Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4 (Q28505325)

Europe PubMed Central

PubMed ID

14512019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14512019

14 March 2024

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00355-5

14 March 2024

4

Irma Thesleff

1 reference

24 January 2017

1

Ritva Rice

1 reference

24 January 2017

David P. C. Rice

2

1 reference

24 January 2017

Bjorn R. Olsen

series ordinal

3

1 reference

24 January 2017

language of work or name

English

0 references

publication date

1 October 2003

1 reference

24 January 2017

full work available at URL

https://api.elsevier.com/content/article/PII:S0012160603003555?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00355-5

https://api.elsevier.com/content/article/PII:S0012160603003555?httpAccept=text/plain

14 March 2024

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00355-5

The developmental effects of congenital hydrocephalus (ch) in the mouse

14 March 2024

published in

Developmental Biology

1 reference

24 January 2017

262

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24 January 2017

75–87

1 reference

24 January 2017

1

1 reference

24 January 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

The membranous skeleton: the role of cell condensations in vertebrate skeletogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

The mouse Fkh1/Mf1 gene: cDNA sequence, chromosomal localization and expression in adult tissues.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Expression of the mouse Fkh1/Mf1 and Mfh1 genes in late gestation embryos is restricted to mesoderm derivatives.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Epidermal dysplasia and abnormal hair follicles in transgenic mice overexpressing homeobox gene MSX-2.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Studies in cranial suture biology: regional dura mater determines overlying suture biology.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Cranial sutures require tissue interactions with dura mater to resist osseous obliteration in vitro.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Ectopic expression of the nude gene induces hyperproliferation and defects in differentiation: implications for the self-renewal of cutaneous epithelia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Apoptosis in murine calvarial bone and suture development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Parietal foramina in Saethre-Chotzen syndrome.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Bone morphogenetic protein: the molecularization of skeletal system development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Identification of BMP-4 as a signal mediating secondary induction between epithelial and mesenchymal tissues during early tooth development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900355-5

A re-examination of two skeletal mutants of the mouse, vestigial-tail (vt) and congenital hydrocephalus (ch)

7 January 2021

series ordinal

6

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00355-5

14 March 2024

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