Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2
Top Cited Papers
- 1 January 2009
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 84 (1) , 44-51
- https://doi.org/10.1016/j.ajhg.2008.12.009
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Acute Necrotizing Encephalopathy of Childhood in Non-Asian Patients: Report of Three Cases and Literature ReviewJournal of Child Neurology, 2006
- Nuclear Envelope Breakdown Is Coordinated by Both Nup358/RanBP2 and Nup153, Two Nucleoporins with Zinc Finger ModulesMolecular Biology of the Cell, 2006
- Diagnostic criteria for multiple sclerosis: 2005 revisions to the “McDonald Criteria”Annals of Neurology, 2005
- Generation and annotation of the DNA sequences of human chromosomes 2 and 4Nature, 2005
- Complex genomic rearrangements lead to novel primate gene functionGenome Research, 2005
- The RanGAP1-RanBP2 Complex Is Essential for Microtubule-Kinetochore Interactions In VivoCurrent Biology, 2004
- A novel amino acid substitution at the receptor-binding site on the hemagglutinin of H3N2 influenza A viruses isolated from 6 cases with acute encephalopathy during the 1997-1998 season in Tokyo.Archiv für die gesamte Virusforschung, 1999
- Acute necrotizing encephalopathy of childhood: a novel form of acute encephalopathy prevalent in Japan and TaiwanBrain & Development, 1997
- Homozygous Defect in HIV-1 Coreceptor Accounts for Resistance of Some Multiply-Exposed Individuals to HIV-1 InfectionCell, 1996
- A giant nucleopore protein that binds Ran/TC4Nature, 1995