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MATN3 gene
Known as:
MATRILIN 3
, EDM5
, HOA
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National Institutes of Health
Create Alert
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Related topics
Related topics
2 relations
EPIPHYSEAL DYSPLASIA, MULTIPLE, 5
Narrower (1)
matrilin 3
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
KRT15, INHBA, MATN3, and AGT are aberrantly methylated and differentially expressed in gastric cancer and associated with prognosis.
Cheng Zhang
,
Yu Liang
,
Ming-Hui Ma
,
Kun-Zhe Wu
,
D. Dai
Pathology, Research and Practice
2019
Corpus ID: 73449051
Review
2018
Review
2018
Genotype–phenotype correlation of hereditary erythrocytosis mutations, a single center experience
J. Oliveira
,
Lea M. Coon
,
+10 authors
J. Hoyer
American journal of hematology/oncology
2018
Corpus ID: 46897435
Hereditary erythrocytosis is associated with high oxygen affinity hemoglobin variants (HOAs), 2,3‐bisphosphoglycerate deficiency…
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2016
2016
Yield of chest radiograph in tuberculosis screening for HIV-infected persons at a district-level HIV clinic.
D. Nguyen
,
N. D. Bang
,
N. Hung
,
R. Beasley
,
L. Hwang
,
E. Graviss
The International Journal of Tuberculosis and…
2016
Corpus ID: 20851354
SETTING An Hoa Clinic, a district-level human immunodeficiency virus (HIV) clinic in Ho Chi Minh City, Viet Nam. OBJECTIVE To…
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2012
2012
Matrilin-3 switches from anti- to pro-anabolic upon integration to the extracellular matrix.
Jean-Baptiste Vincourt
,
S. Etienne
,
+7 authors
J. Magdalou
Matrix Biology
2012
Corpus ID: 25673040
2011
2011
Revisit of multiple epiphyseal dysplasia: Ethnic difference in genotypes and comparison of radiographic features linked to the COMP and MATN3 genes
O. Kim
,
Hyunwoong Park
,
+20 authors
S. Park
American Journal of Medical Genetics. Part A
2011
Corpus ID: 22047303
Multiple epiphyseal dysplasia (MED) is a genetically heterogeneous group of diseases characterized by variable degrees of…
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Highly Cited
2008
Highly Cited
2008
Enhancing and maintaining chondrogenesis of synovial fibroblasts by cartilage extracellular matrix protein matrilins.
Ming Pei
,
Junming Luo
,
Qian Chen
Osteoarthritis and Cartilage
2008
Corpus ID: 25984539
Highly Cited
2007
Highly Cited
2007
Unique matrix structure in the rough endoplasmic reticulum cisternae of pseudoachondroplasia chondrocytes.
Thomas M. Merritt
,
R. Bick
,
B. Poindexter
,
J. Alcorn
,
J. Hecht
American Journal of Pathology
2007
Corpus ID: 34751253
Mutations in cartilage oligomeric matrix protein (COMP) cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple…
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Highly Cited
2006
Highly Cited
2006
Feeding behavior, diet, and the functional consequences of jaw form in orangutans, with implications for the evolution of Pongo.
Andrea B. Taylor
Journal of Human Evolution
2006
Corpus ID: 39576008
Highly Cited
2005
Highly Cited
2005
COMP mutations, chondrocyte function and cartilage matrix.
J. Hecht
,
E. Hayes
,
R. Haynes
,
W. Cole
Matrix Biology
2005
Corpus ID: 41481072
Highly Cited
2004
Highly Cited
2004
Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasia
A. Mabuchi
,
N. Haga
,
+8 authors
S. Ikegawa
Human Mutation
2004
Corpus ID: 29416307
Multiple epiphyseal dysplasia (MED) is a common skeletal dysplasia characterized by joint pain and stiffness, delayed and…
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