Keratinocyte cell lines derived from severe generalized recessive Epidermolysis Bullosa patients carrying a highly recurrentCOL7A1homozygous mutation: models to assess cell and gene therapiesin vitroandin vivo-Reference-Cited by-同舟云学术

Keratinocyte cell lines derived from severe generalized recessive Epidermolysis Bullosa patients carrying a highly recurrentCOL7A1homozygous mutation: models to assess cell and gene therapiesin vitroandin vivo

Published:2013-08-16 Issue:9 Volume:22 Page:601-603
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Chamorro Cristina¹,Almarza David¹,Duarte Blanca,Llames Sara G.²,Murillas Rodolfo,García Marta,Cigudosa Juan C.³,Espinosa-Hevia Luis³,Escámez Maria José,Mencía Ángeles⁴,Meana Álvaro²,García-Escudero Ramón⁵,Moro Rosa¹,Conti Claudio J.,Del Río Marcela,Larcher Fernando

Affiliation:

1. Epithelial Biomedicine Division; Cutaneous Disease Modelling Unit; CIEMAT; Madrid; Spain

2. Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER- U714); Madrid; Spain

3. Centro de Investigaciones Oncológicas; Molecular Cytogenetics Group; Human Cancer Genetics Program; Spanish National Cancer Research Centre (CNIO-CIBERER); Madrid; Spain

4. Department of Bioengineering; Universidad Carlos III de Madrid; Madrid; Spain

5. Molecular Oncology Unit; CIEMAT; Madrid; Spain

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/exd.12203/fullpdf

Reference30 articles.

1. Epidermolysis bullosa - a group of skin diseases with different causes but commonalities in gene expression

2. The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations

3. A prevalent mutation with founder effect in Spanish Recessive Dystrophic Epidermolysis Bullosa families

4. Molecular Therapeutics for Heritable Skin Diseases

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