Dominance of SOX9 function over RUNX2 during skeletogenesis (Q35539737)

8 August 2017

title

Dominance of SOX9 function over RUNX2 during skeletogenesis (English)

1 reference

8 August 2017

Feyza Engin

3

1 reference

ORCID Public Data File 2021

author name string

Guang Zhou

1

1 reference

8 August 2017

Qiping Zheng

2

1 reference

8 August 2017

Elda Munivez

4

1 reference

8 August 2017

Yuqing Chen

5

1 reference

8 August 2017

Eiman Sebald

6

1 reference

8 August 2017

Deborah Krakow

7

1 reference

8 August 2017

Brendan Lee

8

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 December 2006

1 reference

Proceedings of the National Academy of Sciences of the United States of America

8 August 2017

published in

1 reference

8 August 2017

volume

103

1 reference

8 August 2017

issue

50

1 reference

8 August 2017

page(s)

19004-19009

1 reference

Osteo-chondroprogenitor cells are derived from Sox9 expressing precursors

8 August 2017

cites work

1 reference

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Runx2: a master organizer of gene transcription in developing and maturing osteoblasts

12 July 2018

1 reference

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Dysregulation of chondrogenesis in human cleidocranial dysplasia

12 July 2018

1 reference

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The high mobility group transcription factor Sox8 is a negative regulator of osteoblast differentiation

12 July 2018

1 reference

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Histone deacetylase 4 controls chondrocyte hypertrophy during skeletogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Overlapping expression of Runx1(Cbfa2) and Runx2(Cbfa1) transcription factors supports cooperative induction of skeletal development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Hierarchy revealed in the specification of three skeletal fates by Sox9 and Runx2.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Possible roles of Runx1 and Sox9 in incipient intramembranous ossification

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Interactions between Sox9 and beta-catenin control chondrocyte differentiation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

A twist code determines the onset of osteoblast differentiation

12 July 2018

1 reference

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Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

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

12 July 2018

1 reference

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Reaching a genetic and molecular understanding of skeletal development

12 July 2018

1 reference

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Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

A Cbfa1-dependent genetic pathway controls bone formation beyond embryonic development

12 July 2018

1 reference

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Woodchuck hepatitis virus posttranscriptional regulatory element enhances expression of transgenes delivered by retroviral vectors.

12 July 2018

1 reference

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Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Two distinct osteoblast-specific cis-acting elements control expression of a mouse osteocalcin gene

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Separate cis-acting DNA elements of the mouse pro-alpha 1(I) collagen promoter direct expression of reporter genes to different type I collagen-producing cells in transgenic mice

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

Coat color-tagged green mouse with EGFP expressed from the RNA polymerase II promoter

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1748167

CBFA1 Mutation Analysis and Functional Correlation with Phenotypic Variability in Cleidocranial Dysplasia

26 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17142326

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Transcriptional mechanisms in osteoblast differentiation and bone formation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17142326

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0605170103

1 reference

8 August 2017

0 references

1 reference

8 August 2017

1 reference