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Fujio Takeuchi

Showing results (1-10 of 32) with videos related to

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Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[PRPP synthetase deficiency]Kaname Kawasugi, Fujio Takeuchi
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[PRPP synthetase superactivity]Kaname Kawasugi, Fujio Takeuchi
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Phosphoribosylpyrophosphate(PRPP) synthetase]Kaname Kawasugi, Fujio Takeuchi
The Journal of Rheumatology|October 6, 2005
CTLA-4 -1661A/G and -1772T/C dimorphisms in Japanese patients with systemic lupus erythematosusFujio Takeuchi, Shoji Kuwata, Masaki Mori
Endocrine Journal|November 15, 2005
Enhanced expression of CD69 and CD25 antigen on human peripheral blood mononuclear cells by prolactinKenji Takizawa, Seiichi Kitani, Fujio Takeuchi, et al.
Experimental Gerontology|June 28, 2002
Comparison of the level of mitochondrial DNA A3243G mutation in esophageal epithelium and myocardium from individuals of very advanced ageShinji Harihara, Kenichi Nakamura, Kaiyo Takubo, et al.
Mitochondrial DNA|October 18, 2012
Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twinsShinji Harihara, Kennichi Nakamura, Kaiyo Takubo, et al.
Human Immunology|February 1, 2015
Distribution of HLA-DR alleles among Thai patients with rheumatoid arthritisWorawit Louthrenoo, Nuntana Kasitanon, Suparaporn Wangkaew, et al.
International Journal of Rheumatic Diseases|September 17, 2021
CTLA-4 polymorphisms in Thai patients with rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosisWorawit Louthrenoo, Nuntana Kasitanon, Antika Wongthanee, et al.
Experimental Gerontology|February 13, 2003
The mitochondrial DNA A3243G mutation in Werner's syndromeFujio Takeuchi, Shinji Harihara, Kenichi Nakamura, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[PRPP synthetase deficiency]Kaname Kawasugi, Fujio Takeuchi
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[PRPP synthetase superactivity]Kaname Kawasugi, Fujio Takeuchi
Nihon Rinsho. Japanese Journal of Clinical Medicine|March 13, 2003
[Phosphoribosylpyrophosphate(PRPP) synthetase]Kaname Kawasugi, Fujio Takeuchi
The Journal of Rheumatology|October 6, 2005
CTLA-4 -1661A/G and -1772T/C dimorphisms in Japanese patients with systemic lupus erythematosusFujio Takeuchi, Shoji Kuwata, Masaki Mori
Endocrine Journal|November 15, 2005
Enhanced expression of CD69 and CD25 antigen on human peripheral blood mononuclear cells by prolactinKenji Takizawa, Seiichi Kitani, Fujio Takeuchi, et al.
Experimental Gerontology|June 28, 2002
Comparison of the level of mitochondrial DNA A3243G mutation in esophageal epithelium and myocardium from individuals of very advanced ageShinji Harihara, Kenichi Nakamura, Kaiyo Takubo, et al.
Mitochondrial DNA|October 18, 2012
Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twinsShinji Harihara, Kennichi Nakamura, Kaiyo Takubo, et al.
Human Immunology|February 1, 2015
Distribution of HLA-DR alleles among Thai patients with rheumatoid arthritisWorawit Louthrenoo, Nuntana Kasitanon, Suparaporn Wangkaew, et al.
International Journal of Rheumatic Diseases|September 17, 2021
CTLA-4 polymorphisms in Thai patients with rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosisWorawit Louthrenoo, Nuntana Kasitanon, Antika Wongthanee, et al.
Experimental Gerontology|February 13, 2003
The mitochondrial DNA A3243G mutation in Werner's syndromeFujio Takeuchi, Shinji Harihara, Kenichi Nakamura, et al.
Pageof 4