Proprotein convertase subtilisin/kexin-type 1 (PCSK1) activates precursors pro-opiomelanocortin (POMC), proinsulin and prorenin. We investigated if common variants in the PCSK1 gene influence blood pressure and risk of hypertension. Additionally, we investigated the risk of obesity and type 2 diabetes (T2D). In the Rotterdam Study (RS1), a prospective, population-based cohort (n = 5974), four single-nucleotide polymorphisms (rs10515237, rs6232, rs436321 and rs3792747) in PCSK1 were studied. Linear and Cox regression models served to analyze associations between variants and end points. Replication was performed in the Rotterdam Study Plus1 (RSPlus1, n = 1895). Rs436321 was significantly associated with systolic and diastolic blood pressure ...
Proprotein convertase subtilisin/kexin (PCSK) enzymes cleave and convert their immature substrates i...
Insulin and glucagon-like peptide 1 (GLP-1), converted by proprotein convertase 1 (PC1/3) from proin...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
[[abstract]]Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recentl...
Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recently been assoc...
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which enco...
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body...
Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity ...
BackgroundCommon single nucleotide polymorphisms (SNPs) in proprotein convertase subtilisin/kexin ty...
Abstract Objective Many different genetic variants of proprotein convertase subtilisin kexin 9 (PCSK...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
[[abstract]]Proprotein convertase subtilisin/kexin type 2 (PCSK2) is a prohormone processing enzyme ...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
Common variants in PCSK1 have been reported to be associated with obesity in populations of European...
Variants in Proprotein Convertase Subtilisin/Kexin Type 1 (PCSK1) may be causative for obesity as su...
Proprotein convertase subtilisin/kexin (PCSK) enzymes cleave and convert their immature substrates i...
Insulin and glucagon-like peptide 1 (GLP-1), converted by proprotein convertase 1 (PC1/3) from proin...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...
[[abstract]]Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recentl...
Prohormone convertase subtilisin/kexin type 1 (PCSK1) genetic polymorphisms have recently been assoc...
Congenital deficiency of the proprotein convertase subtilisine/kexin type 1 gene (PCSK1), which enco...
Polymorphisms rs6232 and rs6234/rs6235 in PCSK1 have been associated with extreme obesity [e.g. body...
Recently, the rs6232 (N221D) and rs6235 (S690T) SNPs in the PCSK1 gene were associated with obesity ...
BackgroundCommon single nucleotide polymorphisms (SNPs) in proprotein convertase subtilisin/kexin ty...
Abstract Objective Many different genetic variants of proprotein convertase subtilisin kexin 9 (PCSK...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
[[abstract]]Proprotein convertase subtilisin/kexin type 2 (PCSK2) is a prohormone processing enzyme ...
Common PCSK1 variants (notably rs6232 and rs6235) have been shown to be associated with obesity in E...
Common variants in PCSK1 have been reported to be associated with obesity in populations of European...
Variants in Proprotein Convertase Subtilisin/Kexin Type 1 (PCSK1) may be causative for obesity as su...
Proprotein convertase subtilisin/kexin (PCSK) enzymes cleave and convert their immature substrates i...
Insulin and glucagon-like peptide 1 (GLP-1), converted by proprotein convertase 1 (PC1/3) from proin...
International audienceBackground: Rare biallelic pathogenic mutations in PCSK1 (encoding proprotein ...