Nature Search

Associations of family history of hypertension, genetic, and lifestyle risks with incident hypertension

Masato Takase
Takumi Hirata
Masayuki Yamamoto
ResearchOpen Access13 Aug 2025
Hypertension Research

Volume: 48, P: 2606-2617
Lysine-arginine imbalance overcomes therapeutic tolerance governed by the transcription factor E3-lysosome axis in glioblastoma

Glioblastoma (GBM) treatment faces challenges due to drug resistance. Here, the authors show that lysine-arginine balance supports lysosomes mediated tolerance to temozolomide and lysine restriction mimetic increases anticancer therapies in GBM preclinical models.

Yongwei Jing
Masahiko Kobayashi
Atsushi Hirao
ResearchOpen Access01 Apr 2025
Nature Communications

Volume: 16, P: 1-20
Synthesis and Conformations of A-B-A Tri-Block Copolymers with Hydrophobic Poly(γ-benzyl l-glutamate) and Hydrophilic Poly(ethylene oxide)

Kohei Kugo
Atsushi Ohji
Jun Nishino
Research01 Apr 1987
Polymer Journal

Volume: 19, P: 375-381
Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobank

Aye Ko Ko Minn
Motomichi Matsuzaki
Gen Tamiya
ResearchOpen Access03 Apr 2025
Journal of Human Genetics

Volume: 70, P: 287-296
Features of sacral alar fatigue fractures in adolescent athletes with overuse

Masaki Tatsumura
Fumihiko Eto
Masashi Yamazaki
ResearchOpen Access19 Apr 2021
Scientific Reports

Volume: 11, P: 1-6
Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay

Kohei Hamanaka
Atsushi Fujita
Naomichi Matsumoto
ResearchOpen Access26 Aug 2025
npj Genomic Medicine

Volume: 10, P: 1-12
Simulating metabolic pathways to enhance interpretations of metabolome genome-wide association studies

Shun Kodate
Mitsuharu Sato
Kengo Kinoshita
ResearchOpen Access16 May 2025
Scientific Reports

Volume: 15, P: 1-11
Blood pressure during long-term cilostazol-based dual antiplatelet therapy after stroke: a post hoc analysis of the CSPS.com trial

Kazunori Toyoda
Masatoshi Koga
Hiroaki Tanaka
ResearchOpen Access09 Jul 2024
Hypertension Research

Volume: 47, P: 2238-2249
Biallelic TEDC1 variants cause a new syndrome with severe growth impairment and endocrine complications

Noriko Miyake
Kentaro Shiga
Naomichi Matsumoto
Research20 Feb 2025
European Journal of Human Genetics

Volume: 33, P: 738-746
Extrastriatal dopamine D2/3 receptor binding, functional connectivity, and autism socio-communicational deficits: a PET and fMRI study

Chihiro Murayama
Toshiki Iwabuchi
Hidenori Yamasue
Research18 Feb 2022
Molecular Psychiatry

Volume: 27, P: 2106-2113
Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growth

Makoto Saito
Tomohiro Kamoda
Emiko Noguchi
Research24 Nov 2011
Journal of Human Genetics

Volume: 57, P: 109-114
Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age

Hisato Suzuki
Hiroko Fukushima
Ryo Sumazaki
Research19 May 2016
Journal of Human Genetics

Volume: 61, P: 797-801
53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair

The ATM signalling mediator proteins 53BP1 and KAP-1 are required for heterochromatic double-strand break DNA repair. 53BP1 aids Mre11, NBS1 and ATM accumulation at heterochromatic breaks, leading to localized phosphorylation of KAP-1 by ATM.

Angela T. Noon
Atsushi Shibata
Aaron A. Goodarzi
Research17 Jan 2010
Nature Cell Biology

Volume: 12, P: 177-184
Neural mechanisms underlying rule selection based on response evaluation: a near-infrared spectroscopy study

Taeko Harada
Toshiki Iwabuchi
Yoko Hoshi
ResearchOpen Access30 Nov 2022
Scientific Reports

Volume: 12, P: 1-11
Corticosteroids for hospitalized patients with mild to critically-ill COVID-19: a multicenter, retrospective, propensity score-matched study

Satoshi Ikeda
Toshihiro Misumi
Takashi Ogura
ResearchOpen Access21 May 2021
Scientific Reports

Volume: 11, P: 1-13
Identification of neurodevelopmental transition patterns from infancy to early childhood and risk factors predicting descending transition

Takeo Kato
Tomoko Nishimura
Nori Takei
ResearchOpen Access21 Mar 2022
Scientific Reports

Volume: 12, P: 1-10
Comparative analysis of seven types of superoxide dismutases for their ability to respond to oxidative stress in Bombyx mori

Yuta Kobayashi
Yosui Nojima
Hiroko Tabunoki
ResearchOpen Access18 Feb 2019
Scientific Reports

Volume: 9, P: 1-12
Aquarius is required for proper CtIP expression and homologous recombination repair

Ryo Sakasai
Mayu Isono
Kuniyoshi Iwabuchi
ResearchOpen Access23 Oct 2017
Scientific Reports

Volume: 7, P: 1-11
Methylmercury induces neuronal cell death by inducing TNF-α expression through the ASK1/p38 signaling pathway in microglia

Takashi Toyama
Takayuki Hoshi
Gi-Wook Hwang
ResearchOpen Access10 May 2021
Scientific Reports

Volume: 11, P: 1-13

Search

Associations of family history of hypertension, genetic, and lifestyle risks with incident hypertension

Lysine-arginine imbalance overcomes therapeutic tolerance governed by the transcription factor E3-lysosome axis in glioblastoma

Synthesis and Conformations of A-B-A Tri-Block Copolymers with Hydrophobic Poly(γ-benzyl l-glutamate) and Hydrophilic Poly(ethylene oxide)

Profiling of runs of homozygosity from whole-genome sequence data in Japanese biobank

Features of sacral alar fatigue fractures in adolescent athletes with overuse

Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay

Simulating metabolic pathways to enhance interpretations of metabolome genome-wide association studies

Blood pressure during long-term cilostazol-based dual antiplatelet therapy after stroke: a post hoc analysis of the CSPS.com trial

Biallelic TEDC1 variants cause a new syndrome with severe growth impairment and endocrine complications

Extrastriatal dopamine D2/3 receptor binding, functional connectivity, and autism socio-communicational deficits: a PET and fMRI study

Association of adiponectin polymorphism with cord blood adiponectin concentrations and intrauterine growth

Genotyping NUDT15 can predict the dose reduction of 6-MP for children with acute lymphoblastic leukemia especially at a preschool age

53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair

Neural mechanisms underlying rule selection based on response evaluation: a near-infrared spectroscopy study

Corticosteroids for hospitalized patients with mild to critically-ill COVID-19: a multicenter, retrospective, propensity score-matched study

Identification of neurodevelopmental transition patterns from infancy to early childhood and risk factors predicting descending transition

Comparative analysis of seven types of superoxide dismutases for their ability to respond to oxidative stress in Bombyx mori

Aquarius is required for proper CtIP expression and homologous recombination repair

Methylmercury induces neuronal cell death by inducing TNF-α expression through the ASK1/p38 signaling pathway in microglia

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