-
1
-
-
78349294117
-
Exploration of genetic susceptibility factors for Parkinson's disease in a South American sample
-
Benitez BA, Forero DA, Arboleda GH, Granados LA,Yunis JJ, Fernandez W, Arboleda H. Exploration of genetic susceptibility factors for Parkinson's disease in a South American sample. J Genet 2010; 89: 229-232.
-
(2010)
J Genet
, vol.89
, pp. 229-232
-
-
Benitez, B.A.1
Forero, D.A.2
Arboleda, G.H.3
Granados, L.A.4
Yunis, J.J.5
Fernandez, W.6
Arboleda, H.7
-
3
-
-
79956078781
-
Leprosy susceptibility: Genetic variations regulate innate and adaptive immunity, and disease outcome
-
Cardoso CC, Pereira AC, de Sales Marques C, Moraes MO. Leprosy susceptibility: genetic variations regulate innate and adaptive immunity, and disease outcome. Future Microbiol 2011; 6: 533-549.
-
(2011)
Future Microbiol
, vol.6
, pp. 533-549
-
-
Cardoso, C.C.1
Pereira, A.C.2
De Sales Marques, C.3
Moraes, M.O.4
-
4
-
-
79959330427
-
Efficient allele-specific targeting of LRRK2 R1441 mutations mediated by RNAi
-
de Ynigo-Mojado L, Martin-Ruiz I, Sutherland JD. Efficient allele-specific targeting of LRRK2 R1441 mutations mediated by RNAi. PLoS One 2011; 6: e21352.
-
(2011)
PLoS One
, vol.6
-
-
De Ynigo-Mojado, L.1
Martin-Ruiz, I.2
Sutherland, J.D.3
-
5
-
-
33947622118
-
Ashkenazi Jewish mtDNA haplogroup distribution varies among distinct subpopulations: Lessons of population substructure in a closed group
-
DOI 10.1038/sj.ejhg.5201764, PII 5201764
-
Feder J, Ovadia O, Glaser B, Mishmar D. Ashkenazi Jewish mtDNA haplogroup distribution varies among distinct subpopulations: lessons of population substructure in a closed group. Eur J Hum Genet 2007; 15: 498-500. (Pubitemid 46487706)
-
(2007)
European Journal of Human Genetics
, vol.15
, Issue.4
, pp. 498-500
-
-
Feder, J.1
Ovadia, O.2
Glaser, B.3
Mishmar, D.4
-
6
-
-
33846587090
-
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan
-
Fung HC, Chen CM, Hardy J, Singleton AB, Wu YR. A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan. BMC Neurol 2006; 6: 47.
-
(2006)
BMC Neurol
, vol.6
, pp. 47
-
-
Fung, H.C.1
Chen, C.M.2
Hardy, J.3
Singleton, A.B.4
Wu, Y.R.5
-
7
-
-
84874349443
-
The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: Clinical and demographic characteristics
-
Gatto EM, Parisi V, Converso DP, Poderoso JJ, Carreras MC, Marti-Masso JF, Paisan-Ruiz C. The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: clinical and demographic characteristics. Neurosci Lett 2013; 537: 1-5.
-
(2013)
Neurosci Lett
, vol.537
, pp. 1-5
-
-
Gatto, E.M.1
Parisi, V.2
Converso, D.P.3
Poderoso, J.J.4
Carreras, M.C.5
Marti-Masso, J.F.6
Paisan-Ruiz, C.7
-
8
-
-
84861198221
-
PARK2 variability in Polish Parkinson's disease patients - Interaction with mitochondrial haplogroups
-
Gaweda-Walerych K, Safranow K, Jasinska-Myga B, Bialecka M, Klodowska-Duda G, Rudzinska M, Czyzewski K, Cobb SA, Slawek J, Styczynska M, Opala G, Drozdzik M, Nishioka K, Farrer MJ, Ross OA, Wszolek ZK, Barcikowska M, Zekanowski C. PARK2 variability in Polish Parkinson's disease patients - interaction with mitochondrial haplogroups. Parkinsonism Relat Disord 2012; 18: 520-524.
-
(2012)
Parkinsonism Relat Disord
, vol.18
, pp. 520-524
-
-
Gaweda-Walerych, K.1
Safranow, K.2
Jasinska-Myga, B.3
Bialecka, M.4
Klodowska-Duda, G.5
Rudzinska, M.6
Czyzewski, K.7
Cobb, S.A.8
Slawek, J.9
Styczynska, M.10
Opala, G.11
Drozdzik, M.12
Nishioka, K.13
Farrer, M.J.14
Ross, O.A.15
Wszolek, Z.K.16
Barcikowska, M.17
Zekanowski, C.18
-
9
-
-
65649142038
-
The Parkinson disease-associated protein kinase LRRK2 exhibits MAPKKK activity and phosphorylates MKK3/6 and MKK4/7, in vitro
-
Gloeckner CJ, Schumacher A, Boldt K, Ueffing M. The Parkinson disease-associated protein kinase LRRK2 exhibits MAPKKK activity and phosphorylates MKK3/6 and MKK4/7, in vitro. J Neurochem 2009; 109: 959-968.
-
(2009)
J Neurochem
, vol.109
, pp. 959-968
-
-
Gloeckner, C.J.1
Schumacher, A.2
Boldt, K.3
Ueffing, M.4
-
10
-
-
84869805915
-
Celiac disease: Prevalence, diagnosis, pathogenesis and treatment
-
Gujral N, Freeman HJ, Thomson AB. Celiac disease: prevalence, diagnosis, pathogenesis and treatment. World J Gastroenterol 2012; 18: 6036-6059.
-
(2012)
World J Gastroenterol
, vol.18
, pp. 6036-6059
-
-
Gujral, N.1
Freeman, H.J.2
Thomson, A.B.3
-
11
-
-
0026230139
-
A fast method for high-quality genomic DNA extraction from whole human blood
-
Gustincich S, Manfioletti G, Del Sal G, Schneider C, Carninci P. A fast method for high-quality genomic DNA extraction from whole human blood. Biotechniques 1991; 11: 298-300, 302.
-
(1991)
Biotechniques
, vol.11
-
-
Gustincich, S.1
Manfioletti, G.2
Del Sal, G.3
Schneider, C.4
Carninci, P.5
-
12
-
-
79956199220
-
Parkinson's disease-linked LRRK2 is expressed in circulating and tissue immune cells and upregulated following recognition of microbial structures
-
Hakimi M, Selvanantham T, Swinton E, Padmore RF, Tong Y, Kabbach G, Venderova K, Girardin SE, Bulman DE, Scherzer CR, LaVoie MJ, Gris D, Park DS, Angel JB, Shen J, Philpott DJ, Schlossmacher MG. Parkinson's disease-linked LRRK2 is expressed in circulating and tissue immune cells and upregulated following recognition of microbial structures. J Neural Transm 2011; 118: 795-808.
-
(2011)
J Neural Transm
, vol.118
, pp. 795-808
-
-
Hakimi, M.1
Selvanantham, T.2
Swinton, E.3
Padmore, R.F.4
Tong, Y.5
Kabbach, G.6
Venderova, K.7
Girardin, S.E.8
Bulman, D.E.9
Scherzer, C.R.10
LaVoie, M.J.11
Gris, D.12
Park, D.S.13
Angel, J.B.14
Shen, J.15
Philpott, D.J.16
Schlossmacher, M.G.17
-
13
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study
-
Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, Brice A, Aasly J, Zabetian CP, Goldwurm S, Ferreira JJ, Tolosa E, Kay DM, Klein C, Williams DR, Marras C, Lang AE, Wszolek ZK, Berciano J, Schapira AH, Lynch T, Bhatia KP, Gasser T, Lees AJ, Wood NW. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008; 7: 583-590.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
Bonifati, V.4
Durr, A.5
Bressman, S.6
Brice, A.7
Aasly, J.8
Zabetian, C.P.9
Goldwurm, S.10
Ferreira, J.J.11
Tolosa, E.12
Kay, D.M.13
Klein, C.14
Williams, D.R.15
Marras, C.16
Lang, A.E.17
Wszolek, Z.K.18
Berciano, J.19
Schapira, A.H.20
Lynch, T.21
Bhatia, K.P.22
Gasser, T.23
Lees, A.J.24
Wood, N.W.25
more..
-
14
-
-
56849094704
-
Test for LRRK2 mutations in patients with Parkinson's disease
-
Healy DG, Wood NW, Schapira AH. Test for LRRK2 mutations in patients with Parkinson's disease. Pract Neurol 2008; 8: 381-385.
-
(2008)
Pract Neurol
, vol.8
, pp. 381-385
-
-
Healy, D.G.1
Wood, N.W.2
Schapira, A.H.3
-
15
-
-
24044555258
-
Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population
-
DOI 10.1016/j.jns.2005.04.016, PII S0022510X0500184X
-
Huerta C, Castro MG, Coto E, Blazquez M, Ribacoba R, Guisasola LM, Salvador C, Martinez C, Lahoz CH, Alvarez V. Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population. J Neurol Sci 2005; 236: 49-54. (Pubitemid 41218692)
-
(2005)
Journal of the Neurological Sciences
, vol.236
, Issue.1-2
, pp. 49-54
-
-
Huerta, C.1
Castro, M.G.2
Coto, E.3
Blazquez, M.4
Ribacoba, R.5
Guisasola, L.M.6
Salvador, C.7
Martinez, C.8
Lahoz, C.H.9
Alvarez, V.10
-
16
-
-
0036209085
-
The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service
-
Hughes AJ, Daniel SE, Ben-Shlomo Y, Lees AJ. The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. Brain 2002; 125: 861-870. (Pubitemid 34279780)
-
(2002)
Brain
, vol.125
, Issue.4
, pp. 861-870
-
-
Hughes, A.J.1
Daniel, S.E.2
Ben-Shlomo, Y.3
Lees, A.J.4
-
17
-
-
38549106125
-
Pathogenic mutations and non-pathogenic DNA polymorphisms in the most common neurodegenerative disorders
-
Kochanski A. Pathogenic mutations and non-pathogenic DNA polymorphisms in the most common neurodegenerative disorders. Folia Neuropathol 2007; 45: 164-169. (Pubitemid 351149041)
-
(2007)
Folia Neuropathologica
, vol.45
, Issue.4
, pp. 164-169
-
-
Kochanski, A.1
-
18
-
-
70350447105
-
LRRK2 in Parkinson's disease: Genetic and clinical studies from patients
-
Kumari U, Tan EK. LRRK2 in Parkinson's disease: genetic and clinical studies from patients. FEBS J 2009; 276: 6455-6463.
-
(2009)
FEBS J
, vol.276
, pp. 6455-6463
-
-
Kumari, U.1
Tan, E.K.2
-
19
-
-
79960981876
-
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population
-
Liu X, Cheng R, Verbitsky M, Kisselev S, Browne A, Mejia-Sanatana H, Louis ED, Cote LJ, Andrews H, Waters C, Ford B, Frucht S, Fahn S, Marder K, Clark LN, Lee JH. Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. BMC Med Genet 2011; 12: 104.
-
(2011)
BMC Med Genet
, vol.12
, pp. 104
-
-
Liu, X.1
Cheng, R.2
Verbitsky, M.3
Kisselev, S.4
Browne, A.5
Mejia-Sanatana, H.6
Louis, E.D.7
Cote, L.J.8
Andrews, H.9
Waters, C.10
Ford, B.11
Frucht, S.12
Fahn, S.13
Marder, K.14
Clark, L.N.15
Lee, J.H.16
-
20
-
-
80054933395
-
The kinase LRRK2 is a regulator of the transcription factor NFAT that modulates the severity of inflammatory bowel disease
-
Liu Z, Lee J, Krummey S, Lu W, Cai H, Lenardo MJ. The kinase LRRK2 is a regulator of the transcription factor NFAT that modulates the severity of inflammatory bowel disease. Nat Immunol 2011; 12: 1063-1070.
-
(2011)
Nat Immunol
, vol.12
, pp. 1063-1070
-
-
Liu, Z.1
Lee, J.2
Krummey, S.3
Lu, W.4
Cai, H.5
Lenardo, M.J.6
-
21
-
-
0042415580
-
How much phenotypic variation can be attributed to parkin genotype?
-
DOI 10.1002/ana.10613
-
Lohmann E, Periquet M, Bonifati V, Wood NW, De Michele G, Bonnet AM, Fraix V, Broussolle E, Horstink MW, Vidailhet M, Verpillat P, Gasser T, Nicholl D, Teive H, Raskin S, Rascol O, Destee A, Ruberg M, Gasparini F, Meco G, Agid Y, Durr A, Brice A. How much phenotypic variation can be attributed to parkin genotype? Ann Neurol 2003; 54: 176-185. (Pubitemid 36913573)
-
(2003)
Annals of Neurology
, vol.54
, Issue.2
, pp. 176-185
-
-
Lohmann, E.1
Periquet, M.2
Bonifati, V.3
Wood, N.W.4
De Michele, G.5
Bonnet, A.-M.6
Fraix, V.7
Broussolle, E.8
Horstink, M.W.I.M.9
Vidailhet, M.10
Verpillat, P.11
Gasser, T.12
Nicholl, D.13
Teive, H.14
Raskin, S.15
Rascol, O.16
Destee, A.17
Ruberg, M.18
Gasparini, F.19
Meco, G.20
Agid, Y.21
Durr, A.22
Brice, A.23
more..
-
22
-
-
0032564235
-
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
-
The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group
-
Lucking CB, Abbas N, Durr A, Bonifati V, Bonnet AM, de Broucker T, De Michele G, Wood NW, Agid Y, Brice A. Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group. Lancet 1998; 352: 1355-1356.
-
(1998)
Lancet
, vol.352
, pp. 1355-1356
-
-
Lucking, C.B.1
Abbas, N.2
Durr, A.3
Bonifati, V.4
Bonnet, A.M.5
De Broucker, T.6
De Michele, G.7
Wood, N.W.8
Agid, Y.9
Brice, A.10
-
23
-
-
72249099242
-
PARKIN-coding polymorphisms are not associated with Parkinson's disease in a population from northeastern Mexico
-
Martinez HR, Gonzalez-Gonzalez H, Cantu-Martinez L, Ran-gel- Guerra R, Hernandez-Castillo CD, Vergara-Saavedra JJ, Ramos-Gonzalez MR, Cerda-Flores RM, Morales-Garza MA, Guerrero-Munoz MJ, Montes-de-Oca-Luna R, Saucedo-Cardenas O. PARKIN-coding polymorphisms are not associated with Parkinson's disease in a population from northeastern Mexico. Neurosci Lett 2010; 468: 264-266.
-
(2010)
Neurosci Lett
, vol.468
, pp. 264-266
-
-
Martinez, H.R.1
Gonzalez-Gonzalez, H.2
Cantu-Martinez, L.3
Ran-gel- Guerra, R.4
Hernandez-Castillo, C.D.5
Vergara-Saavedra, J.J.6
Ramos-Gonzalez, M.R.7
Cerda-Flores, R.M.8
Morales-Garza, Ma.9
Guerrero-Munoz, M.J.10
Montes-de-Oca-Luna, R.11
Saucedo-Cardenas, O.12
-
24
-
-
77953054123
-
Genetic screening for the LRRK2, G2019S and R1441 codon mutations in Parkinson's disease patients from Extremadura, Spain
-
Moran JM, Castellanos-Pinedo F, Casado-Naranjo I, Duran-Herrera C, Ramirez-Moreno JM, Gomez M, Zurdo-Hernandez JM, Fuentes E, Ortiz-Ortiz MA, Moreno AD, Gonzalez-Polo RA, Niso-Santano M, Bravo-Sanpedro JM, Perez-Tur J, Ruiz-Mesa LM, Fuentes JM. Genetic screening for the LRRK2, G2019S and R1441 codon mutations in Parkinson's disease patients from Extremadura, Spain. Rev Neurol 2010; 50: 591-594.
-
(2010)
Rev Neurol
, vol.50
, pp. 591-594
-
-
Moran, J.M.1
Castellanos-Pinedo, F.2
Casado-Naranjo, I.3
Duran-Herrera, C.4
Ramirez-Moreno, J.M.5
Gomez, M.6
Zurdo-Hernandez, J.M.7
Fuentes, E.8
Ortiz-Ortiz, M.A.9
Moreno, A.D.10
Gonzalez-Polo, R.A.11
Niso-Santano, M.12
Bravo-Sanpedro, J.M.13
Perez-Tur, J.14
Ruiz-Mesa, L.M.15
Fuentes, J.M.16
-
25
-
-
67649637695
-
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population
-
Nuytemans K, Meeus B, Crosiers D, Brouwers N, Goossens D, Engelborghs S, Pals P, Pickut B, Van den Broeck M, Corsmit E, Cras P, De Deyn PP, Del-Favero J, Van Broeckhoven C, Theuns J. Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population. Hum Mutat 2009; 30: 1054-1061.
-
(2009)
Hum Mutat
, vol.30
, pp. 1054-1061
-
-
Nuytemans, K.1
Meeus, B.2
Crosiers, D.3
Brouwers, N.4
Goossens, D.5
Engelborghs, S.6
Pals, P.7
Pickut, B.8
Van Den Broeck, M.9
Corsmit, E.10
Cras, P.11
De Deyn, P.P.12
Del-Favero, J.13
Van Broeckhoven, C.14
Theuns, J.15
-
26
-
-
24644431901
-
LRRK2 gene in Parkinson disease: Mutation analysis and case control association study
-
DOI 10.1212/01.WNL.0000167552.79769.b3
-
Paisan-Ruiz C, Lang AE, Kawarai T, Sato C, Salehi-Rad S, Fis- man GK, Al-Khairallah T, St George-Hyslop P, Singleton A, Rogaeva E. LRRK2 gene in Parkinson disease: mutation analysis and case control association study. Neurology 2005; 65: 696-700. (Pubitemid 41285847)
-
(2005)
Neurology
, vol.65
, Issue.5
, pp. 696-700
-
-
Paisan-Ruiz, C.1
Lang, A.E.2
Kawarai, T.3
Sato, C.4
Salehi-Rad, S.5
Fisman, G.K.6
Al-Khairallah, T.7
St G.-Hyslop, P.8
Singleton, A.9
Rogaeva, E.10
-
27
-
-
3342996696
-
parkin mutation analysis in clinic patients with early-onset Parkinson's disease
-
Poorkaj P, Nutt JG, James D, Gancher S, Bird TD, Steinbart E, Schellenberg GD, Payami H. Parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease. Am J Med Genet A 2004; 129A: 44-50. (Pubitemid 38989043)
-
(2004)
American Journal of Medical Genetics
, vol.129 A
, Issue.1
, pp. 44-50
-
-
Poorkaj, P.1
Nutt, J.G.2
James, D.3
Gancher, S.4
Bird, T.D.5
Steinbart, E.6
Schellenberg, G.D.7
Payami, H.8
-
28
-
-
34347218275
-
Frecuencia del polimorfismo IVS4+66A-G en el gen alfa-sinucleína en pacientes con enfermedad de Parkinson del noroccidente de México
-
Ramirez-Jirano LJ, Ruiz-Sandoval JL, Jimenez-Gil FJ, Ramirez-Vega J, Vargas-Frutos E, Gallegos-Arreola MP. Frequency of the IVS4+66A-G polymorphism in the alpha-synuclein gene in patients with Parkinson's disease in north-western Mexico. Rev Neurol 2007; 44: 15-17. (Pubitemid 350304982)
-
(2007)
Revista de Neurologia
, vol.44
, Issue.1
, pp. 15-17
-
-
Ramirez-Jirano, L.J.1
Ruiz-Sandoval, J.L.2
Jimenez-Gil, F.J.3
Ramirez-Vega, J.4
Vargas-Frutos, E.5
Gallegos-Arreola, M.P.6
-
29
-
-
67649616741
-
Pre-Hispanic Mesoamerican demography approximates the present-day ancestry of Mestizos throughout the territory of Mexico
-
Rubi-Castellanos R, Martinez-Cortes G, Munoz-Valle JF, Gonzalez-Martin A, Cerda-Flores RM, Anaya-Palafox M, Rangel-Villalobos H. Pre-Hispanic Mesoamerican demography approximates the present-day ancestry of Mestizos throughout the territory of Mexico. Am J Phys Anthropol 2009; 139: 284-294.
-
(2009)
Am J Phys Anthropol
, vol.139
, pp. 284-294
-
-
Rubi-Castellanos, R.1
Martinez-Cortes, G.2
Munoz-Valle, J.F.3
Gonzalez-Martin, A.4
Cerda-Flores, R.M.5
Anaya-Palafox, M.6
Rangel-Villalobos, H.7
-
30
-
-
79955528480
-
Pain in Parkinson's disease: Prevalence, characteristics, associated factors, and relation with other non motor symptoms, quality of life, autonomy, and caregiver burden
-
Santos-Garcia D, Abella-Corral J, Aneiros-Diaz A, Santos-Canelles H, Llaneza-Gonzalez MA, Macias-Arribi M. Pain in Parkinson's disease: prevalence, characteristics, associated factors, and relation with other non motor symptoms, quality of life, autonomy, and caregiver burden. Rev Neurol 2011; 52: 385-393.
-
(2011)
Rev Neurol
, vol.52
, pp. 385-393
-
-
Santos-Garcia, D.1
Abella-Corral, J.2
Aneiros-Diaz, A.3
Santos-Canelles, H.4
Llaneza-Gonzalez, M.A.5
Macias-Arribi, M.6
-
31
-
-
70549084415
-
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
-
Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009; 41: 1303-1307.
-
(2009)
Nat Genet
, vol.41
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
Hirota, Y.4
Ito, C.5
Kubo, M.6
Kawaguchi, T.7
Tsunoda, T.8
Watanabe, M.9
Takeda, A.10
Tomiyama, H.11
Nakashima, K.12
Hasegawa, K.13
Obata, F.14
Yoshikawa, T.15
Kawakami, H.16
Sakoda, S.17
Yamamoto, M.18
Hattori, N.19
Murata, M.20
Nakamura, Y.21
Toda, T.22
more..
-
32
-
-
0035743004
-
Case-control studies of genetic markers: Power and sample size approximations for Armitage's test for trend
-
DOI 10.1159/000053370
-
Slager SL, Schaid DJ. Case-control studies of genetic markers: power and sample size approximations for Armitage's test for trend. Hum Hered 2001; 52: 149-153. (Pubitemid 34701500)
-
(2001)
Human Heredity
, vol.52
, Issue.3
, pp. 149-153
-
-
Slager, S.L.1
Schaid, D.J.2
-
33
-
-
84455162099
-
Alteration of GSK-3beta in the hippocampus and other brain structures after chronic paraquat administration in rats
-
Songin M, Ossowska K, Kuter K, Strosznajder JB. Alteration of GSK-3beta in the hippocampus and other brain structures after chronic paraquat administration in rats. Folia Neuropathol 2011; 49: 319-327.
-
(2011)
Folia Neuropathol
, vol.49
, pp. 319-327
-
-
Songin, M.1
Ossowska, K.2
Kuter, K.3
Strosznajder, J.B.4
-
34
-
-
0347635418
-
Neuroprotection by monoamine oxidase B inhibitors: A therapeutic strategy for Parkinson's disease?
-
DOI 10.1002/bies.10378
-
Tabakman R, Lecht S, Lazarovici P. Neuroprotection by monoamine oxidase B inhibitors: a therapeutic strategy for Parkinson's disease? Bioessays 2004; 26: 80-90. (Pubitemid 38095352)
-
(2004)
BioEssays
, vol.26
, Issue.1
, pp. 80-90
-
-
Tabakman, R.1
Lecht, S.2
Lazarovici, P.3
-
35
-
-
33846358949
-
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: Genetic and functional evidence
-
DOI 10.1007/s00439-006-0268-0
-
Tan EK, Zhao Y, Skipper L, Tan MG, Di Fonzo A, Sun L, Fook-Chong S, Tang S, Chua E, Yuen Y, Tan L, Pavanni R, Wong MC, Kolatkar P, Lu CS, Bonifati V, Liu JJ. The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence. Hum Genet 2007; 120: 857-863. (Pubitemid 46128841)
-
(2007)
Human Genetics
, vol.120
, Issue.6
, pp. 857-863
-
-
Tan, E.K.1
Zhao, Y.2
Skipper, L.3
Tan, M.G.4
Di, F.A.5
Sun, L.6
Fook-Chong, S.7
Tang, S.8
Chua, E.9
Yuen, Y.10
Tan, L.11
Pavanni, R.12
Wong, M.C.13
Kolatkar, P.14
Lu, C.S.15
Bonifati, V.16
Liu, J.J.17
-
36
-
-
34548023737
-
Clinical molecular genetics for PARK8 (LRRK2)
-
.Tomiyama H, Hatano T, Hattori N. Clinical molecular genetics for PARK8 (LRRK2)]. Brain Nerve 2007; 59: 839-850. (Pubitemid 47280223)
-
(2007)
Brain and Nerve
, vol.59
, Issue.8
, pp. 839-850
-
-
Tomiyama, H.1
Hatano, T.2
Hattori, N.3
-
37
-
-
84873388282
-
Association of monoamine oxidase B and catechol-O-methyltransferase polymorphisms with sporadic Parkinson's disease in an Iranian population
-
Torkaman-Boutorabi A, Ali Shahidi G, Choopani S, Reza Zarrindast M. Association of monoamine oxidase B and catechol-O-methyltransferase polymorphisms with sporadic Parkinson's disease in an Iranian population. Folia Neuropathol 2012; 50: 382-389.
-
(2012)
Folia Neuropathol
, vol.50
, pp. 382-389
-
-
Torkaman-Boutorabi, A.1
Ali Shahidi, G.2
Choopani, S.3
Reza Zarrindast, M.4
-
38
-
-
0037385480
-
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
-
van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nan- ce MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Stajich JM, McLaurin AC, Middleton LT, Scott BL, Schmechel DE, Pericak-Vance MA, Vance JM. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. Am J Hum Genet 2003; 72: 804-811.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 804-811
-
-
Van Der Walt, J.M.1
Nicodemus, K.K.2
Martin, E.R.3
Scott, W.K.4
Nan- Ce, Ma.5
Watts, R.L.6
Hubble, J.P.7
Haines, J.L.8
Koller, W.C.9
Lyons, K.10
Pahwa, R.11
Stern, M.B.12
Colcher, A.13
Hiner, B.C.14
Jankovic, J.15
Ondo, W.G.16
Allen Jr., F.H.17
Goetz, C.G.18
Small, G.W.19
Mastaglia, F.20
Stajich, J.M.21
McLaurin, A.C.22
Middleton, L.T.23
Scott, B.L.24
Schmechel, D.E.25
Pericak-Vance, Ma.26
Vance, J.M.27
more..
-
39
-
-
75949104449
-
Mitochondria get a Parkin' ticket
-
Wild P, Dikic I. Mitochondria get a Parkin' ticket. Nat Cell Biol 2010; 12: 104-106.
-
(2010)
Nat Cell Biol
, vol.12
, pp. 104-106
-
-
Wild, P.1
Dikic, I.2
-
40
-
-
77957347508
-
Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease
-
.Yescas P, Lopez M, Monroy N, Boll MC, Rodriguez-Violante M, Rodriguez U, Ochoa A, Alonso ME. Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease. Neurosci Lett 2010; 485: 79-82.
-
(2010)
Neurosci Lett
, vol.485
, pp. 79-82
-
-
Yescas, P.1
Lopez, M.2
Monroy, N.3
Boll, M.C.4
Rodriguez-Violante, M.5
Rodriguez, U.6
Ochoa, A.7
Alonso, M.E.8
-
41
-
-
79955567288
-
Identification of chemicals to inhibit the kinase activity of leucine-rich repeat kinase 2 (LRRK2), a Parkinson's disease-associated protein
-
Yun H, Heo HY, Kim HH, DooKim N, Seol W. Identification of chemicals to inhibit the kinase activity of leucine-rich repeat kinase 2 (LRRK2), a Parkinson's disease-associated protein. Bioorg Med Chem Lett 2011; 21: 2953-2957.
-
(2011)
Bioorg Med Chem Lett
, vol.21
, pp. 2953-2957
-
-
Yun, H.1
Heo, H.Y.2
Kim, H.H.3
DooKim, N.4
Seol, W.5
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