Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model-Reference-Cited by-同舟云学术

Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model

Published:2012-11-18 Issue:12 Volume:18 Page:1797-1804
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Carter Calvin S,Vogel Timothy W,Zhang Qihong,Seo Seongjin,Swiderski Ruth E,Moninger Thomas O,Cassell Martin D,Thedens Daniel R,Keppler-Noreuil Kim M,Nopoulos Peggy,Nishimura Darryl Y,Searby Charles C,Bugge Kevin,Sheffield Val C

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.2996.pdf

Reference54 articles.

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3. Williams, M.A. et al. Priorities for hydrocephalus research: report from a National Institutes of Health–sponsored workshop. J. Neurosurg. 107, 345–357 (2007).

4. Vogel, P. et al. Congenital hydrocephalus in genetically engineered mice. Vet. Pathol. 49, 166–181 (2012).

5. Simon, T.D. et al. Hospital care for children with hydrocephalus in the United States: utilization, charges, comorbidities, and deaths. J. Neurosurg. Pediatr. 1, 131–137 (2008).

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