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COL1A2 wt Allele

Known as: Collagen, Type I, Alpha 2 wt Allele, Osteogenesis Imperfecta Type IV Gene, COL1A2 
Human COL1A2 wild-type allele is located in the vicinity of 7q22.1 and is approximately 37 kb in length. This allele, which encodes collagen alpha-2… Expand
National Institutes of Health

Related topics

Related topics

14 relations
7q22.1COL1A1 geneCOL1A2 geneCell Adhesion
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A feature-based analysis identifies COL1A2 as a regulator in pancreatic cancer
  • J. Wu, J. Liu, +4 authors L. Song
  • Journal of enzyme inhibition and medicinal…
  • 2019
    • Corpus ID: 58011204
Abstract This study aimed to identify genetic biomarkers in pancreatic cancer (PC) and explore its function in PC via a feature… Expand
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2018
2018
The inhibitory effects of COL1A2 on colorectal cancer cell proliferation, migration, and invasion
Purpose: Collagen type I alpha 2 chain (COL1A2) has been shown to participate in the development of various human malignancies… Expand
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2017
2017
Inhibition of DNA Methylation in the COL1A2 Promoter by Anacardic Acid Prevents UV-Induced Decrease of Type I Procollagen Expression.
UV radiation decreases type I procollagen production mainly by inhibiting the transforming growth factor-β/Smad signaling pathway… Expand
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2015
2015
940 miRNA and mRNA Profiles From Nondysplastic Mucosa Distinguish UC Patients Harboring Remote Neoplasia and Uncover MiR-4728-3p, a Predicted Regulator of Focal Adhesion, As a Tumor Suppressor in UC
Introduction: In prior studies, we identified RNAs in non-dysplastic mucosa that distinguished patients with ulcerative colitis… Expand
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2015
2015
articleTranscriptional regulation of matrix metalloproteinase-1 and collagen 1 A 2 explains the anti-fibrotic effect exerted by proteasome inhibition in human dermal fibroblasts
Introduction: Extracellular matrix (ECM) turnover is controlled by the synthetic rate of matrix proteins, including type I… Expand
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2013
2013
Skelett und Bewegungssystem
Wichtigste monogene Krankheit mit abnormer Knochenbruchigkeit ist die Osteogenesis imperfecta, auch »Glasknochenkrankheit… Expand
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1991
1991
Assignment of the YT blood group locus to chromosome 7q.
The antithetical antigens YT1 and YT2 constitute the YT blood group system (International Society of Blood Transfusion system… Expand
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