相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients
Teresa Lee et al.
HUMAN MOLECULAR GENETICS (2011)
Epidemiology of Alzheimer disease
Christiane Reitz et al.
NATURE REVIEWS NEUROLOGY (2011)
PolyQ Repeat Expansions in ATXN2 Associated with ALS Are CAA Interrupted Repeats
Zhenming Yu et al.
PLOS ONE (2011)
Non-ATG-initiated translation directed by microsatellite expansions
Tao Zu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Prion-like disorders: blurring the divide between transmissibility and infectivity
Mimi Cushman et al.
JOURNAL OF CELL SCIENCE (2010)
TDP-43 Mediates Degeneration in a Novel Drosophila Model of Disease Caused by Mutations in VCP/p97
Gillian P. Ritson et al.
JOURNAL OF NEUROSCIENCE (2010)
Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS
Andrew C. Elden et al.
NATURE (2010)
TAR DNA-binding protein 43 in neurodegenerative disease
Alice S. Chen-Plotkin et al.
NATURE REVIEWS NEUROLOGY (2010)
Genetic Animal Models of Parkinson's Disease
Ted M. Dawson et al.
NEURON (2010)
TDP-43-Mediated Neuron Loss In Vivo Requires RNA-Binding Activity
Aaron Voigt et al.
PLOS ONE (2010)
Tar DNA Binding Protein-43 (TDP-43) Associates with Stress Granules: Analysis of Cultured Cells and Pathological Brain Tissue
Liqun Liu-Yesucevitz et al.
PLOS ONE (2010)
A Drosophila model for TDP-43 proteinopathy
Yan Li et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Roles of trinucleotide-repeat RNA in neurological disease and degeneration
Ling-Bo Li et al.
TRENDS IN NEUROSCIENCES (2010)
Rethinking ALS: The FUS about TDP-43
Clotilde Lagier-Tourenne et al.
CELL (2009)
Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior
Fabian Feiguin et al.
FEBS LETTERS (2009)
TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity
Brian S. Johnson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature
Lorenzo Nanetti et al.
JOURNAL OF NEUROLOGY (2009)
α-Synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity
Aaron D. Gitler et al.
NATURE GENETICS (2009)
Bridging high-throughput genetic and transcriptional data reveals cellular responses to alpha-synuclein toxicity
Esti Yeger-Lotem et al.
NATURE GENETICS (2009)
Intrafamilial variability of Parkinson phenotype in SCAs: Novel cases due to SCA2 and SCA3 expansions
M. P. Socal et al.
PARKINSONISM & RELATED DISORDERS (2009)
RNA toxicity is a component of ataxin-3 degeneration in Drosophila
Ling-Bo Li et al.
NATURE (2008)
A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDR-43 aggregation and cellular toxicity
Brian S. Johnson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Lysosomes: fusion and function
J. Paul Luzio et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)
Exploring genetic interactions and networks with yeast
Charles Boone et al.
NATURE REVIEWS GENETICS (2007)
Prevalence of spinocerebellar ataxia type 2 mutation among Italian parkinsonian patients
Anna Modoni et al.
MOVEMENT DISORDERS (2007)
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules
Ute Nonhoff et al.
MOLECULAR BIOLOGY OF THE CELL (2007)
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann et al.
SCIENCE (2006)
Drosophila in the study of neurodegenerative disease
J. Lawrence Marsh et al.
NEURON (2006)
α-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models
Antony A. Cooper et al.
SCIENCE (2006)
Drosophila, the golden bug, emerges as a tool for human genetics
E Bier
NATURE REVIEWS GENETICS (2005)
Spinocerebellar ataxia type 2 with levodopa-responsive parkinsonism culminating in motor neuron disease
J Infante et al.
MOVEMENT DISORDERS (2004)
The parkinsonian phenotype of spinocerebellar ataxia type 2
CS Lu et al.
ARCHIVES OF NEUROLOGY (2004)
Complex phenotypes in an Indian family with homozygous SCA2 mutations
M Ragothaman et al.
ANNALS OF NEUROLOGY (2004)
'Men are but worms:' neuronal cell death in C-elegans and vertebrates
G Putcha et al.
CELL DEATH AND DIFFERENTIATION (2004)
SCA-2 presenting as parkinsonism in an Alberta family -: Clinical, genetic, and PET findings
S Furtado et al.
NEUROLOGY (2002)
Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism
DE Shan et al.
ANNALS OF NEUROLOGY (2001)
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
K Gwinn-Hardy et al.
NEUROLOGY (2000)
The genome sequence of Drosophila melanogaster
MD Adams et al.
SCIENCE (2000)
A Drosophila model of Parkinson's disease
MB Feany et al.
NATURE (2000)