about
A single P-loop glutamate point mutation to either lysine or arginine switches the cation-anion selectivity of the CNGA2 channelIdentification of intracellular and extracellular domains mediating signal transduction in the inhibitory glycine receptor chloride channelRole of charged residues in coupling ligand binding and channel activation in the extracellular domain of the glycine receptor.A nonsense mutation in the alpha1 subunit of the inhibitory glycine receptor associated with bovine myoclonus.Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.Impact of the AGTR1 A1166C polymorphism on subcortical hyperintensities and cognition in healthy older adults.Genetic markers of cholesterol transport and gray matter diffusion: a preliminary study of the CETP I405V polymorphism.Neuromarkers of the common angiotensinogen polymorphism in healthy older adults: A comprehensive assessment of white matter integrity and cognitionCation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion-charge selectivity.BDNF Genotype Interacts with Motor Function to Influence Rehabilitation Responsiveness PoststrokeNeuronal fiber bundle lengths in healthy adult carriers of the ApoE4 allele: a quantitative tractography DTI study.In vivo somatic delivery of plasmid DNA and retrograde transport to obtain cell-specific gene expression in the central nervous system.Preliminary evidence of the short allele of the serotonin transporter gene predicting poor response to cognitive behavior therapy in posttraumatic stress disorder.Triallelic relationships between the serotonin transporter polymorphism and cognition among healthy older adults.Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain aging.Association between serotonin transporter promoter polymorphisms and psychological distress in a diabetic population.An examination of multiple classes of rare variants in extended families with bipolar disorder.Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.Bovine myoclonus: Model of human hyperekplexia (Startle disease)Genotyping cattle for inherited congenital myoclonus and maple syrup urine disease
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Kerrie D Pierce
@ast
Kerrie D Pierce
@en
Kerrie D Pierce
@es
Kerrie D Pierce
@nl
type
label
Kerrie D Pierce
@ast
Kerrie D Pierce
@en
Kerrie D Pierce
@es
Kerrie D Pierce
@nl
prefLabel
Kerrie D Pierce
@ast
Kerrie D Pierce
@en
Kerrie D Pierce
@es
Kerrie D Pierce
@nl
P108
P106
P108
P1153
7101864140
P31
P496
0000-0003-0636-4836