Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Otolaryngology/Audiology"'
1
Evidence of Key Tinnitus-Related Brain Regions Documented by a Unique Combination of Manganese-Enhanced MRI and Acoustic Startle Reflex Testing
Autor: Bruce A. Berkowitz, Gary Rajah, David Bissig, Najab Mirza, Avril Genene Holt
Publikováno v: PLoS ONE
PLoS ONE, Vol 5, Iss 12, p e14260 (2010)
Animal models continue to improve our understanding of tinnitus pathogenesis and aid in development of new treatments. However, there are no diagnostic biomarkers for tinnitus-related pathophysiology for use in awake, freely moving animals. To addres
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2d5974eb43b876a636e31072be233ba
http://europepmc.org/articles/PMC3002264
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2
Genetic inactivation of Trpml3 does not lead to hearing and vestibular impairment in mice
Autor: Lars Becker, Christian Grimm, Stefan Heller, Simone Jörs
Publikováno v: PLoS ONE, Vol 5, Iss 12, p e14317 (2010)
PLoS ONE
TRPML3, a member of the transient receptor potential (TRP) family, is an inwardly rectifying, non-selective Ca2+-permeable cation channel that is regulated by extracytosolic Na+ and H+ and can be activated by a variety of small molecules. The severe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acaa5a2b0a5b077a08b95e421c7d3a19
http://europepmc.org/articles/PMC3001452?pdf=render
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3
Central Crosstalk for Somatic Tinnitus: Abnormal Vergence Eye Movements
Autor: Pierre Bonfils, Marine Vernet, Alain Londero, Qing Yang, Zoï Kapoula, Christophe Orssaud
Publikováno v: PLoS ONE
PLoS ONE, Public Library of Science, 2010, 5 (7), pp.e11845. ⟨10.1371/journal.pone.0011845⟩
PLoS ONE, Vol 5, Iss 7, p e11845 (2010)
Background: Frequent oulomotricity problems with orthoptic testing were reported in patients with tinnitus. This study examines with objective recordings vergence eye movements in patients with somatic tinnitus patients with ability to modify their s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::287e12a735efc6d4cbb7bbadac540841
https://hal.archives-ouvertes.fr/hal-02384248
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4
Gene expression analysis of forskolin treated basilar papillae identifies microRNA181a as a mediator of proliferation
Autor: Dhasakumar Navaratnam, Joseph Santos-Sacchi, Mohamed Uduman, Steven H. Kleinstein, Jamie L. Duke, Corey S. Frucht
Publikováno v: PLoS ONE, Vol 5, Iss 7, p e11502 (2010)
PLoS ONE
Background Auditory hair cells spontaneously regenerate following injury in birds but not mammals. A better understanding of the molecular events underlying hair cell regeneration in birds may allow for identification and eventually manipulation of r
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddbd3f9ce1ecce36179791e491f0344d
http://europepmc.org/articles/PMC2901389?pdf=render
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5
Biological markers of auditory gap detection in young, middle-aged, and older adults
Autor: Bruce A. Schneider, Joel S. Snyder, Bernhard Ross, Claude Alain
Publikováno v: PLoS ONE, Vol 5, Iss 4, p e10101 (2010)
PLoS ONE
The capability of processing rapid fluctuations in the temporal envelope of sound declines with age and this contributes to older adults' difficulties in understanding speech. Although, changes in central auditory processing during aging have been pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c7fe7b8e9625daaea8522a35f768898
http://europepmc.org/articles/PMC2852420?pdf=render
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6
RNA microarray analysis in prenatal mouse cochlea reveals novel IGF-I target genes: implication of MEF2 and FOXM1 transcription factors
Autor: José G. Pichel, Lourdes Rodriguez-de la Rosa, Hortensia Sánchez-Calderón, Marta Milo, Matthew C. Holley, Isabel Varela-Nieto
Publikováno v: PLoS One
PLoS ONE, Vol 5, Iss 1, p e8699 (2010)
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSIC
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17 páginas, 8 figuras.-- et al.
[Background]: Insulin-like growth factor-I (IGF-I) provides pivotal cell survival and differentiation signals during inner ear development throughout evolution. Homozygous mutations of human IGF1 cause syndromic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8af8d6596062bb539cc62e979c21110
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7
PLoS One
Autor: María Rodríguez Aburto, Isabel Varela-Nieto, Ulf R. Rapp, Carmen Muñoz-Agudo, Hortensia Sánchez-Calderón, Marta Magariños
Publikováno v: PLoS ONE, Vol 5, Iss 12, p e14435 (2010)
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSIC
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[Background]: Early inner ear development requires the strict regulation of cell proliferation, survival, migration and differentiation, coordinated by the concerted action of extrinsic and intrinsic factors. Deregulation of these processes is associ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72432d4f161ce192618fc183bd374ead
http://europepmc.org/articles/PMC3010996?pdf=render
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8
A Claudin-9–Based Ion Permeability Barrier Is Essential for Hearing
Autor: Yoko Nakano, Yuzhou Zhang, Richard J.H. Smith, Botond Banfi, Hyoung-Mi Kim, Daniel C. Marcus, Sung Huhn Kim, Joel D. Sanneman, Randy Alan Nessler, Philine Wangemann
Publikováno v: PLoS Genetics
PLoS Genetics, Vol 5, Iss 8, p e1000610 (2009)
Hereditary hearing loss is one of the most common birth defects, yet the majority of genes required for audition is thought to remain unidentified. Ethylnitrosourea (ENU)–mutagenesis has been a valuable approach for generating new animal models of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1403fe3a56ef1363c13464615012961
http://europepmc.org/articles/PMC2720454
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9
Carrier Status for the Common R501X and 2282del4 Filaggrin Mutations Is Not Associated with Hearing Phenotypes in 5377 Children from the ALSPAC Cohort
Autor: Ian N. M. Day, W.H. Irwin McLean, Raquel Granell, George Davey Smith, Santiago Rodriguez, Alan D. Irvine, Colin N. A. Palmer, Amanda Hall, John Henderson
Publikováno v: PLoS ONE
PLoS ONE, Vol 4, Iss 6, p e5784 (2009)
BACKGROUND: Filaggrin is a major protein in the epidermis. Several mutations in the filaggrin gene (FLG) have been associated with a number of conditions. Filaggrin is expressed in the tympanic membrane and could alter its mechanical properties, but
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42d4f759d6e88e334f264a34e165ad39
http://europepmc.org/articles/PMC2685991
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10
Association of Tinnitus and Electromagnetic Hypersensitivity: Hints for a Shared Pathophysiology?
Autor: Berthold Langguth, Ulrich Frick, Michael Landgrebe, Simone Hauser, Goeran Hajak
Publikováno v: PLoS ONE
PLoS ONE, Vol 4, Iss 3, p e5026 (2009)
BACKGROUND: Tinnitus is a frequent condition with high morbidity and impairment in quality of life. The pathophysiology is still incompletely understood. Electromagnetic fields are discussed to be involved in the multi-factorial pathogenesis of tinni
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6e064d64e4344111a12c29efcb378e5
http://europepmc.org/articles/PMC2657824
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Plný text Recenzováno Digitální knihovna AV ČR
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