A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes.
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Association of a specific haplotype across the genes MMP1 and MMP3 with radiographic joint destruction in rheumatoid arthritisGenetic Influences on the Development of Fibrosis in Crohn's DiseaseIs there a role for probiotics in the prevention of preterm birth?Association between promoter -1607 polymorphism of MMP1 and lumbar disc disease in Southern ChineseA population-based study of race-specific risk for placental abruption.Polymorphism +17 C/G in matrix metalloprotease MMP8 decreases lung cancer risk.California Very Preterm Birth Study: design and characteristics of the population- and biospecimen bank-based nested case-control study.Vaginal and oral microbes, host genotype and preterm birthBiglycan and decorin differentially regulate signaling in the fetal membranesUbiquitin-Proteasome-Collagen (CUP) Pathway in Preterm Premature Rupture of Fetal Membranes.The matrix metalloproteases and endothelin-1 in infection-associated preterm birth.Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranes.dbPTB: a database for preterm birth.A bioinformatics approach to preterm birth.Role of matrix metalloproteinase, tissue inhibitor of metalloproteinase and tumor necrosis factor-alpha single nucleotide gene polymorphisms in inflammatory bowel diseaseGenetic susceptibility to total hip arthroplasty failure: a case-control study on the influence of MMP 1 gene polymorphismPathway analysis of genetic factors associated with spontaneous preterm birth and pre-labor preterm rupture of membranes.Promoter polymorphisms in matrix metallopeptidase 1 and risk of cutaneous melanoma.A genetic association study of maternal and fetal candidate genes that predispose to preterm prelabor rupture of membranes (PROM).The role of genetic polymorphisms in antioxidant enzymes and potential antioxidant therapies in neonatal lung diseaseFunctional polymorphisms of matrix metalloproteinases 1 and 9 genes in women with spontaneous preterm birthSingle blastomere removal from murine embryos is associated with activation of matrix metalloproteinases and Janus kinase/signal transducers and activators of transcription pathways of placental inflammation.Matrix metalloproteinase 1, 3, and 9 polymorphisms and esophageal squamous cell carcinoma risk.Connective tissue and related disorders and preterm birth: clues to genes contributing to prematurity.A functional SNP in the promoter of the SERPINH1 gene increases risk of preterm premature rupture of membranes in African Americans.Impaired collagen chaperone results in preterm PROMIntrauterine infection and preterm labor.Compensatory fetal membrane mechanisms between biglycan and decorin in inflammation.Altered Expression Levels of MMP1, MMP9, MMP12, TIMP1, and IL-1β as a Risk Factor for the Elevated IOP and Optic Nerve Head Damage in the Primary Open-Angle Glaucoma Patients.Targeted Sequencing and Meta-Analysis of Preterm Birth.Biomarkers for the prediction of preterm delivery.The clinical significance of a positive Amnisure test in women with preterm labor and intact membranesGenetic variation associated with preterm birth: a HuGE review.Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm premature rupture of membranesAssociation of MMP1-1607 1G/2G and TIMP1 372 T/C gene polymorphisms with risk of primary open angle glaucoma in a Polish populationEvidence for a role for the adaptive immune response in human term parturitionPrevention of PPROM: current and future strategies.Genetic polymorphisms associated with intervertebral disc degeneration.Matrix metalloproteinases and their tissue inhibitors in preterm perinatal complications.Different secretion patterns of matrix metalloproteinases and IL-8 and effect of corticotropin-releasing hormone in preterm and term cervical fibroblasts.
P2860
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P2860
A single nucleotide polymorphism in the matrix metalloproteinase-1 (MMP-1) promoter influences amnion cell MMP-1 expression and risk for preterm premature rupture of the fetal membranes.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
A single nucleotide polymorphi ...... upture of the fetal membranes.
@en
type
label
A single nucleotide polymorphi ...... upture of the fetal membranes.
@en
prefLabel
A single nucleotide polymorphi ...... upture of the fetal membranes.
@en
P2093
P2860
P50
P356
P1476
A single nucleotide polymorphi ...... rupture of the fetal membranes
@en
P2093
George Macones
Jerome F Strauss
Mary Sammel
Samuel Parry
Toshio Fujimoto
P2860
P304
P356
10.1074/JBC.M107865200
P407
P577
2001-12-11T00:00:00Z