Connection

FREDERICK PEREIRA to Animals

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

0.420
  1. Membrane prestin expression correlates with the magnitude of prestin-associated charge movement. Hear Res. 2016 09; 339:50-9.
    View in: PubMed
    Score: 0.030
  2. Survival of auditory hair cells. Cell Tissue Res. 2015 Jul; 361(1):59-63.
    View in: PubMed
    Score: 0.027
  3. A coregulatory network of NR2F1 and microRNA-140. PLoS One. 2013; 8(12):e83358.
    View in: PubMed
    Score: 0.025
  4. Head bobber: an insertional mutation causes inner ear defects, hyperactive circling, and deafness. J Assoc Res Otolaryngol. 2012 Jun; 13(3):335-49.
    View in: PubMed
    Score: 0.022
  5. Genome-wide analysis of binding sites and direct target genes of the orphan nuclear receptor NR2F1/COUP-TFI. PLoS One. 2010 Jan 27; 5(1):e8910.
    View in: PubMed
    Score: 0.019
  6. Glycosylation regulates prestin cellular activity. J Assoc Res Otolaryngol. 2010 Mar; 11(1):39-51.
    View in: PubMed
    Score: 0.019
  7. Essential helix interactions in the anion transporter domain of prestin revealed by evolutionary trace analysis. J Neurosci. 2006 Dec 06; 26(49):12727-34.
    View in: PubMed
    Score: 0.015
  8. COUP-TFI controls Notch regulation of hair cell and support cell differentiation. Development. 2006 Sep; 133(18):3683-93.
    View in: PubMed
    Score: 0.015
  9. 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: 0.014
  10. Evolution of a novel nuclear receptor subfamily with emphasis on the member from the Pacific oyster Crassostrea gigas. Gene. 2015 Aug 10; 567(2):164-72.
    View in: PubMed
    Score: 0.014
  11. Glial-Specific Deletion of Med12 Results in Rapid Hearing Loss via Degradation of the Stria Vascularis. J Neurosci. 2021 08 25; 41(34):7171-7181.
    View in: PubMed
    Score: 0.011
  12. 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: 0.011
  13. Whole-mount histochemical detection of beta-galactosidase activity. Curr Protoc Mol Biol. 2001 May; Chapter 14:Unit 14.14.
    View in: PubMed
    Score: 0.010
  14. 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: 0.010
  15. COUP-TF orphan nuclear receptors in development and differentiation. Cell Mol Life Sci. 2000 Sep; 57(10):1388-98.
    View in: PubMed
    Score: 0.010
  16. Nr2f1 heterozygous knockout mice recapitulate neurological phenotypes of Bosch-Boonstra-Schaaf optic atrophy syndrome and show impaired hippocampal synaptic plasticity. Hum Mol Genet. 2020 03 27; 29(5):705-715.
    View in: PubMed
    Score: 0.010
  17. The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development. Genes Dev. 1999 Apr 15; 13(8):1037-49.
    View in: PubMed
    Score: 0.009
  18. Trehalose reduces retinal degeneration, neuroinflammation and storage burden caused by a lysosomal hydrolase deficiency. Autophagy. 2018; 14(8):1419-1434.
    View in: PubMed
    Score: 0.009
  19. Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. Am J Hum Genet. 2018 02 01; 102(2):296-308.
    View in: PubMed
    Score: 0.008
  20. Diflunisal inhibits prestin by chloride-dependent mechanism. PLoS One. 2017; 12(8):e0183046.
    View in: PubMed
    Score: 0.008
  21. An Atoh1-S193A Phospho-Mutant Allele Causes Hearing Deficits and Motor Impairment. J Neurosci. 2017 09 06; 37(36):8583-8594.
    View in: PubMed
    Score: 0.008
  22. mTORC1-independent TFEB activation via Akt inhibition promotes cellular clearance in neurodegenerative storage diseases. Nat Commun. 2017 02 06; 8:14338.
    View in: PubMed
    Score: 0.008
  23. Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders. Elife. 2016 06 21; 5.
    View in: PubMed
    Score: 0.007
  24. Chicken ovalbumin upstream promoter transcription factor (COUP-TF): expression during mouse embryogenesis. J Steroid Biochem Mol Biol. 1995 Jun; 53(1-6):503-8.
    View in: PubMed
    Score: 0.007
  25. Prestin regulation and function in residual outer hair cells after noise-induced hearing loss. PLoS One. 2013; 8(12):e82602.
    View in: PubMed
    Score: 0.006
  26. Conditional deletion of Atoh1 reveals distinct critical periods for survival and function of hair cells in the organ of Corti. J Neurosci. 2013 Jun 12; 33(24):10110-22.
    View in: PubMed
    Score: 0.006
  27. An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions. PLoS One. 2013; 8(2):e57460.
    View in: PubMed
    Score: 0.006
  28. Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome. Adv Exp Med Biol. 1993; 328:45-50.
    View in: PubMed
    Score: 0.006
  29. Ablation of ghrelin receptor in leptin-deficient ob/ob mice has paradoxical effects on glucose homeostasis when compared with ablation of ghrelin in ob/ob mice. Am J Physiol Endocrinol Metab. 2012 Aug 01; 303(3):E422-31.
    View in: PubMed
    Score: 0.006
  30. Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation. Dis Model Mech. 2010 Mar-Apr; 3(3-4):209-23.
    View in: PubMed
    Score: 0.005
  31. Cysteine mutagenesis reveals transmembrane residues associated with charge translocation in prestin. J Biol Chem. 2010 Jan 29; 285(5):3103-13.
    View in: PubMed
    Score: 0.005
  32. 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: 0.005
  33. Membrane composition modulates prestin-associated charge movement. J Biol Chem. 2008 Aug 15; 283(33):22473-81.
    View in: PubMed
    Score: 0.004
  34. Functional prestin transduction of immature outer hair cells from normal and prestin-null mice. J Assoc Res Otolaryngol. 2008 Sep; 9(3):307-20.
    View in: PubMed
    Score: 0.004
  35. Helper-dependent adenovirus-mediated gene transfer into the adult mouse cochlea. Otol Neurotol. 2007 Dec; 28(8):1100-8.
    View in: PubMed
    Score: 0.004
  36. Tuning of the outer hair cell motor by membrane cholesterol. J Biol Chem. 2007 Dec 14; 282(50):36659-70.
    View in: PubMed
    Score: 0.004
  37. 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: 0.004
  38. Assessment of prestin self-association using fluorescence resonance energy transfer. Brain Res. 2006 May 26; 1091(1):140-50.
    View in: PubMed
    Score: 0.004
  39. 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: 0.004
  40. Presenilins are required for the formation of comma- and S-shaped bodies during nephrogenesis. Development. 2003 Oct; 130(20):5019-29.
    View in: PubMed
    Score: 0.003
  41. Deletion of the cancer-amplified coactivator AIB3 results in defective placentation and embryonic lethality. J Biol Chem. 2002 Nov 22; 277(47):45356-60.
    View in: PubMed
    Score: 0.003
  42. Loss of orphan receptor germ cell nuclear factor function results in ectopic development of the tail bud and a novel posterior truncation. Mol Cell Biol. 2001 Jan; 21(2):663-77.
    View in: PubMed
    Score: 0.003
  43. 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: 0.003
  44. The nuclear orphan receptor COUP-TFI is required for differentiation of subplate neurons and guidance of thalamocortical axons. Neuron. 1999 Dec; 24(4):847-59.
    View in: PubMed
    Score: 0.002
  45. Mediation of Sonic hedgehog-induced expression of COUP-TFII by a protein phosphatase. Science. 1997 Dec 12; 278(5345):1947-50.
    View in: PubMed
    Score: 0.002
  46. Null mutation of mCOUP-TFI results in defects in morphogenesis of the glossopharyngeal ganglion, axonal projection, and arborization. Genes Dev. 1997 Aug 01; 11(15):1925-37.
    View in: PubMed
    Score: 0.002
  47. Chicken ovalbumin upstream promoter-transcription factors and their regulation. J Steroid Biochem Mol Biol. 1996 Jan; 56(1-6 Spec No):81-5.
    View in: PubMed
    Score: 0.002
  48. Leu-676-Pro mutation of the androgen receptor causes complete androgen insensitivity syndrome in a large Hutterite kindred. Hum Mutat. 1995; 5(1):28-33.
    View in: PubMed
    Score: 0.002
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.