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Gen Tamiya

Showing results (31-40 of 169) with videos related to

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International Journal of Epidemiology|March 9, 2019
Outlier detection for questionnaire data in biobanksRieko Sakurai, Masao Ueki, Satoshi Makino, et al.
Journal of Human Genetics|April 2, 2025
Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobankAye Ko Ko Minn, Motomichi Matsuzaki, Akira Narita, et al.
American Journal of Human Genetics|January 2, 2003
Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritisKoichi Okamoto, Satoshi Makino, Yoko Yoshikawa, et al.
Gastroenterology|February 28, 2004
Pioglitazone prevents alcohol-induced fatty liver in rats through up-regulation of c-MetKengo Tomita, Toshifumi Azuma, Naoto Kitamura, et al.
Journal of Human Genetics|October 16, 2015
Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysisDaisuke Ogino, Taeko Hashimoto, Motoshi Hattori, et al.
Journal of Human Genetics|September 28, 2012
Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feedingHiroko Sato, Toshihiko Uchida, Kentaro Toyota, et al.
American Journal of Medical Genetics. Part A|October 19, 2024
A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus ArteriosusNaoya Saijo, Hisao Yaoita, Jun Takayama, et al.
Journal of Human Genetics|November 14, 2014
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphismsHiroko Sato, Toshihiko Uchida, Kentaro Toyota, et al.
Pediatric Hematology and Oncology|September 25, 2024
Comprehensive genetic analysis for identification of monogenic disorders and selection of appropriate treatments in pediatric patients with persistent thrombocytopeniaDaichi Sato, Hinako Kirikae, Tomohiro Nakano, et al.
Internal Medicine (Tokyo, Japan)|August 16, 2011
Impaired glucose metabolism slows executive function independent of cerebral ischemic lesions in Japanese elderly: the Takahata studyYoshimi Takahashi, Chifumi Iseki, Manabu Wada, et al.
Pageof 17

Showing results (31-40 of 169) with videos related to

Sort By:
Pageof 17
International Journal of Epidemiology|March 9, 2019
Outlier detection for questionnaire data in biobanksRieko Sakurai, Masao Ueki, Satoshi Makino, et al.
Journal of Human Genetics|April 2, 2025
Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobankAye Ko Ko Minn, Motomichi Matsuzaki, Akira Narita, et al.
American Journal of Human Genetics|January 2, 2003
Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritisKoichi Okamoto, Satoshi Makino, Yoko Yoshikawa, et al.
Gastroenterology|February 28, 2004
Pioglitazone prevents alcohol-induced fatty liver in rats through up-regulation of c-MetKengo Tomita, Toshifumi Azuma, Naoto Kitamura, et al.
Journal of Human Genetics|October 16, 2015
Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysisDaisuke Ogino, Taeko Hashimoto, Motoshi Hattori, et al.
Journal of Human Genetics|September 28, 2012
Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feedingHiroko Sato, Toshihiko Uchida, Kentaro Toyota, et al.
American Journal of Medical Genetics. Part A|October 19, 2024
A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus ArteriosusNaoya Saijo, Hisao Yaoita, Jun Takayama, et al.
Journal of Human Genetics|November 14, 2014
Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphismsHiroko Sato, Toshihiko Uchida, Kentaro Toyota, et al.
Pediatric Hematology and Oncology|September 25, 2024
Comprehensive genetic analysis for identification of monogenic disorders and selection of appropriate treatments in pediatric patients with persistent thrombocytopeniaDaichi Sato, Hinako Kirikae, Tomohiro Nakano, et al.
Internal Medicine (Tokyo, Japan)|August 16, 2011
Impaired glucose metabolism slows executive function independent of cerebral ischemic lesions in Japanese elderly: the Takahata studyYoshimi Takahashi, Chifumi Iseki, Manabu Wada, et al.
Pageof 17