Generation of Xeroderma Pigmentosum-A Patient-Derived Induced Pluripotent Stem Cell Line for Use As Future Disease Model-Reference-Cited by-同舟云学术

Generation of Xeroderma Pigmentosum-A Patient-Derived Induced Pluripotent Stem Cell Line for Use As Future Disease Model

Published:2015-08 Issue:4 Volume:17 Page:268-274
ISSN:2152-4971
Container-title:Cellular Reprogramming
language:en
Short-container-title:Cellular Reprogramming

Author:

Ohnishi Hiroe¹²,Kawasaki Takashi³,Deguchi Tomonori⁴,Yuba Shunsuke¹

Affiliation:

1. Tissue Engineering Research Group, Health Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Amagasaki, Hyogo 661-0974, Japan.

2. Present address: Department of Otolaryngology, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.

3. Functional Biomolecular Research Group, Health Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Amagasaki, Hyogo 661-0974, Japan.

4. Stress Signal Research Group, Health Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka 563-8577, Japan.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Developmental Biology,Biotechnology

Link

http://www.liebertpub.com/doi/pdf/10.1089/cell.2014.0104

Reference33 articles.

1. Generation of Induced Pluripotent Stem Cells from Human Adipose-Derived Stem Cells Without c-MYC

2. Damage recognition in nucleotide excision repair of DNA

3. The case for 8,5′-cyclopurine-2′-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum

4. The Oxidative DNA Lesion 8,5′-(S)-Cyclo-2′-deoxyadenosine Is Repaired by the Nucleotide Excision Repair Pathway and Blocks Gene Expression in Mammalian Cells

5. Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA

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