-
1
-
-
0029938472
-
A novel class of murine semaphorins with homology to thrombospondin is differentially expressed during early embryogenesis
-
Adams R.H., et al. A novel class of murine semaphorins with homology to thrombospondin is differentially expressed during early embryogenesis. Mech. Dev. 57 (1996) 33-45
-
(1996)
Mech. Dev.
, vol.57
, pp. 33-45
-
-
Adams, R.H.1
-
2
-
-
4444252172
-
Plexin-B3 is a functional receptor for semaphorin 5A
-
Artigiani S., et al. Plexin-B3 is a functional receptor for semaphorin 5A. EMBO Rep. 5 (2004) 710-714
-
(2004)
EMBO Rep.
, vol.5
, pp. 710-714
-
-
Artigiani, S.1
-
3
-
-
33646081289
-
Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk
-
Bialecka M., et al. Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk. Neurosci. Lett. 399 (2006) 121-123
-
(2006)
Neurosci. Lett.
, vol.399
, pp. 121-123
-
-
Bialecka, M.1
-
4
-
-
0026695663
-
Criteria for diagnosing Parkinson's disease
-
Calne D.B., et al. Criteria for diagnosing Parkinson's disease. Ann. Neurol. 32 (Suppl) (1992) S125-S127
-
(1992)
Ann. Neurol.
, vol.32 SUPPL.
-
-
Calne, D.B.1
-
5
-
-
85058202401
-
Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease
-
author reply 1092-4
-
Clarimon J., et al. Conflicting results regarding the semaphorin gene (SEMA5A) and the risk for Parkinson disease. Am. J. Hum. Genet. 78 (2006) 1082-1084 author reply 1092-4
-
(2006)
Am. J. Hum. Genet.
, vol.78
, pp. 1082-1084
-
-
Clarimon, J.1
-
6
-
-
33749667971
-
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study
-
Elbaz A., et al. Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study. Lancet Neurol. 5 (2006) 917-923
-
(2006)
Lancet Neurol.
, vol.5
, pp. 917-923
-
-
Elbaz, A.1
-
7
-
-
2542609986
-
An oligodendrocyte lineage-specific semaphorin, Sema5A, inhibits axon growth by retinal ganglion cells
-
Goldberg J.L., et al. An oligodendrocyte lineage-specific semaphorin, Sema5A, inhibits axon growth by retinal ganglion cells. J. Neurosci. 24 (2004) 4989-4999
-
(2004)
J. Neurosci.
, vol.24
, pp. 4989-4999
-
-
Goldberg, J.L.1
-
8
-
-
0038434116
-
Aberrant trajectory of ascending dopaminergic pathway in mice lacking Nkx2.1
-
Kawano H., et al. Aberrant trajectory of ascending dopaminergic pathway in mice lacking Nkx2.1. Exp. Neurol. 182 (2003) 103-112
-
(2003)
Exp. Neurol.
, vol.182
, pp. 103-112
-
-
Kawano, H.1
-
9
-
-
34347338776
-
A genomic pathway approach to a complex disease: axon guidance and Parkinson disease
-
Lesnick T.G., et al. A genomic pathway approach to a complex disease: axon guidance and Parkinson disease. PLoS Genet. 3 (2007) e98
-
(2007)
PLoS Genet.
, vol.3
-
-
Lesnick, T.G.1
-
10
-
-
39049162392
-
Beyond Parkinson disease: amyotrophic lateral sclerosis and the axon guidance pathway
-
Lesnick T.G., et al. Beyond Parkinson disease: amyotrophic lateral sclerosis and the axon guidance pathway. PLoS ONE 3 (2008) e1449
-
(2008)
PLoS ONE
, vol.3
-
-
Lesnick, T.G.1
-
11
-
-
27244451809
-
High-resolution whole-genome association study of Parkinson disease
-
Maraganore D.M., et al. High-resolution whole-genome association study of Parkinson disease. Am. J. Hum. Genet. 77 (2005) 685-693
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 685-693
-
-
Maraganore, D.M.1
-
12
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols W.C., et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet 365 (2005) 410-412
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
-
13
-
-
0037324590
-
Invariant Sema5A inhibition serves an ensheathing function during optic nerve development
-
Oster S.F., et al. Invariant Sema5A inhibition serves an ensheathing function during optic nerve development. Development 130 (2003) 775-784
-
(2003)
Development
, vol.130
, pp. 775-784
-
-
Oster, S.F.1
-
14
-
-
24344469023
-
Semaphorin5A expression in the developing chick telencephalon
-
Pineda D., et al. Semaphorin5A expression in the developing chick telencephalon. Brain Res. Bull. 66 (2005) 436-440
-
(2005)
Brain Res. Bull.
, vol.66
, pp. 436-440
-
-
Pineda, D.1
-
15
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M.H., et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 276 (1997) 2045-2047
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
-
16
-
-
0035068574
-
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36
-
Valente E.M., et al. Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36. Am. J. Hum. Genet. 68 (2001) 895-900
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 895-900
-
-
Valente, E.M.1
-
17
-
-
2442668926
-
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
-
Valente E.M., et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 304 (2004) 1158-1160
-
(2004)
Science
, vol.304
, pp. 1158-1160
-
-
Valente, E.M.1
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