「Aberrant interaction between FUS and SFPQ in neurons in a wide range of FTLD spectrum diseases」の関連論文
-
Conformational change of RNA‐helicase DHX30 by ALS/FTD‐linked FUS induces mitochondrial dysfunction and cytosolic aggregates
-
TDP-43 regulates cholesterol biosynthesis by inhibiting sterol regulatory element-binding protein 2
-
The stimulator of interferon genes (STING) pathway is upregulated in striatal astrocytes of patients with multiple system atrophy
-
Conformational change of RNA-helicase DHX30 by ALS/FTD-linked FUS induces mitochondrial dysfunction and cytosolic aggregates.
-
Discrepancy between distribution of alpha-synuclein oligomers and Lewy-related pathology in Parkinson’s disease
-
Pathogenic mutation of TDP-43 impairs RNA processing in a cell type-specific manner : implications for the pathogenesis of ALS/FTLD (本文)
-
Neuroinflammation in neurodegenerative disease
-
Interactions of amyloid coaggregates with biomolecules and its relevance to neurodegeneration
-
Human induced pluripotent stem cells generated from a patient with idiopathic basal ganglia calcification
-
UBAP1 mutations cause juvenile-onset hereditary spastic paraplegias (SPG80) and impair UBAP1 targeting to endosomes
-
Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2 (本文)
-
LC3/FtMt Colocalization Patterns Reveal the Progression of FtMt Accumulation in Nigral Neurons of Patients with Progressive Supranuclear Palsy.
-
Failure of DNA double-strand break repair by tau mediates Alzheimer's disease pathology in vitro
-
Presenilin is essential for ApoE secretion, a novel role of presenilin involved in Alzheimer’s disease pathogenesis
-
Iinfluence of plasma cytokine levels on the conversion risk from MCI to dementia in the Alzheimer's disease neuroimaging initiative database
-
Optimized sonoreactor for accelerative amyloid-fibril assays through enhancement of primary nucleation and fragmentation
-
Ndufs4 ablation shows an elevated GFAP and a decreased synaptophysin expression in mouse hippocampus.
-
Is Generalized and Segmental Dystonia Accompanied by Impairments in the Dopaminergic System?
-
Long-Surviving Adult Siblings With Joubert Syndrome Harboring a Novel Compound Heterozygous CPLANE1 Variant
-
Tooth Loss Induces Memory Impairment and Gliosis in App Knock-in Mouse Models of Alzheimer's disease
-
SAK3 Administration Improves Spine Abnormalities and Cognitive Deficits in AppNL-G-F/NL-G-F Knock-in Mice by Increasing Proteasome Activity through CaMKII/Rpt6 Signaling
-
Pattern of THK 5351 retention in normal aging involves core regions of resting state networks associated with higher cognitive function
-
A cerebrospinal fluid microRNA analysis: Progressive supranuclear palsy
-
Cell migration is impaired in XPA-deficient cells
-
Prickle2 and Igsf9b coordinately regulate the cytoarchitecture of the axon initial segment
-
A clinical and genetic study of SPG31 in Japan
-
Pharmacological Studies on the Roles of M1 Muscarinic Acetylcholine Receptors in the Cognitive Function of the Rodent Brain
-
Neuronal glutathione loss leads to neurodegeneration involving gasdermin activation
-
Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor
-
Molecular genetic study of the FMR1 CGG repeat configurations in the Japanese population and patients with Fragile X-Associated Tremor/Ataxia Syndrome
-
Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy
-
FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
-
Histone Deacetylase 2 Knockdown Ameliorates Morphological Abnormalities of Dendritic Branches and Spines to Improve Synaptic Plasticity in an APP/PS1 Transgenic Mouse Model
-
Elderly patient with 5q spinal muscular atrophy type 4 markedly improved by Nusinersen
-
Analyses of genetic and retinal lesions in Ccdc85c knockout rats: a rat model of genetic hydrocephalus
-
Constitutive activation of mTORC1 signaling induced by biallelic loss-of-function mutations in SZT2 underlies a discernible neurodevelopmental disease
-
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
-
Cellular senescence in white matter microglia is induced during ageing in mice and exacerbates the neuroinflammatory phenotype
-
SMN promotes mitochondrial metabolic maturation during myogenesis by regulating the MYOD-miRNA axis
-
Motor Progression and Nigrostriatal Neurodegeneration in Parkinson Disease
-
Case report: Late middle-aged features of FAM111A variant, Kenny–Caffey syndrome type 2-suggestive symptoms during a long follow-up
-
Altered functional connectivity associated with striatal dopamine depletion in Parkinson’s disease
-
Cryptotanshinone is a candidate therapeutic agent for interstitial lung disease associated with a BRICHOS-domain mutation of SFTPC
-
α-Synuclein BAC transgenic mice exhibit RBD-like behaviour and hyposmia: a prodromal Parkinson’s disease model
-
A case of Cockayne syndrome with unusually mild clinical manifestations
-
Clinical and serological features of dermatomyositis and systemic lupus erythematosus patients with autoantibodies to ADAR1
-
Reverse Genetic Studies on Mitochondrial tRNA-related Disorders
-
Lack of association between seropositivity of vasculopathy-related viruses and moyamoya disease
-
Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency
-
Study of Mitochonic Acid 5 to improve neuromuscular dysfunction associated with aging and diseases using C. elegans