Renal cystic diseases: Diverse phenotypes converge on the cilium/centrosome complex

Pediatric Nephrology

Volumn 21, Issue 10, 2006, Pages 1369-1376

  Guay Woodford, Lisa M ^a,b  

^a University of Alabama at Birmingham   (United States)

^b UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

Centrosome; Primary cilium; Renal cystic disease

Indexed keywords

CYCLIC AMP; CYSTOPROTEIN; GENE PRODUCT; UNCLASSIFIED DRUG;

AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; BARDET BIEDL SYNDROME; CELL DIFFERENTIATION; CENTROSOME; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; DYSOSTOSIS; EUKARYOTIC FLAGELLUM; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; JOUBERT SYNDROME; KIDNEY EPITHELIUM; KIDNEY FAILURE; KIDNEY POLYCYSTIC DISEASE; KIDNEY TUBULE; MECKEL SYNDROME; NEPHRONOPHTHISIS; ONSET AGE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN LOCALIZATION; REVIEW; SIGNAL TRANSDUCTION; TRANSCRIPTION REGULATION; X CHROMOSOME LINKED DISORDER;

ADOLESCENT; CALCIUM; CENTROSOME; CHILD; CHILD, PRESCHOOL; CILIA; CYCLIC AMP; HUMANS; KIDNEY DISEASES, CYSTIC; PHENOTYPE; WNT PROTEINS;

EID: 33747851112     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-006-0164-9     Document Type: Review

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