-
1
-
-
0032544674
-
Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1
-
Bruijn L.I., Houseweart M.K., Kato S., Anderson K.L., Anderson S.D., Ohama E., et al. Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1. Science 1998, 281:1851-1854.
-
(1998)
Science
, vol.281
, pp. 1851-1854
-
-
Bruijn, L.I.1
Houseweart, M.K.2
Kato, S.3
Anderson, K.L.4
Anderson, S.D.5
Ohama, E.6
-
2
-
-
0032533958
-
Persyn, a member of the synuclein family, has a distinct pattern of expression in the developing nervous system
-
Buchman V.L., Hunter H.J., Pinon L.G., Thompson J., Privalova E.M., Ninkina N.N., et al. Persyn, a member of the synuclein family, has a distinct pattern of expression in the developing nervous system. J. Neurosci. 1998, 18:9335-9341.
-
(1998)
J. Neurosci.
, vol.18
, pp. 9335-9341
-
-
Buchman, V.L.1
Hunter, H.J.2
Pinon, L.G.3
Thompson, J.4
Privalova, E.M.5
Ninkina, N.N.6
-
3
-
-
0037167167
-
Organization of the mouse Ruk locus and expression of isoforms in mouse tissues
-
Buchman V.L., Luke C., Borthwick E.B., Gout I., Ninkina N. Organization of the mouse Ruk locus and expression of isoforms in mouse tissues. Gene 2002, 295:13-17.
-
(2002)
Gene
, vol.295
, pp. 13-17
-
-
Buchman, V.L.1
Luke, C.2
Borthwick, E.B.3
Gout, I.4
Ninkina, N.5
-
4
-
-
40849088250
-
Progressive ganglion cell degeneration precedes neuronal loss in a mouse model of glaucoma
-
Buckingham B.P., Inman D.M., Lambert W., Oglesby E., Calkins D.J., Steele M.R., et al. Progressive ganglion cell degeneration precedes neuronal loss in a mouse model of glaucoma. J. Neurosci. 2008, 28:2735-2744.
-
(2008)
J. Neurosci.
, vol.28
, pp. 2735-2744
-
-
Buckingham, B.P.1
Inman, D.M.2
Lambert, W.3
Oglesby, E.4
Calkins, D.J.5
Steele, M.R.6
-
5
-
-
4644290985
-
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease
-
Chartier-Harlin M.C., Kachergus J., Roumier C., Mouroux V., Douay X., Lincoln S., et al. Alpha-synuclein locus duplication as a cause of familial Parkinson's disease. Lancet 2004, 364:1167-1169.
-
(2004)
Lancet
, vol.364
, pp. 1167-1169
-
-
Chartier-Harlin, M.C.1
Kachergus, J.2
Roumier, C.3
Mouroux, V.4
Douay, X.5
Lincoln, S.6
-
6
-
-
64549117768
-
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
-
Chio A., Schymick J.C., Restagno G., Scholz S.W., Lombardo F., Lai S.L., et al. A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Hum. Mol. Genet. 2009, 18:1524-1532.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1524-1532
-
-
Chio, A.1
Schymick, J.C.2
Restagno, G.3
Scholz, S.W.4
Lombardo, F.5
Lai, S.L.6
-
7
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
DeJesus-Hernandez M., Mackenzie I.R., Boeve B.F., Boxer A.L., Baker M., Rutherford N.J., et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011, 72:245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
Boxer, A.L.4
Baker, M.5
Rutherford, N.J.6
-
8
-
-
80052580969
-
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
-
Deng H.X., Chen W., Hong S.T., Boycott K.M., Gorrie G.H., Siddique N., et al. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature 2011, 477:211-215.
-
(2011)
Nature
, vol.477
, pp. 211-215
-
-
Deng, H.X.1
Chen, W.2
Hong, S.T.3
Boycott, K.M.4
Gorrie, G.H.5
Siddique, N.6
-
9
-
-
77951185469
-
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease
-
Edwards T.L., Scott W.K., Almonte C., Burt A., Powell E.H., Beecham G.W., et al. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Ann. Hum. Genet. 2010, 74:97-109.
-
(2010)
Ann. Hum. Genet.
, vol.74
, pp. 97-109
-
-
Edwards, T.L.1
Scott, W.K.2
Almonte, C.3
Burt, A.4
Powell, E.H.5
Beecham, G.W.6
-
10
-
-
73049098692
-
A systematic study of brainstem motor nuclei in a mouse model of ALS, the effects of lithium
-
Ferrucci M., Spalloni A., Bartalucci A., Cantafora E., Fulceri F., Nutini M., et al. A systematic study of brainstem motor nuclei in a mouse model of ALS, the effects of lithium. Neurobiol. Dis. 2010, 37:370-383.
-
(2010)
Neurobiol. Dis.
, vol.37
, pp. 370-383
-
-
Ferrucci, M.1
Spalloni, A.2
Bartalucci, A.3
Cantafora, E.4
Fulceri, F.5
Nutini, M.6
-
11
-
-
0033539664
-
Axon pathology in Parkinson's disease and Lewy body dementia hippocampus contains alpha-, beta-, and gamma-synuclein
-
Galvin J.E., Uryu K., Lee V.M., Trojanowski J.Q. Axon pathology in Parkinson's disease and Lewy body dementia hippocampus contains alpha-, beta-, and gamma-synuclein. Proc. Natl. Acad. Sci. U. S. A. 1999, 96:13450-13455.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 13450-13455
-
-
Galvin, J.E.1
Uryu, K.2
Lee, V.M.3
Trojanowski, J.Q.4
-
12
-
-
0033897735
-
Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology
-
Galvin J.E., Giasson B., Hurtig H.I., Lee V.M., Trojanowski J.Q. Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathology. Am. J. Pathol. 2000, 157:361-368.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 361-368
-
-
Galvin, J.E.1
Giasson, B.2
Hurtig, H.I.3
Lee, V.M.4
Trojanowski, J.Q.5
-
13
-
-
65949109907
-
Sensory involvement in the SOD1-G93A mouse model of amyotrophic lateral sclerosis
-
Guo Y.S., Wu D.X., Wu H.R., Wu S.Y., Yang C., Li B., et al. Sensory involvement in the SOD1-G93A mouse model of amyotrophic lateral sclerosis. Exp. Mol. Med. 2009, 41:140-150.
-
(2009)
Exp. Mol. Med.
, vol.41
, pp. 140-150
-
-
Guo, Y.S.1
Wu, D.X.2
Wu, H.R.3
Wu, S.Y.4
Yang, C.5
Li, B.6
-
14
-
-
37349093418
-
Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS
-
Hammad M., Silva A., Glass J., Sladky J.T., Benatar M. Clinical, electrophysiologic, and pathologic evidence for sensory abnormalities in ALS. Neurology 2007, 69:2236-2242.
-
(2007)
Neurology
, vol.69
, pp. 2236-2242
-
-
Hammad, M.1
Silva, A.2
Glass, J.3
Sladky, J.T.4
Benatar, M.5
-
15
-
-
4644236043
-
Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease
-
Ibanez P., Bonnet A.M., Debarges B., Lohmann E., Tison F., Pollak P., et al. Causal relation between alpha-synuclein gene duplication and familial Parkinson's disease. Lancet 2004, 364:1169-1171.
-
(2004)
Lancet
, vol.364
, pp. 1169-1171
-
-
Ibanez, P.1
Bonnet, A.M.2
Debarges, B.3
Lohmann, E.4
Tison, F.5
Pollak, P.6
-
16
-
-
34347212891
-
Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
-
Isaacs J.D., Dean A.F., Shaw C.E., Al-Chalabi A., Mills K.R., Leigh P.N. Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?. J. Neurol. Neurosurg. Psychiatry 2007, 78:750-753.
-
(2007)
J. Neurol. Neurosurg. Psychiatry
, vol.78
, pp. 750-753
-
-
Isaacs, J.D.1
Dean, A.F.2
Shaw, C.E.3
Al-Chalabi, A.4
Mills, K.R.5
Leigh, P.N.6
-
17
-
-
0019784990
-
Morphometric comparison of the vulnerability of peripheral motor and sensory neurons in amyotrophic lateral sclerosis
-
Kawamura Y., Dyck P.J., Shimono M., Okazaki H., Tateishi J., Doi H. Morphometric comparison of the vulnerability of peripheral motor and sensory neurons in amyotrophic lateral sclerosis. J. Neuropathol. Exp. Neurol. 1981, 40:667-675.
-
(1981)
J. Neuropathol. Exp. Neurol.
, vol.40
, pp. 667-675
-
-
Kawamura, Y.1
Dyck, P.J.2
Shimono, M.3
Okazaki, H.4
Tateishi, J.5
Doi, H.6
-
18
-
-
0032079517
-
Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1
-
Kong J., Xu Z. Massive mitochondrial degeneration in motor neurons triggers the onset of amyotrophic lateral sclerosis in mice expressing a mutant SOD1. J. Neurosci. 1998, 18:3241-3250.
-
(1998)
J. Neurosci.
, vol.18
, pp. 3241-3250
-
-
Kong, J.1
Xu, Z.2
-
19
-
-
0031990490
-
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
-
Kruger R., Kuhn W., Muller T., Woitalla D., Graeber M., Kosel S., et al. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. Nat. Genet. 1998, 18:106-108.
-
(1998)
Nat. Genet.
, vol.18
, pp. 106-108
-
-
Kruger, R.1
Kuhn, W.2
Muller, T.3
Woitalla, D.4
Graeber, M.5
Kosel, S.6
-
20
-
-
61349156118
-
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
-
Kwiatkowski T.J., Bosco D.A., Leclerc A.L., Tamrazian E., Vanderburg C.R., Russ C., et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science 2009, 323:1205-1208.
-
(2009)
Science
, vol.323
, pp. 1205-1208
-
-
Kwiatkowski, T.J.1
Bosco, D.A.2
Leclerc, A.L.3
Tamrazian, E.4
Vanderburg, C.R.5
Russ, C.6
-
21
-
-
77952419246
-
Mutations of optineurin in amyotrophic lateral sclerosis
-
Maruyama H., Morino H., Ito H., Izumi Y., Kato H., Watanabe Y., et al. Mutations of optineurin in amyotrophic lateral sclerosis. Nature 2010, 465:223-226.
-
(2010)
Nature
, vol.465
, pp. 223-226
-
-
Maruyama, H.1
Morino, H.2
Ito, H.3
Izumi, Y.4
Kato, H.5
Watanabe, Y.6
-
22
-
-
79551638445
-
Myelination transition zone astrocytes are constitutively phagocytic and have synuclein dependent reactivity in glaucoma
-
Nguyen J.V., Soto I., Kim K.Y., Bushong E.A., Oglesby E., Valiente-Soriano F.J., et al. Myelination transition zone astrocytes are constitutively phagocytic and have synuclein dependent reactivity in glaucoma. Proc. Natl. Acad. Sci. U. S. A. 2011, 108:1176-1181.
-
(2011)
Proc. Natl. Acad. Sci. U. S. A.
, vol.108
, pp. 1176-1181
-
-
Nguyen, J.V.1
Soto, I.2
Kim, K.Y.3
Bushong, E.A.4
Oglesby, E.5
Valiente-Soriano, F.J.6
-
23
-
-
0242412282
-
Neurons expressing the highest levels of gamma-synuclein are unaffected by targeted inactivation of the gene
-
Ninkina N., Papachroni K., Robertson D.C., Schmidt O., Delaney L., O'Neill F., et al. Neurons expressing the highest levels of gamma-synuclein are unaffected by targeted inactivation of the gene. Mol. Cell. Biol. 2003, 23:8233-8245.
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 8233-8245
-
-
Ninkina, N.1
Papachroni, K.2
Robertson, D.C.3
Schmidt, O.4
Delaney, L.5
O'Neill, F.6
-
24
-
-
65449181204
-
Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein
-
Ninkina N., Peters O., Millership S., Salem H., van der Putten H., Buchman V.L. Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein. Hum. Mol. Genet. 2009, 18:1779-1794.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1779-1794
-
-
Ninkina, N.1
Peters, O.2
Millership, S.3
Salem, H.4
van der Putten, H.5
Buchman, V.L.6
-
25
-
-
77955447233
-
Association of alpha-, beta-, and gamma-Synuclein with diffuse Lewy body disease
-
Nishioka K., Wider C., Vilarino-Guell C., Soto-Ortolaza A.I., Lincoln S.J., Kachergus J.M., et al. Association of alpha-, beta-, and gamma-Synuclein with diffuse Lewy body disease. Arch. Neurol. 2010, 67:970-975.
-
(2010)
Arch. Neurol.
, vol.67
, pp. 970-975
-
-
Nishioka, K.1
Wider, C.2
Vilarino-Guell, C.3
Soto-Ortolaza, A.I.4
Lincoln, S.J.5
Kachergus, J.M.6
-
26
-
-
67651160721
-
Alpha-synuclein and familial Parkinson's disease
-
Pankratz N., Nichols W.C., Elsaesser V.E., Pauciulo M.W., Marek D.K., Halter C.A., et al. Alpha-synuclein and familial Parkinson's disease. Mov. Disord. 2009, 24:1125-1131.
-
(2009)
Mov. Disord.
, vol.24
, pp. 1125-1131
-
-
Pankratz, N.1
Nichols, W.C.2
Elsaesser, V.E.3
Pauciulo, M.W.4
Marek, D.K.5
Halter, C.A.6
-
27
-
-
0037426346
-
Beta-synuclein inhibits formation of alpha-synuclein protofibrils: a possible therapeutic strategy against Parkinson's disease
-
Park J.Y., Lansbury P.T. Beta-synuclein inhibits formation of alpha-synuclein protofibrils: a possible therapeutic strategy against Parkinson's disease. Biochemistry 2003, 42:3696-3700.
-
(2003)
Biochemistry
, vol.42
, pp. 3696-3700
-
-
Park, J.Y.1
Lansbury, P.T.2
-
28
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M.H., Lavedan C., Leroy E., Ide S.E., Dehejia A., Dutra A., et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997, 276:2045-2047.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
Ide, S.E.4
Dehejia, A.5
Dutra, A.6
-
29
-
-
34347247316
-
Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study
-
Pugdahl K., Fuglsang-Frederiksen A., de Carvalho M., Johnsen B., Fawcett P.R., Labarre-Vila A., et al. Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study. J. Neurol. Neurosurg. Psychiatry 2007, 78:746-749.
-
(2007)
J. Neurol. Neurosurg. Psychiatry
, vol.78
, pp. 746-749
-
-
Pugdahl, K.1
Fuglsang-Frederiksen, A.2
de Carvalho, M.3
Johnsen, B.4
Fawcett, P.R.5
Labarre-Vila, A.6
-
30
-
-
80054837386
-
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
-
Renton A.E., Majounie E., Waite A., Simon-Sanchez J., Rollinson S., Gibbs J.R., et al. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 2011, 72:257-268.
-
(2011)
Neuron
, vol.72
, pp. 257-268
-
-
Renton, A.E.1
Majounie, E.2
Waite, A.3
Simon-Sanchez, J.4
Rollinson, S.5
Gibbs, J.R.6
-
31
-
-
0027401203
-
Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
-
Rosen D.R., Siddique T., Patterson D., Figlewicz D.A., Sapp P., Hentati A., et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature 1993, 362:59-62.
-
(1993)
Nature
, vol.362
, pp. 59-62
-
-
Rosen, D.R.1
Siddique, T.2
Patterson, D.3
Figlewicz, D.A.4
Sapp, P.5
Hentati, A.6
-
32
-
-
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., et al. 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
-
33
-
-
77958022745
-
Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice
-
Shan X., Chiang P.M., Price D.L., Wong P.C. Altered distributions of Gemini of coiled bodies and mitochondria in motor neurons of TDP-43 transgenic mice. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:16325-16330.
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 16325-16330
-
-
Shan, X.1
Chiang, P.M.2
Price, D.L.3
Wong, P.C.4
-
34
-
-
70549088602
-
Genome-wide association study reveals genetic risk underlying Parkinson's disease
-
Simon-Sanchez J., Schulte C., Bras J.M., Sharma M., Gibbs J.R., Berg D., Paisan, et al. Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat. Genet. 2009, 41:1308-1312.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1308-1312
-
-
Simon-Sanchez, J.1
Schulte, C.2
Bras, J.M.3
Sharma, M.4
Gibbs, J.R.5
Berg, D.6
Paisan7
-
35
-
-
11144357471
-
Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplication
-
Singleton A., Gwinn-Hardy K., Sharabi Y., Li S.T., Holmes C., Dendi R., et al. Association between cardiac denervation and parkinsonism caused by alpha-synuclein gene triplication. Brain 2004, 127:768-772.
-
(2004)
Brain
, vol.127
, pp. 768-772
-
-
Singleton, A.1
Gwinn-Hardy, K.2
Sharabi, Y.3
Li, S.T.4
Holmes, C.5
Dendi, R.6
-
36
-
-
38349070853
-
Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model
-
Soto I., Oglesby E., Buckingham B.P., Son J.L., Roberson E.D., Steele M.R., et al. Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model. J. Neurosci. 2008, 28:548-561.
-
(2008)
J. Neurosci.
, vol.28
, pp. 548-561
-
-
Soto, I.1
Oglesby, E.2
Buckingham, B.P.3
Son, J.L.4
Roberson, E.D.5
Steele, M.R.6
-
37
-
-
41149180753
-
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
-
Sreedharan J., Blair I.P., Tripathi V.B., Hu X., Vance C., Rogelj B., et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008, 319:1668-1672.
-
(2008)
Science
, vol.319
, pp. 1668-1672
-
-
Sreedharan, J.1
Blair, I.P.2
Tripathi, V.B.3
Hu, X.4
Vance, C.5
Rogelj, B.6
-
38
-
-
0036221254
-
Synucleins in glaucoma: implication of gamma-synuclein in glaucomatous alterations in the optic nerve
-
Surgucheva I., McMahan B., Ahmed F., Tomarev S., Wax M.B., Surguchov A. Synucleins in glaucoma: implication of gamma-synuclein in glaucomatous alterations in the optic nerve. J. Neurosci. Res. 2002, 68:97-106.
-
(2002)
J. Neurosci. Res.
, vol.68
, pp. 97-106
-
-
Surgucheva, I.1
McMahan, B.2
Ahmed, F.3
Tomarev, S.4
Wax, M.B.5
Surguchov, A.6
-
39
-
-
70349592269
-
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
-
van Es M.A., Veldink J.H., Saris C.G., Blauw H.M., van Vught P.W., Birve A., et al. Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 2009, 41:1083-1087.
-
(2009)
Nat. Genet.
, vol.41
, pp. 1083-1087
-
-
van Es, M.A.1
Veldink, J.H.2
Saris, C.G.3
Blauw, H.M.4
van Vught, P.W.5
Birve, A.6
-
40
-
-
61349162349
-
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
-
Vance C., Rogelj B., Hortobagyi T., De Vos K.J., Nishimura A.L., Sreedharan J., et al. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science 2009, 323:1208-1211.
-
(2009)
Science
, vol.323
, pp. 1208-1211
-
-
Vance, C.1
Rogelj, B.2
Hortobagyi, T.3
De Vos, K.J.4
Nishimura, A.L.5
Sreedharan, J.6
-
41
-
-
77949529252
-
The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci
-
Wain L.V., Pedroso I., Landers J.E., Breen G., Shaw C.E., Leigh P.N., et al. The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci. PLoS One 2009, 4:e8175.
-
(2009)
PLoS One
, vol.4
-
-
Wain, L.V.1
Pedroso, I.2
Landers, J.E.3
Breen, G.4
Shaw, C.E.5
Leigh, P.N.6
-
42
-
-
4043089794
-
Accumulation of beta- and gamma-synucleins in the ubiquitin carboxyl-terminal hydrolase L1-deficient gad mouse
-
Wang Y.L., Takeda A., Osaka H., Hara Y., Furuta A., Setsuie R., et al. Accumulation of beta- and gamma-synucleins in the ubiquitin carboxyl-terminal hydrolase L1-deficient gad mouse. Brain Res. 2004, 1019:1-9.
-
(2004)
Brain Res.
, vol.1019
, pp. 1-9
-
-
Wang, Y.L.1
Takeda, A.2
Osaka, H.3
Hara, Y.4
Furuta, A.5
Setsuie, R.6
-
44
-
-
10744230149
-
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia
-
Zarranz J.J., Alegre J., Gomez-Esteban J.C., Lezcano E., Ros R., Ampuero I., et al. The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia. Ann. Neurol. 2004, 55:164-173.
-
(2004)
Ann. Neurol.
, vol.55
, pp. 164-173
-
-
Zarranz, J.J.1
Alegre, J.2
Gomez-Esteban, J.C.3
Lezcano, E.4
Ros, R.5
Ampuero, I.6
|