We detected an interaction of the N-terminus of huntingtin (htt171) with the C-terminal region
of the nuclear receptor co-repressor (N-CoR) using the yeast two-hybrid system. This …

Age of onset (AO) of Huntington disease (HD) is known to be correlated with the length of an
expanded CAG repeat in the HD gene. Apolipoprotein E (APOE) genotype, in turn, is known …

We have screened a rat brain library to identify proteins which interact with the 5′-end of
huntingtin (amino acids 1–171), including the polyglutamine tract, in the yeast two-hybrid …

Huntington's disease (HD) is an inherited neurodegenerative disorder caused by the
expansion of a CAG repeat in a gene coding for a protein of unknown function. We have …

Huntington's disease is a dominantly inherited neurological disorder where specific
neurodegeneration is caused by an extended polyglutamine stretch in the huntingtin protein …

The lipid composition of the two brown marine algae, Fucus vesiculosus and Ascophyllum
nodosum, was very similar. The major acyl lipids were monogalactosyldiacylglycerol …

Huntingtin was localized by using a series of antibodies that detected different areas of the
protein from the immediate N–terminus to the C–terminal region of the protein. The more C …

Lipid metabolism and environmental effects on this process have been studied in the marine
brown algae Fucus vesiculosus and Ascophyllum nodosum. These algae showed very …

The type II fatty acid synthases (FASs) of higher plants (and Escherichia coli) contain three
condensing enzymes called β-ketoacyl-ACP synthases (KAS), where ACP is acyl-carrier …

Recently, an inherited spinocerebellar ataxia (SCA17) has been attributed to polyglutamine
coding expansions within the gene coding for human TATA-box binding protein (TBP). The …