Connection

FREDERICK PEREIRA to Male

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

0.077
  1. 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: 0.016
  2. 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: 0.008
  3. 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: 0.007
  4. 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: 0.007
  5. 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: 0.006
  6. 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: 0.006
  7. 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: 0.004
  8. 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: 0.004
  9. Human cytosolic aldehyde dehydrogenase in androgen insensitivity syndrome. Adv Exp Med Biol. 1993; 328:45-50.
    View in: PubMed
    Score: 0.004
  10. 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: 0.004
  11. The 56 kDa androgen binding protein is an aldehyde dehydrogenase. Biochem Biophys Res Commun. 1991 Mar 29; 175(3):831-8.
    View in: PubMed
    Score: 0.004
  12. 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: 0.003
  13. 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
  14. 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: 0.001
  15. Replacement of arginine 773 by cysteine or histidine in the human androgen receptor causes complete androgen insensitivity with different receptor phenotypes. Am J Hum Genet. 1992 Jul; 51(1):143-55.
    View in: PubMed
    Score: 0.001
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.