Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
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Neuroacanthocytosis associated with a defect of the 4.1R membrane proteinConcise review: Patient-derived olfactory stem cells: new models for brain diseases.Biochemical and morphological consequences of human α-synuclein expression in a mouse α-synuclein null background.The H50Q mutation induces a 10-fold decrease in the solubility of α-synuclein.Neurodegenerative disorders: Parkinson's disease and Huntington's diseaseEvolution of neurodegeneration.α-Synuclein is localized to mitochondria-associated ER membranes.Genetic variability in SNCA and Parkinson's disease.α-Synuclein in Parkinson's disease.Lithium-responsive genes and gene networks in bipolar disorder patient-derived lymphoblastoid cell lines.
P2860
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P2860
Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
description
2003 nî lūn-bûn
@nan
2003年の論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年論文
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2003年论文
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2003年论文
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2003年论文
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name
Haploinsufficiency at the alph ...... familial Parkinson's disease.
@en
type
label
Haploinsufficiency at the alph ...... familial Parkinson's disease.
@en
prefLabel
Haploinsufficiency at the alph ...... familial Parkinson's disease.
@en
P2093
P2860
P50
P921
P356
P1433
P1476
Haploinsufficiency at the alph ...... familial Parkinson's disease.
@en
P2093
Bruce Chase
Hikaru Taka
Hirokazu Kobayashi
Katerina Markopoulou
Kimie Murayama
Reiko Mineki
P2860
P356
10.1093/BRAIN/AWG010
P407
P577
2003-01-01T00:00:00Z