Genetics, Hearing loss, Mutation, Cell biology and Missense mutation are his primary areas of study. As part of his studies on Genetics, Shin-ichi Usami often connects relevant areas like Sensorineural hearing loss. Shin-ichi Usami has researched Hearing loss in several fields, including Pendred syndrome, Point mutation, Mitochondrial DNA and Genotype.
His work in the fields of Mutation, such as Gene mutation, overlaps with other areas such as Connexin. His Cell biology research is multidisciplinary, incorporating perspectives in Organ of Corti, Cochlea, Biochemistry, Postsynaptic density and Immunogold labelling. His studies in Missense mutation integrate themes in fields like Frameshift mutation and Usher syndrome.
His primary areas of investigation include Hearing loss, Audiology, Genetics, Sensorineural hearing loss and Mutation. The Hearing loss study combines topics in areas such as Missense mutation, Mitochondrial DNA, Pediatrics and Point mutation. His Audiology study frequently links to other fields, such as Etiology.
His studies in Gene, Mutation, Genetic testing, DNA sequencing and Allele frequency are all subfields of Genetics research. His Sensorineural hearing loss study frequently draws connections to other fields, such as Compound heterozygosity. As part of his studies on Mutation, Shin-ichi Usami frequently links adjacent subjects like Genotype.
Shin-ichi Usami mostly deals with Hearing loss, Audiology, Genetics, Cochlear implant and Sensorineural hearing loss. His work deals with themes such as Mutation, Proband, Gene, Gene mutation and Mutation, which intersect with Hearing loss. His work on Point mutation as part of general Mutation study is frequently linked to Erythropoietin-producing hepatocellular receptor, Pendrin and EPH receptor A2, bridging the gap between disciplines.
His Genetics study frequently links to adjacent areas such as Congenital hearing loss. His Cochlear implant research is multidisciplinary, relying on both Surgery, Implant, Hearing preservation and Dentistry. His Sensorineural hearing loss research incorporates elements of Thrombocytopenic purpura, Nephritis and Rare disease.
Shin-ichi Usami spends much of his time researching Hearing loss, Audiology, Gene, Genetics and Sensorineural hearing loss. His Hearing loss study incorporates themes from Proband, Internal medicine, Cohort, Haplotype and Cochlear implant. His study in Audiology is interdisciplinary in nature, drawing from both Magnetic resonance imaging and Locus.
Shin-ichi Usami is involved in the study of Gene that focuses on Mutation in particular. The study incorporates disciplines such as Audiometry, Wolfram syndrome, Family history and Gene family in addition to Mutation. His Sensorineural hearing loss research is multidisciplinary, incorporating elements of STRC and Bioinformatics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Prevalent connexin 26 gene (GJB2) mutations in Japanese
Satoko Abe;Shin-ichi Usami;Hideichi Shinkawa;Philip M Kelley.
Journal of Medical Genetics (2000)
Organization of AMPA Receptor Subunits at a Glutamate Synapse: A Quantitative Immunogold Analysis of Hair Cell Synapses in the Rat Organ of Corti
Atsushi Matsubara;Jon H. Laake;Svend Davanger;Shin Ichi Usami.
The Journal of Neuroscience (1996)
Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations
Shin Ichi Usami;Satoko Abe;Mike D. Weston;Hideichi Shinkawa.
Human Genetics (1999)
Differential Localization of δ Glutamate Receptors in the Rat Cerebellum: Coexpression with AMPA Receptors in Parallel Fiber–Spine Synapses and Absence from Climbing Fiber–Spine Synapses
Alf Sommer Landsend;Mahmood Amiry-Moghaddam;Atsushi Matsubara;Linda Bergersen.
The Journal of Neuroscience (1997)
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
Park Hj;Shaukat S;Liu Xz;Hahn Sh.
Journal of Medical Genetics (2003)
Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese
Koji Tsukamoto;Hiroaki Suzuki;Daisuke Harada;Atsushi Namba.
European Journal of Human Genetics (2003)
Prevalence of mitochondrial gene mutations among hearing impaired patients.
Shin-ichi Usami;Satoko Abe;Jiro Akita;Atsushi Namba.
Journal of Medical Genetics (2000)
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation.
Akihiro Ohtsuka;Isamu Yuge;Shinobu Kimura;Atsushi Namba.
Human Genetics (2003)
Expression of the P2X(2) receptor subunit of the ATP-gated ion channel in the cochlea: implications for sound transduction and auditory neurotransmission.
Gary D. Housley;Refik Kanjhan;Nicholas P. Raybould;Denise Greenwood.
The Journal of Neuroscience (1999)
Congenital hearing loss.
Anna M.H. Korver;Richard J.H. Smith;Guy Van Camp;Mark R. Schleiss.
Nature Reviews Disease Primers (2017)
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