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Summary Expression Phenotypes Gene Literature (117) GO Terms (12) Nucleotides (141) Proteins (57) Interactants (613) Wiki
XB--484854

Papers associated with gli3 (and OMIM)



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Endosome-Mediated Epithelial Remodeling Downstream of Hedgehog-Gli Is Required for Tracheoesophageal Separation., Nasr T, Mancini P, Rankin SA, Rankin SA, Edwards NA, Agricola ZN, Kenny AP, Kinney JL, Daniels K, Vardanyan J, Han L, Trisno SL, Cha SW, Wells JM, Kofron MJ, Zorn AM., Dev Cell. December 16, 2019; 51 (6): 665-674.e6.                  

Folate-dependent methylation of septins governs ciliogenesis during neural tube closure., Toriyama M, Toriyama M, Wallingford JB, Finnell RH., FASEB J. August 1, 2017; 31 (8): 3622-3635.                    

The amino-terminal region of Gli3 antagonizes the Shh response and acts in dorsoventral fate specification in the developing spinal cord., Meyer NP, Roelink H., Dev Biol. May 15, 2003; 257 (2): 343-55.

Human genetic disease caused by de novo mitochondrial-nuclear DNA transfer., Turner C, Killoran C, Thomas NS, Rosenberg M, Chuzhanova NA, Johnston J, Kemel Y, Cooper DN, Biesecker LG., Hum Genet. March 1, 2003; 112 (3): 303-9.

Pallister-Hall syndrome phenotype in mice mutant for Gli3., Böse J, Grotewold L, Rüther U., Hum Mol Genet. May 1, 2002; 11 (9): 1129-35.

Point mutations in human GLI3 cause Greig syndrome., Wild A, Kalff-Suske M, Vortkamp A, Bornholdt D, König R, Grzeschik KH., Hum Mol Genet. October 1, 1997; 6 (11): 1979-84.

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