FREDERICK PEREIRA to Molecular Sequence Data
This is a "connection" page, showing publications FREDERICK PEREIRA has written about Molecular Sequence Data.
Connection Strength
0.209
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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: 0.067
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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: 0.047
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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: 0.042
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Selective cell-surface labeling of the molecular motor protein prestin. Biochem Biophys Res Commun. 2011 Jun 24; 410(1):134-9.
Score: 0.016
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Identification of functionally important residues/domains in membrane proteins using an evolutionary approach coupled with systematic mutational analysis. Methods Mol Biol. 2009; 493:287-97.
Score: 0.014
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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: 0.009
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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: 0.005
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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: 0.005
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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: 0.004