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COL1A2 wt Allele
Known as:
Collagen, Type I, Alpha 2 wt Allele
, Osteogenesis Imperfecta Type IV Gene
, COL1A2
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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…
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National Institutes of Health
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Related topics
Related topics
14 relations
7q22.1
COL1A1 gene
COL1A2 gene
Cell 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
Jie Wu
,
Jing Liu
,
+4 authors
Lei 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…
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2018
2018
The inhibitory effects of COL1A2 on colorectal cancer cell proliferation, migration, and invasion
Yifan Yu
,
Dongliang Liu
,
+4 authors
Baolin Liu
Journal of Cancer
2018
Corpus ID: 52030354
Purpose: Collagen type I alpha 2 chain (COL1A2) has been shown to participate in the development of various human malignancies…
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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.
Min-Kyoung Kim
,
Eun Ju Kim
,
+4 authors
J. Chung
The Journal of investigative dermatology
2017
Corpus ID: 36125305
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
J. Pekow
,
Alan L. Hutchison
,
+4 authors
M. Bissonnette
2015
Corpus ID: 74854159
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
L. Goffin
,
Queralt Seguı́n-Estévez
,
M. Alvarez
,
W. Reith
,
C. Chizzolini
2015
Corpus ID: 2436688
Introduction: Extracellular matrix (ECM) turnover is controlled by the synthetic rate of matrix proteins, including type I…
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2013
2013
Skelett und Bewegungssystem
Christian Schaaf
,
J. Zschocke
2013
Corpus ID: 160224159
Wichtigste monogene Krankheit mit abnormer Knochenbruchigkeit ist die Osteogenesis imperfecta, auch »Glasknochenkrankheit…
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1991
1991
Assignment of the YT blood group locus to chromosome 7q.
T. Zelinski
,
L. White
,
G. Coghlan
,
S. Philipps
Genomics
1991
Corpus ID: 2920989
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