(Q53438975)

14 May 2018

title

Peeling skin syndrome: genetic defects in late terminal differentiation of the epidermis. (English)

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14 May 2018

main subject

peeling skin syndrome

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Paul E Bowden

1

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14 May 2018

language of work or name

English

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publication date

1 March 2011

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14 May 2018

Journal of Investigative Dermatology

published in

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14 May 2018

volume

131

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14 May 2018

issue

3

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14 May 2018

page(s)

561-564

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14 May 2018

Localized peeling skin syndrome: case report with ultrastructural study

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Homo-oligomerization of human corneodesmosin is mediated by its N-terminal glycine loop domain

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

A 4.2 kb upstream region of the human corneodesmosin gene directs site-specific expression in hair follicles and hyperkeratotic epidermis of transgenic mice

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Acral peeling skin syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Polymorphisms in the SEEK1 and SPR1 genes on 6p21.3 associate with psoriasis in the Swedish population

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Corneodesmosin, a component of epidermal corneocyte desmosomes, displays homophilic adhesive properties

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

A missense mutation in TGM5 causes acral peeling skin syndrome in a Tunisian family.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction.

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

The peeling skin syndrome

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Identification of Late Differentiation Antigens of Human Cornified Epithelia, Expressed in Re-Organized Desmosomes and Bound to Cross-Linked Envelope

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Characterization and purification of human corneodesmosin, an epidermal basic glycoprotein associated with corneocyte-specific modified desmosomes

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Epidermal detachment, desmosomal dissociation, and destabilization of corneodesmosin in Spink5-/- mice

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Identification in the HLA class I region of a gene expressed late in keratinocyte differentiation

1 reference

https://api.crossref.org/works/10.1038%2FJID.2010.434

7 January 2021

Identifiers

DOI

10.1038/JID.2010.434

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14 May 2018

Dimensions Publication ID

1051075796

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1 reference

14 May 2018