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。Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
Daniel J. Klionsky et al.
AUTOPHAGY (2021)
Enhancement of Autophagy and Solubilization of Ataxin-2 Alleviate Apoptosis in Spinocerebellar Ataxia Type 2 Patient Cells
Jonathan Henry Wardman et al.
CEREBELLUM (2020)
ALS-associated genes in SCA2 mouse spinal cord transcriptomes
Daniel R. Scoles et al.
HUMAN MOLECULAR GENETICS (2020)
The microcircuits of striatum in silico
J. J. Johannes Hjorth et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
Cordycepin activates autophagy through AMPK phosphorylation to reduce abnormalities in Machado-Joseph disease models
Adriana Marcelo et al.
HUMAN MOLECULAR GENETICS (2019)
RNA Interference Therapy for Machado-Joseph Disease: Long-Term Safety Profile of Lentiviral Vectors Encoding Short Hairpin RNAs Targeting Mutant Ataxin-3
Clevio Nobrega et al.
HUMAN GENE THERAPY (2019)
Autophagy in Neurons
Andrea K. H. Stavoe et al.
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 35 (2019)
Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation
Nesli-Ece Sen et al.
NEUROBIOLOGY OF DISEASE (2019)
Molecular Mechanisms and Therapeutics for Spinocerebellar Ataxia Type 2
Polina A. Egorova et al.
NEUROTHERAPEUTICS (2019)
Peripheral markers of autophagy in polyglutamine diseases
Giorgia Puorro et al.
NEUROLOGICAL SCIENCES (2018)
Association Between Autophagy and Neurodegenerative Diseases
Nobuhiro Fujikake et al.
FRONTIERS IN NEUROSCIENCE (2018)
Non-ataxic manifestations of Spinocerebellar ataxia-2, their determinants and predictors
Albert Stezin et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2018)
Staufen1 links RNA stress granules and autophagy in a model of neurodegeneration
Sharan Paul et al.
NATURE COMMUNICATIONS (2018)
On the distribution of intranuclear and cytoplasmic aggregates in the brainstem of patients with spinocerebellar ataxia type 2 and 3
Kay Seidel et al.
BRAIN PATHOLOGY (2017)
Effects of the enlargement of polyglutamine segments on the structure and folding of ataxin-2 and ataxin-3 proteins
Jingran Wen et al.
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS (2017)
Protein Misfolding and Aggregation as a Therapeutic Target for Polyglutamine Diseases
Toshihide Takeuchi et al.
BRAIN SCIENCES (2017)
Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review
Joao M. Da Conceicao Alves-Cruzeiro et al.
FRONTIERS IN NEUROSCIENCE (2016)
Pathophysiological Role of Neuroinflammation in Neurodegenerative Diseases and Psychiatric Disorders
Heeok Hong et al.
INTERNATIONAL NEUROUROLOGY JOURNAL (2016)
Re-establishing ataxin-2 downregulates translation of mutant ataxin-3 and alleviates Machado-Joseph disease
Clevio Nobrega et al.
BRAIN (2015)
p62/SQSTM1 functions as a signaling hub and an autophagy adaptor
Yoshinori Katsuragi et al.
FEBS JOURNAL (2015)
The Role of the Immune System in Triplet Repeat Expansion Diseases
Marta Olejniczak et al.
MEDIATORS OF INFLAMMATION (2015)
Autophagy in polyglutamine disease: Imposing order on disorder or contributing to the chaos?
Constanza J. Cortes et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2015)
Ataxin-2 Regulates RGS8 Translation in a New BAC-SCA2 Transgenic Mouse Model
Warunee Dansithong et al.
PLOS GENETICS (2015)
Transplantation of cerebellar neural stem cells improves motor coordination and neuropathology in Machado-Joseph disease mice
Liliana S. Mendonca et al.
BRAIN (2015)
Neuropathological Staging of Spinocerebellar Ataxia Type 2 by Semiquantitative 1C2-Positive Neuron Typing. Nuclear Translocation of Cytoplasmic 1C2 Underlies Disease Progression of Spinocerebellar Ataxia Type 2
Shigeru Koyano et al.
BRAIN PATHOLOGY (2014)
Beyond and below the cortex: the contribution of striatal dysfunction to cognition and behaviour in neurodegeneration
Claire O'Callaghan et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2014)
The role of protein clearance mechanisms in organismal ageing and age-related diseases
David Vilchez et al.
NATURE COMMUNICATIONS (2014)
Overexpression of Mutant Ataxin-3 in Mouse Cerebellum Induces Ataxia and Cerebellar Neuropathology
Clevio Nobrega et al.
CEREBELLUM (2013)
Changes in Purkinje cell firing and gene expression precede behavioral pathology in a mouse model of SCA2
Stephen T. Hansen et al.
HUMAN MOLECULAR GENETICS (2013)
Spinocerebellar Ataxia Type 2: Clinical Presentation, Molecular Mechanisms, and Therapeutic Perspectives
J. J. Magana et al.
MOLECULAR NEUROBIOLOGY (2013)
Caspase Functions in Cell Death and Disease
David R. McIlwain et al.
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2013)
Brain pathology of spinocerebellar ataxias
Kay Seidel et al.
ACTA NEUROPATHOLOGICA (2012)
Four factors underlying mouse behavior in an open field
Shoji Tanaka et al.
BEHAVIOURAL BRAIN RESEARCH (2012)
ATXN2-CAG42 Sequesters PABPC1 into Insolubility and Induces FBXW8 in Cerebellum of Old Ataxic Knock-In Mice
Ewa Damrath et al.
PLOS GENETICS (2012)
Overexpression of the autophagic beclin-1 protein clears mutant ataxin-3 and alleviates Machado-Joseph disease
Isabel Nascimento-Ferreira et al.
BRAIN (2011)
Repeat expansion disease: progress and puzzles in disease pathogenesis
Albert R. La Spada et al.
NATURE REVIEWS GENETICS (2010)
Striatal and nigral pathology in a lentiviral rat model of Machado-Joseph disease
Sandro Alves et al.
HUMAN MOLECULAR GENETICS (2008)
Involvement of the auditory brainstem system in spinocerebellar ataxia type 2 (SCA2), type 3 (SCA3) and type 7 (SCA7)
F. Hoche et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2008)
Dissection of the autophagosome maturation process by a novel reporter protein, tandem fluorescent-tagged LC3
Shunsuke Kimura et al.
AUTOPHAGY (2007)
Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes
Terrence F. Satterfield et al.
HUMAN MOLECULAR GENETICS (2006)
Ubiquitous expression of human SCA2 gene under the regulation of the SCA2 self promoter cause specific Purkinje cell degeneration in transgenic mice
J Aguiar et al.
NEUROSCIENCE LETTERS (2006)
p62/SQSTM1 forms protein aggregates degraded by autophagy and has a protective effect on huntingtin-induced cell death
G Bjorkoy et al.
JOURNAL OF CELL BIOLOGY (2005)
Bcl-2 antiapoptotic proteins inhibit Beclin 1-dependent autophagy
S Pattingre et al.
CELL (2005)
Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA2)
K Gierga et al.
ACTA NEUROPATHOLOGICA (2005)
Reduced striatal [123I]FP-CIT binding in SCA2 patients without Parkinsonism
A Varrone et al.
ANNALS OF NEUROLOGY (2004)
Long-term lentiviral-mediated expression of ciliary neurotrophic factor in the striatum of Huntington's disease transgenic mice
D Zala et al.
EXPERIMENTAL NEUROLOGY (2004)
Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell death
DP Huynh et al.
HUMAN MOLECULAR GENETICS (2003)
Chronic thalamic stimulation in a patient with spinocerebellar ataxia type 2
W Pirker et al.
MOVEMENT DISORDERS (2003)
Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases
JT Pang et al.
BRAIN (2002)
Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease
LP de Almeida et al.
NEUROBIOLOGY OF DISEASE (2001)
The ortholog of human ataxin-2 is essential for early embryonic patterning in C-elegans
TR Kiehl et al.
JOURNAL OF MOLECULAR NEUROSCIENCE (2000)
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human
DP Huynh et al.
NATURE GENETICS (2000)
分享论文
