Search Results - "PLEASANT, N"
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Resistance exercise and lipoproteins in postmenopausal women
Published in International journal of sports medicine (01-01-2011)“…The specific aims of this study were to quantify the effects of 12 weeks of resistance training, as well as a single session of resistance exercise on lipids…”
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Hairpin-Bisulfite PCR: Assessing Epigenetic Methylation Patterns on Complementary Strands of Individual DNA Molecules
Published in Proceedings of the National Academy of Sciences - PNAS (06-01-2004)“…Epigenetic inheritance, the transmission of gene expression states from parent to daughter cells, often involves methylation of DNA. In eukaryotes, cytosine…”
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3
A Novel, Heritable, Expanding CTG Repeat in an Intron of the SEF2-1 Gene on Chromosome 18q21.1
Published in Human molecular genetics (01-10-1997)“…There are currently 13 diseases known to be caused by unstable triplet repeat mutations; however, there are some instances (as with FRAXF and FRA16) when these…”
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Expression of the mutant allele of IT-15 (the HD gene) in striatum and cortex of Huntington's disease patients
Published in Human molecular genetics (01-01-1995)“…Huntington's disease (HD) is an inherited neurodegenerative disorder expressed when a trinucleotide repeat in the gene IT-15 is expanded. The mechanism by…”
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Anticipation and instability of IT-15 (CAG)N repeats in parent-offspring pairs with Huntington disease
Published in American journal of human genetics (01-09-1995)“…Huntington disease (HD) is an autosomal dominant degenerative disorder caused by an expanded and unstable trinucleotide repeat (CAG)n in a gene (IT-15) on…”
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Macrokinetic analysis of blockade of NMDA-gated currents by substituted alcohols, alkanes and ethers
Published in Brain research (23-07-2004)“…Volatile hydrocarbon based CNS depressants including short chain alcohols and anesthetics act, in part, by inhibition of the excitatory effect of glutamate at…”
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Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15
Published in Human molecular genetics (01-10-1993)“…Huntington's disease (HD) is an autosomal dominant disorder with a variable age of onset that is influenced by the sex of the affected parent. The recent…”
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