Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects

Human Molecular Genetics

Volumn 10, Issue 21, 2001, Pages 2385-2396

  Lu, Weining ^a,e   Shen, Xiaohua ^a   Pavlova, Anna ^a   Lakkis, Montaha ^a   Ward, Christopher J ^b   Pritchard, Lynn ^c   Harris, Peter C ^b   Genest, David R ^a   Perez Atayde, Antonio R ^a   Zhou, Jing ^d  

^a HARVARD MEDICAL SCHOOL   (United States)

^b MAYO CLINIC   (United States)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d HARVARD INSTITUTES OF MEDICINE   (United States)

^e BRIGHAM AND WOMEN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POLYCYSTIC KIDNEY DISEASE PROTEIN 1; POLYCYSTIN; POLYCYSTIN 1; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DEFECT; BONE DEVELOPMENT; CARTILAGE CELL; CHONDRODYSPLASIA; COMPARATIVE STUDY; CONTROLLED STUDY; EPITHELIUM; FETUS HYDROPS; GENE DELETION; GENE MUTATION; GENE OVEREXPRESSION; GENE TARGETING; HETEROZYGOSITY; HOMOZYGOSITY; HYDRAMNIOS; IMMUNOREACTIVITY; KIDNEY CYST; KIDNEY POLYCYSTIC DISEASE; MOUSE; MOUSE MUTANT; NEURAL TUBE DEFECT; NEWBORN; NONHUMAN; PANCREAS CYST; PANCREAS DISEASE; PHENOTYPE; PRIORITY JOURNAL;

ANIMALIA; HYDROPS;

EID: 0035504102     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.21.2385     Document Type: Article

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