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Kenichiro Hata

Showing results (51-60 of 266) with videos related to

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Modern Rheumatology|January 17, 2012
Good response to infliximab in a patient with deep vein thrombosis associated with Behçet diseaseShuzo Yoshida, Tohru Takeuchi, Ayaka Yoshikawa, et al.
Human Genome Variation|December 12, 2022
A novel FLNA variant in a fetus with skeletal dysplasiaKyoko Oshina, Yoshimasa Kamei, Asuka Hori, et al.
Journal of Neurology|April 15, 2019
Occurrence of cerebral small vessel disease at diagnosis of MPO-ANCA-associated vasculitisHiroki Tani, Koji Nagai, Takafumi Hosokawa, et al.
European Journal of Medical Genetics|September 2, 2018
Molecular genetic analysis reveals atypical confined placental mosaicism with a small supernumerary marker chromosome derived from chromosome 18: A clinical report of discordant results from three prenatal testsTaisuke Sato, Osamu Samura, Tomona Matsuoka, et al.
Human Genome Variation|June 13, 2023
Genome-wide association study of preterm birth and gestational age in a Japanese populationKeita Hasegawa, Natsuhiko Kumasaka, Kazuhiko Nakabayashi, et al.
Neonatology|January 31, 2015
Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6Tomohito Takimoto, Hidetoshi Takada, Masataka Ishimura, et al.
Frontiers in Medicine|August 7, 2023
Gene expression signatures associated with chronic endometritis revealed by RNA sequencingKyoko Oshina, Keiji Kuroda, Kazuhiko Nakabayashi, et al.
Nature Communications|November 15, 2014
The role of maternal-specific H3K9me3 modification in establishing imprinted X-chromosome inactivation and embryogenesis in miceAtsushi Fukuda, Junko Tomikawa, Takumi Miura, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|September 27, 2006
Dnmt3a2 targets endogenous Dnmt3L to ES cell chromatin and induces regional DNA methylationKeisuke Nimura, Chisaki Ishida, Hiroshi Koriyama, et al.
Human Genome Variation|June 15, 2018
Genitopatellar syndrome: the first reported case in JapanSatomi Okano, Akie Miyamoto, Ikue Fukuda, et al.
Pageof 27

Showing results (51-60 of 266) with videos related to

Sort By:
Pageof 27
Modern Rheumatology|January 17, 2012
Good response to infliximab in a patient with deep vein thrombosis associated with Behçet diseaseShuzo Yoshida, Tohru Takeuchi, Ayaka Yoshikawa, et al.
Human Genome Variation|December 12, 2022
A novel FLNA variant in a fetus with skeletal dysplasiaKyoko Oshina, Yoshimasa Kamei, Asuka Hori, et al.
Journal of Neurology|April 15, 2019
Occurrence of cerebral small vessel disease at diagnosis of MPO-ANCA-associated vasculitisHiroki Tani, Koji Nagai, Takafumi Hosokawa, et al.
European Journal of Medical Genetics|September 2, 2018
Molecular genetic analysis reveals atypical confined placental mosaicism with a small supernumerary marker chromosome derived from chromosome 18: A clinical report of discordant results from three prenatal testsTaisuke Sato, Osamu Samura, Tomona Matsuoka, et al.
Human Genome Variation|June 13, 2023
Genome-wide association study of preterm birth and gestational age in a Japanese populationKeita Hasegawa, Natsuhiko Kumasaka, Kazuhiko Nakabayashi, et al.
Neonatology|January 31, 2015
Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6Tomohito Takimoto, Hidetoshi Takada, Masataka Ishimura, et al.
Frontiers in Medicine|August 7, 2023
Gene expression signatures associated with chronic endometritis revealed by RNA sequencingKyoko Oshina, Keiji Kuroda, Kazuhiko Nakabayashi, et al.
Nature Communications|November 15, 2014
The role of maternal-specific H3K9me3 modification in establishing imprinted X-chromosome inactivation and embryogenesis in miceAtsushi Fukuda, Junko Tomikawa, Takumi Miura, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|September 27, 2006
Dnmt3a2 targets endogenous Dnmt3L to ES cell chromatin and induces regional DNA methylationKeisuke Nimura, Chisaki Ishida, Hiroshi Koriyama, et al.
Human Genome Variation|June 15, 2018
Genitopatellar syndrome: the first reported case in JapanSatomi Okano, Akie Miyamoto, Ikue Fukuda, et al.
Pageof 27