Nature Search

Retraction Note: GlcNAcylation of a histone methyltransferase in retinoic-acid-induced granulopoiesis

Ryoji Fujiki
Toshihiro Chikanishi
Shigeaki Kato
Amendments and Corrections11 Dec 2013
Nature

Volume: 505, P: 574
GlcNAcylation of histone H2B facilitates its monoubiquitination

Genome-wide analysis shows that H2B S112 O-linked to N-acetylglucosamine is frequently located near transcribed genes, suggesting that histone GlcNAcylation facilitates transcription of the genes.

Ryoji Fujiki
Waka Hashiba
Shigeaki Kato
Research27 Nov 2011
Nature

Volume: 480, P: 557-560
Galactose mutarotase deficiency as the galactosemia type IV

Yoichi Wada
Yu Aihara
Shigeo Kure
ReviewsOpen Access15 Dec 2025
Journal of Human Genetics

P: 1-6
Attenuated fusogenicity and pathogenicity of SARS-CoV-2 Omicron variant

In vitro studies in human cell lines and in vivo studies in a hamster model show that the SARS-CoV-2 Omicron variant is less pathogenic than both the Delta variant and an ancestral strain of SARS-CoV-2.

Rigel Suzuki
Daichi Yamasoba
Kei Sato
ResearchOpen Access01 Feb 2022
Nature

Volume: 603, P: 700-705
GlcNAcylation of a histone methyltransferase in retinoic-acid-induced granulopoiesis

The post-translational modifications of histone tails generate a 'histone code' that defines local and global chromatin states. Here it is shown that nuclear GlcNAcylation of a histone lysine methyltransferase, MLL5, by O-linked β-N-acetylglucosamine transferase, facilitates retinoic-acid-induced granulopoiesis.

Ryoji Fujiki
Toshihiro Chikanishi
Shigeaki Kato
Research19 Apr 2009
Nature

Volume: 459, P: 455-459
TET2 promotes histone O-GlcNAcylation during gene transcription

TET2 is shown to associate with OGT, which catalyses O-GlcNAcylation, and the two enzymes are found together at transcription start sites; TET2 facilitates the activity of OGT in O-GlcNAcylation of histone 2B, and epigenetic modifications to both DNA and histones by TET2 and OGT may be important in gene transcription regulation.

Qiang Chen
Yibin Chen
Xiaochun Yu
Research09 Dec 2012
Nature

Volume: 493, P: 561-564
Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia

Yoichi Wada
Atsuo Kikuchi
Shigeo Kure
Amendments and Corrections05 Jun 2020
Genetics in Medicine

Volume: 22, P: 1281
Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutation

Tomoko Lee
Maiko Misaki
Yasuhiro Takeshima
ResearchOpen Access16 Aug 2018
Human Genome Variation

Volume: 5, P: 1-4
Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiency

Mina Nakama
Hideo Sasai
Toshiyuki Fukao
ResearchOpen Access02 Apr 2020
Human Genome Variation

Volume: 7, P: 1-4
Biallelic GALM pathogenic variants cause a novel type of galactosemia

Yoichi Wada
Atsuo Kikuchi
Shigeo Kure
Research19 Oct 2018
Genetics in Medicine

Volume: 21, P: 1286-1294

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Retraction Note: GlcNAcylation of a histone methyltransferase in retinoic-acid-induced granulopoiesis

GlcNAcylation of histone H2B facilitates its monoubiquitination

Galactose mutarotase deficiency as the galactosemia type IV

Attenuated fusogenicity and pathogenicity of SARS-CoV-2 Omicron variant

GlcNAcylation of a histone methyltransferase in retinoic-acid-induced granulopoiesis

TET2 promotes histone O-GlcNAcylation during gene transcription

Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia

Late-onset ornithine transcarbamylase deficiency caused by a somatic mosaic mutation

Novel HADHB mutations in a patient with mitochondrial trifunctional protein deficiency

Biallelic GALM pathogenic variants cause a novel type of galactosemia

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