Talpid3-binding centrosomal protein Cep120 is required for centriole duplication and proliferation of cerebellar granule neuron progenitors

PLoS ONE

Volumn 9, Issue 9, 2014, Pages

  Wu, Chuanqing ^a,b   Yang, Mei ^b,c   Li, Juan ^b,d,f   Wang, Chengbing ^b   Cao, Ting ^b,e   Tao, Kaixiong ^a   Wang, Baolin ^b  

^a UNION HOSPITAL   (China)

^b WEILL CORNELL MEDICAL COLLEGE   (United States)

^c CHONGQING MEDICAL UNIVERSITY   (China)

^d SHANDONG UNIVERSITY   (China)

^e NANJING UNIVERSITY   (China)

^f CLIN RESEARCH INSTITUTE OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CELL PROTEIN; CEP120 PROTEIN; SONIC HEDGEHOG PROTEIN; TALPID3 PROTEIN; UNCLASSIFIED DRUG; CELL CYCLE PROTEIN; CEP120 PROTEIN, MOUSE; TALPID3 PROTEIN, MOUSE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CELL PROLIFERATION; CENTRAL NERVOUS SYSTEM; CENTRIOLE; CEREBELLUM CELL; CEREBELLUM HYPOPLASIA; CONGENITAL HEART MALFORMATION; CONTROLLED STUDY; CYTOLOGY; DEATH; DISEASE SEVERITY; EMBRYO; EPENDYMA CELL; EUKARYOTIC FLAGELLUM; FEMALE; GENE INACTIVATION; GENE MUTATION; GESTATION PERIOD; GRANULE NEURAL STEM CELL; HYDROCEPHALUS; MALE; MOUSE; MOUSE MUTANT; NEURAL STEM CELL; NEWBORN; NONHUMAN; PROTEIN BINDING; PROTEIN DEPLETION; PROTEIN INTERACTION; PROTEIN LOCALIZATION; ANIMAL; C57BL MOUSE; CELL CULTURE; CEREBELLUM; CONGENITAL MALFORMATION; DEVELOPMENTAL DISORDER; GENE DELETION; GENETICS; METABOLISM; NERVOUS SYSTEM MALFORMATION; PROTEIN PROTEIN INTERACTION; SIGNAL TRANSDUCTION; ULTRASTRUCTURE;

ANIMALS; CELL CYCLE PROTEINS; CELL PROLIFERATION; CELLS, CULTURED; CENTRIOLES; CEREBELLUM; DEVELOPMENTAL DISABILITIES; FEMALE; GENE DELETION; HYDROCEPHALUS; MALE; MICE; MICE, INBRED C57BL; NERVOUS SYSTEM MALFORMATIONS; NEURAL STEM CELLS; PROTEIN INTERACTION MAPS; SIGNAL TRANSDUCTION;

EID: 84907457202     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0107943     Document Type: Article

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