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Yutaka Nishigaki

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Nihon Rinsho. Japanese Journal of Clinical Medicine|July 14, 2009
[Mitochondrial genome and longevity]Yutaka Nishigaki, Masashi Tanaka
Geriatrics & Gerontology International|July 2, 2010
Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese populationYutaka Nishigaki, Noriyuki Fuku, Masashi Tanaka
The Neurologist|January 15, 2004
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomesMichio Hirano, Yutaka Nishigaki, Ramon Martí
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|July 4, 2006
[Mitochondrial dysfunctions and age-associated diseases]Yutaka Nishigaki, Noriyuki Fuku, Masashi Tanaka
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|December 2, 2005
[Human mitochondrial genome polymorphism database (mtSNP)]Noriyuki Fuku, Yutaka Nishigaki, Masashi Tanaka
Human Molecular Genetics|November 14, 2003
ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathyYutaka Nishigaki, Ramon Marti, Michio Hirano
Biochemical and Biophysical Research Communications|March 21, 2003
Elevated plasma deoxyuridine in patients with thymidine phosphorylase deficiencyRamon Martí, Yutaka Nishigaki, Michio Hirano
Internal Medicine (Tokyo, Japan)|November 2, 2006
Thymidine phosphorylase gene mutations cause mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Michio Hirano, Ichizo Nishino, Yutaka Nishigaki, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Development of an image processing support system based on fluorescent dye to prevent elderly people with dementia from wanderingYutaka Nishigaki, Kentaro Tanaka, Juhyon Kim, et al.
The Journal of Clinical Investigation|June 19, 2003
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiencyYutaka Nishigaki, Ramon Martí, William C Copeland, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Nihon Rinsho. Japanese Journal of Clinical Medicine|July 14, 2009
[Mitochondrial genome and longevity]Yutaka Nishigaki, Masashi Tanaka
Geriatrics & Gerontology International|July 2, 2010
Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese populationYutaka Nishigaki, Noriyuki Fuku, Masashi Tanaka
The Neurologist|January 15, 2004
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a disease of two genomesMichio Hirano, Yutaka Nishigaki, Ramon Martí
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|July 4, 2006
[Mitochondrial dysfunctions and age-associated diseases]Yutaka Nishigaki, Noriyuki Fuku, Masashi Tanaka
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|December 2, 2005
[Human mitochondrial genome polymorphism database (mtSNP)]Noriyuki Fuku, Yutaka Nishigaki, Masashi Tanaka
Human Molecular Genetics|November 14, 2003
ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathyYutaka Nishigaki, Ramon Marti, Michio Hirano
Biochemical and Biophysical Research Communications|March 21, 2003
Elevated plasma deoxyuridine in patients with thymidine phosphorylase deficiencyRamon Martí, Yutaka Nishigaki, Michio Hirano
Internal Medicine (Tokyo, Japan)|November 2, 2006
Thymidine phosphorylase gene mutations cause mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)Michio Hirano, Ichizo Nishino, Yutaka Nishigaki, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Development of an image processing support system based on fluorescent dye to prevent elderly people with dementia from wanderingYutaka Nishigaki, Kentaro Tanaka, Juhyon Kim, et al.
The Journal of Clinical Investigation|June 19, 2003
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiencyYutaka Nishigaki, Ramon Martí, William C Copeland, et al.
Pageof 7