Epidermal barrier disorders and corneodesmosome defects.

about

Junctions in human health and inherited disease.Physiological and functional changes in the stratum corneum restored by oestrogen in an ovariectomized mice model of climacterium.

P2860

Q41808374-5A691AB7-F317-4CE0-9A00-A93AD2CC3FDA Q52675349-E1655E90-D849-4D7B-9ABF-3386CF0E5793

P2860

Epidermal barrier disorders and corneodesmosome defects.

Item

http://www.wikidata.org/entity/Q38265975

description

2014 nî lūn-bûn

@nan

2014年の論文

@ja

2014年学术文章

@wuu

2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

@zh-sg

2014年學術文章

@yue

2014年學術文章

@zh

2014年學術文章

@zh-hant

name

Epidermal barrier disorders and corneodesmosome defects.

@en

type

Item

label

Epidermal barrier disorders and corneodesmosome defects.

@en

prefLabel

Epidermal barrier disorders and corneodesmosome defects.

@en

P1476

Epidermal barrier disorders and corneodesmosome defects.

@en

P2093

Marek Haftek

http://www.w3.org/2001/XMLSchema#string

P2860

Refined characterization of corneodesmosin proteolysis during terminal differentiation of human epidermis and its relationship to desquamation

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

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

Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing

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

LEKTI fragments specifically inhibit KLK5, KLK7, and KLK14 and control desquamation through a pH-dependent interaction

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

Basis for abnormal desquamation and permeability barrier dysfunction in RXLI

Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations

Degradation of corneodesmosome proteins by two serine proteases of the kallikrein family, SCTE/KLK5/hK5 and SCCE/KLK7/hK7

P2888

s00441-014-2019-1

P304

483-490

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

review article

P356

10.1007/S00441-014-2019-1

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

360

http://www.w3.org/2001/XMLSchema#string

P577

2014-11-07T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

2015-06-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

267931440

http://www.w3.org/2001/XMLSchema#string

P6179

1032142130

http://www.w3.org/2001/XMLSchema#string

P698

25378284

http://www.w3.org/2001/XMLSchema#string

P921

P932

4452581

http://www.w3.org/2001/XMLSchema#string

Epidermal barrier disorders and corneodesmosome defects.

about

P2860

P2860

Epidermal barrier disorders and corneodesmosome defects.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P5875

P6179

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P5875

P6179

P698

P921

P932