Disease model: heritable skin blistering (Q34351479)

1 August 2017

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title

Disease model: heritable skin blistering (English)

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1 August 2017

Arin MJ

1

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PubMed ID

11530338

1 August 2017

Roop DR

series ordinal

2

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1 August 2017

1 September 2001

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Trends in Molecular Medicine

1 August 2017

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1 August 2017

7

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1 August 2017

422-424

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1 August 2017

9

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The molecular basis for inherited bullous diseases

1 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Epidermolysis bullosa: a spectrum of clinical phenotypes explained by molecular heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Gene targeting at the mouse cytokeratin 10 locus: severe skin fragility and changes of cytokeratin expression in the epidermis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Targeted inactivation of plectin reveals essential function in maintaining the integrity of skin, muscle, and heart cytoarchitecture

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Targeted disruption of the LAMA3 gene in mice reveals abnormalities in survival and late stage differentiation of epithelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Beta4 integrin is required for hemidesmosome formation, cell adhesion and cell survival

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Absence of integrin alpha 6 leads to epidermolysis bullosa and neonatal death in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Epithelial detachment due to absence of hemidesmosomes in integrin beta 4 null mice

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

An inducible mouse model for epidermolysis bullosa simplex: implications for gene therapy

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902095-0

7 January 2021

10.1016/S1471-4914(01)02095-0

Identifiers

DOI

1 reference

1 August 2017

1 reference

PubMed ID

11530338