Medical dictionary. 2011.
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
Proteinfehlfaltungserkrankung — Als Proteinfehlfaltungserkrankungen, auch Proteinfaltungserkrankungen (engl. protein misfolding diseases oder protein misfolding disorders oder conformational diseases) genannt, bezeichnet man solche Erkrankungen, die durch falsche gefaltete… … Deutsch Wikipedia
Huntingtin — PBB Summary section title = summary text =The Huntingtin gene, also called HD (Huntington disease) gene, or the IT15 ( interesting transcript 15 ) gene codes for a 348 kDa protein called huntingtin protein. The exact function of this protein is… … 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
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
Dentatorubral-pallidoluysian atrophy — Classification and external resources OMIM 125370 DiseasesDB 32909 MeSH … 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
Spinocerebellar ataxia type-6 — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 12339 ICD10 = ICD10|G|11|2|g|10 ICD9 = ICD9|334.9 ICDO = OMIM = 183086 MedlinePlus = eMedicineSubj = neuro eMedicineTopic = 556 Spinocerebellar ataxia type 6 (SCA6) is a rare, late onset,… … Wikipedia
