(Q33815908)

29 July 2017

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title

Molecular genetics of the hair follicle: the state of the art. (English)

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29 July 2017

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Van Steensel MA

1

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29 July 2017

Happle R

series ordinal

2

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29 July 2017

Steijlen PM

series ordinal

3

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29 July 2017

publication date

1 January 2000

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Experimental Biology and Medicine

29 July 2017

published in

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29 July 2017

volume

223

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29 July 2017

issue

1

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29 July 2017

page(s)

1-7

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

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Induction of a beta-catenin-LEF-1 complex by wnt-1 and transforming mutants of beta-catenin

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

A new member of the frizzled family from Drosophila functions as a Wingless receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

De Novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Tyrosine phosphorylation and src family kinases control keratinocyte cell-cell adhesion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Nuclear localization of beta-catenin by interaction with transcription factor LEF-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Alopecia universalis associated with a mutation in the human hairless gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Towards defining the pathogenesis of the hairless phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

FGF5 as a regulator of the hair growth cycle: evidence from targeted and spontaneous mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Defining the interactions between intermediate filaments and desmosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Analysis of Apoptotic Cell Death in Human Hair Follicles In Vivo andIn Vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Mineral water and spas in Korea

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1525-1373.2000.22301.X

10.1046/J.1525-1373.2000.22301.X

21 January 2018

Identifiers

DOI

1 reference

29 July 2017

1 reference