SHOX interacts with the chondrogenic transcription factors SOX5 and SOX6 to activate the aggrecan enhancer (Q24338206)

Angel Campos-Barros

10

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Karen E Heath

Karen E Heath

12

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Jesús Argente

Jesús Argente

9

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Peter J Scambler

Peter J Scambler

11

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author name string

Miriam Aza-Carmona

1

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Debbie J Shears

2

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Patricia Yuste-Checa

3

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Verónica Barca-Tierno

4

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Alfonso Hisado-Oliva

5

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Alberta Belinchón

6

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J Ignacio Rodríguez

The combination of SOX5, SOX6, and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage

8

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language of work or name

English

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publication date

15 April 2011

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published in

Human Molecular Genetics

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volume

20

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issue

8

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page(s)

1547-59

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cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

PAR1 deletions downstream ofSHOX are the most frequent defect in a Spanish cohort of Léri-Weill dyschondrosteosis (LWD) probands

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Altered bone turnover in chlorpromazine-challenged rats and its effect on 1alpha-hydroxyvitamin D3 administration in vivo

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The transcription factors L-Sox5 and Sox6 are essential for cartilage formation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

S100A1 and S100B, transcriptional targets of SOX trio, inhibit terminal differentiation of chondrocytes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The short stature homeodomain protein SHOX induces cellular growth arrest and apoptosis and is expressed in human growth plate chondrocytes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Sox5 and Sox6 are needed to develop and maintain source, columnar, and hypertrophic chondrocytes in the cartilage growth plate

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

PHOG, a candidate gene for involvement in the short stature of Turner syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

BNP is a transcriptional target of the short stature homeobox gene SHOX.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The high-mobility-group domain of Sox proteins interacts with DNA-binding domains of many transcription factors

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The transcription factor Sox9 has essential roles in successive steps of the chondrocyte differentiation pathway and is required for expression of Sox5 and Sox6

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

The homozygous deletion of the 3' enhancer of the SHOX gene causes Langer mesomelic dysplasia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

L-Sox5 and Sox6 drive expression of the aggrecan gene in cartilage by securing binding of Sox9 to a far-upstream enhancer

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

High incidence of SHOX anomalies in individuals with short stature.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Enhancer deletions of the SHOX gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Consensus statement on the diagnosis and treatment of children with idiopathic short stature: a summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Wor

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021

Transcriptional activation of cartilage oligomeric matrix protein by Sox9, Sox5, and Sox6 transcription factors and CBP/p300 coactivators

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDR032

7 January 2021