Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes.

Tabler, Jacqueline M

Fuz mutant mice reveal shared mechanisms between ciliopathies and FGF-related syndromes. [electronic resource] - Developmental cell Jun 2013 - 623-35 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

1878-1551

10.1016/j.devcel.2013.05.021 doi


Animals
Bardet-Biedl Syndrome--genetics
Cell Movement--physiology
Ciliary Motility Disorders--genetics
Craniofacial Abnormalities--genetics
Cytoskeletal Proteins
Disease Models, Animal
Fibroblast Growth Factor 8--genetics
Intracellular Signaling Peptides and Proteins--genetics
Kruppel-Like Transcription Factors--genetics
Maxilla--abnormalities
Mice
Mice, Mutant Strains
Neural Crest--abnormalities
Orofaciodigital Syndromes--genetics
Palate--abnormalities
Phenotype
Zinc Finger Protein GLI1