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Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Zusätzlich bieten wir Ihnen Matrix Metallopeptidase 13 (Collagenase 3) Antikörper (290) und Matrix Metallopeptidase 13 (Collagenase 3) Kits (144) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 42 products:
A strong association between the -77 MMP-13 polymorphism and posterior tibial tendinopathy insufficiency.
Data show that AJUBA (zeige AJUBA Proteine) upregulated MMP10 (zeige MMP10 Proteine) and MMP13 expression in esophageal squamous cell carcinoma (ESCC).
TGF-beta1 (zeige TGFB1 Proteine) stimulates the phosphorylation of Runx2 (zeige RUNX2 Proteine) at three serine amino acids, and this event is required for MMP-13 expression in osteoblastic cells.
IL-6 (zeige IL6 Proteine)-stimulated MMP-13 expression was independent of IL-1beta (zeige IL1B Proteine) stimulation and was blocked by SAHA, suggesting that SAHA inhibits IL-6 (zeige IL6 Proteine) signaling in Osteoarthritis (OA) chondrocytes.
High MMP13 expression is associated with intervertebral disc degeneration.
data demonstrate that MMP-13 is critical for the development of osteolytic lesions in Multiple myeloma and that targeting the MMP-13 protein - rather than its catalytic activity - constitutes a potential approach to mitigating bone disease in affected patients.
Endoplasmic reticulum stress participates in the progress of senescence and apoptosis of osteoarthritic chondrocytes, which manifested in increased expression of ADAMTS5 (zeige ADAMTS5 Proteine), MMP13, and decreased COL2A1 (zeige COL2A1 Proteine) expression.
Matrix metalloprotease (MMP) regulation was the top pathway involved in gingival aging. MMP3 (zeige MMP3 Proteine), MMP9 (zeige MMP9 Proteine), MMP12 (zeige MMP12 Proteine), and MMP13 were upregulated in old gingival tissues, concomitantly with interleukin-1 beta (IL1B (zeige IL1B Proteine)) expression.
these findings support roles for both cFOS (indirect) and ATF3 (zeige ATF3 Proteine) (direct) in effecting MMP13 transcription in human chondrocytes.
Oxytocin prevents cartilage matrix destruction via regulating MMP1 (zeige MMP1 Proteine) and MMP13.
the phenotype seen in the Hdac4 (zeige HDAC5 Proteine)(-/-) mice is partially derived from elevation in MMP-13 and may be due to a bone remodeling disorder caused by overexpression of this enzyme.
MEF2C (zeige MEF2C Proteine) is necessary for Mmp13 gene expression at the transcriptional level and participates in PTH (zeige PTH Proteine)-stimulated Mmp13 gene expression by increased binding to c-FOS at the AP-1 (zeige JUN Proteine) site in the Mmp13 promoter.
data reveal a novel involvement of MMP-13 in regulating dendritic cell (DC) immunobiology through moderating MHC-I surface presentation, endocytosis and cytokine/chemokine (zeige CCL1 Proteine) secretion; furthermore, the reduced MHC-I surface presentation by DCs resulted in a poor CD8 (zeige CD8A Proteine)(+) T-cell response in vitro; MMP-13 might be a promising target for therapeutic intervention in inflammatory diseases
The progressive process of articular cartilage degeneration was significantly delayed in the knee joints of Ddr2 (zeige DDR2 Proteine)-deficient mice in comparison to their control littermates. Articular cartilage damage in the knee joints of the mice was associated with increased expression profiles of both Ddr2 (zeige DDR2 Proteine) and matrix metalloproteinase 13.
Postnatal chondrocyte-specific deletion of Hdac3 (zeige HDAC3 Proteine) with an inducible Col2a1 (zeige COL2A1 Proteine)-Cre caused premature production of pErk1/2 and Mmp13 in the growth plate.
Mmp13 is selectively regulated of by 1,25-Dihydroxyvitamin D3, PTH (zeige PTH Proteine), and Osterix (zeige SP7 Proteine) through distal enhancers.
Our study contributes to the understanding of the role of HIF1alpha (zeige HIF1A Proteine) in OA and highlights the HIF1alpha (zeige HIF1A Proteine)-beta-catenin (zeige CTNNB1 Proteine) interaction, thus providing new insights into the impact of hypoxia in articular cartilage.
Matrix metalloproteinases (MMP) are effectors of hippocampal neuroplasticity in the adult central nervous system and that the MMP-1 (zeige MMP1 Proteine)/protease-activated receptor-1 (zeige F2R Proteine) axis may play a role in neurogenesis following physiological and/or pathological stimuli.
IL-1Ra (zeige IL1RN Proteine) is associated with MMP-13 expression and has a novel function in such regulation without interference of the IL-1 (zeige IL1A Proteine) signaling cascade.
We reveal a novel role of AP-2epsilon in the regulation of gene expression in articular chondrocytes, as well as in osteoarthritis development, through modulation of Mmp13 expression and activity.
p38 (zeige MAPK14 Proteine) phosphorylation and MMP13 expression are regulated by Rho/ROCK activation, and support the potential novel pathway that Rho/ROCK is in the upper part of the mechanical stress-induced matrix degeneration cascade in cartilage.
These data identify atypical PKC isozymes as STAT and ERK activators that mediate c-fos and collagenase expression.
MMP-13 treatment of fresh articular cartilage results in cleaved fibromodulin (zeige FMOD Proteine) fragments
increased in bovine preovulatory follicles following the gonadotropin surge but no up-regulation of MMP-1 (zeige MMP1 Proteine) and MMP-13 (follicular apex (zeige APEX1 Proteine) vs. base) for the preovulatory collagenolysis required for follicle rupture
involvement of p38 MAP kinase (zeige MAPK14 Proteine) in the hyaluronan oligosaccharide induction of MMP-13
MMP-13 and collagenase have roles in chondrocyte hypertrophy induced by type II collagen (zeige COL2A1 Proteine)
At high but naturally occurring concentrations the collagen peptide CB12-II induced an increase in the expressions of MMP-13 and cleavage of type II collagen (zeige COL2A1 Proteine) by collagenase in the mid zone and also in the superficial zone.
XCL3 and XCL4 can be differentially induced by prolactin (zeige PRL Proteine) and thyroid hormone (zeige PTH Proteine)(3)
MeHg impairs tail development at least partially by activation of the tissue remodeling proteases Mmp9 (zeige MMP9 Proteine) and Mmp13.
Zebra fish embryogenesis requires MMP-13 and dexamethasone and hydrocortisone modulate the expression of this gene, leading to increased activity and potentially contributing to subsequent dysmorphogenesis.
JNK (zeige MAPK8 Proteine)-Mmp13 signaling pathway plays an essential role in regulating the innate immune cell migration in response to severe injury in vivo
These results suggest that PEP-1-SIRT2 (zeige SIRT2 Proteine) promotes matrix metalloproteinases-induced dedifferentiation via ERK (zeige MAPK1 Proteine) signaling in articular chondrocytes.
chitosan-pDNA nanoparticles encoding shRNA targeting MMP-3 (zeige MMP3 Proteine) and -13 had great potential in silencing the dedifferentiation-related genes for regenerating prolonged and endurable cartilage.
Leptin (zeige LEP Proteine) can induce MMP-13 and have a synergistic induction effect on NO with TNF-alpha (zeige TNF Proteine) in rabbit articular chondrocytes in vitro.
The DNA microarray analysis for matrix metalloproteinase (MMP)-related mRNA expression in equine superficial digital flexor tendinitis indicated that mRNA level of MMP-13 was apparently up-regulated in the tendinitis as compared to normal tendon.
TNF-alpha (zeige TNF Proteine) induced MMP-13 expression by condylar cells might be involved in the degradation of the juvenile condyle.
Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. The protein encoded by this gene cleaves type II collagen more efficiently than types I and III. It may be involved in articular cartilage turnover and cartilage pathophysiology associated with osteoarthritis. The gene is part of a cluster of MMP genes which localize to chromosome 11q22.3.
, collagenase 3
, matrix metalloproteinase 13 (collagenase 3)
, interstitial collagenase
, matrix metalloproteinase 13
, matrix metalloproteinase-13
, gene 11
, matrix metallopeptidase 13 (collagenase 3)
, gene A
, collagenase 3-like