embryonic myogenesis., Della Gaspera B., Dev Dyn. May 1, 2012; 241 (5): 995-1007.                                    

MIM regulates vertebrate neural tube closure., Liu W., Development. May 1, 2011; 138 (10): 2035-47.                            

Functional analysis of novel mutations in y(+)LAT-1 amino acid transporter gene causing lysinuric protein intolerance (LPI)., Mykkänen J., Hum Mol Genet. February 12, 2000; 9 (3): 431-8.

Boy with syndactylies, macrocephaly, and severe skeletal dysplasia: not a new syndrome, but two dominant mutations (GLI3 E543X and COL2A1 G973R) in the same individual., Sobetzko D., Am J Med Genet. January 31, 2000; 90 (3): 239-42.

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome., Kalff-Suske M., Hum Mol Genet. September 1, 1999; 8 (9): 1769-77.

Point mutations in human GLI3 cause Greig syndrome., Wild A., Hum Mol Genet. October 1, 1997; 6 (11): 1979-84.

Developmental potential., Holmgren RA., Genes Dev. February 1, 1992; 6 (2): 161-5.

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