Author

Kazunori Namba

Observed name: Namba, Kazunori

Institution: National Institute of Japanese Literature

Observed institutions: Nihon University, National Institute of Japanese Literature, Sapporo Medical University, RIKEN Center for Brain Science, Tokyo Medical Center, Tokyo Metropolitan Institute of Medical Science, Eiju General Hospital, RIKEN, National Hospital Organization, Institute for Protein Research, The University of Osaka, The University of Osaka

OpenAlex ID: A5103804392

The Crystal Structure of a Virus-like Particle from the Hyperthermophilic Archaeon Pyrococcus furiosus Provides Insight into the Evolution of Viruses

2007 · Fusamichi Akita, Khoon Tee Chong, et al. · Journal of Molecular Biology · 135

Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study

2013 · Hideki Mutai, Naohiro Suzuki, et al. · Orphanet Journal of Rare Diseases · 90

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Regulation of pharmacology by hetero-oligomerization between A1 adenosine receptor and P2Y2 receptor

2006 · Tokiko Suzuki, Kazunori Namba, et al. · Biochemical and Biophysical Research Communications · 74

Close correlation between the birth date of purkinje cells and the longitudinal compartmentalization of the mouse adult cerebellum

2011 · Kazunori Namba, Izumi Sugihara, et al. · The Journal of Comparative Neurology · 55

High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss

2015 · Kunio Mizutari, Hideki Mutai, et al. · Orphanet Journal of Rare Diseases · 47

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A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss

2014 · Sawako Masuda, Kazunori Namba, et al. · Biochemical and Biophysical Research Communications · 31

Assembly of single-shelled cores and double-shelled virus-like particles after baculovirus expression of major structural proteins P3, P7 and P8 of Rice dwarf virus

2003 · Kyoji Hagiwara, Takahiko Higashi, et al. · Journal of General Virology · 31

Dimerization of G protein-coupled purinergic receptors: increasing the diversity of purinergic receptor signal responses and receptor functions

2010 · Hiroyasu Nakata, Tokiko Suzuki, et al. · Journal of Receptors and Signal Transduction · 30

Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients With Distinct Clinical and Genetic Backgrounds

2018 · Kyoko Kitao, Hideki Mutai, et al. · Ear and Hearing · 29

Immunogold electron microscopic evidence of in situ formation of homo- and heteromeric purinergic adenosine A1 and P2Y2 receptors in rat brain

2010 · Kazunori Namba, Tokiko Suzuki, et al. · BMC Research Notes · 28

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Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

2017 · Nobuko Yamamoto, Hideki Mutai, et al. · Orphanet Journal of Rare Diseases · 27

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Expression and Molecular Characterization of Spherical Particles Derived from the Genome of the Hyperthermophilic Euryarchaeote Pyrococcus furiosus

2005 · Kazunori Namba, Kyoji Hagiwara, et al. · The Journal of Biochemistry · 22

Homozygous EDNRB mutation in a patient with Waardenburg syndrome type 1

2017 · Noriko Morimoto, Hideki Mutai, et al. · Auris Nasus Larynx · 21

Epha4 controls the midline crossing and contralateral axonal projections of inferior olive neurons

2011 · Mitsuhiro Hashimoto, Rie Ito, et al. · The Journal of Comparative Neurology · 21

Genetic analysis ofPAX3for diagnosis of Waardenburg syndrome type I

2012 · Tatsuo Matsunaga, Hideki Mutai, et al. · Acta Oto-Laryngologica · 19

A highly conserved tryptophan residue in the fourth transmembrane domain of the A1 adenosine receptor is essential for ligand binding but not receptor homodimerization

2009 · Tokiko Suzuki, Kazunori Namba, et al. · Journal of Neurochemistry · 19

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Vestibular dysfunction in a Japanese patient with a mutation in the gene OPA1

2010 · Kunio Mizutari, Tatsuo Matsunaga, et al. · Journal of the Neurological Sciences · 18

In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing loss

2012 · Kazunori Namba, Hideki Mutai, et al. · BMC Research Notes · 15

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Frequency and specific characteristics of the incomplete partition type III anomaly in children

2016 · Ayako Kanno, Hideki Mutai, et al. · The Laryngoscope · 14

Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD1

2016 · Shujiro B. Minami, Hideki Mutai, et al. · Auris Nasus Larynx · 13

Molecular Impairment Mechanisms of Novel OPA1 Mutations Predicted by Molecular Modeling in Patients With Autosomal Dominant Optic Atrophy and Auditory Neuropathy Spectrum Disorder

2016 · Kazunori Namba, Hideki Mutai, et al. · Otology & Neurotology · 13

Hetero-oligomerization and Specificity Changes of G Protein-Coupled Purinergic Receptors

2013 · Tokiko Suzuki, Kazunori Namba, et al. · Methods in enzymology on CD-ROM/Methods in enzymology · 12

Moderate hearing loss associated with a novel KCNQ4 non-truncating mutation located near the N-terminus of the pore helix

2013 · Takahisa Watabe, Tatsuo Matsunaga, et al. · Biochemical and Biophysical Research Communications · 10

Novel OTOF pathogenic variant segregating with non-syndromic hearing loss in a consanguineous family from tribal Rajouri in Jammu and Kashmir

2019 · Raja A.H. Kuchay, Yaser Rafiq Mir, et al. · International Journal of Pediatric Otorhinolaryngology · 8

Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome

2014 · Yukiko Arimoto, Kazunori Namba, et al. · Gene · 7

Works count: 53

Citation count: 807

H-index: 17

I10-index: 23