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Ken Higashimoto

Showing results (41-50 of 50) with videos related to

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Gene|February 26, 2016
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infantsJanette Mareska Rumbajan, Yuko Yamaguchi, Kazuhiko Nakabayashi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2020
DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancerHidetaka Watanabe, Ken Higashimoto, Noriko Miyake, et al.
Journal of Medical Genetics|August 30, 2017
<i>CTCF</i> deletion syndrome: clinical features and epigenetic delineationIkumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, et al.
European Journal of Human Genetics : EJHG|March 15, 2013
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndromeKen Higashimoto, Toshiyuki Maeda, Junichiro Okada, et al.
Genomics|December 31, 2002
Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouseKen Higashimoto, Hidenobu Soejima, Hitomi Yatsuki, et al.
Oncogene|December 3, 2003
Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancerTetsuji Nakagawachi, Hidenobu Soejima, Takeshi Urano, et al.
Human Mutation|February 24, 2017
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndromeEri Imagawa, Ken Higashimoto, Yasunari Sakai, et al.
BMC Cancer|December 31, 2013
Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastomaJanette Mareska Rumbajan, Toshiyuki Maeda, Ryota Souzaki, et al.
Gynecologic and Obstetric Investigation|November 26, 2015
Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform MoleYuki Ito, Kayoko Maehara, Eisuke Kaneki, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsToshiyuki Maeda, Ken Higashimoto, Kosuke Jozaki, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Gene|February 26, 2016
The HUS1B promoter is hypomethylated in the placentas of low-birth-weight infantsJanette Mareska Rumbajan, Yuko Yamaguchi, Kazuhiko Nakabayashi, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2020
DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancerHidetaka Watanabe, Ken Higashimoto, Noriko Miyake, et al.
Journal of Medical Genetics|August 30, 2017
<i>CTCF</i> deletion syndrome: clinical features and epigenetic delineationIkumi Hori, Rie Kawamura, Kazuhiko Nakabayashi, et al.
European Journal of Human Genetics : EJHG|March 15, 2013
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndromeKen Higashimoto, Toshiyuki Maeda, Junichiro Okada, et al.
Genomics|December 31, 2002
Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouseKen Higashimoto, Hidenobu Soejima, Hitomi Yatsuki, et al.
Oncogene|December 3, 2003
Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancerTetsuji Nakagawachi, Hidenobu Soejima, Takeshi Urano, et al.
Human Mutation|February 24, 2017
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndromeEri Imagawa, Ken Higashimoto, Yasunari Sakai, et al.
BMC Cancer|December 31, 2013
Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastomaJanette Mareska Rumbajan, Toshiyuki Maeda, Ryota Souzaki, et al.
Gynecologic and Obstetric Investigation|November 26, 2015
Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform MoleYuki Ito, Kayoko Maehara, Eisuke Kaneki, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2014
Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsToshiyuki Maeda, Ken Higashimoto, Kosuke Jozaki, et al.
Pageof 5