(Q28240418)

English

More than one gene involved in monilethrix: intracellular but also extracellular players

scientific article (publication date: June 2006)

In more languages

edit

Statements

instance of

scholarly article

0 references

title

More than one gene involved in monilethrix: intracellular but also extracellular players (English)

0 references

author name string

Jurgen Schweizer

series ordinal

1

0 references

language of work or name

English

0 references

publication date

June 2006

0 references

published in

Journal of Investigative Dermatology

0 references

volume

126

0 references

issue

6

0 references

page(s)

1216-9

0 references

cites work

Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo "hairless" rat

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Keratins of the human hair follicle

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Human hair abnormalities resulting from inherited desmosome gene mutations.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense mutation in the cadherin interaction site of the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat model.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Lanceolate hair (lah): a recessive mouse mutation with alopecia and abnormal hair.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A locus for hereditary hypotrichosis localized to human chromosome 18q21.1.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for genetic heterogeneity in monilethrix

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Lanceolate hair-J (lahJ): a mouse model for human hair disorders

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense mutation in the type II hair keratin hHb3 is associated with monilethrix

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

An autosomal recessive form of monilethrix is caused by mutations in DSG4: clinical overlap with localized autosomal recessive hypotrichosis

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.JID.5700266

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.JID.5700266

0 references

Dimensions Publication ID

1013001255

0 references

PubMed ID

16702971

0 references

ResearchGate publication ID

7078599

0 references

(Q28240418)

More than one gene involved in monilethrix: intracellular but also extracellular players

Statements

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)