(Q24291250)

4 July 2017

title

A nonsense mutation in MSX1 causes Witkop syndrome (English)

1 reference

embryonic nail plate morphogenesis

4 July 2017

main subject

1 reference

Gene Ontology release 2020-05-02

1 reference

GOA release 2020-03-11

odontogenesis of dentin-containing tooth

1 reference

GOA release 2020-03-11

Msh homeobox 1

1 reference

GOA release 2020-03-11

9

J G Seidman

1 reference

4 July 2017

D Jumlongras

1

1 reference

4 July 2017

M Bei

2

1 reference

4 July 2017

J M Stimson

3

1 reference

4 July 2017

W F Wang

4

1 reference

4 July 2017

S R DePalma

5

1 reference

4 July 2017

C E Seidman

6

1 reference

4 July 2017

U Felbor

7

1 reference

4 July 2017

R Maas

8

1 reference

4 July 2017

B R Olsen

10

1 reference

4 July 2017

language of work or name

English

0 references

publication date

16 May 2001

1 reference

American Journal of Human Genetics

4 July 2017

published in

1 reference

4 July 2017

volume

69

1 reference

4 July 2017

issue

1

1 reference

4 July 2017

page(s)

67-74

1 reference

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

4 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

A role for the Msx-1 homeodomain in transcriptional regulation: residues in the N-terminal arm mediate TATA binding protein interaction and transcriptional repression

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Mutations in GJB6 cause hidrotic ectodermal dysplasia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Association of developmental regulatory genes with the development of different molar tooth shapes in two species of rodents

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Haploinsufficiency of MSX1: a mechanism for selective tooth agenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Hidrotic ectodermal dysplasia of hair, teeth, and nails: case reports and review.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Structure and sequence of the human homeobox gene HOX7.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Features of oligodontia in three generations.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Patterning of the mammalian dentition in development and evolution

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Digit tip regeneration correlates with regions of Msx1 (Hox 7) expression in fetal and newborn mice.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

The “tooth and nail” type of autosomal dominant ectodermal dysplasia

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

The homeobox gene Hox 7.1 has specific regional and temporal expression patterns during early murine craniofacial embryogenesis, especially tooth development in vivo and in vitro.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

Dual roles of Wnt signaling during chondrogenesis in the chicken limb

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1226049

FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development

29 November 2018

1 reference

12 December 2020

Witkop tooth and nail syndrome: report of two cases in a family

1 reference

12 December 2020

Autosomal dominant hypodontia with nail dysgenesis. Report of twenty-nine cases in six families

1 reference

12 December 2020

Nail is produced by the normal nail bed: a controversy resolved

1 reference

12 December 2020

Hypodontia and nail dysplasia syndrome. Report of a case

1 reference

12 December 2020

Multiple amino acids determine the DNA binding specificity of the Msx-1 homeodomain

1 reference

12 December 2020

Identifiers

DOI

10.1086/321271

1 reference

4 July 2017

1 reference

4 July 2017

1 reference