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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
  • Rainer Benndorf, Katrin Hayess, S V Ryazantsev, Martin Wieske, Joachim Behlke, Gudrun Lutsch
  • Chemistry, Medicine
  • The Journal of biological chemistry
  • 1994 (First Publication: 12 August 1994)
  • Characteristic features of mammalian small heat shock proteins are their rapid phosphorylation in response to stress and mitogenic signals and their ability to form multimeric particles of 200-700Expand
  • Tatyana Gurlo, S V Ryazantsev, +6 authors Peter C Butler
  • Medicine, Biology
  • The American journal of pathology
  • 2010 (First Publication: 1 February 2010)
  • The islet in type 2 diabetes mellitus (T2DM) is characterized by a deficit in beta cells and islet amyloid derived from islet amyloid polypeptide (IAPP), a protein co-expressed with insulin by betaExpand
  • Yi Zheng, Nora Rozengurt, S V Ryazantsev, Donald B. Kohn, Noriko Satake, Elizabeth F. Neufeld
  • Biology, Medicine
  • Molecular genetics and metabolism
  • 2003 (First Publication: 1 August 2003)
  • Mucopolysaccharidosis I is a lysosomal storage disorder caused by mutations in the IDUA gene, resulting in deficiency of alpha-L-iduronidase and accumulation of glycosaminoglycans. Bone marrowExpand
  • Kazuhiro Ohmi, Lili C. Kudo, S V Ryazantsev, Hui-Zhi Zhao, Stanislav L Karsten, Elizabeth F. Neufeld
  • Medicine, Biology
  • Proceedings of the National Academy of Sciences
  • 2009 (First Publication: 19 May 2009)
  • Sanfilippo syndrome type B (mucopolysaccharidosis III B, MPS III B) is an autosomal recessive, neurodegenerative disease of children, characterized by profound mental retardation and dementia. TheExpand
  • Yi Zheng, S V Ryazantsev, +4 authors Elizabeth F. Neufeld
  • Biology, Medicine
  • Molecular genetics and metabolism
  • 2004 (First Publication: 1 August 2004)
  • Mucopolysaccharidosis IIIB (MPS IIIB) is a lysosomal storage disorder caused by mutations in NAGLU, the gene encoding alpha-N-acetylglucosaminidase. The disease is characterized by profound mentalExpand