polyglutamine

polyglutamine

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  • polyglutamine — poly·glu·ta·mine (pol″e glooґtə mēn) a stretch of glutamine residues in a protein; expanded numbers of such residues are associated with several triplet repeat disorders. See also polyglutamine disorders, under disorder …   Medical dictionary

  • polyglutamine disorders — polyQ disorders any of the triplet repeat disorders in which a CAG triplet repeat sequence is expanded, yielding a large polyglutamine tract in the protein product. Although the affected protein differs, all have a toxic gain of function, the… …   Medical dictionary

  • polyglutamine diseases — see under disorder …   Medical dictionary

  • PQBP1 — Polyglutamine binding protein 1, also known as PQBP1, is a human gene.cite web | title = Entrez Gene: PQBP1 polyglutamine binding protein 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=10084| accessdate …   Wikipedia

  • Trinucleotide repeat disorder — Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation …   Wikipedia

  • Androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

  • Mild androgen insensitivity syndrome — Classification and external resources AIS results when the function of the androgen receptor (AR) is impaired. The AR protein (pictured) mediates the effects of androgens in the human body. ICD 10 E …   Wikipedia

  • Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH …   Wikipedia

  • Huntington's disease — Classification and external resources A microscope image of …   Wikipedia

  • Neurodegeneration — Classification and external resources Para sagittal MRI of the head in a patient with benign familial macrocephaly. ICD 10 G30 G32 …   Wikipedia

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