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Guanine nucleotide‐binding protein 1 is one of the key molecules contributing to cancer cell radioresistance

Cancer science, 2014-10, Vol.105 (10), p.1351-1359

2014

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Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures

Journal of human genetics, 2022-09, Vol.67 (9), p.505-513

2022

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Successful cochlear implantation in a patient with Epstein syndrome during long-term follow-up

Auris, nasus, larynx, 2022-04, Vol.49 (2), p.308-312

2022

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Effects of salicylate derivatives on localization of p.H723R allele product of SLC26A4

Auris, nasus, larynx, 2022-12, Vol.49 (6), p.928-937

2022

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(Life) Saved by Health Informatics―Real World Data to Precision Medicine

Japan Journal of Medical Informatics, 2018/04/25, Vol.38(1), pp.25-32

2018

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Salicylate restores transport function and anion exchanger activity of missense pendrin mutations

Hearing research, 2010-12, Vol.270 (1), p.110-118

2010

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Clinical characteristics of delayed endolymphatic hydrops in Japan: A nationwide survey by the Peripheral Vestibular Disorder Research Committee of Japan

Acta oto-laryngologica, 2010-10, Vol.130 (10), p.1135-1140

2010

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Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct

Journal of human genetics, 2006-09, Vol.51 (9), p.805-810

2006

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Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients

PloS one, 2016-09, Vol.11 (9), p.e0162230-e0162230

2016

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Deafness gene expression patterns in the mouse cochlea found by microarray analysis

PloS one, 2014-03, Vol.9 (3), p.e92547-e92547

2014

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Problem and Assignment for Distinguishing the Usher Syndrome Type

Nippon Jibiinkoka Gakkai Kaiho, 2012, Vol.115(10), pp.894-901

2012

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μ-Crystallin as an Intracellular 3,5,3′-Triiodothyronine Holder in Vivo

Molecular endocrinology (Baltimore, Md.), 2007-04, Vol.21 (4), p.885-894

2007

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High-throughput screening for GJB2 mutations—its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations

Auris, nasus, larynx, 2002-07, Vol.29 (3), p.231-239

2002

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μ-Crystallin, New Candidate Protein in Endotoxin-Induced Uveitis

Investigative ophthalmology & visual science, 2010-07, Vol.51 (7), p.3554

2010

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Multicenter Clinical Study of Vibrant Soundbridge® in Japan: Analysis of Subjective Questionnaires

Nippon Jibiinkoka Gakkai Kaiho, 2015/11/20, Vol.118(11), pp.1309-1318

2015

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Round Window VIBROPLASTY® for Patients with Mixed or Conductive Hearing Loss: A Comparative Study of Middle Ear Disease and Congenital Aural Atresia

Nippon Jibiinkoka Gakkai Kaiho, 2016/01/20, Vol.119(1), pp.37-45

2016

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（いのち）医療情報が救ういのち―リアルワールドデータからプレシジョンメディシンへ

医療情報学, 2018/04/25, Vol.38(1), pp.25-32

2018

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Future of cochlear implants: a new approach to cochlear implants, low stress, and preservation of residual hearing acuity

Nippon Jibi Inkoka Gakkai Kaiho, 2011-10, Vol.114 (10), p.801-806

2011

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micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo

Molecular endocrinology (Baltimore, Md.), 2007-04, Vol.21 (4), p.885-894

2007

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A case of enlarged vestibular aqueduct syndrome with PDS gene mutations

Nippon Jibi Inkoka Gakkai Kaiho, 2002-02, Vol.105 (2), p.174-177

2002

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{mu}-Crystallin, new candidate protein in endotoxin-induced uveitis

Investigative ophthalmology & visual science, 2010-07, Vol.51 (7), p.3554-3559

2010

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Multicenter Clinical Study of Bone-anchored Hearing Aids in Japan —Application for Congenital Auricular Atresia

Nippon Jibiinkoka Gakkai Kaiho, 2011, Vol.114(9), pp.761-767

2011

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Multicenter clinical study of bone-anchored hearing aids in Japan-comparison with conventional hearing aids

Audiology Japan, 2010, Vol.53 (3), p.224-231

2010

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Effective case of genetic testing in a bilateral deafness patient

AUDIOLOGY JAPAN, 2009, Vol.52(4), pp.214-219

2009

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EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family

Journal of human genetics, 1999-01, Vol.44 (4), p.261-265

1999

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Guanine nucleotide‐binding protein 1 is one of the key molecules contributing to cancer cell radioresistance

Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures

Successful cochlear implantation in a patient with Epstein syndrome during long-term follow-up

Effects of salicylate derivatives on localization of p.H723R allele product of SLC26A4

(Life) Saved by Health Informatics―Real World Data to Precision Medicine

Salicylate restores transport function and anion exchanger activity of missense pendrin mutations

Clinical characteristics of delayed endolymphatic hydrops in Japan: A nationwide survey by the Peripheral Vestibular Disorder Research Committee of Japan

Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients

Deafness gene expression patterns in the mouse cochlea found by microarray analysis

Problem and Assignment for Distinguishing the Usher Syndrome Type

μ-Crystallin as an Intracellular 3,5,3′-Triiodothyronine Holder in Vivo

High-throughput screening for GJB2 mutations—its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations

μ-Crystallin, New Candidate Protein in Endotoxin-Induced Uveitis

Multicenter Clinical Study of Vibrant Soundbridge® in Japan: Analysis of Subjective Questionnaires

Round Window VIBROPLASTY® for Patients with Mixed or Conductive Hearing Loss: A Comparative Study of Middle Ear Disease and Congenital Aural Atresia

（いのち）医療情報が救ういのち―リアルワールドデータからプレシジョンメディシンへ

Future of cochlear implants: a new approach to cochlear implants, low stress, and preservation of residual hearing acuity

micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo

A case of enlarged vestibular aqueduct syndrome with PDS gene mutations

{mu}-Crystallin, new candidate protein in endotoxin-induced uveitis

Multicenter Clinical Study of Bone-anchored Hearing Aids in Japan —Application for Congenital Auricular Atresia

Multicenter clinical study of bone-anchored hearing aids in Japan-comparison with conventional hearing aids

Effective case of genetic testing in a bilateral deafness patient

EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family

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