Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size-Reference-Cited by-同舟云学术

Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size

Published:2018-04 Issue:7701 Volume:556 Page:370-375
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Johnson Matthew B.,Sun Xingshen,Kodani Andrew,Borges-Monroy Rebeca,Girskis Kelly M.,Ryu Steven C.,Wang Peter P.,Patel Komal,Gonzalez Dilenny M.,Woo Yu Mi,Yan Ziying,Liang Bo,Smith Richard S.,Chatterjee Manavi,Coman Daniel,Papademetris Xenophon,Staib Lawrence H.,Hyder Fahmeed,Mandeville Joseph B.,Grant P. Ellen,Im Kiho,Kwak Hojoong,Engelhardt John F.,Walsh Christopher A.,Bae Byoung-Il

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41586-018-0035-0.pdf

Reference43 articles.

1. Faheem, M. et al. Molecular genetics of human primary microcephaly: an overview. BMC Med. Genomics 8, S4 (2015).

2. Bond, J. et al. ASPM is a major determinant of cerebral cortical size. Nat. Genet. 32, 316–320 (2002).

3. Passemard, S. et al. Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory. Cortex 74, 158–176 (2016).

4. Desir, J., Cassart, M., David, P., Van Bogaert, P. & Abramowicz, M. Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally. Am. J. Med. Genet. A 146A, 1439–1443 (2008).

5. Pulvers, J. N. et al. Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline. Proc. Natl Acad. Sci. USA 107, 16595–16600 (2010).

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