Neural Stem Cell Engraftment and Myelination in the Human Brain-Reference-Cited by-同舟云学术

Neural Stem Cell Engraftment and Myelination in the Human Brain

Published:2012-10-10 Issue:155 Volume:4 Page:
ISSN:1946-6234
Container-title:Science Translational Medicine
language:en
Short-container-title:Sci. Transl. Med.

Author:

Gupta Nalin¹²,Henry Roland G.³⁴⁵,Strober Jonathan²³,Kang Sang-Mo⁶,Lim Daniel A.¹,Bucci Monica³,Caverzasi Eduardo³,Gaetano Laura³,Mandelli Maria Luisa³,Ryan Tamara⁷,Perry Rachel⁷,Farrell Jody⁷,Jeremy Rita J.⁸,Ulman Mary²,Huhn Stephen L.⁹,Barkovich A. James²³⁴,Rowitch David H.¹²¹⁰

Affiliation:

1. Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.

2. Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94143, USA.

3. Department of Neurology, University of California, San Francisco, San Francisco, CA 94143, USA.

4. Department of Radiology, University of California, San Francisco, San Francisco, CA 94143, USA.

5. Bioengineering Graduate Group, University of California, San Francisco, San Francisco, CA 94143, USA.

6. Division of Transplantation, Department of Surgery, University of California, San Francisco, San Francisco, CA 94143, USA.

7. Fetal Treatment Center, University of California, San Francisco, San Francisco, CA 94143, USA.

8. Clinical & Translational Science Institute, University of California, San Francisco, San Francisco, CA 94143, USA.

9. StemCells Inc., Newark, CA 94560, USA.

10. Howard Hughes Medical Institute.

Abstract

Neural stem cell transplantation study suggests myelin formation in children with a severe hypomyelination disorder.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

Reference36 articles.

1. Pelizaeus-Merzbacher disease: An X-linked neurologic disorder of myelin metabolism with a novel mutation in the gene encoding proteolipid protein.;Gencic S.;Am. J. Hum. Genet.,1989

2. Invited Article: An MRI-based approach to the diagnosis of white matter disorders

3. Pelizaeus-Merzbacher disease: Genetic and cellular pathogenesis

4. Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene

5. Misalignment of PLP/DM20 Transmembrane Domains Determines Protein Misfolding in Pelizaeus-Merzbacher Disease

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