Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,166,815 papers from all fields of science
Search
Sign In
Create Free Account
COL6A2 gene
Known as:
COL6A2
, COLLAGEN, TYPE VI, ALPHA-2
, collagen type VI alpha 2
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
COL6A1 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
A Revisited Diagnosis of Collagen VI Related Muscular Dystrophy in a Patient with a Novel COL6A2 Variant and 21q22.3 Deletion
P. Simsek-Kiper
,
S. Oğuz
,
F. Ergen
,
G. Utine
,
M. Alikaşifoğlu
,
G. Haliloglu
Neuropediatrics
2020
Corpus ID: 220531455
Abstract The genetic etiology of collagen VI related muscular dystrophies is heterogenous. Genomic deletions in one allele…
Expand
2017
2017
Collagen type VI-related myopathy
P. S. D. de Souza
,
T. Bortholin
,
J. Pinheiro
,
F. Naylor
,
W. B. Pinto
,
A. Oliveira
Practical Neurology
2017
Corpus ID: 755149
A 15-year-old Brazilian boy presented with slowly progressive infancy-onset global amyotrophy and limb-girdle pattern of weakness…
Expand
2014
2014
ACollagen-Remodeling Gene Signature Regulated by TGF-b Signaling Is Associated with Metastasis and Poor Survival in Serous Ovarian Cancer
Dong-Joo Cheon
,
Yun-guang Tong
,
+9 authors
S. Orsulic
2014
Corpus ID: 313541
Purpose: To elucidate molecular pathways contributing to metastatic cancer progression and poor clinical outcome in serous…
Expand
2013
2013
serous ovarian cancer signaling is associated with metastasis and poor survival in β A collagen-remodeling gene signature regulated by TGF
Dong-Joo Cheon
,
Yun-guang Tong
,
+9 authors
S. Orsulic
2013
Corpus ID: 207785604
2012
2012
578: Gene expression analysis of VEZF1, a lymphatic transcription factor, in fetal cystic hygromas and increased nuchal translucency
Inna V. Landres
,
Elizabeth Looke-Stewart
,
+4 authors
H. Stuhlmann
2012
Corpus ID: 58146059
2012
2012
Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome
S. Karkheiran
,
Catharine E. Krebs
,
+7 authors
C. Paisán-Ruiz
Human Genetics
2012
Corpus ID: 253984085
In this study, a consanguineous family with progressive myoclonus epilepsy (PME) was clinically examined and molecularly…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE