Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorder-Reference-Cited by-同舟云学术

Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorder

Published:2019-04-08 Issue:7 Volume:3 Page:571-582
ISSN:2157-846X
Container-title:Nature Biomedical Engineering
language:en
Short-container-title:Nat Biomed Eng

Author:

Mukherjee-Clavin Bipasha,Mi Ruifa,Kern Barbara,Choi In Young,Lim Hotae,Oh Yohan^ORCID,Lannon Benjamin^ORCID,Kim Kevin J.,Bell Shaughn,Hur Junho K.,Hwang Woochang,Che Young Hyun,Habib Omer,Baloh Robert H.,Eggan Kevin^ORCID,Brandacher Gerald,Hoke Ahmet^ORCID,Studer Lorenz^ORCID,Kim Yong Jun^ORCID,Lee Gabsang^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Computer Science Applications,Biomedical Engineering,Medicine (miscellaneous),Bioengineering,Biotechnology

Link

http://www.nature.com/articles/s41551-019-0381-8.pdf

Reference48 articles.

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3. Mertens, J. et al. Directly reprogrammed human neurons retain aging-associated transcriptomic signatures and reveal age-related nucleocytoplasmic defects. Cell Stem Cell 17, 705–718 (2015).

4. van Paassen, B. W. et al. PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies. Orphanet J. Rare Dis. 9, 38 (2014).

5. Robaglia-Schlupp, A. et al. PMP22 overexpression causes dysmyelination in mice. Brain 125, 2213–2221 (2002).

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