-
2
-
-
0030669689
-
Polyglutamines, nuclear inclusions and neurodegeneration
-
Lunkes, A. & Mandel, J-L. Polyglutamines, nuclear inclusions and neurodegeneration. Nature Med. 3, 1201-1202 (1997).
-
(1997)
Nature Med.
, vol.3
, pp. 1201-1202
-
-
Lunkes, A.1
Mandel, J.-L.2
-
3
-
-
0032191848
-
Neuronal intranuclear inclusions in polyglutamine diseases: Nuclear weapons or nuclear fallout?
-
Kim, T-W. & Tanzi, R.E. Neuronal Intranuclear inclusions in polyglutamine diseases: Nuclear Weapons or Nuclear Fallout? Neuron 21, 657-659 (1998).
-
(1998)
Neuron
, vol.21
, pp. 657-659
-
-
Kim, T.-W.1
Tanzi, R.E.2
-
4
-
-
6844254538
-
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)
-
David, C. et al. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). Hum. Mol. Genet. 7, 165-170 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 165-170
-
-
David, C.1
-
5
-
-
9844263366
-
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
-
Jodice, C. et al. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. Hum. Mol. Genet. 6, 1973-1978 (1997).
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1973-1978
-
-
Jodice, C.1
-
6
-
-
0032900772
-
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
-
Koob, M.D. et al. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8). Nature Genet. 21, 379-384 (1999).
-
(1999)
Nature Genet.
, vol.21
, pp. 379-384
-
-
Koob, M.D.1
-
7
-
-
0027256423
-
Direct detection of novel expanded trinucleotide repeats in the human genome
-
Schalling, M. et al. Direct detection of novel expanded trinucleotide repeats in the human genome. Nature. Genet. 4, 135-139 (1993).
-
(1993)
Nature. Genet.
, vol.4
, pp. 135-139
-
-
Schalling, M.1
-
8
-
-
0031712686
-
Two commonly expanded CAG/CTG repeat loci: Involvement in affective disorders?
-
Lindblad, K. et al. Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders? Mol. Psychiatry 3, 405-410 (1998).
-
(1998)
Mol. Psychiatry
, vol.3
, pp. 405-410
-
-
Lindblad, K.1
-
9
-
-
0032231668
-
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
-
Takano, H. et al. Close Associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am. J. Hum. Genet. 63, 1060-1066 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1060-1066
-
-
Takano, H.1
-
10
-
-
0031647246
-
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
-
Moseley, M.L. et al. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology 51, 1666-1671 (1998).
-
(1998)
Neurology
, vol.51
, pp. 1666-1671
-
-
Moseley, M.L.1
|