Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome. [electronic resource]
Producer: 20110818Description: 726-31 p. digitalISSN:- 1546-170X
- Abnormalities, Multiple
- Adaptor Proteins, Vesicular Transport
- Animals
- Antigens, Neoplasm
- Cell Cycle Proteins
- Cerebellar Diseases -- etiology
- Cerebellum -- abnormalities
- Cytoskeletal Proteins
- Disease Models, Animal
- Eye Abnormalities -- etiology
- Humans
- Kidney Diseases, Cystic -- etiology
- Lithium -- pharmacology
- Magnetic Resonance Imaging
- Mice
- Mice, Mutant Strains
- Nuclear Proteins -- genetics
- Phenotype
- Proto-Oncogene Proteins -- genetics
- Retina -- abnormalities
- Signal Transduction -- drug effects
- Wnt Proteins -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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