FREDERICK PEREIRA to Animals
This is a "connection" page, showing publications FREDERICK PEREIRA has written about Animals.
Connection Strength
0.420
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Membrane prestin expression correlates with the magnitude of prestin-associated charge movement. Hear Res. 2016 09; 339:50-9.
Score: 0.030
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Survival of auditory hair cells. Cell Tissue Res. 2015 Jul; 361(1):59-63.
Score: 0.027
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A coregulatory network of NR2F1 and microRNA-140. PLoS One. 2013; 8(12):e83358.
Score: 0.025
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Head bobber: an insertional mutation causes inner ear defects, hyperactive circling, and deafness. J Assoc Res Otolaryngol. 2012 Jun; 13(3):335-49.
Score: 0.022
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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.
Score: 0.019
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Glycosylation regulates prestin cellular activity. J Assoc Res Otolaryngol. 2010 Mar; 11(1):39-51.
Score: 0.019
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Essential helix interactions in the anion transporter domain of prestin revealed by evolutionary trace analysis. J Neurosci. 2006 Dec 06; 26(49):12727-34.
Score: 0.015
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COUP-TFI controls Notch regulation of hair cell and support cell differentiation. Development. 2006 Sep; 133(18):3683-93.
Score: 0.015
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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: 0.014
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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.
Score: 0.014
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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.
Score: 0.011
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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: 0.011
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Whole-mount histochemical detection of beta-galactosidase activity. Curr Protoc Mol Biol. 2001 May; Chapter 14:Unit 14.14.
Score: 0.010
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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: 0.010
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COUP-TF orphan nuclear receptors in development and differentiation. Cell Mol Life Sci. 2000 Sep; 57(10):1388-98.
Score: 0.010
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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.
Score: 0.010
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The orphan nuclear receptor COUP-TFII is required for angiogenesis and heart development. Genes Dev. 1999 Apr 15; 13(8):1037-49.
Score: 0.009
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Trehalose reduces retinal degeneration, neuroinflammation and storage burden caused by a lysosomal hydrolase deficiency. Autophagy. 2018; 14(8):1419-1434.
Score: 0.009
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Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. Am J Hum Genet. 2018 02 01; 102(2):296-308.
Score: 0.008
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Diflunisal inhibits prestin by chloride-dependent mechanism. PLoS One. 2017; 12(8):e0183046.
Score: 0.008
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An Atoh1-S193A Phospho-Mutant Allele Causes Hearing Deficits and Motor Impairment. J Neurosci. 2017 09 06; 37(36):8583-8594.
Score: 0.008
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mTORC1-independent TFEB activation via Akt inhibition promotes cellular clearance in neurodegenerative storage diseases. Nat Commun. 2017 02 06; 8:14338.
Score: 0.008
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Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders. Elife. 2016 06 21; 5.
Score: 0.007
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Chicken ovalbumin upstream promoter transcription factor (COUP-TF): expression during mouse embryogenesis. J Steroid Biochem Mol Biol. 1995 Jun; 53(1-6):503-8.
Score: 0.007
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Prestin regulation and function in residual outer hair cells after noise-induced hearing loss. PLoS One. 2013; 8(12):e82602.
Score: 0.006
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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.
Score: 0.006
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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.
Score: 0.006
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Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome. Adv Exp Med Biol. 1993; 328:45-50.
Score: 0.006
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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.
Score: 0.006
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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.
Score: 0.005
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Cysteine mutagenesis reveals transmembrane residues associated with charge translocation in prestin. J Biol Chem. 2010 Jan 29; 285(5):3103-13.
Score: 0.005
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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: 0.005
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Membrane composition modulates prestin-associated charge movement. J Biol Chem. 2008 Aug 15; 283(33):22473-81.
Score: 0.004
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Functional prestin transduction of immature outer hair cells from normal and prestin-null mice. J Assoc Res Otolaryngol. 2008 Sep; 9(3):307-20.
Score: 0.004
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Helper-dependent adenovirus-mediated gene transfer into the adult mouse cochlea. Otol Neurotol. 2007 Dec; 28(8):1100-8.
Score: 0.004
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Tuning of the outer hair cell motor by membrane cholesterol. J Biol Chem. 2007 Dec 14; 282(50):36659-70.
Score: 0.004
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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: 0.004
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Assessment of prestin self-association using fluorescence resonance energy transfer. Brain Res. 2006 May 26; 1091(1):140-50.
Score: 0.004
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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: 0.004
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Presenilins are required for the formation of comma- and S-shaped bodies during nephrogenesis. Development. 2003 Oct; 130(20):5019-29.
Score: 0.003
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Deletion of the cancer-amplified coactivator AIB3 results in defective placentation and embryonic lethality. J Biol Chem. 2002 Nov 22; 277(47):45356-60.
Score: 0.003
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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.
Score: 0.003
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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: 0.003
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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.
Score: 0.002
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Mediation of Sonic hedgehog-induced expression of COUP-TFII by a protein phosphatase. Science. 1997 Dec 12; 278(5345):1947-50.
Score: 0.002
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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.
Score: 0.002
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Chicken ovalbumin upstream promoter-transcription factors and their regulation. J Steroid Biochem Mol Biol. 1996 Jan; 56(1-6 Spec No):81-5.
Score: 0.002
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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.
Score: 0.002