A single nucleotide polymorphism in the promoter of the LOXL1 gene and its relationship to pelvic organ prolapse and preterm premature rupture of membranes
about
Genetic epidemiology of pelvic organ prolapse: a systematic reviewSpontaneous preterm birth and single nucleotide gene polymorphisms: a recent updatePseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1.The association between sex-related interleukin-6 gene polymorphisms and the risk for cerebral palsyMajor LOXL1 risk allele is reversed in exfoliation glaucoma in a black South African population.Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse?A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).Mutation screen of LOXL1 in patients with female pelvic organ prolapseLOXL1 promoter haplotypes are associated with exfoliation syndrome in a U.S. Caucasian population.Systematic review and metaanalysis of genetic association studies of urinary symptoms and prolapse in women.Identification of six loci associated with pelvic organ prolapse using genome-wide association analysisLOXL1 gene variants and their association with pseudoexfoliation glaucoma (XFG) in Spanish patients.Verification of the Chromosome Region 9q21 Association with Pelvic Organ Prolapse Using RegulomeDB AnnotationsCircumferential iris transillumination defects in exfoliation syndrome.Review: The role of LOXL1 in exfoliation syndrome/glaucomaGenetics of pelvic organ prolapse: crossing the bridge between bench and bedside in urogynecologic research.Molecular genetics in glaucoma.Uterine prolapse in pregnancy: risk factors, complications and management.Genetics of exfoliation syndrome and glaucomaLysyl oxidase-like 1 polymorphisms in a southwestern Greek cataract population with pseudoexfoliation syndrome.Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome.
P2860
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P2860
A single nucleotide polymorphism in the promoter of the LOXL1 gene and its relationship to pelvic organ prolapse and preterm premature rupture of membranes
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 30 January 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
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name
A single nucleotide polymorphi ...... premature rupture of membranes
@en
A single nucleotide polymorphi ...... remature rupture of membranes.
@nl
type
label
A single nucleotide polymorphi ...... premature rupture of membranes
@en
A single nucleotide polymorphi ...... remature rupture of membranes.
@nl
prefLabel
A single nucleotide polymorphi ...... premature rupture of membranes
@en
A single nucleotide polymorphi ...... remature rupture of membranes.
@nl
P2093
P2860
P356
P1476
A single nucleotide polymorphi ...... premature rupture of membranes
@en
P2093
Catherine A Matthews
Georgia Ferrell
Jerome F Strauss
Mary D Sammel
Paul Stoddard
Roberto Romero
P2860
P304
P356
10.1177/1933719108330567
P577
2009-01-30T00:00:00Z