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Hiroyuki Awano

Showing results (91-100 of 152) with videos related to

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Endocrine|October 28, 2018
The prescription rates of glucagon for hypoglycemia by pediatricians and physicians are low in JapanMasaaki Matsumoto, Hiroyuki Awano, Yushi Hirota, et al.
Rheumatology (Oxford, England)|July 23, 2021
Identification of plexin D1 on circulating extracellular vesicles as a potential biomarker of polymyositis and dermatomyositisKenichi Uto, Koji Ueda, Takaichi Okano, et al.
Animal Models and Experimental Medicine|March 1, 2022
A sandwich ELISA kit reveals marked elevation of titin N-terminal fragment levels in the urine of mdx miceTaku Shirakawa, Ayumu Ikushima, Nobuhiro Maruyama, et al.
Genes|October 23, 2021
Detection of Spinal Muscular Atrophy Patients Using Dried Saliva SpotsYogik Onky Silvana Wijaya, Hisahide Nishio, Emma Tabe Eko Niba, et al.
Molecular Genetics and Metabolism|July 20, 2010
A Japanese child with asymptomatic elevation of serum creatine kinase shows PTRF-CAVIN mutation matching with congenital generalized lipodystrophy type 4Ery Kus Dwianingsih, Yasuhiro Takeshima, Kyoko Itoh, et al.
Vaccines|November 11, 2022
Impact after the Change from Voluntary to Universal Oral Rotavirus Vaccination on Consecutive Emergency Department Visits for Acute Gastroenteritis among Children in Kobe City, Japan (2016-2022)Hiroshi Yamaguchi, Kandai Nozu, Hiroaki Hanafusa, et al.
Histochemistry and Cell Biology|April 26, 2016
HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71abAtsushi Nishida, Sato Yasuno, Atsuko Takeuchi, et al.
Genes|December 23, 2023
Newborn Screening for Spinal Muscular Atrophy: A 2.5-Year Experience in Hyogo Prefecture, JapanShoko Sonehara, Ryosuke Bo, Yoshinori Nambu, et al.
International Journal of Neonatal Screening|June 25, 2026
A Four-Year Prospective Pilot Study of Newborn Screening for Late-Onset Proximal Urea-Cycle Disorders in Hyogo Prefecture in JapanTomoko Lee, Miki Matsui, Yoko Yokoyama, et al.
Journal of Human Genetics|January 20, 2017
Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGSEmma Tabe Eko Niba, Atsushi Nishida, Van Khanh Tran, et al.
Pageof 16

Showing results (91-100 of 152) with videos related to

Sort By:
Pageof 16
Endocrine|October 28, 2018
The prescription rates of glucagon for hypoglycemia by pediatricians and physicians are low in JapanMasaaki Matsumoto, Hiroyuki Awano, Yushi Hirota, et al.
Rheumatology (Oxford, England)|July 23, 2021
Identification of plexin D1 on circulating extracellular vesicles as a potential biomarker of polymyositis and dermatomyositisKenichi Uto, Koji Ueda, Takaichi Okano, et al.
Animal Models and Experimental Medicine|March 1, 2022
A sandwich ELISA kit reveals marked elevation of titin N-terminal fragment levels in the urine of mdx miceTaku Shirakawa, Ayumu Ikushima, Nobuhiro Maruyama, et al.
Genes|October 23, 2021
Detection of Spinal Muscular Atrophy Patients Using Dried Saliva SpotsYogik Onky Silvana Wijaya, Hisahide Nishio, Emma Tabe Eko Niba, et al.
Molecular Genetics and Metabolism|July 20, 2010
A Japanese child with asymptomatic elevation of serum creatine kinase shows PTRF-CAVIN mutation matching with congenital generalized lipodystrophy type 4Ery Kus Dwianingsih, Yasuhiro Takeshima, Kyoko Itoh, et al.
Vaccines|November 11, 2022
Impact after the Change from Voluntary to Universal Oral Rotavirus Vaccination on Consecutive Emergency Department Visits for Acute Gastroenteritis among Children in Kobe City, Japan (2016-2022)Hiroshi Yamaguchi, Kandai Nozu, Hiroaki Hanafusa, et al.
Histochemistry and Cell Biology|April 26, 2016
HEK293 cells express dystrophin Dp71 with nucleus-specific localization of Dp71abAtsushi Nishida, Sato Yasuno, Atsuko Takeuchi, et al.
Genes|December 23, 2023
Newborn Screening for Spinal Muscular Atrophy: A 2.5-Year Experience in Hyogo Prefecture, JapanShoko Sonehara, Ryosuke Bo, Yoshinori Nambu, et al.
International Journal of Neonatal Screening|June 25, 2026
A Four-Year Prospective Pilot Study of Newborn Screening for Late-Onset Proximal Urea-Cycle Disorders in Hyogo Prefecture in JapanTomoko Lee, Miki Matsui, Yoko Yokoyama, et al.
Journal of Human Genetics|January 20, 2017
Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGSEmma Tabe Eko Niba, Atsushi Nishida, Van Khanh Tran, et al.
Pageof 16