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Department of Otorhinolaryngology,
Head and Neck Surgery,
Department of Otorhinolaryngology, Head and Neck Surgery
Masato Fujioka has not added Biography.
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Proinflammatory cytokines expression in noise-induced damaged cochlea.
Journal of neuroscience research Mar, 2006 | Pubmed ID: 16429448
Blockade of interleukin-6 signaling suppressed cochlear inflammatory response and improved hearing impairment in noise-damaged mice cochlea.
Neuroscience research Apr, 2010 | Pubmed ID: 20026135
Generating mouse models of degenerative diseases using Cre/lox-mediated in vivo mosaic cell ablation.
The Journal of clinical investigation Jun, 2011 | Pubmed ID: 21576819
Notch inhibition induces cochlear hair cell regeneration and recovery of hearing after acoustic trauma.
Neuron Jan, 2013 | Pubmed ID: 23312516
A psychometric validation of the Japanese versions of new questionnaires on tinnitus (THI-12, TRS, TRSw, TSS, and TSSw).
Acta oto-laryngologica May, 2013 | Pubmed ID: 23320814
The autophagy pathway maintained signaling crosstalk with the Keap1-Nrf2 system through p62 in auditory cells under oxidative stress.
Cellular signalling Feb, 2015 | Pubmed ID: 25435427
Manipulating cell fate in the cochlea: a feasible therapy for hearing loss.
Trends in neurosciences Mar, 2015 | Pubmed ID: 25593106
ERK2 mediates inner hair cell survival and decreases susceptibility to noise-induced hearing loss.
Scientific reports Nov, 2015 | Pubmed ID: 26577290
Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea.
Scientific reports Feb, 2016 | Pubmed ID: 26915689
Overlapping expression of anion exchangers in the cochlea of a non-human primate suggests functional compensation.
Neuroscience research Sep, 2016 | Pubmed ID: 27091614
Expression pattern of wolframin, the WFS1 (Wolfram syndrome-1 gene) product, in common marmoset (Callithrix jacchus) cochlea.
Neuroreport 08, 2016 | Pubmed ID: 27341211
Distinct Expression Pattern of a Deafness Gene, KIAA1199, in a Primate Cochlea.
BioMed research international , 2016 | Pubmed ID: 27403418
Cochlear Cell Modeling Using Disease-Specific iPSCs Unveils a Degenerative Phenotype and Suggests Treatments for Congenital Progressive Hearing Loss.
Cell reports 01, 2017 | Pubmed ID: 28052261
Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss.
Orphanet journal of rare diseases Sep, 2017 | Pubmed ID: 28946916
Expression pattern of EYA4 in the common marmoset (Callithrix jacchus) cochlea.
Neuroscience letters Jan, 2018 | Pubmed ID: 29054432
Engraftment of Human Pluripotent Stem Cell-derived Progenitors in the Inner Ear of Prenatal Mice.
Scientific reports Jan, 2018 | Pubmed ID: 29386634
Keio University School of Medicine
Sho Kurihara*,1,2,
Masato Fujioka*,3,
Tomohiko Yoshida*,1,2,
Makoto Koizumi4,
Kaoru Ogawa3,
Hiromi Kojima2,
Hirotaka James Okano1
1Division of Regenerative Medicine, Jikei University School of Medicine,
2Department of Otorhinolaryngology, Jikei University School of Medicine,
3Department of Otorhinolaryngology, Head and Neck Surgery, Keio University School of Medicine,
4Laboratory Animal Facilities, Jikei University School of Medicine
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