Role of cilia in structural birth defects: Insights from ciliopathy mutant mouse models

Birth Defects Research Part C - Embryo Today: Reviews

Volumn 102, Issue 2, 2014, Pages 115-125

  Rao Damerla, Rama ^a   Gabriel, George C ^a   Li, You ^a   Klena, Nikolai T ^a   Liu, Xiaoqin ^a   Chen, Yu ^a   Cui, Cheng ^a   Pazour, Gregory J ^b   Lo, Cecilia W ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

Author keywords

Cilia; Ciliopathies; Congenital heart disease; ENU mutagenesis screen; Structural birth defects

Indexed keywords

ALSTROM SYNDROME; ARTICLE; BARDET BIEDL SYNDROME; BIRTH DEFECT; BRAIN MALFORMATION; CALCIUM SIGNALING; CELL ORGANELLE; CELL TYPE; CILIARY DYSKINESIA; CILIARY MOTILITY; CILIOPATHY; CLEFT PALATE; CRANIOFACIAL MALFORMATION; DISEASE MODEL; EUKARYOTIC FLAGELLUM; GENE LOCUS; GENE MUTATION; HUMAN; JOUBERT SYNDROME; KIDNEY POLYCYSTIC DISEASE; LEBER CONGENITAL AMAUROSIS; MECKEL SYNDROME; MOUSE MUTANT; MULTIPLE MALFORMATION SYNDROME; NEPHRONOPHTHISIS; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; RETINA DYSTROPHY; RETINITIS PIGMENTOSA; SECKEL SYNDROME; SIGNAL TRANSDUCTION; ANIMAL; BRAIN; CONGENITAL DISORDER; CONGENITAL HEART MALFORMATION; DYSKINESIA; GENETICS; HIGH THROUGHPUT SEQUENCING; MOUSE; MUTATION; PATHOLOGY;

ANIMALS; BRAIN; CILIA; CONGENITAL ABNORMALITIES; DISEASE MODELS, ANIMAL; DYSKINESIAS; HEART DEFECTS, CONGENITAL; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; MICE; MUTATION; ORGANELLES; SIGNAL TRANSDUCTION;

EID: 84903155477     PISSN: 1542975X     EISSN: 15429768     Source Type: Journal    
DOI: 10.1002/bdrc.21067     Document Type: Article

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