-
1
-
-
39349105603
-
The role for oxidative stress in neurodegenerative diseases
-
Shibata N, Kobayashi M. The role for oxidative stress in neurodegenerative diseases. Brain Nerve 2008; 60:157-170.
-
(2008)
Brain Nerve
, vol.60
, pp. 157-170
-
-
Shibata, N.1
Kobayashi, M.2
-
2
-
-
33846358949
-
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: Genetic and functional evidence
-
Tan EK, Zhao Y, Skipper L, Tan MG, Di Fonzo A, Sun L, et al. The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence. Hum Genet 2007; 120:857-863.
-
(2007)
Hum Genet
, vol.120
, pp. 857-863
-
-
Tan, E.K.1
Zhao, Y.2
Skipper, L.3
Tan, M.G.4
Di Fonzo, A.5
Sun, L.6
-
3
-
-
34447289622
-
Pathogenic mutations in Parkinson disease
-
Tan EK, Skipper LM. Pathogenic mutations in Parkinson disease. Hum Mutat 2007; 28:641-653.
-
(2007)
Hum Mutat
, vol.28
, pp. 641-653
-
-
Tan, E.K.1
Skipper, L.M.2
-
4
-
-
0028964602
-
Association between the oxidative polymorphism and early onset of Parkinson's disease
-
Agundez JA, Jimenez-Jimenez FJ, Luengo A, Bernal ML, Molina JA, Ayuso L, et al. Association between the oxidative polymorphism and early onset of Parkinson's disease. Clin Pharmacol Ther 1995; 57:291-298.
-
(1995)
Clin Pharmacol Ther
, vol.57
, pp. 291-298
-
-
Agundez, J.A.1
Jimenez-Jimenez, F.J.2
Luengo, A.3
Bernal, M.L.4
Molina, J.A.5
Ayuso, L.6
-
5
-
-
17444452570
-
Slow allotypic variants of the NAT2 gene and susceptibility to early-onset Parkinson's disease
-
Agundez JA, Jimenez-Jimenez FJ, Luengo A, Molina JA, Orti-Pareja M, Vazquez A, et al. Slow allotypic variants of the NAT2 gene and susceptibility to early-onset Parkinson's disease. Neurology 1998; 5:1587-1592.
-
(1998)
Neurology
, vol.5
, pp. 1587-1592
-
-
Agundez, J.A.1
Jimenez-Jimenez, F.J.2
Luengo, A.3
Molina, J.A.4
Orti-Pareja, M.5
Vazquez, A.6
-
6
-
-
33748602367
-
Genetic testing in Parkinson disease: Promises and pitfalls
-
Tan EK, Jankovic J. Genetic testing in Parkinson disease: promises and pitfalls. Arch Neurol 2006; 63:1232-1237.
-
(2006)
Arch Neurol
, vol.63
, pp. 1232-1237
-
-
Tan, E.K.1
Jankovic, J.2
-
7
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisan-Ruiz C, Jain S, Evans EW, Gilks WP, Simon J, van der Brug M, et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004; 44:595-600.
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
Gilks, W.P.4
Simon, J.5
van der Brug, M.6
-
8
-
-
0036830525
-
A susceptibility gene for late-onset idiopathic Parkinson's disease
-
Hicks AA, Petursson H, Jonsson T, Stefansson H, Johannsdottir HS, Sainz J, et al. A susceptibility gene for late-onset idiopathic Parkinson's disease. Ann Neurol 2002; 52:549-555.
-
(2002)
Ann Neurol
, vol.52
, pp. 549-555
-
-
Hicks, A.A.1
Petursson, H.2
Jonsson, T.3
Stefansson, H.4
Johannsdottir, H.S.5
Sainz, J.6
-
9
-
-
22544472702
-
Identification of risk and age-onset genes on chromosome 1p in Parkinson disease
-
Oliveira SA, Li YJ, Noureddine MA, Zuchner S, Qin X, Pericak-Vance MA, et al. Identification of risk and age-onset genes on chromosome 1p in Parkinson disease. Am J Hum Genet 2005; 77:252-264.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 252-264
-
-
Oliveira, S.A.1
Li, Y.J.2
Noureddine, M.A.3
Zuchner, S.4
Qin, X.5
Pericak-Vance, M.A.6
-
10
-
-
0035987204
-
Catechol-O-Methyltransferase (COMT)-mediated methylation metabolism of endogenous bioactive catechols and modulation by endobiotics and xenobiotics: Importance in pathophysiology and pathogenesis
-
Zhu BT. Catechol-O-Methyltransferase (COMT)-mediated methylation metabolism of endogenous bioactive catechols and modulation by endobiotics and xenobiotics: importance in pathophysiology and pathogenesis. Curr Drug Metab 2002; 3:321-349.
-
(2002)
Curr Drug Metab
, vol.3
, pp. 321-349
-
-
Zhu, B.T.1
-
11
-
-
20544449204
-
Catechol-O-methyltransferase (COMT) and monoamine oxidase B (MAOB) genes and susceptibility to sporadic Parkinson's disease in a Polish population
-
Białecka M, Drozdzik M, Honczarenko K, Gawrońska-Szklarz B, Stankiewicz J, Da̧browska E, et al. Catechol-O-methyltransferase (COMT) and monoamine oxidase B (MAOB) genes and susceptibility to sporadic Parkinson's disease in a Polish population. Eur Neurol 2005; 53:68-73.
-
(2005)
Eur Neurol
, vol.53
, pp. 68-73
-
-
Białecka, M.1
Drozdzik, M.2
Honczarenko, K.3
Gawrońska-Szklarz, B.4
Stankiewicz, J.5
Da̧browska, E.6
-
12
-
-
0026666528
-
Iron-melanin complex in substantia nigra of parkinsonian brains: An X-ray microanalysis
-
Jellinger K, Kienzl E, Rumpelmaier G, Riederer P, Paulus W, Stachelberger H, et al. Iron-melanin complex in substantia nigra of parkinsonian brains: an X-ray microanalysis. J Neurochem 1993; 59:1168-1171.
-
(1993)
J Neurochem
, vol.59
, pp. 1168-1171
-
-
Jellinger, K.1
Kienzl, E.2
Rumpelmaier, G.3
Riederer, P.4
Paulus, W.5
Stachelberger, H.6
-
13
-
-
38149073317
-
Aggregation of alpha-synuclein by DOPAL, the monoamine oxidase metabolite of dopamine
-
Burke WJ, Kumar VB, Pandey N, Panneton WM, Gan Q, Franko MW, et al. Aggregation of alpha-synuclein by DOPAL, the monoamine oxidase metabolite of dopamine. Acta Neuropathol 2008; 115:193-203.
-
(2008)
Acta Neuropathol
, vol.115
, pp. 193-203
-
-
Burke, W.J.1
Kumar, V.B.2
Pandey, N.3
Panneton, W.M.4
Gan, Q.5
Franko, M.W.6
-
14
-
-
0021201021
-
Difference in erythrocyte catechol-O-methyltransferase activity between Orientals and Caucasians: Difference in levodopa tolerance
-
Ricera-Caliman L, Reilly DK. Difference in erythrocyte catechol-O-methyltransferase activity between Orientals and Caucasians: difference in levodopa tolerance. Clin Pharmacol Ther 1984; 35:804-809.
-
(1984)
Clin Pharmacol Ther
, vol.35
, pp. 804-809
-
-
Ricera-Caliman, L.1
Reilly, D.K.2
-
15
-
-
0037176816
-
COMT genotype and effectiveness of entacapone in patients with fluctuating Parkinson's disease
-
Lee MS, Kim HS, Cho EK, Lim JH, Rinne JO. COMT genotype and effectiveness of entacapone in patients with fluctuating Parkinson's disease. Neurology 2002; 58:564-567.
-
(2002)
Neurology
, vol.58
, pp. 564-567
-
-
Lee, M.S.1
Kim, H.S.2
Cho, E.K.3
Lim, J.H.4
Rinne, J.O.5
-
16
-
-
0028918413
-
Kinetics of human soluble and membrane-bound catechol-O- methyltransferase: A revised mechanism and description of the termolabile variant of the enzyme
-
Lotta T, Vidgren J, Tilgmann C, Ulmanen I, Melen K, Julkunen I, et al. Kinetics of human soluble and membrane-bound catechol-O- methyltransferase: a revised mechanism and description of the termolabile variant of the enzyme. Biochemistry 1995; 34:4202-4210.
-
(1995)
Biochemistry
, vol.34
, pp. 4202-4210
-
-
Lotta, T.1
Vidgren, J.2
Tilgmann, C.3
Ulmanen, I.4
Melen, K.5
Julkunen, I.6
-
17
-
-
0031015324
-
High and low activity alleles of catechol-O-methyltransferase gene: Ethnic difference and possible association with Parkinson's disease
-
Kunugi H, Nanko S, Ueki A, Otsuka E, Hattori M, Hoda F, et al. High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease. Neurosci Lett 1997; 221:202-204.
-
(1997)
Neurosci Lett
, vol.221
, pp. 202-204
-
-
Kunugi, H.1
Nanko, S.2
Ueki, A.3
Otsuka, E.4
Hattori, M.5
Hoda, F.6
-
18
-
-
0030611325
-
G/A1947 polymorphism in catechol-O- methyltransferase (COMT) gene in Parkinson's disease
-
Xie T, Ho SL, Li SW, Ma OC. G/A1947 polymorphism in catechol-O- methyltransferase (COMT) gene in Parkinson's disease. Mov Disord 1997; 12:426-427.
-
(1997)
Mov Disord
, vol.12
, pp. 426-427
-
-
Xie, T.1
Ho, S.L.2
Li, S.W.3
Ma, O.C.4
-
19
-
-
0031436062
-
Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan
-
Yoritaka A, Hattori N, Yoshino H, Mizuno Y. Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. J Neural Transm 1997; 104:1313-1317.
-
(1997)
J Neural Transm
, vol.104
, pp. 1313-1317
-
-
Yoritaka, A.1
Hattori, N.2
Yoshino, H.3
Mizuno, Y.4
-
20
-
-
0031777394
-
Ethnic differences in catechol-O-methyltransferase pharmacogenetics: Frequency of the codon 108/158 low activity allele is lower in Kenyan than Caucasian or South-west Asian individuals
-
McLeod HL, Syvanen AC, Githang A, Indalo A, Ismail D, Dewar K, et al. Ethnic differences in catechol-O-methyltransferase pharmacogenetics: frequency of the codon 108/158 low activity allele is lower in Kenyan than Caucasian or South-west Asian individuals. Pharmacogenetics 1998; 8:195-199.
-
(1998)
Pharmacogenetics
, vol.8
, pp. 195-199
-
-
McLeod, H.L.1
Syvanen, A.C.2
Githang, A.3
Indalo, A.4
Ismail, D.5
Dewar, K.6
-
21
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
Nackley AG, Shabalina SA, Tchivileva IE, Satterfield K, Korchynskyi O, Makarov SS, et al. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 2006; 314:1930-1933.
-
(2006)
Science
, vol.314
, pp. 1930-1933
-
-
Nackley, A.G.1
Shabalina, S.A.2
Tchivileva, I.E.3
Satterfield, K.4
Korchynskyi, O.5
Makarov, S.S.6
-
22
-
-
19944427292
-
Genetic basis for individual variations in pain perception and the development of a chronic pain condition
-
Diatchenko L, Slade GD, Nackley AG, Bhalang K, Sigurdsson A, Belfer I, et al. Genetic basis for individual variations in pain perception and the development of a chronic pain condition. Hum Mol Genet 2005; 14:135-143.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 135-143
-
-
Diatchenko, L.1
Slade, G.D.2
Nackley, A.G.3
Bhalang, K.4
Sigurdsson, A.5
Belfer, I.6
-
23
-
-
33846504706
-
A silent polymorphism in the MDR1 gene changes substrate specificity
-
Kimchi-Sarfaty C, Oh JM, Kim IW, Sauna ZE, Calcagno AM, Ambudkar SV, et al. A silent polymorphism in the MDR1 gene changes substrate specificity. Science 2007; 315:525-528.
-
(2007)
Science
, vol.315
, pp. 525-528
-
-
Kimchi-Sarfaty, C.1
Oh, J.M.2
Kim, I.W.3
Sauna, Z.E.4
Calcagno, A.M.5
Ambudkar, S.V.6
-
24
-
-
0027337422
-
Parkinson's disease society brain bank, London: Overview and research
-
Daniel SE, Lees AJ. Parkinson's disease society brain bank, London: overview and research. J Neural Transm Suppl 1993; 39:165-172.
-
(1993)
J Neural Transm Suppl
, vol.39
, pp. 165-172
-
-
Daniel, S.E.1
Lees, A.J.2
-
25
-
-
0014082977
-
Parkinsonism: Onset, progression, and mortality
-
Hoehn MM, Yahr MD. Parkinsonism: onset, progression, and mortality. Neurology 1967; 17:427-442.
-
(1967)
Neurology
, vol.17
, pp. 427-442
-
-
Hoehn, M.M.1
Yahr, M.D.2
-
26
-
-
0035852840
-
The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese
-
Wu RM, Cheng CW, Chen KH, Lu SL, Shan DE, Ho YF, et al. The COMT L allele modifies the association between MAOB polymorphism and PD in Taiwanese. Neurology 2002; 56:375-382.
-
(2002)
Neurology
, vol.56
, pp. 375-382
-
-
Wu, R.M.1
Cheng, C.W.2
Chen, K.H.3
Lu, S.L.4
Shan, D.E.5
Ho, Y.F.6
-
27
-
-
0037183750
-
Apolipoprotein E (APOE), PARKIN and catechol-O-methyltransferase (COMT) genes and susceptibility to sporadic Parkinson's disease in Finland
-
Eerola J, Launes J, Hellstrom O, Tienari PJ. Apolipoprotein E (APOE), PARKIN and catechol-O-methyltransferase (COMT) genes and susceptibility to sporadic Parkinson's disease in Finland. Neurosci Lett 2002; 330:296-298.
-
(2002)
Neurosci Lett
, vol.330
, pp. 296-298
-
-
Eerola, J.1
Launes, J.2
Hellstrom, O.3
Tienari, P.J.4
-
28
-
-
4644328053
-
The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphism on levodopa therapy in patients with sporadic Parkinson disease
-
Białecka M, Drozdzik M, Kłodowska-Duda G, Honczarenko K, Gawrońska-Szklarz B, Opala G, et al. The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphism on levodopa therapy in patients with sporadic Parkinson disease. Acta Neurol Scand 2004; 110:260-266.
-
(2004)
Acta Neurol Scand
, vol.110
, pp. 260-266
-
-
Białecka, M.1
Drozdzik, M.2
Kłodowska-Duda, G.3
Honczarenko, K.4
Gawrońska-Szklarz, B.5
Opala, G.6
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