A Mutation in the Mouse Ttc26 Gene Leads to Impaired Hedgehog Signaling

PLoS Genetics

Volumn 10, Issue 10, 2014, Pages

  Swiderski, Ruth E ^a   Nakano, Yoko ^a   Mullins, Robert F ^a   Seo, Seongjin ^a   Bánfi, Botond ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

INTRAFLAGELLAR TRANSPORT COMPLEX B; PROTEIN; SUFU PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GLI; TTC26 PROTEIN; UNCLASSIFIED DRUG; GLI PROTEIN, MOUSE; HOMEODOMAIN PROTEIN; HOP PROTEIN, MOUSE; KRUPPEL LIKE FACTOR; REPRESSOR PROTEIN; SIGNAL PEPTIDE; SONIC HEDGEHOG PROTEIN; SUFU PROTEIN, MOUSE; TTC26 PROTEIN, MOUSE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BALB CBY MOUSE; CONTROLLED STUDY; EMBRYO; EMBRYO CELL; EMBRYO PATTERN FORMATION; EUKARYOTIC FLAGELLUM; FIBROBLAST; GAIT; GENE; GENE ACTIVATION; GENE EXPRESSION; HEDGEHOG SIGNALING; HYDROCEPHALUS; MALE STERILITY; MOUSE; MOUSE MUTANT; NEURAL TUBE; NONHUMAN; NONSENSE MUTATION; POLYDACTYLY; PROTEIN BINDING; PROTEIN DEFECT; PROTEIN PROTEIN INTERACTION; PROTEIN SUBUNIT; SIGNAL TRANSDUCTION; TTC26 GENE; ANIMAL; GENETICS; GROWTH, DEVELOPMENT AND AGING; MALE; METABOLISM; MUTATION; PATHOLOGY; PHENOTYPE;

ANIMALS; CILIA; HEDGEHOG PROTEINS; HOMEODOMAIN PROTEINS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; KRUPPEL-LIKE TRANSCRIPTION FACTORS; MALE; MICE; MUTATION; NEURAL TUBE; PHENOTYPE; REPRESSOR PROTEINS; SIGNAL TRANSDUCTION;

EID: 84908315689     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1004689     Document Type: Article

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