Molecular and diagnostic aspects of genetic skin fragility.

Molecular and diagnostic aspects of genetic skin fragility.

Item
http://www.wikidata.org/entity/Q36601695
Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytesPlakophilin 2 affects cell migration by modulating focal adhesion dynamics and integrin protein expression.Rare presentation of Rothmund-Thomson syndrome with predominantly cutaneous findings.Mechanisms of fibroblast cell therapy for dystrophic epidermolysis bullosa: high stability of collagen VII favors long-term skin integrityDynamic interactions of epidermal collagen XVII with the extracellular matrix: laminin 332 as a major binding partnerIntegrin α3 mutations with kidney, lung, and skin disease.A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome.A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy.The skinny on Slug.Biology and function of fetal and pediatric skin.Global remodelling of cellular microenvironment due to loss of collagen VII.
P2860

Molecular and diagnostic aspects of genetic skin fragility.

Item
http://www.wikidata.org/entity/Q36601695
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Molecular and diagnostic aspects of genetic skin fragility.
@ast
Molecular and diagnostic aspects of genetic skin fragility.
@en
type
label
Molecular and diagnostic aspects of genetic skin fragility.
@ast
Molecular and diagnostic aspects of genetic skin fragility.
@en
prefLabel
Molecular and diagnostic aspects of genetic skin fragility.
@ast
Molecular and diagnostic aspects of genetic skin fragility.
@en
P1433
P1476
P304
P31
P356
P433
P478
P50
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P698
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P1433
P1476
Molecular and diagnostic aspects of genetic skin fragility
@en
P304
P31
P356
10.1016/J.JDERMSCI.2006.08.003
P433
P478
P50
P577
P698