Post-natal treatment by a blood-brain-barrier permeable calpain inhibitor, SNJ1945 rescued defective function in lissencephaly-Reference-Cited by-同舟云学术

Post-natal treatment by a blood-brain-barrier permeable calpain inhibitor, SNJ1945 rescued defective function in lissencephaly

Published:2013-02-06 Issue:1 Volume:3 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Toba Shiori,Tamura Yasuhisa,Kumamoto Kanako,Yamada Masami,Takao Keizo,Hattori Satoko,Miyakawa Tsuyoshi,Kataoka Yosky,Azuma Mitsuyoshi,Hayasaka Kiyoshi,Amamoto Masano,Tominaga Keiko,Wynshaw-Boris Anthony,Wanibuchi Hideki,Oka Yuichiro,Sato Makoto,Kato Mitsuhiro,Hirotsune Shinji

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep01224.pdf

Reference29 articles.

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2. Reiner, O. et al. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature 364, 717–721 (1993).

3. Hattori, M., Adachi, H., Tsujimoto, M., Arai, H. & Inoue, K. Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]. Nature 370, 216–218 (1994).

4. Vallee, R. B., Tai, C. & Faulkner, N. E. LIS1: cellular function of a disease-causing gene. Trends Cell Biol 11, 155–160 (2001).

5. Wynshaw-Boris, A. Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development. Clin Genet 72, 296–304 (2007).

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