-
1
-
-
0034077041
-
Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system
-
(2000)
Neuron
, vol.25
, pp. 239-252
-
-
Abeliovich, A.1
Schmitz, Y.2
Farinas, I.3
Choi-Lundberg, D.4
Ho, W.H.5
Castillo, P.E.6
Shinksy, N.7
Verdugo, J.M.8
Armanini, M.9
Ryan, A.10
Hynes, M.11
Phillips, H.12
Sulzer, D.13
Rosenthal, A.14
-
4
-
-
0028965513
-
The NACP/ synuclein screening for alteration in Alzheimer disease
-
(1995)
Genomics
, vol.26
, pp. 254-257
-
-
Campion, D.1
Martin, C.2
Heilig, R.3
Charbonnier, F.4
Moreau, V.5
Flaman, J.M.6
Petit, J.L.7
Hannequin, D.8
Brice, A.9
Frebourg, T.10
-
6
-
-
0032102455
-
The synucleins: A family of proteins involved in synaptic function, plasticity, neurodegeneration and disease
-
(1998)
TINS
, vol.21
, pp. 249-254
-
-
Clayton, D.F.1
George, J.M.2
-
11
-
-
0033678217
-
Widespread nitration of pathological inclusions in neurodegenerative synucleinopathies
-
(2000)
Am J Pathol
, vol.157
, pp. 1439-1445
-
-
Duda, J.E.1
Giasson, B.I.2
Chen, Q.3
Gur, T.L.4
Hurtig, H.I.5
Stern, M.B.6
Gollomp, S.M.7
Ischiropoulos, H.8
Lee, V.M.9
Trojanowski, J.Q.10
-
12
-
-
0032573597
-
Aggregates from mutant and wild-type alpha-synuclein proteins and NAC peptide induce apoptotic cell death in human neuroblastoma cells by formation of beta-sheet and amyloid-like filaments
-
(1998)
FEBS Lett
, vol.440
, pp. 71-75
-
-
El-Agnaf, O.M.1
Jakes, R.2
Curran, M.D.3
Middleton, D.4
Ingenito, R.5
Bianchi, E.6
Pessi, A.7
Neill, D.8
Wallace, A.9
-
15
-
-
2642607011
-
Low frequency of α-synuclein mutations in familial Parkinson's disease
-
(1998)
Ann Neurol
, vol.43
, pp. 394-397
-
-
Farrer, M.1
Wavrant-De Vrieze, F.2
Crook, R.3
Boles, L.4
Perez-Tur, J.5
Hardy, J.6
Johnson, W.G.7
Steele, J.8
Maraganore, D.9
Gwinn, K.10
Lynch, T.11
-
17
-
-
0034602442
-
Oxidative damage linked to neurodegeneration by selective alpha-synuclein nitration in synucleinopathy lesions
-
(2000)
Science
, vol.290
, pp. 985-998
-
-
Giasson, B.I.1
Duda, J.E.2
Murray, I.V.3
Chen, Q.4
Souza, J.M.5
Hurtig, H.I.6
Ischiropoulos, H.7
Trojanowski, J.Q.8
Lee, V.M.9
-
20
-
-
0028985267
-
The precursor protein of non-A beta component of Alzheimer's disease amyloid is a presynaptic protein of the central nervous system
-
(1995)
Neuron
, vol.14
, pp. 467-475
-
-
Iwai, A.1
Masliah, E.2
Yoshimoto, M.3
Ge, N.4
Flanagan, L.5
De Silva, H.A.6
Kittel, A.7
Saitoh, T.8
-
22
-
-
0030932673
-
Binding of Abeta to alpha- and beta-synucleins: Identification of segments in alpha-synuclein/NAC precursor that bind Abeta and NAC
-
(1997)
Biochem J
, vol.323
, pp. 539-546
-
-
Jensen, P.H.1
Hojrup, P.2
Hager, H.3
Nielsen, M.S.4
Jacobsen, L.5
Olesen, O.F.6
Gliemann, J.7
Jakes, R.8
-
23
-
-
0031045589
-
Identification of a breast cancer-specific gene. BCSG1, by direct differential cDNA sequencing
-
(1997)
Cancer Res
, vol.57
, pp. 759-764
-
-
Ji, H.1
Liu, Y.E.2
Jia, T.3
Wang, M.4
Liu, J.5
Xiao, G.6
Joseph, B.K.7
Rosen, C.8
Shi, Y.9
-
25
-
-
0031990490
-
A1a30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
-
(1998)
Nature Genet
, vol.18
, pp. 106-108
-
-
Kruger, R.1
Kuhn, W.2
Müller, T.3
Woitalla, D.4
Graeber, M.5
Kosel, S.6
Przuntek, H.7
Epplen, J.T.8
Schols, L.9
Riess, O.10
-
26
-
-
0031705984
-
Identification, localization and characterization of the human γ-synuclein gene
-
(1998)
Hum Genet
, vol.103
, pp. 106-112
-
-
Lavedan, C.1
Leroy, E.2
Dehejia, A.3
Buchholtz, S.4
Dutra, A.5
Nussbaum, R.L.6
Polymeropoulos, M.H.7
-
29
-
-
0034681471
-
Dopaminergic loss and inclusion body formation in alpha synuclein mice: Implications for neurodegenerative disorders
-
(2000)
Science
, vol.287
, pp. 1265
-
-
Masliah, E.1
Rockenstein, E.2
Veinbergs, J.3
Mallory, M.4
Hashimoto, M.5
Takeda, A.6
Sagara, Y.7
Sisk, A.8
Mucke, L.9
-
32
-
-
0031715527
-
Organization, expression and polymorphism of the human persyn gene
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1417-1424
-
-
Ninkina, N.N.1
Alimova-Kost, M.V.2
Paterson, J.W.E.3
Delaney, L.4
Cohen, B.B.5
Imreh, S.6
Gnuchev, N.V.7
Davies, A.M.8
Buchman, V.L.9
-
34
-
-
0033777330
-
2 in PC12 cells
-
(2000)
J Neurochem
, vol.75
, pp. 2445-2454
-
-
Oh, S.O.1
Hong, J.H.2
Kim, Y.R.3
Yoo, H.S.4
Lee, S.H.5
Kin, K.6
Hwang, B.D.7
Exton, J.H.8
Park, S.K.9
-
39
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
(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
Pike, B.7
Root, H.8
Rubenstein, J.9
Boyer, R.10
Stenroos, E.11
Chandrasekharappa, S.12
Athanassiadou, A.13
Papapetropoulos, T.14
Johnson, W.G.15
Lazzarini, A.M.16
Duvoisin, R.C.17
Dilorio, G.18
Golbe, L.I.19
Nussbaum, R.L.20
more..
-
44
-
-
0027162243
-
Cell and tissue distribution and developmental change of neuron specific 14 kDa protein (phosphoneuroprotein 14)
-
(1993)
Brain Res
, vol.17
, pp. 17-25
-
-
Shibayama-Imazu, T.1
Okahashi, I.2
Omata, K.3
Nakajo, S.4
Ochiai, H.5
Nakai, Y.6
Hama, T.7
Nakamura, Y.8
Nakaya, K.9
-
45
-
-
0031861285
-
Distribution of PNP 14 (beta-synuclein) in neuroendocrine tissues: Localization in Sertoli cells
-
(1998)
Mol Reprod Dev
, vol.50
, pp. 163-169
-
-
Shibayama-Imazu, T.1
Ogane, K.2
Hasegawa, Y.3
Nakajo, S.4
Shioda, S.5
Ochiai, H.6
Nakai, Y.7
Nakaya, K.8
-
51
-
-
0027489773
-
Molecular cloning of cDNA encoding an unrecognized component of amyloid in Alzheimer disease
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 11282-11286
-
-
Ueda, K.1
Fukushima, H.2
Masliah, E.3
Xia, Y.4
Iwai, A.5
Yashimoto, M.6
Otero, D.A.C.7
Kondo, J.8
Ihara, Y.9
Saitoh, T.10
-
52
-
-
15444338952
-
The alpha-synuclein A1a53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease
-
(1998)
Ann Neurol
, vol.44
, pp. 270-273
-
-
Vaughan, J.1
Durr, A.2
Tassin, J.3
Bereznai, B.4
Gasser, T.5
Bonifati, V.6
De Michele, G.7
Fabrizio, E.8
Volpe, G.9
Bandmann, O.10
Johnson, W.G.11
Golbe, L.I.12
Breteler, M.13
Meco, G.14
Agid, Y.15
Brice, A.16
Marsden, C.D.17
Wood, N.W.18
-
53
-
-
6844236385
-
Sequencing of the α-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations
-
(1998)
Hum Mol Genet
, vol.7
, pp. 751-753
-
-
Vaughan, J.R.1
Fatter, M.J.2
Wszolek, Z.K.3
Gasser, T.4
Durr, A.5
Agid, Y.6
Bonifati, V.7
DeMichele, G.8
Volpe, G.9
Lincoln, S.10
Breteler, M.11
Meco, G.12
Brice, A.13
Marsden, C.D.14
Hardy, J.15
Wood, N.W.16
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