Kanako Goto

Yushima, Japan

Last Updated: 09/26/2026

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Found 12 publications

Visualization and quantification of RANK-RANKL binding for application to disease investigations and drug discovery.

Visualization and quantification of RANK-RANKL binding for application to disease investigations and drug discovery.

Journal: Bone

Published: January 26, 2025

Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation.

Characteristics of Japanese Patients with Becker Muscular Dystrophy and Intermediate Muscular Dystrophy in a Japanese National Registry of Muscular Dystrophy (Remudy): Heterogeneity and Clinical Variation.

Journal: Journal of neuromuscular diseases

Published: April 05, 2018

Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Journal: Journal of human genetics

Published: September 26, 2017

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.

Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.

Journal: Orphanet journal of rare diseases

Published: June 14, 2017

Corrigendum to "Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations": [Neuromuscular Disorders 26/4-5 (2016) 300-308].

Corrigendum to "Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations": [Neuromuscular Disorders 26/4-5 (2016) 300-308].

Journal: Neuromuscular disorders : NMD

Published: June 18, 2016

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations.

Journal: Journal of human genetics

Published: November 16, 2015

Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations.

Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations.

Journal: Neuromuscular disorders : NMD

Published: September 17, 2015

Congenital fiber type disproportion myopathy caused by LMNA mutations.

Congenital fiber type disproportion myopathy caused by LMNA mutations.

Journal: Journal of the neurological sciences

Published: December 05, 2013

Association between a C8orf13-BLK polymorphism and polymyositis/dermatomyositis in the Japanese population: an additive effect with STAT4 on disease susceptibility.

Association between a C8orf13-BLK polymorphism and polymyositis/dermatomyositis in the Japanese population: an additive effect with STAT4 on disease susceptibility.

Journal: PloS one

Published: October 10, 2013

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy).

Journal: Orphanet journal of rare diseases

Published: January 04, 2013

Teaching NeuroImages: unilateral arm and contralateral leg amyotrophy in FSHD: unusual presentation.

Teaching NeuroImages: unilateral arm and contralateral leg amyotrophy in FSHD: unusual presentation.

Journal: Neurology

Published: August 02, 2012

Positive association between STAT4 polymorphisms and polymyositis/dermatomyositis in a Japanese population.

Positive association between STAT4 polymorphisms and polymyositis/dermatomyositis in a Japanese population.

Journal: Annals of the rheumatic diseases

Published: March 10, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026