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A Oshima

Showing results (161-170 of 205) with videos related to

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American Journal of Human Genetics|November 1, 1990
Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry diseaseH Sakuraba, A Oshima, Y Fukuhara, et al.
Clinical Genetics|March 1, 1991
Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase AY Nagao, H Nakashima, Y Fukuhara, et al.
Human Mutation|April 23, 2008
Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type IA Oshima, T Jaijo, E Aller, et al.
Journal of Clinical Gastroenterology|January 1, 1991
Gastric microcirculation and its regulating factors in stressM Kitajima, A Shimizu, N Sakai, et al.
Nihon Geka Hokan. Archiv Fur Japanische Chirurgie|November 1, 1988
[Hyperbilirubinemia due to hepatic failure following open-heart surgery]N Nishiwaki, J Nishizawa, M Matsumoto, et al.
Journal of Psychiatric Research|June 26, 2007
Relationship between age at onset and magnetic resonance image-defined hyperintensities in mood disordersK Takahashi, A Oshima, I Ida, et al.
Clinical Genetics|August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B diseaseN Ishii, T Oohira, A Oshima, et al.
Clinical Cardiology|June 1, 1995
Myocardial damage after successful thrombolysis is associated with the duration of ST re-elevation at reperfusionM Ochiai, T Isshiki, Y Hirose, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|April 1, 1989
[Recovery of marrow myeloid progenitors (CFU-GM) after bone marrow transplantation, especially associated with chronic graft-versus-host disease (GVHD)]H Takatsu, M Hirokawa, A Oshima, et al.
Neuroscience|May 2, 2008
The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochleaS Usami, Y Takumi, N Suzuki, et al.
Pageof 21

Showing results (161-170 of 205) with videos related to

Sort By:
Pageof 21
American Journal of Human Genetics|November 1, 1990
Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry diseaseH Sakuraba, A Oshima, Y Fukuhara, et al.
Clinical Genetics|March 1, 1991
Hypertrophic cardiomyopathy in late-onset variant of Fabry disease with high residual activity of alpha-galactosidase AY Nagao, H Nakashima, Y Fukuhara, et al.
Human Mutation|April 23, 2008
Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type IA Oshima, T Jaijo, E Aller, et al.
Journal of Clinical Gastroenterology|January 1, 1991
Gastric microcirculation and its regulating factors in stressM Kitajima, A Shimizu, N Sakai, et al.
Nihon Geka Hokan. Archiv Fur Japanische Chirurgie|November 1, 1988
[Hyperbilirubinemia due to hepatic failure following open-heart surgery]N Nishiwaki, J Nishizawa, M Matsumoto, et al.
Journal of Psychiatric Research|June 26, 2007
Relationship between age at onset and magnetic resonance image-defined hyperintensities in mood disordersK Takahashi, A Oshima, I Ida, et al.
Clinical Genetics|August 1, 1995
Clinical and molecular analysis of a Japanese boy with Morquio B diseaseN Ishii, T Oohira, A Oshima, et al.
Clinical Cardiology|June 1, 1995
Myocardial damage after successful thrombolysis is associated with the duration of ST re-elevation at reperfusionM Ochiai, T Isshiki, Y Hirose, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|April 1, 1989
[Recovery of marrow myeloid progenitors (CFU-GM) after bone marrow transplantation, especially associated with chronic graft-versus-host disease (GVHD)]H Takatsu, M Hirokawa, A Oshima, et al.
Neuroscience|May 2, 2008
The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochleaS Usami, Y Takumi, N Suzuki, et al.
Pageof 21