|
1
|
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.
|
Nat Genet
|
1993
|
5.82
|
|
2
|
Cleavage of huntingtin by apopain, a proapoptotic cysteine protease, is modulated by the polyglutamine tract.
|
Nat Genet
|
1996
|
3.08
|
|
3
|
Forskolin and dopamine D1 receptor activation increase huntingtin's association with endosomes in immortalized neuronal cells of striatal origin.
|
Neuroscience
|
1999
|
0.90
|
|
4
|
Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript.
|
Hum Mol Genet
|
1996
|
0.87
|
|
5
|
Structural analysis of the 5' region of mouse and human Huntington disease genes reveals conservation of putative promoter region and di- and trinucleotide polymorphisms.
|
Genomics
|
1995
|
0.83
|