COL10A1 gene

Known as: collagen type X alpha 1, Schmid metaphyseal chondrodysplasia, COL10A1 
 

Topic mentions per year

Topic mentions per year

1992-2017
051019922017

Papers overview

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Highly Cited
2011
Highly Cited
2011
Despite significant progress in the identification of genetic loci for age-related macular degeneration (AMD), not all of the… (More)
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Highly Cited
2010
Highly Cited
2010
Chondrocyte hypertrophy followed by cartilage matrix degradation and vascular invasion, characterized by expression of type X… (More)
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2010
2010
OBJECTIVES To elucidate disease-specific molecular changes occurring in osteoarthritis (OA) by analysing the differential gene… (More)
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2008
2008
OBJECTIVE Human articular chondrocytes do not express COL10A1 and do not undergo hypertrophy except in close vicinity to… (More)
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2007
2007
Suppression of type II collagen (COL2A1) cleavage by transforming growth factor (TGF)-beta2 in cultured human osteoarthritic… (More)
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2007
2007
Missense, nonsense and frame-shift mutations in the collagen X gene (COL10A1) result in metaphyseal chondrodysplasia type Schmid… (More)
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2005
2005
Schmid metaphyseal chondrodysplasia (SMCD) is a dominantly inherited cartilage disorder caused by mutations in the gene for the… (More)
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2002
2002
PTH and PTHrP have been shown to inhibit maturation of growth plate chondrocytes and the expression of type X collagen. In order… (More)
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1998
1998
Spondylometaphyseal dysplasia (SMD) comprises a heterogeneous group of heritable skeletal dysplasias characterized by… (More)
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1996
1996
Type X collagen is a homotrimer of alpha 1 (X) chains encoded by the COL10A1 gene. It is synthesised specifically and transiently… (More)
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