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Showing 1-17 of 17 results for "SRP3117" within Papers
Regulation of matrix metalloproteinase expression in tumor invasion.
Westermarck J and Kahari VM
Faseb Journal, 13, 781-792 (1999)
Annie Pardo et al.
The international journal of biochemistry & cell biology, 37(2), 283-288 (2004-10-12)
The matrix metalloproteinases (MMPs) are a family of zinc-containing endopeptidases that play a key role in both physiological and pathological tissue remodeling. Human fibroblast collagenase (MMP-1) was the first vertebrate collagenase purified as a protein and cloned as a cDNA
Expression profiles of MMP-1 and TIMP-1 in lumbar intervertebral disc degeneration.
Deng B
Genetics and molecular research : GMR, 14, 19080-19086 (2015)
Haplotypes in matrix metalloproteinase gene cluster on chromosome 11q22 contribute to the risk of lung cancer development and progression.
Clinical Cancer Research, 12, 7009-7017 (2006)
Dynamics of matrix turnover during pathologic remodeling of the extracellular matrix.
Stetler-Stevenson WG
The American Journal of Pathology, 148, 1345-1350 (1996)
S M Wojtowicz-Praga et al.
Investigational new drugs, 15(1), 61-75 (1997-01-01)
The matrix metalloproteinases (MMPs) are a family of at least fifteen secreted and membrane-bound zinc-endopeptidases. Collectively, these enzymes can degrade all of the components of the extracellular matrix, including fibrallar and non-fibrallar collagens, fibronectin, laminin and basement membrane glycoproteins. MMPs
Activated interstitial myofibroblasts express catabolic enzymes and mediate matrix remodeling in myxomatous heart valves.
Rabkin E
Circulation, 104, 2525-2532 (2001)
Transcriptional regulation of collagenase (MMP-1, MMP-13) genes in arthritis: integration of complex signaling pathways for the recruitment of gene-specific transcription factors.
Vincenti MP and Brinckerhoff CE
Arthritis Research, 4, 157-164 (2002)
Matrix metalloproteinases in coronary artery disease.
Mittal B
Advances in Clinical Chemistry, 64, 1-72 (2014)
Chi Huu Nguyen et al.
Oncotarget, 6(36), 39262-39275 (2015-10-30)
RELA, RELB, CREL, NFKB1 and NFKB2, and the upstream regulators NEMO and NIK were knocked-down in lymph endothelial cells (LECs) and in MDA-MB231 breast cancer spheroids to study the contribution of NF-κB in vascular barrier breaching. Suppression of RELA, NFKB1
Matrix metalloproteinases: role in skeletal development and growth plate disorders.
Malemud CJ
Frontiers in Bioscience, 11, 1702-1715 (2006)
MMP-2, MMP-9, TIMP-1 and TIMP-2 levels in patients with rheumatoid arthritis and psoriatic arthritis.
Giannelli G
Clinical and Experimental Rheumatology, 22, 335-338 (2004)
High MMP-1, MMP-2, and MMP-9 protein levels in osteoarthritis.
Zeng GQ
Genetics and molecular research : GMR, 14, 14811-14822 (2015)
Joanna Sikora et al.
Journal of biomedical optics, 20(5), 051039-051039 (2015-03-13)
The concentration of collagen degradation products (CDPs) may reflect the process of left ventricular remodeling (LVR). The aim of this study was to evaluate the potential diagnostic usefulness of time-resolved fluorescence spectroscopy (TRFS) in assessment of CDPs. The preliminary experiment
Influence of Matrix metalloproteinase 1 and 3 genetic variations on susceptibility and severity of juvenile idiopathic arthritis.
Abd-Allah SH
IUBMB Life, 67, 934-942 (2015)
MMP-2 functions as an early response protein in ovarian cancer metastasis.
Kenny HA
Cell Cycle, 8, 683-688 (2009)
Meagan E Ita et al.
Frontiers in bioengineering and biotechnology, 10, 926675-926675 (2022-08-23)
Chronic joint pain is a major healthcare challenge with a staggering socioeconomic burden. Pain from synovial joints is mediated by the innervated collagenous capsular ligament that surrounds the joint and encodes nociceptive signals. The interstitial collagenase MMP-1 is elevated in
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