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Ken Higashimoto

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Journal of Human Genetics|May 31, 2013
Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disordersHidenobu Soejima, Ken Higashimoto
Methods in Molecular Biology (Clifton, N.J.)|September 29, 2022
DNA Methylation Analysis Using Bisulfite PyrosequencingKen Higashimoto, Satoshi Hara, Hidenobu Soejima
Cancers|November 26, 2022
Placental Mesenchymal Dysplasia and Beckwith-Wiedemann SyndromeHidenobu Soejima, Satoshi Hara, Takashi Ohba, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2007
Phosphorylation-mediated inactivation of coactivator-associated arginine methyltransferase 1Ken Higashimoto, Peter Kuhn, Dhaval Desai, et al.
Journal of Biochemistry|September 19, 2009
Antisense transcription occurs at the promoter of a mouse imprinted gene, commd1, on the repressed paternal alleleKeiichiro Joh, Hitomi Yatsuki, Ken Higashimoto, et al.
Pediatric Blood & Cancer|July 1, 2010
Acute megakaryocytic leukemia (AMKL,FAB;M7) with Beckwith-Wiedemann syndromeShohei Yamamoto, Daisuke Toyama, Hitomi Yatsuki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 19, 2014
Fibroadenoma in Beckwith-Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5Yuichi Takama, Akio Kubota, Masahiro Nakayama, et al.
The Journal of Obstetrics and Gynaecology Research|September 30, 2011
Beckwith-Wiedemann syndrome with placental chorangioma due to H19-differentially methylated region hypermethylation: a case reportAiko Aoki, Arihiro Shiozaki, Azusa Sameshima, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Long term survival of a patient with Perlman syndrome due to novel compound heterozygous missense mutations in RNB domain of DIS3L2Noriko Soma, Ken Higashimoto, Masaru Imamura, et al.
American Journal of Medical Genetics. Part A|May 26, 2021
Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndromeFeifei Sun, Satoshi Hara, Chiyoko Tomita, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Journal of Human Genetics|May 31, 2013
Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disordersHidenobu Soejima, Ken Higashimoto
Methods in Molecular Biology (Clifton, N.J.)|September 29, 2022
DNA Methylation Analysis Using Bisulfite PyrosequencingKen Higashimoto, Satoshi Hara, Hidenobu Soejima
Cancers|November 26, 2022
Placental Mesenchymal Dysplasia and Beckwith-Wiedemann SyndromeHidenobu Soejima, Satoshi Hara, Takashi Ohba, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 21, 2007
Phosphorylation-mediated inactivation of coactivator-associated arginine methyltransferase 1Ken Higashimoto, Peter Kuhn, Dhaval Desai, et al.
Journal of Biochemistry|September 19, 2009
Antisense transcription occurs at the promoter of a mouse imprinted gene, commd1, on the repressed paternal alleleKeiichiro Joh, Hitomi Yatsuki, Ken Higashimoto, et al.
Pediatric Blood & Cancer|July 1, 2010
Acute megakaryocytic leukemia (AMKL,FAB;M7) with Beckwith-Wiedemann syndromeShohei Yamamoto, Daisuke Toyama, Hitomi Yatsuki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 19, 2014
Fibroadenoma in Beckwith-Wiedemann syndrome with paternal uniparental disomy of chromosome 11p15.5Yuichi Takama, Akio Kubota, Masahiro Nakayama, et al.
The Journal of Obstetrics and Gynaecology Research|September 30, 2011
Beckwith-Wiedemann syndrome with placental chorangioma due to H19-differentially methylated region hypermethylation: a case reportAiko Aoki, Arihiro Shiozaki, Azusa Sameshima, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Long term survival of a patient with Perlman syndrome due to novel compound heterozygous missense mutations in RNB domain of DIS3L2Noriko Soma, Ken Higashimoto, Masaru Imamura, et al.
American Journal of Medical Genetics. Part A|May 26, 2021
Phenotypically concordant but epigenetically discordant monozygotic dichorionic diamniotic twins with Beckwith-Wiedemann syndromeFeifei Sun, Satoshi Hara, Chiyoko Tomita, et al.
Pageof 5