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1 . Academic Journal
Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome
저자
by
Hitomi Yatsuki
;
Ken Higashimoto
;
Kosuke Jozaki
;
Kayoko Koide
;
Junichiro Okada
, et al.
소스
Genes & Genomics, 35(2), pp.141-147 Apr, 2013
Web of Science
Scopus
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7 . Academic Journal
Donor cord blood aging accelerates in recipients after transplantation
저자
by
Makoto Onizuka
;
Tadashi Imanishi
;
Kaito Harada
;
Yasuyuki Aoyama
;
Jun Amaki
, et al.
소스
Scientific Reports, Vol 13, Iss 1, Pp 1-6 (2023)
Open Access (DOAJ)
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7 . Academic Journal
Placental Mesenchymal Dysplasia and Beckwith–Wiedemann Syndrome
저자
by
Hidenobu Soejima
;
Satoshi Hara
;
Takashi Ohba
;
Ken Higashimoto
.
소스
Cancers, Vol 14, Iss 22, p 5563 (2022)
Open Access (DOAJ)
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6 . Academic Journal
Birt-Hogg-Dubé症候群1家系内2例の臨床的特徴 / Clinical Characteristics of Birt-Hogg-Dubé Syndrome for Two Cases in a Family
저자
by
Chiho Nakashima
;
Hidenobu Soejima
;
Hiroki Tashiro
;
Koichiro Takahashi
;
Mitsuko Furuya
, et al.
소스
日本内科学会雑誌 / Nihon Naika Gakkai Zasshi. 2021, 110(2):274
Open Access (JSTAGE)
Find it @ DONGA
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7 . Academic Journal
Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer
저자
by
Hidenori Hidaka
;
Ken Higashimoto
;
Saori Aoki
;
Hiroyuki Mishima
;
Chisa Hayashida
, et al.
소스
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-11 (2018)
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7 . Academic Journal
Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR
저자
by
Keiichiro Joh
;
Fumikazu Matsuhisa
;
Shuji Kitajima
;
Kenichi Nishioka
;
Ken Higashimoto
, et al.
소스
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-11 (2018)
Open Access (BioMed Central)
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Web of Science
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7 . Academic Journal
TYK2 Promoter Variant Is Associated with Impaired Insulin Secretion and Lower Insulin Resistance in Japanese Type 2 Diabetes Patients
저자
by
Hitoe Mori
;
Hirokazu Takahashi
;
Keiichiro Mine
;
Ken Higashimoto
;
Kanako Inoue
, et al.
소스
Genes, Vol 12, Iss 3, p 400 (2021)
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7 . Academic Journal
Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan
저자
by
Hidenobu SOEJIMA
;
Ken HIGASHIMOTO
;
Masatou KAWASHIMA
;
Muneaki MATSUO
;
Tatsuya ABE
, et al.
소스
Neurologia medico-chirurgica. 2017, 57(11):607
Open Access (JSTAGE)
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7 . Academic Journal
An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression.
저자
by
Tokiho Akiyama
;
Takafumi Katsumura
;
Shigeki Nakagome
;
Sang-Il Lee
;
Keiichiro Joh
, et al.
소스
PLoS ONE, Vol 12, Iss 6, p e0178373 (2017)
Open Access (DOAJ)
Web of Science
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7 . Academic Journal
Ash1l methylates Lys36 of histone H3 independently of transcriptional elongation to counteract polycomb silencing.
저자
by
Hitomi Miyazaki
;
Ken Higashimoto
;
Yukari Yada
;
Takaho A Endo
;
Jafar Sharif
, et al.
소스
PLoS Genetics, Vol 9, Iss 11, p e1003897 (2013)
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