Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Ken Higashimoto

Showing results (11-20 of 50) with videos related to

Pageof 5
Sort By:
Pediatrics and Neonatology|December 6, 2017
Hepatoblastoma in an extremely low birth-weight infant with Beckwith-Wiedemann syndromeYukako Kawasaki, Masami Makimoto, Azusa Samejima, et al.
Communications Biology|December 2, 2024
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowthSatoshi Hara, Fumikazu Matsuhisa, Shuji Kitajima, et al.
The Journal of Obstetrics and Gynaecology Research|January 19, 2021
Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case seriesChisato Kodera, Saori Aoki, Takashi Ohba, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|October 21, 2018
Beckwith-Wiedemann syndrome with asymmetric mosaic of paternal disomy causing hemihyperplasiaTomohiro Yamada, Goro Sugiyama, Ken Higashimoto, et al.
Neurologia Medico-Chirurgica|September 22, 2017
Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, JapanYuichiro Takamatsu, Ken Higashimoto, Toshiyuki Maeda, et al.
Glycoconjugate Journal|March 10, 2023
Possible regulation of ganglioside GD3 synthase gene expression with DNA methylation in human glioma cellsYurie Yamamoto, Ken Higashimoto, Yuki Ohkawa, et al.
Journal of Medical Genetics|May 25, 2020
Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndromeKen Higashimoto, Hijiri Watanabe, Yuka Tanoue, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Primary palmar hyperhidrosis locus maps to 14q11.2-q13Ikuyo Higashimoto, Koh-ichiro Yoshiura, Naomi Hirakawa, et al.
European Journal of Human Genetics : EJHG|August 19, 2007
Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterationsKensaku Sasaki, Hidenobu Soejima, Ken Higashimoto, et al.
Gene|November 25, 2005
Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in miceZhongming Zhang, Keiichiro Joh, Hitomi Yatsuki, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
Pediatrics and Neonatology|December 6, 2017
Hepatoblastoma in an extremely low birth-weight infant with Beckwith-Wiedemann syndromeYukako Kawasaki, Masami Makimoto, Azusa Samejima, et al.
Communications Biology|December 2, 2024
Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith-Wiedemann syndrome-like overgrowthSatoshi Hara, Fumikazu Matsuhisa, Shuji Kitajima, et al.
The Journal of Obstetrics and Gynaecology Research|January 19, 2021
Clinical manifestations of placental mesenchymal dysplasia in Japan: A multicenter case seriesChisato Kodera, Saori Aoki, Takashi Ohba, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|October 21, 2018
Beckwith-Wiedemann syndrome with asymmetric mosaic of paternal disomy causing hemihyperplasiaTomohiro Yamada, Goro Sugiyama, Ken Higashimoto, et al.
Neurologia Medico-Chirurgica|September 22, 2017
Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, JapanYuichiro Takamatsu, Ken Higashimoto, Toshiyuki Maeda, et al.
Glycoconjugate Journal|March 10, 2023
Possible regulation of ganglioside GD3 synthase gene expression with DNA methylation in human glioma cellsYurie Yamamoto, Ken Higashimoto, Yuki Ohkawa, et al.
Journal of Medical Genetics|May 25, 2020
Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndromeKen Higashimoto, Hijiri Watanabe, Yuka Tanoue, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Primary palmar hyperhidrosis locus maps to 14q11.2-q13Ikuyo Higashimoto, Koh-ichiro Yoshiura, Naomi Hirakawa, et al.
European Journal of Human Genetics : EJHG|August 19, 2007
Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterationsKensaku Sasaki, Hidenobu Soejima, Ken Higashimoto, et al.
Gene|November 25, 2005
Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in miceZhongming Zhang, Keiichiro Joh, Hitomi Yatsuki, et al.
Pageof 5