The molecular basis of human keratin disorders.

The molecular basis of human keratin disorders.

Item
http://www.wikidata.org/entity/Q37402486
Essential role of the keratinocyte-specific endonuclease DNase1L2 in the removal of nuclear DNA from hair and nailsDLA class II alleles are associated with risk for canine symmetrical lupoid onychodystrophy [corrected](SLO).[The ichthyoses. Pathophysiological models of epidermal differentiation].Keratin gene mutations in disorders of human skin and its appendages.Regulation of keratin expression by retinoids.Seven kinds of intermediate filament networks in the cytoplasm of polarized cells: structure and function.Keratins and skin disease.Sodium fluoride influences the expression of keratins in cultured keratinocytes.Culture of human intestinal epithelial cell using the dissociating enzyme thermolysin and endothelin-3.Spatiotemporal regulation of keratin 5 and 17 in the axolotl limb.A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene.Annotation of sheep keratin intermediate filament genes and their patterns of expression.Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
P2860

The molecular basis of human keratin disorders.

Item
http://www.wikidata.org/entity/Q37402486
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 27 February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
The molecular basis of human keratin disorders.
@en
The molecular basis of human keratin disorders.
@nl
type
label
The molecular basis of human keratin disorders.
@en
The molecular basis of human keratin disorders.
@nl
prefLabel
The molecular basis of human keratin disorders.
@en
The molecular basis of human keratin disorders.
@nl
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P433
P478
P577
P698
P356
P1433
P1476
The molecular basis of human keratin disorders.
@en
P2093
P2860
P2888
P304
P31
P356
P433
P478
P577
P698