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Pathologic Features of Anti-Mi-2 Dermatomyositis

Neurology, 2021-01, Vol.96 (3), p.e448

2021

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Anti-nuclear matrix protein 2 antibody-positive inflammatory myopathies represent extensive myositis without dermatomyositis-specific rash

Rheumatology (Oxford, England), 2022-03, Vol.61 (3), p.1222-1227

2022

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HIV-1 gag recruits PACSIN2 to promote virus spreading

Proceedings of the National Academy of Sciences - PNAS, 2018-07, Vol.115 (27), p.7093-7098

2018

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Redox-assisted regulation of Ca2+ homeostasis in the endoplasmic reticulum by disulfide reductase ERdj5

Proceedings of the National Academy of Sciences - PNAS, 2016-10, Vol.113 (41), p.E6055-E6063

2016

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Deep convolutional neural network-based algorithm for muscle biopsy diagnosis

Laboratory investigation, 2022-03, Vol.102 (3), p.220-226

2022

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Causative variant profile of collagen VI-related dystrophy in Japan

Orphanet journal of rare diseases, 2021-06, Vol.16 (1), p.1-284, Article 284

2021

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The oxidative folding of nascent polypeptides provides electrons for reductive reactions in the ER

Cell reports (Cambridge), 2023-07, Vol.42 (7), p.112742-112742, Article 112742

2023

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Reliability of antinuclear matrix protein 2 antibody assays in idiopathic inflammatory myopathies is dependent on target protein properties

Journal of dermatology, 2022-04, Vol.49 (4), p.441-447

2022

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Cryo-EM structures of human zinc transporter ZnT7 reveal the mechanism of Zn2+ uptake into the Golgi apparatus

Nature communications, 2023-08, Vol.14 (1), p.4770-4770, Article 4770

2023

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A recurrent homozygous ACTN2 variant associated with core myopathy

Acta neuropathologica, 2021-10, Vol.142 (4), p.785-788

2021

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COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency

Annals of neurology, 2019-08, Vol.86 (2), p.193-202

2019

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HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis

PloS one, 2020-08, Vol.15 (8), p.e0237890-e0237890

2020

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Structural Basis of Sarco/Endoplasmic Reticulum Ca2+-ATPase 2b Regulation via Transmembrane Helix Interplay

Cell reports (Cambridge), 2019-04, Vol.27 (4), p.1221-1230.e3

2019

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Mutations in the J domain of DNAJB6 cause dominant distal myopathy

Neuromuscular disorders : NMD, 2020-01, Vol.30 (1), p.38-46

2020

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The Highly Dynamic Nature of ERdj5 Is Key to Efficient Elimination of Aberrant Protein Oligomers through ER-Associated Degradation

Structure (London), 2017-06, Vol.25 (6), p.846-857.e4

2017

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Radically Different Thioredoxin Domain Arrangement of ERp46, an Efficient Disulfide Bond Introducer of the Mammalian PDI Family

Structure (London), 2014-03, Vol.22 (3), p.431-443

2014

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The ESCRT pathway and HIV-1 budding

Biochemical Society transactions, 2009-02, Vol.37 (Pt 1), p.181

2009

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Cryo-EM structures of SERCA2b reveal the mechanism of regulation by the luminal extension tail

Science advances, 2020-08, Vol.6 (33), p.eabb0147-eabb0147

2020

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Human Immunodeficiency Virus Type 1 Gag Engages the Bro1 Domain of ALIX/AIP1 through the Nucleocapsid

Journal of Virology, 2008-02, Vol.82 (3), p.1389-1398

2008

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Divergent Bro1 Domains Share the Capacity To Bind Human Immunodeficiency Virus Type 1 Nucleocapsid and To Enhance Virus-Like Particle Production

Journal of Virology, 2009-07, Vol.83 (14), p.7185-7193

2009

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Nucleotide-Dependent Conformational Changes and Assembly of the AAA ATPase SKD1/VPS4B

Traffic (Copenhagen, Denmark), 2008-12, Vol.9 (12), p.2180-2189

2008

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Dermatomyositis: Muscle Pathology According to Antibody Subtypes

Neurology, 2022-02, Vol.98 (7), p.e739

2022

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Physician-Level Aggregated Classifier for Genetic Muscle Disorders

2019 IEEE 16th International Symposium on Biomedical Imaging (ISBI 2019), 2019, p.1850-1854

2019

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IEEE_Xplore

Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy

Human genome variation, 2018-01, Vol.5 (1), p.9-5, Article 9

2018

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A Fatal Case of Congenital Langerhans Cell Histiocytosis with Disseminated Cutaneous Lesions in a Premature Neonate

Case reports in pediatrics, 2016-01, Vol.2016, p.4972180-4

2016

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Pathologic Features of Anti-Mi-2 Dermatomyositis

Anti-nuclear matrix protein 2 antibody-positive inflammatory myopathies represent extensive myositis without dermatomyositis-specific rash

HIV-1 gag recruits PACSIN2 to promote virus spreading

Redox-assisted regulation of Ca2+ homeostasis in the endoplasmic reticulum by disulfide reductase ERdj5

Deep convolutional neural network-based algorithm for muscle biopsy diagnosis

Causative variant profile of collagen VI-related dystrophy in Japan

The oxidative folding of nascent polypeptides provides electrons for reductive reactions in the ER

Reliability of antinuclear matrix protein 2 antibody assays in idiopathic inflammatory myopathies is dependent on target protein properties

Cryo-EM structures of human zinc transporter ZnT7 reveal the mechanism of Zn2+ uptake into the Golgi apparatus

A recurrent homozygous ACTN2 variant associated with core myopathy

COX6A2 variants cause a muscle‐specific cytochrome c oxidase deficiency

HLA-DRB1 allele and autoantibody profiles in Japanese patients with inclusion body myositis

Structural Basis of Sarco/Endoplasmic Reticulum Ca2+-ATPase 2b Regulation via Transmembrane Helix Interplay

Mutations in the J domain of DNAJB6 cause dominant distal myopathy

The Highly Dynamic Nature of ERdj5 Is Key to Efficient Elimination of Aberrant Protein Oligomers through ER-Associated Degradation

Radically Different Thioredoxin Domain Arrangement of ERp46, an Efficient Disulfide Bond Introducer of the Mammalian PDI Family

The ESCRT pathway and HIV-1 budding

Cryo-EM structures of SERCA2b reveal the mechanism of regulation by the luminal extension tail

Human Immunodeficiency Virus Type 1 Gag Engages the Bro1 Domain of ALIX/AIP1 through the Nucleocapsid

Divergent Bro1 Domains Share the Capacity To Bind Human Immunodeficiency Virus Type 1 Nucleocapsid and To Enhance Virus-Like Particle Production

Nucleotide-Dependent Conformational Changes and Assembly of the AAA ATPase SKD1/VPS4B

Dermatomyositis: Muscle Pathology According to Antibody Subtypes

Physician-Level Aggregated Classifier for Genetic Muscle Disorders

Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy

A Fatal Case of Congenital Langerhans Cell Histiocytosis with Disseminated Cutaneous Lesions in a Premature Neonate

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