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COL10A1 gene

Known as: collagen type X alpha 1, Schmid metaphyseal chondrodysplasia, COL10A1 
National Institutes of Health

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COL15A1 gene

Papers overview

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Highly Cited
2014
Highly Cited
2014
Identification and characterization of the novel Col10a1 regulatory mechanism during chondrocyte hypertrophic differentiation
The majority of human skeleton develops through the endochondral pathway, in which cartilage-forming chondrocytes proliferate and… 
2013
2013
Interleukin 6 mediates selected effects of Notch in chondrocytes.
Highly Cited
2007
Highly Cited
2007
Differential effects of BMP‐2 and TGF‐β1 on chondrogenic differentiation of adipose derived stem cells
Abstract.  Objectives: This article addresses the interaction of transforming growth factor β1 (TGF‐β1) and bone morphogenic… 
Highly Cited
2006
Highly Cited
2006
Inhibition of BMP signaling during zebrafish fin regeneration disrupts fin growth and scleroblasts differentiation and function.
Highly Cited
2005
Highly Cited
2005
Misfolding of Collagen X Chains Harboring Schmid Metaphyseal Chondrodysplasia Mutations Results in Aberrant Disulfide Bond Formation, Intracellular Retention, and Activation of the Unfolded Protein…
Collagen X is a short chain collagen expressed specifically by the hypertrophic chondrocytes of the cartilage growth plate during… 
2002
2002
Collagen X Chains Harboring Schmid Metaphyseal Chondrodysplasia NC1 Domain Mutations Are Selectively Retained and Degraded in Stably Transfected Cells*
Collagen X is a short chain, homotrimeric collagen expressed specifically by hypertrophic chondrocytes during endochondral bone… 
Highly Cited
1998
Highly Cited
1998
A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.
Type X collagen is a short-chain homotrimeric collagen expressed in the hypertrophic zone of calcifying cartilage. The clustering… 
Highly Cited
1998
Highly Cited
1998
Mutation of the type X collagen gene (COL10A1) causes spondylometaphyseal dysplasia.
Spondylometaphyseal dysplasia (SMD) comprises a heterogeneous group of heritable skeletal dysplasias characterized by… 
Highly Cited
1997
Highly Cited
1997
Mutations in the N‐terminal globular domain of the type X collagen gene (COL10A1) in patients with Schmid metaphyseal chondrodysplasia
Schmid metaphyseal chondrodysplasia (SMCD) is a relatively common, heritable osteochondrodysplasia characterized by short‐limbed… 
1993
1993
Characterization of the mouse type X collagen gene.
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