A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats.
Boy, Jana
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats. [electronic resource] - Neurobiology of disease Feb 2010 - 284-93 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1095-953X
10.1016/j.nbd.2009.08.002 doi
Age of Onset
Animals
Ataxin-3
Brain--metabolism
Chromosomal Instability--genetics
Disease Models, Animal
Disease Progression
Gene Expression--genetics
Genetic Predisposition to Disease--genetics
Intranuclear Inclusion Bodies--genetics
Machado-Joseph Disease--genetics
Mice
Mice, Transgenic
Movement Disorders--genetics
Mutation--genetics
Nuclear Proteins--genetics
Rats
Sex Characteristics
Transcription Factors--genetics
Trinucleotide Repeats--genetics
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats. [electronic resource] - Neurobiology of disease Feb 2010 - 284-93 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1095-953X
10.1016/j.nbd.2009.08.002 doi
Age of Onset
Animals
Ataxin-3
Brain--metabolism
Chromosomal Instability--genetics
Disease Models, Animal
Disease Progression
Gene Expression--genetics
Genetic Predisposition to Disease--genetics
Intranuclear Inclusion Bodies--genetics
Machado-Joseph Disease--genetics
Mice
Mice, Transgenic
Movement Disorders--genetics
Mutation--genetics
Nuclear Proteins--genetics
Rats
Sex Characteristics
Transcription Factors--genetics
Trinucleotide Repeats--genetics