FREDERICK PEREIRA to Mutation
This is a "connection" page, showing publications FREDERICK PEREIRA has written about Mutation.
Connection Strength
0.082
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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: 0.032
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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: 0.031
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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: 0.008
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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: 0.004
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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: 0.003
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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.
Score: 0.002
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An abundant 56 kD protein with low affinity androgen binding: another member of the steroid/thyroid receptor family? Biochem Biophys Res Commun. 1988 Sep 15; 155(2):907-13.
Score: 0.002