Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene: role of Sp1 in allele-specific transcriptional regulation.
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Quantitative prediction of NF-kappa B DNA-protein interactions.Promoter characterization of the novel human matrix metalloproteinase-26 gene: regulation by the T-cell factor-4 implies specific expression of the gene in cancer cells of epithelial originThe Role of Matrix Metalloproteinase Polymorphisms in Ischemic StrokeMeta-analysis of association of the matrix metalloproteinase 2 (-735 C/T) polymorphism with cancer riskPhyscion, a naturally occurring anthraquinone derivative, induces apoptosis and autophagy in human nasopharyngeal carcinomaHow matrix metalloproteinases regulate cell behaviorGenetic variation in the matrix metalloproteinase genes and diabetic nephropathy in type 1 diabetes.Association of matrix metalloproteinase family gene polymorphisms with lung cancer risk: logistic regression and generalized odds of published dataMatrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung developmentMatrix metalloproteinase-2 polymorphisms and clinical outcome of Chinese patients with nonsmall cell lung cancer treated with first-line, platinum-based chemotherapy.A single nucleotide polymorphism in the matrix metalloproteinase 2 promoter is closely associated with high risk of nasopharyngeal carcinoma in Cantonese from southern ChinaEffects of RNA silencing of matrix metalloproteinase-2 on the growth of esophageal carcinoma cells in vivoHighly Protective Association of MMP-2-1306C/T Promoter Polymorphism With Asthma in a North Indian Population: A Pilot StudyGenetic polymorphisms of matrix metalloproteinases and their inhibitors in potentially malignant and malignant lesions of the head and neck.MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI StudySingle-nucleotide polymorphisms of matrix metalloproteinases and their inhibitors in gastrointestinal cancer.Matrix metalloproteinase-2 promoter genotype as a marker of cutaneous T-cell lymphoma early stageAnalysis of MMP2 promoter polymorphisms in childhood obesity.Genetic analysis of polymorphisms in biologically relevant candidate genes in patients with abdominal aortic aneurysms.Role of functional single nucleotide polymorphisms of MMP1, MMP2, and MMP9 in open angle glaucomasAssociation between polymorphisms in the promoter regions of matrix metalloproteinases (MMPs) and risk of cancer metastasis: a meta-analysis.Role of matrix metalloproteinase, tissue inhibitor of metalloproteinase and tumor necrosis factor-alpha single nucleotide gene polymorphisms in inflammatory bowel diseaseThe GC + CC genotype at position -418 in TIMP-2 promoter and the -1575GA/-1306CC genotype in MMP-2 is genetic predisposing factors for prevalence of moyamoya diseaseMatrix metalloproteinases and atherosclerotic plaque instability.Regeneration of aged rat vocal folds using hepatocyte growth factor therapy.MTHFR Glu429Ala and ERCC5 His46His polymorphisms are associated with prognosis in colorectal cancer patients: analysis of two independent cohorts from Newfoundland.Meta-analysis of MMP2, MMP3, and MMP9 promoter polymorphisms and head and neck cancer risk.Regulatory polymorphisms in extracellular matrix protease genes and susceptibility to rheumatoid arthritis: a case-control study.MMP-2, TNF-α and NLRP1 polymorphisms in Chinese patients with ankylosing spondylitis and rheumatoid arthritis.Genetic variation in TIMP1 but not MMPs predict excess FEV1 decline in two general population-based cohorts.Matrix metalloproteinases and genetic mouse models in cancer research: a mini-review.Active matrix metalloprotease-9 is associated with the collagen capsule surrounding the Madurella mycetomatis grain in mycetoma.Functional polymorphisms in the promoter region of MMP-2 and MMP-9 and susceptibility to obstructive sleep apneaMethylenetetrahydrofolate reductase C667T polymorphism is associated with increased risk of coronary artery disease in a Chinese population.Quantifying DNA-protein binding specificities by using oligonucleotide mass tags and mass spectroscopy.Matrix Metalloproteinase-2 Polymorphisms and Incident Coronary Artery Disease: A Meta-Analysis.The pivotal role of matrix metalloproteinases in the development of human abdominal aortic aneurysms.ProMMP-2: TIMP-1 complexes identified in plasma of healthy individualsIschemia-Reperfusion Injury and Ischemic-Type Biliary Lesions following Liver Transplantation.Genetic susceptibility to periapical disease: conditional contribution of MMP2 and MMP3 genes to the development of periapical lesions and healing response
P2860
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P2860
Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene: role of Sp1 in allele-specific transcriptional regulation.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh
2000年學術文章
@zh-hant
name
Identification of novel, funct ...... ic transcriptional regulation.
@en
type
label
Identification of novel, funct ...... ic transcriptional regulation.
@en
prefLabel
Identification of novel, funct ...... ic transcriptional regulation.
@en
P2860
P356
P1476
Identification of novel, funct ...... ic transcriptional regulation.
@en
P2093
P2860
P304
P356
10.1074/JBC.M010242200
P407
P577
2000-12-12T00:00:00Z