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Microbiology Resource Announcements|January 4, 2023
Genome Sequence of Bjerkandera adusta Strain Dec 1, a Basidiomycete Secreting DyP-Type PeroxidaseKanako Sugawara, Yasushi Sugano
Molecular Genetics and Metabolism|February 6, 2008
Structural and clinical implications of amino acid substitutions in N-acetylgalactosamine-4-sulfatase: insight into mucopolysaccharidosis type VISeiji Saito, Kazuki Ohno, Kanako Sugawara, et al.
FEBS Letters|August 23, 2015
Assembly of human mitochondrial ATP synthase through two separate intermediates, F1-c-ring and b-e-g complexMakoto Fujikawa, Kanako Sugawara, Tsutomu Tanabe, et al.
Molecular Genetics and Metabolism|May 21, 2008
Structural consequences of amino acid substitutions causing Tay-Sachs diseaseKazuki Ohno, Seiji Saito, Kanako Sugawara, et al.
Journal of Human Genetics|July 18, 2008
Structural characterization of mutant alpha-galactosidases causing Fabry diseaseKanako Sugawara, Kazuki Ohno, Seiji Saito, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|December 17, 2013
Population of ATP synthase molecules in mitochondria is limited by available 6.8-kDa proteolipid protein (MLQ)Makoto Fujikawa, Shigenori Ohsakaya, Kanako Sugawara, et al.
Journal of Human Genetics|March 15, 2008
Structural study on mutant alpha-L-iduronidases: insight into mucopolysaccharidosis type IKanako Sugawara, Seiji Saito, Kazuki Ohno, et al.
Journal of Human Genetics|February 9, 2010
Prediction of the clinical phenotype of Fabry disease based on protein sequential and structural informationSeiji Saito, Kazuki Ohno, Jun Sese, et al.
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