Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

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Foxc1 Expression in Early Osteogenic Differentiation Is Regulated by BMP4-SMAD Activity.

P2860

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Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

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2014 nî lūn-bûn

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2014年の論文

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2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

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2014年論文

@zh-tw

2014年论文

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2014年论文

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2014年论文

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Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@en

Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@nl

type

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label

Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@en

Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@nl

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Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@en

Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@nl

P1476

Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

@en

P2093

Akihiko Machida

http://www.w3.org/2001/XMLSchema#string

Kiyoshi Harada

http://www.w3.org/2001/XMLSchema#string

Sachiko Iseki

http://www.w3.org/2001/XMLSchema#string

Shigeru Okuhara

http://www.w3.org/2001/XMLSchema#string

P2860

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

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

Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene

The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus

FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation

Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis.

Initiation of early osteoblast differentiation events through the direct transcriptional regulation of Msx2 by FOXC1

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172-177

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scholarly article

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10.1111/CGA.12053

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2014-08-01T00:00:00Z

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24417671

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Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

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P2860

P2860

Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698