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I Inoue

Showing results (301-310 of 318) with videos related to

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Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|March 1, 1982
[Treatment of chronic biliary typhoid and paratyphoid carriers--results on 78 treated cases obtained in 16 years (1963 to 1978) (author's transl)]K Hiraishi, H Sagara, K Niwano, et al.
Genes and Immunity|May 13, 2005
Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 proteinT Nakajima, S Wooding, Y Satta, et al.
American Journal of Human Genetics|June 1, 1997
Haplotypes of angiotensinogen in essential hypertensionX Jeunemaitre, I Inoue, C Williams, et al.
Neurology|September 30, 2009
De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsiesI Ogiwara, K Ito, Y Sawaishi, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Urocortin expression in synovium of patients with rheumatoid arthritis and osteoarthritis: relation to inflammatory activityM Kohno, Y Kawahito, Y Tsubouchi, et al.
Oral Diseases|June 11, 2013
Genome-wide association study of degenerative bony changes of the temporomandibular jointT Yamaguchi, H Nakaoka, K Yamamoto, et al.
Scientific Reports|November 30, 2018
Nanofocusing of X-ray free-electron laser using wavefront-corrected multilayer focusing mirrorsS Matsuyama, T Inoue, J Yamada, et al.
The Journal of Clinical Investigation|April 1, 1997
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitroI Inoue, T Nakajima, C S Williams, et al.
Neuroscience|May 11, 2010
Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohortB Krischek, A Tajima, H Akagawa, et al.
Diabetes|March 17, 1999
Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteinsS Yamada, H Tomura, H Nishigori, et al.
Pageof 32

Showing results (301-310 of 318) with videos related to

Sort By:
Pageof 32
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases|March 1, 1982
[Treatment of chronic biliary typhoid and paratyphoid carriers--results on 78 treated cases obtained in 16 years (1963 to 1978) (author's transl)]K Hiraishi, H Sagara, K Niwano, et al.
Genes and Immunity|May 13, 2005
Evidence for natural selection in the HAVCR1 gene: high degree of amino-acid variability in the mucin domain of human HAVCR1 proteinT Nakajima, S Wooding, Y Satta, et al.
American Journal of Human Genetics|June 1, 1997
Haplotypes of angiotensinogen in essential hypertensionX Jeunemaitre, I Inoue, C Williams, et al.
Neurology|September 30, 2009
De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsiesI Ogiwara, K Ito, Y Sawaishi, et al.
The Journal of Clinical Endocrinology and Metabolism|September 11, 2001
Urocortin expression in synovium of patients with rheumatoid arthritis and osteoarthritis: relation to inflammatory activityM Kohno, Y Kawahito, Y Tsubouchi, et al.
Oral Diseases|June 11, 2013
Genome-wide association study of degenerative bony changes of the temporomandibular jointT Yamaguchi, H Nakaoka, K Yamamoto, et al.
Scientific Reports|November 30, 2018
Nanofocusing of X-ray free-electron laser using wavefront-corrected multilayer focusing mirrorsS Matsuyama, T Inoue, J Yamada, et al.
The Journal of Clinical Investigation|April 1, 1997
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitroI Inoue, T Nakajima, C S Williams, et al.
Neuroscience|May 11, 2010
Association of the Jun dimerization protein 2 gene with intracranial aneurysms in Japanese and Korean cohorts as compared to a Dutch cohortB Krischek, A Tajima, H Akagawa, et al.
Diabetes|March 17, 1999
Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteinsS Yamada, H Tomura, H Nishigori, et al.
Pageof 32