Function of the Msx2 gene in the morphogenesis of the skull (Q46258979)

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English	Function of the Msx2 gene in the morphogenesis of the skull	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

8702183

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

title

Function of the Msx2 gene in the morphogenesis of the skull (English)

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Europe PubMed Central

PubMed publication ID

8702183

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

main subject

morphogenesis

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based on heuristic

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author name string

Liu YH

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1

1 reference

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

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http://europepmc.org/abstract/MED/8702183

Ma L

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2

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

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http://europepmc.org/abstract/MED/8702183

Kundu R

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3

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

Ignelzi M

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4

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

Sangiorgi F

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5

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

Wu L

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6

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

Luo W

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7

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PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

Snead ML

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8

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stated in

Europe PubMed Central

PubMed publication ID

8702183

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

Maxson R

series ordinal

9

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Europe PubMed Central

PubMed publication ID

8702183

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

language of work or name

English

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publication date

1 June 1996

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PubMed publication ID

8702183

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20 December 2017

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http://europepmc.org/abstract/MED/8702183

published in

Annals of the New York Academy of Sciences

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

volume

785

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Europe PubMed Central

PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

page(s)

48-58

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PubMed publication ID

8702183

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

cites work

Sutural biology and the correlates of craniosynostosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

The function and evolution of Msx genes: pointers and paradoxes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Developmental expression of the endogenous TIMP gene and a TIMP-lacZ fusion gene in transgenic mice.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Regulation of the Msx2 homeobox gene during mouse embryogenesis: a transgene with 439 bp of 5' flanking sequence is expressed exclusively in the apical ectodermal ridge of the developing limb

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Homeodomain Proteins: Cooperating to be different

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Newly recognized autosomal dominant disorder with craniosynostosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1749-6632.1996.TB56243.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8702183

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

PubMed publication ID

8702183

1 reference

stated in

Europe PubMed Central

PubMed publication ID

8702183

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/8702183

 

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