Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development. (Q33767459)

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18 March 2020

title

Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development (English)

1 reference

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18 March 2020

main subject

cleidocranial dysplasia

1 reference

6

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18 March 2020

author name string

Wei Chen

1

1 reference

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18 March 2020

Junqing Ma

2

1 reference

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18 March 2020

Guochun Zhu

3

1 reference

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18 March 2020

Joel Jules

4

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18 March 2020

Mengrui Wu

5

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18 March 2020

Fei Tian

7

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18 March 2020

Christie Paulson

8

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18 March 2020

Xuedong Zhou

9

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18 March 2020

Lin Wang

10

1 reference

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18 March 2020

Yi-Ping Li

11

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18 March 2020

language of work or name

English

0 references

publication date

21 May 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24850862%20AND%20SRC:MED&resulttype=core&format=json

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

18 March 2020

published in

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18 March 2020

volume

111

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issue

23

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18 March 2020

page(s)

8482-8487

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Runx2, osx, and dspp in tooth development

18 March 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

Cbfbeta interacts with Runx2 and has a critical role in bone development

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

The core-binding factor beta subunit is required for bone formation and hematopoietic maturation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

Absence of fetal liver hematopoiesis in mice deficient in transcriptional coactivator core binding factor beta

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

Cbf beta regulates Runx2 function isoform-dependently in postnatal bone development.

14 July 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1310617111

Core-binding factor beta interacts with Runx2 and is required for skeletal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1310617111

Distinct roles for Hedgehog and canonical Wnt signaling in specification, differentiation and maintenance of osteoblast progenitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1310617111

Mouse alpha1(I)-collagen promoter is the best known promoter to drive efficient Cre recombinase expression in osteoblast

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1310617111

Cbfa1 is required for epithelial-mesenchymal interactions regulating tooth development in mice.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4060659

Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24850862

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Core binding factor beta (CBFB) haploinsufficiency due to an interstitial deletion at 16q21q22 resulting in delayed cranial ossification, cleft palate, congenital heart anomalies, and feeding difficulties but favorable outcome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24850862

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1310617111

1 reference

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18 March 2020

0 references

1 reference

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18 March 2020

1 reference

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