-
1
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
Leroy E, Boyer R, Auburger G, et al. The ubiquitin pathway in Parkinson's disease. Nature 1998;395:451-452.
-
(1998)
Nature
, vol.395
, pp. 451-452
-
-
Leroy, E.1
Boyer, R.2
Auburger, G.3
-
2
-
-
0033544368
-
Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease
-
Maraganore DM, Farrer MJ, Hardy JA, et al. Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease. Neurology 1999;53:1858-1860.
-
(1999)
Neurology
, vol.53
, pp. 1858-1860
-
-
Maraganore, D.M.1
Farrer, M.J.2
Hardy, J.A.3
-
3
-
-
0035881339
-
A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population
-
Satoh J, Kuroda Y. A polymorphic variation of serine to tyrosine at codon 18 in the ubiquitin C-terminal hydrolase-L1 gene is associated with a reduced risk of sporadic Parkinson's disease in a Japanese population. J Neurol Sci 2001;189:113-117.
-
(2001)
J Neurol Sci
, vol.189
, pp. 113-117
-
-
Satoh, J.1
Kuroda, Y.2
-
4
-
-
0036135090
-
Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms
-
Momose Y, Murata M, Kobayashi K, et al. Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms. Ann Neurol 2002;51:133-136.
-
(2002)
Ann Neurol
, vol.51
, pp. 133-136
-
-
Momose, Y.1
Murata, M.2
Kobayashi, K.3
-
5
-
-
0034647948
-
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients
-
Wintermeyer P, Kruger R, Kuhn W, et al. Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients. Neuroreport 2000;11:2079-2082.
-
(2000)
Neuroreport
, vol.11
, pp. 2079-2082
-
-
Wintermeyer, P.1
Kruger, R.2
Kuhn, W.3
-
6
-
-
0033947504
-
Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease
-
Zhang J, Hattori N, Leroy E, et al. Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease. Parkinsonism Rel Disord 2000;6:195-197.
-
(2000)
Parkinsonism Rel Disord
, vol.6
, pp. 195-197
-
-
Zhang, J.1
Hattori, N.2
Leroy, E.3
-
7
-
-
0345269293
-
S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: Evidence for an age-dependent relationship
-
Elbaz A, Levecque C, Clavel J, et al. S18Y polymorphism in the UCH-L1 gene and Parkinson's disease: evidence for an age-dependent relationship. Mov Disord 2003;18:130-137.
-
(2003)
Mov Disord
, vol.18
, pp. 130-137
-
-
Elbaz, A.1
Levecque, C.2
Clavel, J.3
-
8
-
-
0034722106
-
The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease
-
Mellick GD, Silburn PA. The ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism does not confer protection against idiopathic Parkinson's disease. Neurosci Lett 2000;293:127-130.
-
(2000)
Neurosci Lett
, vol.293
, pp. 127-130
-
-
Mellick, G.D.1
Silburn, P.A.2
-
9
-
-
0035859766
-
Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD
-
Savettieri G, De Marco EV, Civitelli D, et al. Lack of association between ubiquitin carboxy-terminal hydrolase L1 gene polymorphism and PD. Neurology 2001;57:560-561.
-
(2001)
Neurology
, vol.57
, pp. 560-561
-
-
Savettieri, G.1
De Marco, E.V.2
Civitelli, D.3
-
10
-
-
0036654541
-
ACT and UCHL-1 polymorphisms in Parkinson's disease and age of onset
-
Wang J, Zhao CY, Si YM, et al. ACT and UCHL-1 polymorphisms in Parkinson's disease and age of onset. Mov Disord 2002;17:767-771.
-
(2002)
Mov Disord
, vol.17
, pp. 767-771
-
-
Wang, J.1
Zhao, C.Y.2
Si, Y.M.3
-
11
-
-
0034864346
-
No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease
-
Levecque C, Destee A, Mouroux V, et al. No genetic association of the ubiquitin carboxy-terminal hydrolase-L1 gene S18Y polymorphism with familial Parkinson's disease. J Neural Transm 2001;108:979-984.
-
(2001)
J Neural Transm
, vol.108
, pp. 979-984
-
-
Levecque, C.1
Destee, A.2
Mouroux, V.3
-
12
-
-
0004185387
-
Ubiquitin C-terminal hydrolase L1 in sporadic Parkinson's disease
-
Gasser T, Pilz P, Omasmeier D, et al. Ubiquitin C-terminal hydrolase L1 in sporadic Parkinson's disease. Mov Disord 2000;15:A201.
-
(2000)
Mov Disord
, vol.15
-
-
Gasser, T.1
Pilz, P.2
Omasmeier, D.3
-
13
-
-
12144289221
-
UCHL1 is a Parkinson's disease susceptibility gene
-
Maraganore DM, Lesnick TG, Elbaz A, et al. UCHL1 is a Parkinson's disease susceptibility gene. Ann Neurol 2004;55:512-521.
-
(2004)
Ann Neurol
, vol.55
, pp. 512-521
-
-
Maraganore, D.M.1
Lesnick, T.G.2
Elbaz, A.3
-
14
-
-
0037131567
-
The UCHL-1 gene encodes two opposing enzymatic activities that affect alpha synuclein degradation and Parkinson's disease susceptibility
-
Liu Y, Fallon L, Lashuel HA, Liu Z, Lansbury PT Jr. The UCHL-1 gene encodes two opposing enzymatic activities that affect alpha synuclein degradation and Parkinson's disease susceptibility. Cell 2002;111:209-218.
-
(2002)
Cell
, vol.111
, pp. 209-218
-
-
Liu, Y.1
Fallon, L.2
Lashuel, H.A.3
Liu, Z.4
Lansbury Jr., P.T.5
-
15
-
-
0242380286
-
Genome scans and candidate gene approaches in the study of common diseases and variable drug responses
-
Goldstein DB, Ahmadi KR, Weale ME, Wood NW. Genome scans and candidate gene approaches in the study of common diseases and variable drug responses. Trends Genet 2003;19:615-622.
-
(2003)
Trends Genet
, vol.19
, pp. 615-622
-
-
Goldstein, D.B.1
Ahmadi, K.R.2
Weale, M.E.3
Wood, N.W.4
-
16
-
-
0042387804
-
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mapping
-
Weale ME, Depondt C, Macdonald SJ, et al. Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping. Am J Hum Genet 2003;73:551-565.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 551-565
-
-
Weale, M.E.1
Depondt, C.2
Macdonald, S.J.3
-
17
-
-
0023898945
-
The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease
-
Gibb WR, Lees AJ. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 1988;51:745-754.
-
(1988)
J Neurol Neurosurg Psychiatry
, vol.51
, pp. 745-754
-
-
Gibb, W.R.1
Lees, A.J.2
-
18
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinicopathological study of 100 cases
-
Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinicopathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992;55:181-184.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
20
-
-
84888791276
-
-
Tagging SNP software. Available at: http://www.genome. duke.edu. Accessed.
-
Tagging SNP Software
-
-
-
21
-
-
4444375576
-
The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism
-
Healy DG, Abou-Sleiman PM, Ahmadi KR, et al. The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism. Ann Neurol 2004;56:329-335.
-
(2004)
Ann Neurol
, vol.56
, pp. 329-335
-
-
Healy, D.G.1
Abou-Sleiman, P.M.2
Ahmadi, K.R.3
-
22
-
-
0033990339
-
Model-free analysis and permutation tests for allelic associations
-
Zhao JH, Curtis D, Sham PC. Model-free analysis and permutation tests for allelic associations. Hum Hered 2000;50:133-139.
-
(2000)
Hum Hered
, vol.50
, pp. 133-139
-
-
Zhao, J.H.1
Curtis, D.2
Sham, P.C.3
-
23
-
-
84959801619
-
Statistical aspects of the analysis of data from retrospective studies of disease
-
Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959;22:719-748.
-
(1959)
J Natl Cancer Inst
, vol.22
, pp. 719-748
-
-
Mantel, N.1
Haenszel, W.2
-
26
-
-
12244264435
-
Genetic Power Calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 2003;19:149-150.
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
27
-
-
12244264435
-
Genetic Power Calculator: Design of linkage and association genetic mapping studies of complex traits
-
Purcell S, Cherny SS, Sham PC. Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics 2003;19:149-150.
-
(2003)
Bioinformatics
, vol.19
, pp. 149-150
-
-
Purcell, S.1
Cherny, S.S.2
Sham, P.C.3
-
28
-
-
20144365768
-
Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease
-
Li Y, Hollingworth P, Moore P, et al. Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease. Hum Mutat 2005;25:270-277.
-
(2005)
Hum Mutat
, vol.25
, pp. 270-277
-
-
Li, Y.1
Hollingworth, P.2
Moore, P.3
-
29
-
-
0033609337
-
The homeobox gene Phox2b is essential for the development of autonomie neural crest derivatives
-
Pattyn A, Morin X, Cremer H, et al. The homeobox gene Phox2b is essential for the development of autonomie neural crest derivatives. Nature 1999;399:366-370.
-
(1999)
Nature
, vol.399
, pp. 366-370
-
-
Pattyn, A.1
Morin, X.2
Cremer, H.3
-
30
-
-
18544380387
-
Parameters for reliable results in genetic association studies in common disease
-
Dahlman I, Eaves IA, Kosoy R, et al. Parameters for reliable results in genetic association studies in common disease. Nat Genet 2002;3:149-150.
-
(2002)
Nat Genet
, vol.3
, pp. 149-150
-
-
Dahlman, I.1
Eaves, I.A.2
Kosoy, R.3
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