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Journal of Human Genetics - Table of Contents alert Volume 63 Issue 2

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Journal of Human Genetics

Volume 63, Issue 2 (February 2018)

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Genome editing for dissecting and curing human genetic diseases

Tetsushi Sakuma & Takashi Yamamoto

Journal of Human Genetics 2018 63 :105 - 105; January 25, 2018; 10.1038/s10038-017-0380-0


Abstract | Full Text

Review Article

Genome editing for the reproduction and remedy of human diseases in mice

Satoshi Hara & Shuji Takada

Journal of Human Genetics 2017 63 :107 - 113; November 27, 2017; 10.1038/s10038-017-0360-4


Abstract | Full Text

Application of genome editing technologies in rats for human disease models

Kazuto Yoshimi & Tomoji Mashimo

Journal of Human Genetics 2017 63 :115 - 123; November 20, 2017; 10.1038/s10038-017-0346-2


Abstract | Full Text

Genetic engineering in nonhuman primates for human disease modeling

Kenya Sato & Erika Sasaki

Journal of Human Genetics 2017 63 :125 - 131; December 04, 2017; 10.1038/s10038-017-0351-5


Abstract | Full Text

Updated summary of genome editing technology in human cultured cells linked to human genetics studies

Tatsuo Miyamoto, Silvia Natsuko Akutsu & Shinya Matsuura

Journal of Human Genetics 2017 63 :133 - 143; October 11, 2017; 10.1038/s10038-017-0349-z


Abstract | Full Text

Combinations of chromosome transfer and genome editing for the development of cell/animal models of human disease and humanized animal models

Narumi Uno, Satoshi Abe, Mitsuo Oshimura & Yasuhiro Kazuki

Journal of Human Genetics 2017 63 :145 - 156; November 27, 2017; 10.1038/s10038-017-0378-7


Abstract | Full Text

In vivo genome editing via the HITI method as a tool for gene therapy

Keiichiro Suzuki & Juan Carlos Izpisua Belmonte

Journal of Human Genetics 2017 63 :157 - 164; November 13, 2017; 10.1038/s10038-017-0352-4


Abstract | Full Text

Stem cells and genome editing: approaches to tissue regeneration and regenerative medicine

Nozomu Takata & Mototsugu Eiraku

Journal of Human Genetics 2017 63 :165 - 178; October 11, 2017; 10.1038/s10038-017-0348-0


Abstract | Full Text

CRISPR/Cas9 library screening for drug target discovery


Journal of Human Genetics 2017 63 :179 - 186; November 20, 2017; 10.1038/s10038-017-0376-9


Abstract | Full Text

Cancer induction and suppression with transcriptional control and epigenome editing technologies

Shota Nakade, Takashi Yamamoto & Tetsushi Sakuma

Journal of Human Genetics 2017 63 :187 - 194; November 14, 2017; 10.1038/s10038-017-0377-8


Abstract | Full Text


Regulation of HMGB3 by antitumor miR-205-5p inhibits cancer cell aggressiveness and is involved in prostate cancer pathogenesis

Yasutaka Yamada, Rika Nishikawa, Mayuko Kato, Atsushi Okato, Takayuki Arai et al.

Journal of Human Genetics 2017 63 :195 - 205; December 01, 2017; 10.1038/s10038-017-0371-1


Abstract | Full Text

A novel mutation in SLC1A3 causes episodic ataxia

Kazuhiro Iwama, Aya Iwata, Masaaki Shiina, Satomi Mitsuhashi, Satoko Miyatake et al.

Journal of Human Genetics 2017 63 :207 - 211; December 05, 2017; 10.1038/s10038-017-0365-z


Abstract | Full Text

Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals

Yumi Yamaguchi-Kabata, Jun Yasuda, Osamu Tanabe, Yoichi Suzuki, Hiroshi Kawame et al.

Journal of Human Genetics 2017 63 :213 - 230; December 01, 2017; 10.1038/s10038-017-0347-1


Abstract | Full Text

The Y-chromosome haplogroup C3*-F3918, likely attributed to the Mongol Empire, can be traced to a 2500-year-old nomadic group

Ye Zhang, Xiyan Wu, Jiawei Li, Hongjie Li, Yongbin Zhao et al.

Journal of Human Genetics 2017 63 :231 - 238; December 05, 2017; 10.1038/s10038-017-0357-z


Abstract | Full Text

Characterization of the B-cell receptor repertoires in peanut allergic subjects undergoing oral immunotherapy

Kazuma Kiyotani, Tu H Mai, Rui Yamaguchi, Poh Yin Yew, Mike Kulis et al.

Journal of Human Genetics 2017 63 :239 - 248; November 30, 2017; 10.1038/s10038-017-0364-0


Abstract | Full Text

Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathy

Haruhito Harada, Takeharu Hayashi, Hirofumi Nishi, Ken Kusaba, Yoshinori Koga et al.

Journal of Human Genetics 2017 63 :249 - 254; November 22, 2017; 10.1038/s10038-017-0383-x


Abstract | Full Text


A commentary on band-like calcification with simplified gyration and polymicrogyria: report of 10 new families and identification of five novel OCLN mutations

Rayssa Borges-Medeiros & João Ricardo Mendes de Oliveira

Journal of Human Genetics 2017 63 :255 - 256; November 30, 2017; 10.1038/s10038-017-0390-y


Abstract | Full Text

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