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Ken Higashimoto

Showing results (21-30 of 50) with videos related to

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Epigenetics & Chromatin|June 8, 2018
Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMRKeiichiro Joh, Fumikazu Matsuhisa, Shuji Kitajima, et al.
Journal of Biochemistry|April 6, 2005
The essential role of histone H3 Lys9 di-methylation and MeCP2 binding in MGMT silencing with poor DNA methylation of the promoter CpG islandWei Zhao, Hidenobu Soejima, Ken Higashimoto, et al.
Cancer Letters|June 30, 2006
Retinoic acid receptor beta2 is epigenetically silenced either by DNA methylation or repressive histone modifications at the promoter in cervical cancer cellsZhongming Zhang, Keiichiro Joh, Hitomi Yatsuki, et al.
Cancer Science|September 13, 2006
Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancersSeiji Nakano, Kazuhiro Murakami, Makiko Meguro, et al.
Journal of Human Genetics|June 26, 2019
The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndromeFeifei Sun, Ken Higashimoto, Atsuko Awaji, et al.
Genes & Genetic Systems|May 29, 2008
MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene productsShinya Yakabe, Hidenobu Soejima, Hitomi Yatsuki, et al.
American Journal of Human Genetics|September 2, 2003
Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndromeKen Higashimoto, Takeshi Urano, Kazumitsu Sugiura, et al.
Endocrine Journal|December 1, 2012
Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndromeHiroyuki Adachi, Ikuko Takahashi, Ken Higashimoto, et al.
Journal of Medical Genetics|January 16, 2024
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrumKen Higashimoto, Feifei Sun, Eri Imagawa, et al.
Genome Research|September 24, 2004
Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control regionHitomi Yatsuki, Keiichiro Joh, Ken Higashimoto, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
Epigenetics & Chromatin|June 8, 2018
Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMRKeiichiro Joh, Fumikazu Matsuhisa, Shuji Kitajima, et al.
Journal of Biochemistry|April 6, 2005
The essential role of histone H3 Lys9 di-methylation and MeCP2 binding in MGMT silencing with poor DNA methylation of the promoter CpG islandWei Zhao, Hidenobu Soejima, Ken Higashimoto, et al.
Cancer Letters|June 30, 2006
Retinoic acid receptor beta2 is epigenetically silenced either by DNA methylation or repressive histone modifications at the promoter in cervical cancer cellsZhongming Zhang, Keiichiro Joh, Hitomi Yatsuki, et al.
Cancer Science|September 13, 2006
Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancersSeiji Nakano, Kazuhiro Murakami, Makiko Meguro, et al.
Journal of Human Genetics|June 26, 2019
The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndromeFeifei Sun, Ken Higashimoto, Atsuko Awaji, et al.
Genes & Genetic Systems|May 29, 2008
MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene productsShinya Yakabe, Hidenobu Soejima, Hitomi Yatsuki, et al.
American Journal of Human Genetics|September 2, 2003
Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndromeKen Higashimoto, Takeshi Urano, Kazumitsu Sugiura, et al.
Endocrine Journal|December 1, 2012
Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndromeHiroyuki Adachi, Ikuko Takahashi, Ken Higashimoto, et al.
Journal of Medical Genetics|January 16, 2024
Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrumKen Higashimoto, Feifei Sun, Eri Imagawa, et al.
Genome Research|September 24, 2004
Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control regionHitomi Yatsuki, Keiichiro Joh, Ken Higashimoto, et al.
Pageof 5