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S Usami

Showing results (231-240 of 237) with videos related to

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European Journal of Human Genetics : EJHG|January 15, 1999
Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutationS Abe, S Usami, H Shinkawa, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|September 8, 2011
Outcomes of endoscopic and surgical resection for a second primary cancer in the residual cervical esophagus after thoracic esophagectomyS Usami, S Motoyama, T Matsuhashi, et al.
Clinical Genetics|September 9, 2015
Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss populationH Moteki, H Azaiez, K T Booth, et al.
Journal of Medical Genetics|January 14, 2000
Prevalence of mitochondrial gene mutations among hearing impaired patientsS Usami, S Abe, J Akita, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 24, 1999
Expression of the P2X(2) receptor subunit of the ATP-gated ion channel in the cochlea: implications for sound transduction and auditory neurotransmissionG D Housley, R Kanjhan, N P Raybould, et al.
Acta Oto-Laryngologica. Supplementum|December 17, 2013
Towards a consensus on a hearing preservation classification systemHenryk Skarzynski, P van de Heyning, S Agrawal, et al.
Pageof 24

Showing results (231-240 of 237) with videos related to

Sort By:
Pageof 24
You have reached the last page of results.This site can display upto 237 results.
European Journal of Human Genetics : EJHG|January 15, 1999
Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutationS Abe, S Usami, H Shinkawa, et al.
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus|September 8, 2011
Outcomes of endoscopic and surgical resection for a second primary cancer in the residual cervical esophagus after thoracic esophagectomyS Usami, S Motoyama, T Matsuhashi, et al.
Clinical Genetics|September 9, 2015
Comprehensive genetic testing with ethnic-specific filtering by allele frequency in a Japanese hearing-loss populationH Moteki, H Azaiez, K T Booth, et al.
Journal of Medical Genetics|January 14, 2000
Prevalence of mitochondrial gene mutations among hearing impaired patientsS Usami, S Abe, J Akita, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|September 24, 1999
Expression of the P2X(2) receptor subunit of the ATP-gated ion channel in the cochlea: implications for sound transduction and auditory neurotransmissionG D Housley, R Kanjhan, N P Raybould, et al.
Acta Oto-Laryngologica. Supplementum|December 17, 2013
Towards a consensus on a hearing preservation classification systemHenryk Skarzynski, P van de Heyning, S Agrawal, et al.
Pageof 24