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。Suppression of glycogen synthesis as a treatment for Lafora disease: Establishing the window of opportunity
Olga Varea et al.
NEUROBIOLOGY OF DISEASE (2021)
Gys1 antisense therapy rescues neuropathological bases of murine Lafora disease
Saija Ahonen et al.
BRAIN (2021)
Astrocytic glycogen accumulation drives the pathophysiology of neurodegeneration in Lafora disease
Jordi Duran et al.
BRAIN (2021)
Targeting Gys1 with AAV-SaCas9 Decreases Pathogenic Polyglucosan Bodies and Neuroinflammation in Adult Polyglucosan Body and Lafora Disease Mouse Models
Emrah Gumusgoz et al.
NEUROTHERAPEUTICS (2021)
An inducible glycogen synthase-1 knockout halts but does not reverse Lafora disease progression in mice
Silvia Nitschke et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2021)
The tissue- and developmental stage-specific involvement of autophagy genes in aggrephagy
Hui Zheng et al.
AUTOPHAGY (2020)
Reactive Glia-Derived Neuroinflammation: a Novel Hallmark in Lafora Progressive Myoclonus Epilepsy That Progresses with Age
Marcos Lahuerta et al.
MOLECULAR NEUROBIOLOGY (2020)
The process of Lewy body formation, rather than simply α-synuclein fibrillization, is one of the major drivers of neurodegeneration
Anne-Laure Mahul-Mellier et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2020)
p62: Friend or Foe? Evidences forOncoJanusandNeuroJanusRoles
Sonia Emanuele et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
Lack of Astrocytic Glycogen Alters Synaptic Plasticity but Not Seizure Susceptibility
Jordi Duran et al.
MOLECULAR NEUROBIOLOGY (2020)
Targeting Pathogenic Lafora Bodies in Lafora Disease Using an Antibody-Enzyme Fusion
M. Kathryn Brewer et al.
CELL METABOLISM (2019)
Lack of Neuronal Glycogen Impairs Memory Formation and Learning-Dependent Synaptic Plasticity in Mice
Jordi Duran et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2019)
p62/SQSTM1: 'Jack of all trades' in health and cancer
Pablo Sanchez-Martin et al.
FEBS JOURNAL (2019)
P62/SQSTM1 is a novel leucine-rich repeat kinase 2 (LRRK2) substrate that enhances neuronal toxicity
Alexia F. Kalogeropulou et al.
BIOCHEMICAL JOURNAL (2018)
Polyubiquitin chain-induced p62 phase separation drives autophagic cargo segregation
Daxiao Sun et al.
CELL RESEARCH (2018)
Astrocytes: new players in progressive myoclonus epilepsy of Lafora type
Carla Rubio-Villena et al.
HUMAN MOLECULAR GENETICS (2018)
Lafora disease offers a unique window into neuronal glycogen metabolism
Matthew S. Gentry et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2018)
Glycogen synthase protects neurons from cytotoxicity of mutant huntingtin by enhancing the autophagy flux
Anupama Rai et al.
CELL DEATH & DISEASE (2018)
Astrocytes and neurons produce distinct types of polyglucosan bodies in Lafora disease
Elisabet Auge et al.
GLIA (2018)
Exploring the elusive composition of corpora amylacea of human brain
Elisabet Auge et al.
SCIENTIFIC REPORTS (2018)
Glycogen metabolism and glycogen storage disorders
Shibani Kanungo et al.
ANNALS OF TRANSLATIONAL MEDICINE (2018)
lmerTest Package: Tests in Linear Mixed Effects Models
Alexandra Kuznetsova et al.
JOURNAL OF STATISTICAL SOFTWARE (2017)
Neurotoxic reactive astrocytes are induced by activated microglia
Shane A. Liddelow et al.
NATURE (2017)
Autophagy Receptors and Neurodegenerative Diseases
Zhiqiang Deng et al.
TRENDS IN CELL BIOLOGY (2017)
Huntingtin Inclusions Trigger Cellular Quiescence, Deactivate Apoptosis, and Lead to Delayed Necrosis
Yasmin M. Ramdzan et al.
CELL REPORTS (2017)
YOD1/TRAF6 association balances p62-dependent IL-1 signaling to NF-κB
Gisela Schimmack et al.
ELIFE (2017)
p62 Pathology Model in the Rat Substantia Nigra with Filamentous Inclusions and Progressive Neurodegeneration
Kasey L. Jackson et al.
PLOS ONE (2017)
QuPath: Open source software for digital pathology image analysis
Peter Bankhead et al.
SCIENTIFIC REPORTS (2017)
Brain glycogen in health and disease
Jordi Duran et al.
MOLECULAR ASPECTS OF MEDICINE (2015)
The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy
Michael Lazarou et al.
NATURE (2015)
Cellular and metabolic functions for autophagy in cancer cells
Candia M. Kenific et al.
TRENDS IN CELL BIOLOGY (2015)
Depletion of p62 reduces nuclear inclusions and paradoxically ameliorates disease phenotypes in Huntington's model mice
Masaru Kurosawa et al.
HUMAN MOLECULAR GENETICS (2015)
Neuronal glycogen synthesis contributes to physiological aging
Christopher Sinadinos et al.
AGING CELL (2014)
A New Muscle Glycogen Storage Disease Associated with Glycogenin-1 Deficiency
Edoardo Malfatti et al.
ANNALS OF NEUROLOGY (2014)
Glycogen accumulation underlies neurodegeneration and autophagy impairment in Lafora disease
Jordi Duran et al.
HUMAN MOLECULAR GENETICS (2014)
Neurons have an active glycogen metabolism that contributes to tolerance to hypoxia
Isabel Saez et al.
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM (2014)
Polyglucosan Body Myopathy Caused by Defective Ubiquitin Ligase RBCK1
Johanna Nilsson et al.
ANNALS OF NEUROLOGY (2013)
Metabolic signatures of amyotrophic lateral sclerosis reveal insights into disease pathogenesis
James C. Dodge et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Deleterious effects of neuronal accumulation of glycogen in flies and mice
Jordi Duran et al.
EMBO MOLECULAR MEDICINE (2012)
Dysfunctions in endosomal-lysosomal and autophagy pathways underlie neuropathology in a mouse model for Lafora disease
Rajat Puri et al.
HUMAN MOLECULAR GENETICS (2012)
Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy
Olga Criado et al.
HUMAN MOLECULAR GENETICS (2012)
Neurodegeneration and functional impairments associated with glycogen synthase accumulation in a mouse model of Lafora disease
Jordi Valles-Ortega et al.
EMBO MOLECULAR MEDICINE (2011)
Neuroprotective role of PrPC against kainate-induced epileptic seizures and cell death depends on the modulation of JNK3 activation by GluR6/7-PSD-95 binding
Patricia Carulla et al.
MOLECULAR BIOLOGY OF THE CELL (2011)
PTG Depletion Removes Lafora Bodies and Rescues the Fatal Epilepsy of Lafora Disease
Julie Turnbull et al.
PLOS GENETICS (2011)
Lafora Disease Epidemiology, Pathophysiology and Management
Thomas S. Monaghan et al.
CNS DRUGS (2010)
The selective autophagy substrate p62 activates the stress responsive transcription factor Nrf2 through inactivation of Keap1
Masaaki Komatsu et al.
NATURE CELL BIOLOGY (2010)
p62, an autophagy hero or culprit?
Tor Erik Rusten et al.
NATURE CELL BIOLOGY (2010)
Epilepsy, Regulation of Brain Energy Metabolism and Neurotransmission
Jean-Francois Cloix et al.
CURRENT MEDICINAL CHEMISTRY (2009)
To aggregate or not to aggregate? A new role for p62
Jorge Moscat et al.
EMBO REPORTS (2009)
Regulation of GABAA and Glutamate Receptor Expression, Synaptic Facilitation and Long-Term Potentiation in the Hippocampus of Prion Mutant Mice
Alejandra Rangel et al.
PLOS ONE (2009)
Simultaneous inference in general parametric models
Torsten Hothorn et al.
BIOMETRICAL JOURNAL (2008)
Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice
Masaaki Komatsu et al.
CELL (2007)
Enhanced susceptibility of Prnp-deficient mice to kainate-induced seizures, neuronal apoptosis, and death:: Role of AMPA/kainate receptors
Alejandra Rangel et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2007)
High glycogen levels in the hippocampus of patients with epilepsy
Mads K. Dalsgaard et al.
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM (2007)
Soluble protein oligomers in neurodegeneration:: lessons from the Alzheimer's amyloid β-peptide
Christian Haass et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)
The presence of polyglucosan bodies in temporal lobe epilepsy: its role and significance
A Abubakr et al.
JOURNAL OF CLINICAL NEUROSCIENCE (2005)
Accumulation of high-molecular-weight amylose in Alzheimer's disease brains
LJ Huang et al.
GLYCOBIOLOGY (2004)
Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
M Arrasate et al.
NATURE (2004)
Inherent toxicity of aggregates implies a common mechanism for protein misfolding diseases
M Bucciantini et al.
NATURE (2002)
分享论文
