-
1
-
-
0030744876
-
Mutation in the α-synuclein gene identified in families with Parkinson's disease
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
-
2
-
-
0031990490
-
Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease
-
(1998)
Nat. Genet.
, vol.18
, pp. 106-108
-
-
Kruger, R.1
-
4
-
-
0032190090
-
The ubiquitin pathway in Parkinson's disease
-
(1998)
Nature
, vol.395
, pp. 451-452
-
-
Leroy, E.1
-
5
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
-
6
-
-
18244412384
-
Molecular genetic analysis of a novel parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the parkin gene in affected individuals
-
(1998)
Ann. Neurol.
, vol.44
, pp. 935-941
-
-
Hattori, N.1
-
7
-
-
0342368772
-
Association between early-onset Parkinson's disease and mutations in the parkin gene
-
(2000)
N. Engl. J. Med.
, vol.342
, pp. 1560-1567
-
-
Lucking, C.B.1
-
8
-
-
0033933048
-
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
-
(2000)
Nat. Genet.
, vol.25
, pp. 302-305
-
-
Shimura, H.1
-
10
-
-
0034681471
-
Dopaminergic loss and inclusion body formation in α-synuclein mice: Implications for neurodegenerative disorders
-
(2000)
Science
, vol.287
, pp. 1265-1269
-
-
Masliah, E.1
-
12
-
-
0034280435
-
Subcellular localization of wild-type and Parkinson's disease-associated mutant α-synuclein in human and transgenic mouse brain
-
(2000)
J. Neurosci.
, vol.20
, pp. 6365-6373
-
-
Kahle, P.J.1
-
13
-
-
0031721141
-
Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q
-
(1998)
Neurology
, vol.51
, pp. 890-892
-
-
Mori, H.1
-
14
-
-
0343527226
-
α-Synuclein immunoreactivity in dementia with Lewy bodies: Morphological staging and comparison with ubiquitin immunostaining
-
(2000)
Acta Neuropathol.
, vol.99
, pp. 352-357
-
-
Gomez-Tortosa, E.1
-
16
-
-
0032718068
-
The ubiquitin-conjugating enzymes UbcH7 and UbcH8 interact with RING finger/IBR motif-containing domains of HHARI and H7-AP1
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 30963-30968
-
-
Moynihan, T.P.1
-
18
-
-
0033525589
-
A novel ubiquitination factor, E4, is involved in multiubiquitin chain assembly
-
(1999)
Cell
, vol.96
, pp. 635-644
-
-
Koegl, M.1
-
19
-
-
0032957883
-
Immunohistochemical and subcellular localization of parkin protein: Absence of protein in autosomal recessive juvenile parkinsonism patients
-
(1999)
Ann. Neurol.
, vol.45
, pp. 668-672
-
-
Shimura, H.1
-
20
-
-
0033961490
-
Expression of α-synuclein, parkin, and ubiquitin carboxy-terminal hydrolase L1 mRNA in human brain: Genes associated with familial Parkinson's disease
-
(2000)
Ann. Neurol.
, vol.47
, pp. 201-210
-
-
Solano, S.M.1
-
21
-
-
0033868381
-
Novel, pseudo-dominant inheritance, and possible familial affects in patients with autosomal recessive juvenile parkinsonism
-
(2000)
Ann. Neurol.
, vol.48
, pp. 245-250
-
-
Maruyama, M.1
-
22
-
-
0345490853
-
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 567-574
-
-
Abbas, N.1
-
23
-
-
0031753976
-
Deletions in the parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease
-
(1998)
Hum. Genet.
, vol.103
, pp. 424-427
-
-
Leroy, E.1
-
25
-
-
0343517605
-
A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism
-
(2000)
Neurosci. Lett.
, vol.289
, pp. 66-68
-
-
Munoz, E.1
-
26
-
-
0032564235
-
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism
-
(1998)
Lancet
, vol.352
, pp. 1355-1356
-
-
Lucking, C.B.1
|