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ADAMTS3 encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family.
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Molecular cloning and in silico analysis identify potential transcription factor binding sites in the ADAMTS3 promoter region and show that SP1 (show PSG1 Antibodies) downregulated ADAMTS3 transcriptional activity in osteosarcoma cell lines. As consistent with the transcriptional activity, mRNA, and protein expression levels were also decreased by SP1 (show PSG1 Antibodies).
Results corroborate the recent in vitro and murine data that suggest a close functional interaction between ADAMTS3 and CCBE1 (show CCBE1 Antibodies) in triggering VEGFR3 (show FLT4 Antibodies) signaling, a cornerstone for the differentiation and function of lymphatic endothelial cells.
Findings suggest that these MMP16 (show MMP16 Antibodies) rs10090371, ADAMTS3 rs788935, TLL2 (show TLL2 Antibodies) rs10882807 and MMP9 (show MMP9 Antibodies) rs3918251 may be promising prognostic biomarkers for cutaneous melanoma specific survival (CMSS).
The pregnancy loss rate seems to be affected by both ADAMTS-3 and ADAMTS-16 (show ADAMTS16 Antibodies).
Data indicate that ADAMTS2 (show ADAMTS4 Antibodies) and 3 cleave the amino-propeptide of fibrillar collagens and regulate blood vessels homeostasis and lymphangiogenesis. [review]
ADAMTS-2 (show ADAMTS4 Antibodies), -3, and -13 expression, but not that of ADAMTS-14 (show ADAMTS14 Antibodies), are increased in plaques causing AMI (show CFD Antibodies) compared those associated with stable angina.
ADAMTS-3 was identified as the protease that cleaves and inactivates Reelin in the cerebral cortex and hippocampus. ADAMTS-3 was expressed in the excitatory neurons of the embryonic and postnatal cerebral cortex and hippocampus.
an ADAMTS3 knockout mouse (Adamts3(-/-)) model was created to determine in vivo the actual functions of ADAMTS3.
This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene is the major procollagen II N-propeptidase. A deficiency of this protein may be responsible for dermatosparaxis, a genetic defect of connective tissues.
A disintegrin and metalloproteinase with thrombospondin motifs 3
, ADAM-TS 3
, PC II-NP
, a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 3
, procollagen II N-proteinase
, procollagen II amino propeptide-processing enzyme
, zinc metalloendopeptidase
, ADAM metallopeptidase with thrombospondin type 1 motif, 3