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Proton-Motive Force
MAPK p38 regulates transcriptional activity of NF-kappaB in primary human astrocytes via acetylation of p65.
Diurnal and seasonal molecular rhythms in human neocortex and their relation to Alzheimer's disease.
Optic Lobe, Nonmammalian
KCNE1 mutations cause jervell and Lange-Nielsen syndrome.
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KCNE1 mutations cause jervell and Lange-Nielsen syndrome.
KCNE1 mutations cause jervell and Lange-Nielsen syndrome. Nat Genet. 1997 Nov; 17(3):267-8.
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subject areas
Female
Gene Frequency
Genetic Markers
Heterozygote
Humans
Long QT Syndrome
Male
Microsatellite Repeats
Mutation
Pedigree
Polymorphism, Genetic
Potassium Channels
Potassium Channels, Voltage-Gated