FREDERICK PEREIRA to Cochlea
This is a "connection" page, showing publications FREDERICK PEREIRA has written about Cochlea.
Connection Strength
0.632
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Membrane prestin expression correlates with the magnitude of prestin-associated charge movement. Hear Res. 2016 09; 339:50-9.
Score: 0.128
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Membrane composition modulates prestin-associated charge movement. J Biol Chem. 2008 Aug 15; 283(33):22473-81.
Score: 0.074
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Helper-dependent adenovirus-mediated gene transfer into the adult mouse cochlea. Otol Neurotol. 2007 Dec; 28(8):1100-8.
Score: 0.071
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Altered traveling wave propagation and reduced endocochlear potential associated with cochlear dysplasia in the BETA2/NeuroD1 null mouse. J Assoc Res Otolaryngol. 2007 Dec; 8(4):447-63.
Score: 0.069
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COUP-TFI controls Notch regulation of hair cell and support cell differentiation. Development. 2006 Sep; 133(18):3683-93.
Score: 0.065
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Dynamic expression of COUP-TFI and COUP-TFII during development and functional maturation of the mouse inner ear. Gene Expr Patterns. 2005 Jun; 5(5):587-92.
Score: 0.059
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Erythrocyte adenosine A2B receptor prevents cognitive and auditory dysfunction by promoting hypoxic and metabolic reprogramming. PLoS Biol. 2021 06; 19(6):e3001239.
Score: 0.045
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Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems. Genes Dev. 2000 Nov 15; 14(22):2839-54.
Score: 0.043
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Adenosine A2B receptor: A pathogenic factor and a therapeutic target for sensorineural hearing loss. FASEB J. 2020 12; 34(12):15771-15787.
Score: 0.043
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DNA sequence analysis of SLC26A5, encoding prestin, in a patient-control cohort: identification of fourteen novel DNA sequence variations. PLoS One. 2009 Jun 02; 4(6):e5762.
Score: 0.020
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High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss. BMC Med Genet. 2005 Aug 08; 6:30.
Score: 0.015