Xenografting of human umbilical mesenchymal stem cells from Wharton’s jelly ameliorates mouse spinocerebellar ataxia type 1-Reference-Cited by-同舟云学术

Xenografting of human umbilical mesenchymal stem cells from Wharton’s jelly ameliorates mouse spinocerebellar ataxia type 1

Published:2019-09-05 Issue:1 Volume:8 Page:
ISSN:2047-9158
Container-title:Translational Neurodegeneration
language:en
Short-container-title:Transl Neurodegener

Author:

Tsai Pei-Jiun,Yeh Chang-Ching,Huang Wan-Jhen,Min Ming-Yuan,Huang Tzu-Hao,Ko Tsui-Ling,Huang Pei-Yu,Chen Tien-Hua,Hsu Sanford P. C.,Soong Bing-Wen,Fu Yu-Show^ORCID

Funder

Ministry of Science and Technology, Taiwan

Taipei Veterans General Hospital

Ministry of Education

Development and Construction Plan of the School of Medicine, National Yang-Ming University

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience,Clinical Neurology

Link

http://link.springer.com/content/pdf/10.1186/s40035-019-0166-8.pdf

Reference38 articles.

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2. Soong BW, Morrison PJ. The cerebellum disorders and treatment. In: Manto M, Huisman TAGM, editors. Handbook of clinical neurology, Vol. 155 (3rd series), Chapter 10: Spinocerebellar ataxias. Amsterdam: Elsevier; 2018. p. 143–74.

3. Orr HT, M-y C, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet. 1993;4(3):221–6.

4. Banfi S, Chung MY, Kwiatkowski TJ Jr, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY. Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb. Genomics. 1993;18(3):627–35.

5. Burright EN, Clark HB, Servadio A, Matilla T, Feddersen RM, Yunis WS, Duvick LA, Zoghbi HY, Orr HT. SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat. Cell. 1995;82(6):937–48.

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