-
1
-
-
77952122496
-
Lrrk2 and Parkinson disease
-
20457952 10.1001/archneurol.2010.79
-
Dachsel JC, Farrer MJ (2010) Lrrk2 and Parkinson disease. Arch Neurol 67:542-547
-
(2010)
Arch Neurol
, vol.67
, pp. 542-547
-
-
Dachsel, J.C.1
Farrer, M.J.2
-
2
-
-
33646151866
-
Lrrk2 in Parkinson's disease: Protein domains and functional insights
-
16616379 10.1016/j.tins.2006.03.006 1:CAS:528:DC%2BD28XktVehtb0%3D
-
Mata IF, Wedemeyer WJ, Farrer MJ, Taylor JP, Gallo KA (2006) Lrrk2 in Parkinson's disease: protein domains and functional insights. Trends Neurosci 29:286-293
-
(2006)
Trends Neurosci
, vol.29
, pp. 286-293
-
-
Mata, I.F.1
Wedemeyer, W.J.2
Farrer, M.J.3
Taylor, J.P.4
Gallo, K.A.5
-
3
-
-
70349103837
-
Parkin protects against lrrk2 G2019S mutant-induced dopaminergic neurodegeneration in drosophila
-
19741132 10.1523/JNEUROSCI.2375-09.2009 1:CAS:528:DC%2BD1MXhtFOhu7vO
-
Ng CH, Mok SZ, Koh C et al (2009) Parkin protects against lrrk2 G2019S mutant-induced dopaminergic neurodegeneration in drosophila. J Neurosci 29:11257-11262
-
(2009)
J Neurosci
, vol.29
, pp. 11257-11262
-
-
Ng, C.H.1
Mok, S.Z.2
Koh, C.3
-
4
-
-
57649178295
-
Intramolecular activation mechanism of the dictyostelium lrrk2 homolog roco protein gbpc
-
18703517 10.1074/jbc.M804265200
-
van Egmond WN, Kortholt A, Plak K et al (2008) Intramolecular activation mechanism of the dictyostelium lrrk2 homolog roco protein gbpc. J Biol Chem 283:30412-30420
-
(2008)
J Biol Chem
, vol.283
, pp. 30412-30420
-
-
Van Egmond, W.N.1
Kortholt, A.2
Plak, K.3
-
5
-
-
53749090842
-
Lrrk2 R1628P increases risk of Parkinson's disease: Replication evidence
-
18781329 10.1007/s00439-008-0544-2 1:CAS:528:DC%2BD1cXht1art7jK
-
Tan EK, Tan LC, Lim HQ et al (2008) Lrrk2 R1628P increases risk of Parkinson's disease: replication evidence. Hum Genet 124:287-288
-
(2008)
Hum Genet
, vol.124
, pp. 287-288
-
-
Tan, E.K.1
Tan, L.C.2
Lim, H.Q.3
-
6
-
-
31344432937
-
Lrrk2 G2019S as a cause of Parkinson's disease in North African Arabs
-
16436781 10.1056/NEJMc055540 1:CAS:528:DC%2BD28XnslWisg%3D%3D
-
Lesage S, Durr A, Tazir M et al (2006) Lrrk2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl J Med 354:422-423
-
(2006)
N Engl J Med
, vol.354
, pp. 422-423
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
-
7
-
-
31344439221
-
Lrrk2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
16436782 10.1056/NEJMc055509 1:CAS:528:DC%2BD28XnslWisw%3D%3D
-
Ozelius LJ, Senthil G, Saunders-Pullman R et al (2006) Lrrk2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med 354:424-425
-
(2006)
N Engl J Med
, vol.354
, pp. 424-425
-
-
Ozelius, L.J.1
Senthil, G.2
Saunders-Pullman, R.3
-
8
-
-
80053967546
-
A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease
-
21234781 10.1007/s10072-010-0453-8 1:STN:280:DC%2BC3MnnsVaitQ%3D%3D
-
Hu ZX, Peng DT, Cai M et al (2011) A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease. Neurol Sci 32:741-742
-
(2011)
Neurol Sci
, vol.32
, pp. 741-742
-
-
Hu, Z.X.1
Peng, D.T.2
Cai, M.3
-
9
-
-
33846358949
-
The lrrk2 Gly2385Arg variant is associated with Parkinson's disease: Genetic and functional evidence
-
17019612 10.1007/s00439-006-0268-0 1:CAS:528:DC%2BD2sXnsF2isQ%3D%3D
-
Tan EK, Zhao Y, Skipper L et al (2007) The lrrk2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence. Hum Genet 120:857-863
-
(2007)
Hum Genet
, vol.120
, pp. 857-863
-
-
Tan, E.K.1
Zhao, Y.2
Skipper, L.3
-
10
-
-
48949092066
-
Analysis of lrrk2 R1628P as a risk factor for Parkinson's disease
-
18412265 10.1002/ana.21405 1:CAS:528:DC%2BD1cXhtVKnsrnJ
-
Ross OA, Wu YR, Lee MC et al (2008) Analysis of lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol 64:88-92
-
(2008)
Ann Neurol
, vol.64
, pp. 88-92
-
-
Ross, O.A.1
Wu, Y.R.2
Lee, M.C.3
-
11
-
-
79951653866
-
Confirmation of lrrk2 S1647T variant as a risk factor for parkinson's disease in southern China
-
20629711 10.1111/j.1468-1331.2010.03164.x 1:STN:280: DC%2BC3M7psVagsA%3D%3D
-
Zheng Y, Liu Y, Wu Q et al (2011) Confirmation of lrrk2 S1647T variant as a risk factor for parkinson's disease in southern China. Eur J Neurol 18:538-540
-
(2011)
Eur J Neurol
, vol.18
, pp. 538-540
-
-
Zheng, Y.1
Liu, Y.2
Wu, Q.3
-
12
-
-
79955043145
-
Lrrk2 R1398H polymorphism is associated with decreased risk of Parkinson's disease in a Han Chinese population
-
21159540 10.1016/j.parkreldis.2010.11.012 1:CAS:528:DC%2BC3MXnt12nsro%3D
-
Chen L, Zhang S, Liu Y et al (2011) Lrrk2 R1398H polymorphism is associated with decreased risk of Parkinson's disease in a Han Chinese population. Parkinsonism Relat Disord 17:291-292
-
(2011)
Parkinsonism Relat Disord
, vol.17
, pp. 291-292
-
-
Chen, L.1
Zhang, S.2
Liu, Y.3
-
13
-
-
39149133173
-
Lrrk2 Gly2385Arg variant is a risk factor of parkinson's disease among Han-Chinese from mainland China
-
18201193 10.1111/j.1468-1331.2007.02052.x
-
An XK, Peng R, Li T et al (2008) Lrrk2 Gly2385Arg variant is a risk factor of parkinson's disease among Han-Chinese from mainland China. Eur J Neurol 15:301-305
-
(2008)
Eur J Neurol
, vol.15
, pp. 301-305
-
-
An, X.K.1
Peng, R.2
Li, T.3
-
14
-
-
38549097049
-
The prevalence of lrrk2 Gly2385Arg variant in Chinese Han population with Parkinson's disease
-
17960808 10.1002/mds.21763
-
Li C, Ting Z, Qin X et al (2007) The prevalence of lrrk2 Gly2385Arg variant in Chinese Han population with Parkinson's disease. Mov Disord 22:2439-2443
-
(2007)
Mov Disord
, vol.22
, pp. 2439-2443
-
-
Li, C.1
Ting, Z.2
Qin, X.3
-
15
-
-
84862198228
-
Association of Parkinson's disease with six single nucleotide polymorphisms located in four PARK genes in the Northern Han Chinese population
-
22575062 10.1016/j.jocn.2011.09.028 1:CAS:528:DC%2BC38XntVWhtLg%3D
-
Zhou Y, Luo X, Li F et al (2012) Association of Parkinson's disease with six single nucleotide polymorphisms located in four PARK genes in the Northern Han Chinese population. J Clin Neurosci. 19:1011-1015
-
(2012)
J Clin Neurosci.
, vol.19
, pp. 1011-1015
-
-
Zhou, Y.1
Luo, X.2
Li, F.3
-
16
-
-
52649111119
-
The lrrk2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population
-
18716801 10.1007/s10048-008-0140-6 1:CAS:528:DC%2BD1cXhtFKhu73I
-
Lu CS, Wu-Chou YH, van Doeselaar M et al (2008) The lrrk2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese population. Neurogenetics 9:271-276
-
(2008)
Neurogenetics
, vol.9
, pp. 271-276
-
-
Lu, C.S.1
Wu-Chou, Y.H.2
Van Doeselaar, M.3
-
17
-
-
70349267492
-
Lrrk2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China
-
19699188 10.1016/j.brainres.2009.08.047 1:CAS:528:DC%2BD1MXhtFyqsb%2FK
-
Yu L, Hu F, Zou X et al (2009) Lrrk2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China. Brain Res 1296:113-116
-
(2009)
Brain Res
, vol.1296
, pp. 113-116
-
-
Yu, L.1
Hu, F.2
Zou, X.3
-
18
-
-
70450202383
-
Lrrk2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
-
19672984 10.1002/mds.22371
-
Zhang Z, Burgunder JM, An X et al (2009) Lrrk2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China. Mov Disord 24:1902-1905
-
(2009)
Mov Disord
, vol.24
, pp. 1902-1905
-
-
Zhang, Z.1
Burgunder, J.M.2
An, X.3
-
19
-
-
67651173105
-
Lrrk2 mutations and risk variants in Japanese patients with Parkinson's disease
-
19343804 10.1002/mds.22514
-
Zabetian CP, Yamamoto M, Lopez AN et al (2009) Lrrk2 mutations and risk variants in Japanese patients with Parkinson's disease. Mov Disord 24:1034-1041
-
(2009)
Mov Disord
, vol.24
, pp. 1034-1041
-
-
Zabetian, C.P.1
Yamamoto, M.2
Lopez, A.N.3
-
20
-
-
75949122054
-
The lrrk2 G2385R variant is a risk factor for sporadic Parkinson's disease in the korean population
-
19854095 10.1016/j.parkreldis.2009.10.004
-
Kim JM, Lee JY, Kim HJ et al (2010) The lrrk2 G2385R variant is a risk factor for sporadic Parkinson's disease in the korean population. Parkinsonism Relat Disord 16:85-88
-
(2010)
Parkinsonism Relat Disord
, vol.16
, pp. 85-88
-
-
Kim, J.M.1
Lee, J.Y.2
Kim, H.J.3
-
21
-
-
35348968375
-
Analysis of lrrk2 Gly2385Arg genetic variant in non-Chinese Asians
-
17659642 10.1002/mds.21658
-
Tan EK, Zhao Y, Tan L et al (2007) Analysis of lrrk2 Gly2385Arg genetic variant in non-Chinese Asians. Mov Disord 22:1816-1818
-
(2007)
Mov Disord
, vol.22
, pp. 1816-1818
-
-
Tan, E.K.1
Zhao, Y.2
Tan, L.3
-
22
-
-
55849140881
-
Lrrk2 R1628P in non-Chinese Asian races
-
18688798 10.1002/ana.21467
-
Tan EK, Tang M, Tan LC et al (2008) Lrrk2 R1628P in non-Chinese Asian races. Ann Neurol 64:472-473
-
(2008)
Ann Neurol
, vol.64
, pp. 472-473
-
-
Tan, E.K.1
Tang, M.2
Tan, L.C.3
-
23
-
-
48449089238
-
Is the G2019S lrrk2 mutation common in all southern European populations?
-
18617409 10.1016/j.jocn.2007.08.013 1:CAS:528:DC%2BD1cXps12gs7k%3D
-
Papapetropoulos S, Adi N, Shehadeh L et al (2008) Is the G2019S lrrk2 mutation common in all southern European populations? J Clin Neurosci 15:1027-1030
-
(2008)
J Clin Neurosci
, vol.15
, pp. 1027-1030
-
-
Papapetropoulos, S.1
Adi, N.2
Shehadeh, L.3
-
24
-
-
71149105110
-
Genetic structure of the Han Chinese population revealed by genome-wide snp variation
-
19944401 10.1016/j.ajhg.2009.10.016 1:CAS:528:DC%2BC3cXht1eqtrg%3D
-
Chen J, Zheng H, Bei JX et al (2009) Genetic structure of the Han Chinese population revealed by genome-wide snp variation. Am J Hum Genet 85:775-785
-
(2009)
Am J Hum Genet
, vol.85
, pp. 775-785
-
-
Chen, J.1
Zheng, H.2
Bei, J.X.3
-
25
-
-
80052967403
-
Association of lrrk2 exonic variants with susceptibility to Parkinson's disease: A case-control study
-
21885347 10.1016/S1474-4422(11)70175-2 1:CAS:528:DC%2BC3MXht1ant7zP
-
Ross OA, Soto-Ortolaza AI, Heckman MG et al (2011) Association of lrrk2 exonic variants with susceptibility to Parkinson's disease: a case-control study. Lancet Neurol 10:898-908
-
(2011)
Lancet Neurol
, vol.10
, pp. 898-908
-
-
Ross, O.A.1
Soto-Ortolaza, A.I.2
Heckman, M.G.3
-
26
-
-
77951876814
-
Multiple LRRK2 variants modulate risk of Parkinson disease: A Chinese multicenter study
-
20186690 1:CAS:528:DC%2BC3cXnt1CjtLY%3D
-
Tan EK, Peng R, Teo YY et al (2010) Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study. Hum Mutat 31:561-568
-
(2010)
Hum Mutat
, vol.31
, pp. 561-568
-
-
Tan, E.K.1
Peng, R.2
Teo, Y.Y.3
-
27
-
-
79551495766
-
Lrrk2 S1647T and BDNF V66 M interact with environmental factors to increase risk of Parkinson's disease
-
21167764 10.1016/j.parkreldis.2010.11.011
-
Lin CH, Wu RM, Tai CH et al (2011) Lrrk2 S1647T and BDNF V66 M interact with environmental factors to increase risk of Parkinson's disease. Parkinsonism Relat Disord 17:84-88
-
(2011)
Parkinsonism Relat Disord
, vol.17
, pp. 84-88
-
-
Lin, C.H.1
Wu, R.M.2
Tai, C.H.3
|