Genetically corrected iPSCs as cell therapy for recessive dystrophic epidermolysis bullosa-Reference-Cited by-同舟云学术

Genetically corrected iPSCs as cell therapy for recessive dystrophic epidermolysis bullosa

Published:2014-11-26 Issue:264 Volume:6 Page:
ISSN:1946-6234
Container-title:Science Translational Medicine
language:en
Short-container-title:Sci. Transl. Med.

Author:

Wenzel Daniel¹,Bayerl Jonathan¹,Nyström Alexander²,Bruckner-Tuderman Leena²,Meixner Arabella¹,Penninger Josef M.¹

Affiliation:

1. IMBA—Institute of Molecular Biotechnology of the Austrian Academy of Sciences, Dr. Bohr-Gasse 3, 1030 Vienna, Austria.

2. Department of Dermatology, Medical Center—University of Freiburg, 79104 Freiburg, Germany.

Abstract

iPSCs derived from fibroblasts with mutant type VII collagen were genetically corrected and used as cell therapy in mice with recessive dystrophic epidermolysis bullosa.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference46 articles.

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2. Progress in Epidermolysis Bullosa Research: Summary of DEBRA International Research Conference 2012

3. Molecular Heterogeneity of Blistering Disorders: The Paradigm of Epidermolysis Bullosa

4. Germline Mutation in EXPH5 Implicates the Rab27B Effector Protein Slac2-b in Inherited Skin Fragility

5. Epidermolysis bullosa and the risk of life-threatening cancers: The National EB Registry experience, 1986-2006

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