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Kenichiro Hata

Showing results (11-20 of 266) with videos related to

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Reproductive Biomedicine Online|March 31, 2019
Analysis of chromosome microstructures in products of conception associated with recurrent miscarriageTaisuke Sato, Ohsuke Migita, Hiroka Hata, et al.
Plos One|July 21, 2025
Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in miceEriko Ohnishi, Shiori Kinoshita, Kazuhiko Nakabayashi, et al.
Scientific Reports|August 31, 2019
Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete molesHirokazu Usui, Kazuhiko Nakabayashi, Kayoko Maehara, et al.
Molecular Reproduction and Development|October 8, 2005
Meiotic and epigenetic aberrations in Dnmt3L-deficient male germ cellsKenichiro Hata, Maki Kusumi, Takaaki Yokomine, et al.
Genomics|May 31, 2011
Methylation dynamics of IG-DMR and Gtl2-DMR during murine embryonic and placental developmentShun Sato, Wataru Yoshida, Hidenobu Soejima, et al.
Genomics Data|December 24, 2015
Whole-exome sequencing of fibroblast and its iPS cell lines derived from a patient diagnosed with xeroderma pigmentosumKohji Okamura, Masashi Toyoda, Kenichiro Hata, et al.
Plos One|October 14, 2025
Correction: Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in miceEriko Ohnishi, Shiori Kinoshita, Kazuhiko Nakabayashi, et al.
Archives of Osteoporosis|February 24, 2021
Effects of denosumab on rheumatic diseases and refractory glucocorticoid-induced osteoporosis: a prospective studyTakaaki Ishida, Shuzo Yoshida, Youhei Fujiki, et al.
FEBS Letters|March 28, 2012
Imprinted DNA methylation reprogramming during early mouse embryogenesis at the Gpr1-Zdbf2 locus is linked to long cis-intergenic transcriptionHisato Kobayashi, Takayuki Sakurai, Shun Sato, et al.
Pediatric Neurology|December 3, 2014
Paramagnetic signals in the globus pallidus as late radiographic sign of juvenile-onset GM1 gangliosidosisToshiki Takenouchi, Rika Kosaki, Kazuhiko Nakabayashi, et al.
Pageof 27

Showing results (11-20 of 266) with videos related to

Sort By:
Pageof 27
Reproductive Biomedicine Online|March 31, 2019
Analysis of chromosome microstructures in products of conception associated with recurrent miscarriageTaisuke Sato, Ohsuke Migita, Hiroka Hata, et al.
Plos One|July 21, 2025
Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in miceEriko Ohnishi, Shiori Kinoshita, Kazuhiko Nakabayashi, et al.
Scientific Reports|August 31, 2019
Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete molesHirokazu Usui, Kazuhiko Nakabayashi, Kayoko Maehara, et al.
Molecular Reproduction and Development|October 8, 2005
Meiotic and epigenetic aberrations in Dnmt3L-deficient male germ cellsKenichiro Hata, Maki Kusumi, Takaaki Yokomine, et al.
Genomics|May 31, 2011
Methylation dynamics of IG-DMR and Gtl2-DMR during murine embryonic and placental developmentShun Sato, Wataru Yoshida, Hidenobu Soejima, et al.
Genomics Data|December 24, 2015
Whole-exome sequencing of fibroblast and its iPS cell lines derived from a patient diagnosed with xeroderma pigmentosumKohji Okamura, Masashi Toyoda, Kenichiro Hata, et al.
Plos One|October 14, 2025
Correction: Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in miceEriko Ohnishi, Shiori Kinoshita, Kazuhiko Nakabayashi, et al.
Archives of Osteoporosis|February 24, 2021
Effects of denosumab on rheumatic diseases and refractory glucocorticoid-induced osteoporosis: a prospective studyTakaaki Ishida, Shuzo Yoshida, Youhei Fujiki, et al.
FEBS Letters|March 28, 2012
Imprinted DNA methylation reprogramming during early mouse embryogenesis at the Gpr1-Zdbf2 locus is linked to long cis-intergenic transcriptionHisato Kobayashi, Takayuki Sakurai, Shun Sato, et al.
Pediatric Neurology|December 3, 2014
Paramagnetic signals in the globus pallidus as late radiographic sign of juvenile-onset GM1 gangliosidosisToshiki Takenouchi, Rika Kosaki, Kazuhiko Nakabayashi, et al.
Pageof 27