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Taku Miyagawa

Showing results (1-10 of 55) with videos related to

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Human Genome Variation|January 18, 2019
Genetics of narcolepsyTaku Miyagawa, Katsushi Tokunaga
Sleep|February 10, 2018
Epigenome-wide association study of DNA methylation in narcolepsy: an integrated genetic and epigenetic approachMihoko Shimada, Taku Miyagawa, Hiromi Toyoda, et al.
Sleep|May 16, 2020
Metabolome analysis using cerebrospinal fluid from narcolepsy type 1 patientsMihoko Shimada, Taku Miyagawa, Tohru Kodama, et al.
Sleep|July 10, 2010
Anti-Tribbles homolog 2 autoantibodies in Japanese patients with narcolepsyHiromi Toyoda, Susumu Tanaka, Taku Miyagawa, et al.
Sleep|July 10, 2022
Low carnitine palmitoyltransferase 1 activity is a risk factor for narcolepsy type 1 and other hypersomniaMakoto Honda, Yosuke Shigematsu, Mihoko Shimada, et al.
Journal of Human Genetics|January 17, 2022
A variant in orexin receptor-2 is associated with self-reported daytime sleepiness in the Japanese populationTaku Miyagawa, Mihoko Shimada, Yoshiko Honda, et al.
Plos One|May 1, 2009
Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia)Taku Miyagawa, Makoto Honda, Minae Kawashima, et al.
Journal of Human Genetics|November 21, 2009
Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotypeTaku Miyagawa, Makoto Honda, Minae Kawashima, et al.
Sleep|September 19, 2025
DNA methylation and multi-omics profiling of T cells uncovers chemotactic pathways and proliferation-linked hypomethylation in narcolepsy type 1Mihoko Shimada, Makoto Honda, Yoshiko Honda, et al.
Human Genetics|August 3, 2010
An approach based on a genome-wide association study reveals candidate loci for narcolepsyMihoko Shimada, Taku Miyagawa, Minae Kawashima, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Human Genome Variation|January 18, 2019
Genetics of narcolepsyTaku Miyagawa, Katsushi Tokunaga
Sleep|February 10, 2018
Epigenome-wide association study of DNA methylation in narcolepsy: an integrated genetic and epigenetic approachMihoko Shimada, Taku Miyagawa, Hiromi Toyoda, et al.
Sleep|May 16, 2020
Metabolome analysis using cerebrospinal fluid from narcolepsy type 1 patientsMihoko Shimada, Taku Miyagawa, Tohru Kodama, et al.
Sleep|July 10, 2010
Anti-Tribbles homolog 2 autoantibodies in Japanese patients with narcolepsyHiromi Toyoda, Susumu Tanaka, Taku Miyagawa, et al.
Sleep|July 10, 2022
Low carnitine palmitoyltransferase 1 activity is a risk factor for narcolepsy type 1 and other hypersomniaMakoto Honda, Yosuke Shigematsu, Mihoko Shimada, et al.
Journal of Human Genetics|January 17, 2022
A variant in orexin receptor-2 is associated with self-reported daytime sleepiness in the Japanese populationTaku Miyagawa, Mihoko Shimada, Yoshiko Honda, et al.
Plos One|May 1, 2009
Polymorphism located between CPT1B and CHKB, and HLA-DRB1*1501-DQB1*0602 haplotype confer susceptibility to CNS hypersomnias (essential hypersomnia)Taku Miyagawa, Makoto Honda, Minae Kawashima, et al.
Journal of Human Genetics|November 21, 2009
Polymorphism located in TCRA locus confers susceptibility to essential hypersomnia with HLA-DRB1*1501-DQB1*0602 haplotypeTaku Miyagawa, Makoto Honda, Minae Kawashima, et al.
Sleep|September 19, 2025
DNA methylation and multi-omics profiling of T cells uncovers chemotactic pathways and proliferation-linked hypomethylation in narcolepsy type 1Mihoko Shimada, Makoto Honda, Yoshiko Honda, et al.
Human Genetics|August 3, 2010
An approach based on a genome-wide association study reveals candidate loci for narcolepsyMihoko Shimada, Taku Miyagawa, Minae Kawashima, et al.
Pageof 6