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  • Kazuhiro Ohmi, David S. Greenberg, K S Rajavel, S V Ryazantsev, Hong Li, Elizabeth F. Neufeld
  • Medicine, Biology
  • Proceedings of the National Academy of Sciences…
  • 2003 (First Publication: 7 February 2003)
  • α-N-Acetylglucosaminidase deficiency (mucopolysaccharidosis IIIB, MPS IIIB) and α-l-iduronidase deficiency (MPS I) are heritable lysosomal storage diseases; neurodegeneration is prominent in MPS IIIBExpand
  • Pavel V. Belichenko, E. E. Wright, +4 authors Uta Francke
  • Biology, Medicine
  • The Journal of comparative neurology
  • 2009 (First Publication: 20 May 2009)
  • Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the X-linked gene MECP2. Girls with RTT show dramatic changes in brain function, but relatively few studies have exploredExpand
  • Xiao Feng Cui, Hong Li, +4 authors Norman Arnheim
  • Biology, Medicine
  • Proceedings of the National Academy of Sciences…
  • 1989 (First Publication: 1 December 1989)
  • The frequency of recombination between the G gamma-globin (HBG2) and parathyroid hormone (PTH) loci on the short arm of human chromosome 11 was estimated by typing greater than 700 single-spermExpand
  • Tong Chao Liu, Katherine C. Donahue, +4 authors Stella Elkabes
  • Biology, Medicine
  • Journal of proteome research
  • 2007 (First Publication: 1 July 2007)
  • The present study used isobaric tags for relative and absolute quantitation (iTRAQ) to identify novel targets in experimental autoimmune encephalomyelitis (EAE), an animal model of multipleExpand