(Q52055183)

20 April 2018

title

Runx2 regulates FGF2-induced Bmp2 expression during cranial bone development (English)

1 reference

20 April 2018

author

Tae-Geon Kwon

4

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20 April 2018

author name string

Kang-Young Choi

1

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20 April 2018

Hyun-Jung Kim

2

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20 April 2018

Mi-Hye Lee

3

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20 April 2018

Hyun-Duck Nah

5

1 reference

20 April 2018

Tatsuya Furuichi

6

1 reference

20 April 2018

Toshihisa Komori

7

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20 April 2018

Soon-Hyeun Nam

8

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20 April 2018

Young-Jin Kim

9

1 reference

20 April 2018

Hyun-Jung Kim

10

1 reference

20 April 2018

Hyun-Mo Ryoo

11

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20 April 2018

publication date

1 May 2005

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20 April 2018

published in

Developmental Dynamics

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20 April 2018

volume

233

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20 April 2018

issue

1

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20 April 2018

page(s)

115-121

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20 April 2018

Spatio-temporal expression patterns of Runx2 isoforms in early skeletogenesis

cites work

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

Abnormal bone growth and selective translational regulation in basic fibroblast growth factor (FGF-2) transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

Factors that promote progressive development of the osteoblast phenotype in cultured fetal rat calvaria cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Skeletal disorders associated with fibroblast growth factor receptor mutatios

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https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Stimulatory effects of basic fibroblast growth factor and bone morphogenetic protein-2 on osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

BMP signals regulate Dlx5 during early avian skull development

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

The protein kinase C pathway plays a central role in the fibroblast growth factor-stimulated expression and transactivation activity of Runx2

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Runx2 is a common target of transforming growth factor beta1 and bone morphogenetic protein 2, and cooperation between Runx2 and Smad5 induces osteoblast-specific gene expression in the pluripotent mesenchymal precursor cell line C2C12.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

BMP-2-induced Runx2 expression is mediated by Dlx5, and TGF-beta 1 opposes the BMP-2-induced osteoblast differentiation by suppression of Dlx5 expression

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

BMP-2-induced Osterix expression is mediated by Dlx5 but is independent of Runx2.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Runx1/AML1 hematopoietic transcription factor contributes to skeletal development in vivo.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Disruption of the fibroblast growth factor-2 gene results in decreased bone mass and bone formation

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Differential expression patterns of Runx2 isoforms in cranial suture morphogenesis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

The BMP antagonist noggin regulates cranial suture fusion

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Genomic structure and isoform expression of the mouse, rat and human Cbfa1/Osf2 transcription factor

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

A Pro250Arg substitution in mouse Fgfr1 causes increased expression of Cbfa1 and premature fusion of calvarial sutures

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.20323

7 January 2021

Identifiers

DOI

10.1002/DVDY.20323

1 reference

20 April 2018

1 reference

20 April 2018