Connection

FREDERICK PEREIRA to Cochlea

This is a "connection" page, showing publications FREDERICK PEREIRA has written about Cochlea.
Connection Strength

0.632
  1. Membrane prestin expression correlates with the magnitude of prestin-associated charge movement. Hear Res. 2016 09; 339:50-9.
    View in: PubMed
    Score: 0.128
  2. Membrane composition modulates prestin-associated charge movement. J Biol Chem. 2008 Aug 15; 283(33):22473-81.
    View in: PubMed
    Score: 0.074
  3. Helper-dependent adenovirus-mediated gene transfer into the adult mouse cochlea. Otol Neurotol. 2007 Dec; 28(8):1100-8.
    View in: PubMed
    Score: 0.071
  4. 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.
    View in: PubMed
    Score: 0.069
  5. COUP-TFI controls Notch regulation of hair cell and support cell differentiation. Development. 2006 Sep; 133(18):3683-93.
    View in: PubMed
    Score: 0.065
  6. 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.
    View in: PubMed
    Score: 0.059
  7. Erythrocyte adenosine A2B receptor prevents cognitive and auditory dysfunction by promoting hypoxic and metabolic reprogramming. PLoS Biol. 2021 06; 19(6):e3001239.
    View in: PubMed
    Score: 0.045
  8. Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems. Genes Dev. 2000 Nov 15; 14(22):2839-54.
    View in: PubMed
    Score: 0.043
  9. Adenosine A2B receptor: A pathogenic factor and a therapeutic target for sensorineural hearing loss. FASEB J. 2020 12; 34(12):15771-15787.
    View in: PubMed
    Score: 0.043
  10. 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.
    View in: PubMed
    Score: 0.020
  11. 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.
    View in: PubMed
    Score: 0.015
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.