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Mitsuru Murata

Showing results (31-40 of 142) with videos related to

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Journal of Dermatological Science|December 26, 2016
Validation of chemiluminescent enzyme immunoassay in detection of autoantibodies in pemphigus and pemphigoidYumi Fujio, Kazuo Kojima, Masahiro Hashiguchi, et al.
No to Shinkei = Brain and Nerve|November 26, 2003
[Wilson's disease associated with olfactory paranoid syndrome and idiopathic thrombocytopenic purpura]Morihiko Sagawa, Masaki Takao, Shigeru Nogawa, et al.
Journal of Epidemiology|November 9, 2005
Increased risk of obesity resulting from the interaction between high energy intake and the Trp64Arg polymorphism of the beta3-adrenergic receptor gene in healthy Japanese menKoichi Miyaki, Shinya Sutani, Haruhito Kikuchi, et al.
Neuroscience Letters|January 13, 2005
T280M and V249I polymorphisms of fractalkine receptor CX3CR1 and ischemic cerebrovascular diseaseHidenori Hattori, Daisuke Ito, Norio Tanahashi, et al.
Heart and Vessels|August 13, 2011
Effect of chronic kidney disease on platelet reactivity to dual-antiplatelet therapy in patients treated with drug-eluting stentsTakahide Arai, Akio Kawamura, Yumiko Matsubara, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|January 30, 2019
[Potential Application of Fibrinogen Measurement Based on the Clauss Assay to Monitoring of Dabigatran]Yuta Fujimorl, Masatoshi Wakui, Hisako Katagiri, et al.
American Journal of Human Genetics|January 10, 2002
The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and AfricansNurit Rosenberg, Mitsuru Murata, Yasuo Ikeda, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 19, 2004
Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiencyKeiko Ishii, Shuji Oguchi, Takanori Moriki, et al.
Thrombosis Research|June 23, 2012
Identification of epitopes on ADAMTS13 recognized by a panel of monoclonal antibodies with functional or non-functional effects on catalytic activityAtsuko Igari, Terumichi Nakagawa, Takanori Moriki, et al.
Biochemical and Biophysical Research Communications|January 18, 2006
Telomere length of normal leukocytes is affected by a functional polymorphism of hTERTYumiko Matsubara, Mitsuru Murata, Tadashi Yoshida, et al.
Pageof 15

Showing results (31-40 of 142) with videos related to

Sort By:
Pageof 15
Journal of Dermatological Science|December 26, 2016
Validation of chemiluminescent enzyme immunoassay in detection of autoantibodies in pemphigus and pemphigoidYumi Fujio, Kazuo Kojima, Masahiro Hashiguchi, et al.
No to Shinkei = Brain and Nerve|November 26, 2003
[Wilson's disease associated with olfactory paranoid syndrome and idiopathic thrombocytopenic purpura]Morihiko Sagawa, Masaki Takao, Shigeru Nogawa, et al.
Journal of Epidemiology|November 9, 2005
Increased risk of obesity resulting from the interaction between high energy intake and the Trp64Arg polymorphism of the beta3-adrenergic receptor gene in healthy Japanese menKoichi Miyaki, Shinya Sutani, Haruhito Kikuchi, et al.
Neuroscience Letters|January 13, 2005
T280M and V249I polymorphisms of fractalkine receptor CX3CR1 and ischemic cerebrovascular diseaseHidenori Hattori, Daisuke Ito, Norio Tanahashi, et al.
Heart and Vessels|August 13, 2011
Effect of chronic kidney disease on platelet reactivity to dual-antiplatelet therapy in patients treated with drug-eluting stentsTakahide Arai, Akio Kawamura, Yumiko Matsubara, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology|January 30, 2019
[Potential Application of Fibrinogen Measurement Based on the Clauss Assay to Monitoring of Dabigatran]Yuta Fujimorl, Masatoshi Wakui, Hisako Katagiri, et al.
American Journal of Human Genetics|January 10, 2002
The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and AfricansNurit Rosenberg, Mitsuru Murata, Yasuo Ikeda, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 19, 2004
Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiencyKeiko Ishii, Shuji Oguchi, Takanori Moriki, et al.
Thrombosis Research|June 23, 2012
Identification of epitopes on ADAMTS13 recognized by a panel of monoclonal antibodies with functional or non-functional effects on catalytic activityAtsuko Igari, Terumichi Nakagawa, Takanori Moriki, et al.
Biochemical and Biophysical Research Communications|January 18, 2006
Telomere length of normal leukocytes is affected by a functional polymorphism of hTERTYumiko Matsubara, Mitsuru Murata, Tadashi Yoshida, et al.
Pageof 15