Single-nucleotide polymorphisms of the proprotein convertase subtilisin/kexin type 5 (PCSK5) gene

Journal of Human Genetics

Volumn 46, Issue 12, 2001, Pages 730-732

  Cao, H ^a   Mok, A ^a   Miskie, B ^a   Hegele, R A ^a  

^a ROBARTS RESEARCH INSTITUTE   (Canada)

Author keywords

Cardiovascular disease; Complex traits; Genomic DNA; Inflammation; Sequencing

Indexed keywords

ALPHA INTEGRIN; DNA; INTEGRIN; KEXIN; PROPROTEIN CONVERTASE; SUBTILISIN; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; ETHNIC DIFFERENCE; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENETIC ASSOCIATION; HUMAN; INFLAMMATION; NORMAL HUMAN; NUCLEOTIDE SEQUENCE; PCSK5 GENE; PHENOTYPE; PROTEIN DEGRADATION; PROTEIN PROCESSING; SINGLE NUCLEOTIDE POLYMORPHISM; VASCULAR DISEASE;

ALLELES; BASE SEQUENCE; DNA PRIMERS; GENE FREQUENCY; HUMANS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROPROTEIN CONVERTASES; SACCHAROMYCES CEREVISIAE PROTEINS; SUBTILISINS;

EID: 0035670417     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380170008     Document Type: Article

References (4)

1. Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy
2. Endoproteolytic processing of integrin pro-α subunits involves the redundant function of furin and proprotein convertase (PC) 5A, but not paired basic amino acid converting enzyme (PACE) 4, PC5B or PC7
3. Proprotein and prohormone convertases: A family of subtilases generating diverse bioactive polypeptides
4. Assignment of the human proprotein convertase gene PCSK5 to chromosome 9q21.3