Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes
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Exome sequencing and functional analysis identifies a novel mutation in EXT1 gene that causes multiple osteochondromasA mouse model of osteochondromagenesis from clonal inactivation of Ext1 in chondrocytes.Etiological point mutations in the hereditary multiple exostoses gene EXT1: a functional analysis of heparan sulfate polymerase activityAutoantibody signature differentiates Wilms tumor patients from neuroblastoma patients.No haploinsufficiency but loss of heterozygosity for EXT in multiple osteochondromasA broad spectrum of genomic changes in latinamerican patients with EXT1/EXT2-CDGIdentification of a novel EXT1 mutation in patients with hereditary multiple exostosis by exome sequencingA position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice.Detection of exostosin glycosyltransferase gene mutations in patients with non-hereditary osteochondromas of the mandibular condyleHereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments.Malignant progression in two children with multiple osteochondromasCompound heterozygous loss of Ext1 and Ext2 is sufficient for formation of multiple exostoses in mouse ribs and long bones.Increase of exostosin 1 in plasma as a potential biomarker for opisthorchiasis-associated cholangiocarcinoma.Advances in the pathogenesis and possible treatments for multiple hereditary exostoses from the 2016 international MHE conference.The pathogenic roles of heparan sulfate deficiency in hereditary multiple exostoses.EXT1:EXT2 transfers GlcNAc to the terminal GlcA residueEXT1:EXT2 transfers GlcNAc to heparanEXT1:EXT2 transfer GlcNAc to the heparan chainEXT1:EXT2 transfers GlcA to heparanFamilial case of Potocki-Shaffer syndrome associated with microdeletion of EXT2 and ALX4.Genetic models of osteochondroma onset and neoplastic progression: evidence for mechanisms alternative to EXT genes inactivationThe Role of EXT1 in Nonhereditary Osteochondroma: Identification of Homozygous Deletions
P2860
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P2860
Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@ast
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@en
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@nl
type
label
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@ast
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@en
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@nl
prefLabel
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@ast
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@en
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@nl
P2093
P2860
P1433
P1476
Diminished levels of the putat ...... EXT2 in exostosis chondrocytes
@en
P2093
G A Clines
H J Lüdecke
M B Snuggs
W B Van Winkle
P2860
P304
P356
10.1002/1097-0169(200102)48:2<149::AID-CM1005>3.0.CO;2-3
P407
P50
P577
2001-02-01T00:00:00Z