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Mariko Taniguchi

Showing results (51-60 of 91) with videos related to

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Pediatric Nephrology (Berlin, Germany)|April 9, 2016
Identification of mutations in FN1 leading to glomerulopathy with fibronectin depositsHiromi Ohtsubo, Taro Okada, Kandai Nozu, et al.
Neuromuscular Disorders : NMD|September 18, 2018
National registry of patients with Fukuyama congenital muscular dystrophy in JapanKeiko Ishigaki, Chikoto Ihara, Harumasa Nakamura, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|January 28, 2020
Acute rhabdomyolysis following viral infection with coxsackie A4 in a 50-day-old infant with Fukuyama congenital muscular dystrophyHiroshi Yamaguchi, Mariko Taniguchi-Ikeda, Hiroaki Nagase, et al.
Environmental Health and Preventive Medicine|November 23, 2017
Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children's primary emergency medical centerIchiro Morioka, Naohiro Kamiyoshi, Masahiro Nishiyama, et al.
Clinical and Experimental Nephrology|March 13, 2016
Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencingTomohiko Yamamura, Naoya Morisada, Kandai Nozu, et al.
The Journal of International Medical Research|March 9, 2018
Clinical features predicting group A streptococcal pharyngitis in a Japanese paediatric primary emergency medical centreMasahiro Nishiyama, Ichiro Morioka, Mariko Taniguchi-Ikeda, et al.
Molecular Cytogenetics|December 6, 2014
Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocationDivya Mishra, Takema Kato, Hidehito Inagaki, et al.
Human Genome Variation|April 16, 2016
A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomyXue J Fu, Naoya Morisada, Fusako Hashimoto, et al.
Journal of Human Genetics|April 11, 2025
Regulation of MCCC1 expression by a Parkinson's disease-associated intronic variant: implications for pathogenesisShunsaku Sogabe, Hiroko Nakano, Yusuke Ogasahara, et al.
Brain & Development|June 6, 2017
Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophyTetsushi Yamamoto, Mariko Taniguchi-Ikeda, Hiroyuki Awano, et al.
Pageof 10

Showing results (51-60 of 91) with videos related to

Sort By:
Pageof 10
Pediatric Nephrology (Berlin, Germany)|April 9, 2016
Identification of mutations in FN1 leading to glomerulopathy with fibronectin depositsHiromi Ohtsubo, Taro Okada, Kandai Nozu, et al.
Neuromuscular Disorders : NMD|September 18, 2018
National registry of patients with Fukuyama congenital muscular dystrophy in JapanKeiko Ishigaki, Chikoto Ihara, Harumasa Nakamura, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy|January 28, 2020
Acute rhabdomyolysis following viral infection with coxsackie A4 in a 50-day-old infant with Fukuyama congenital muscular dystrophyHiroshi Yamaguchi, Mariko Taniguchi-Ikeda, Hiroaki Nagase, et al.
Environmental Health and Preventive Medicine|November 23, 2017
Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children's primary emergency medical centerIchiro Morioka, Naohiro Kamiyoshi, Masahiro Nishiyama, et al.
Clinical and Experimental Nephrology|March 13, 2016
Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencingTomohiko Yamamura, Naoya Morisada, Kandai Nozu, et al.
The Journal of International Medical Research|March 9, 2018
Clinical features predicting group A streptococcal pharyngitis in a Japanese paediatric primary emergency medical centreMasahiro Nishiyama, Ichiro Morioka, Mariko Taniguchi-Ikeda, et al.
Molecular Cytogenetics|December 6, 2014
Breakpoint analysis of the recurrent constitutional t(8;22)(q24.13;q11.21) translocationDivya Mishra, Takema Kato, Hidehito Inagaki, et al.
Human Genome Variation|April 16, 2016
A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomyXue J Fu, Naoya Morisada, Fusako Hashimoto, et al.
Journal of Human Genetics|April 11, 2025
Regulation of MCCC1 expression by a Parkinson's disease-associated intronic variant: implications for pathogenesisShunsaku Sogabe, Hiroko Nakano, Yusuke Ogasahara, et al.
Brain & Development|June 6, 2017
Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophyTetsushi Yamamoto, Mariko Taniguchi-Ikeda, Hiroyuki Awano, et al.
Pageof 10