「Aberrant interaction between FUS and SFPQ in neurons in a wide range of FTLD spectrum diseases」の関連論文
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Genetic and chemical inhibition of IRF5 suppresses pre-existing mouse lupus-like disease
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Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population
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Myh9 R702C is associated with erythroid abnormality with splenomegaly in mice
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Disease modeling of pulmonary fibrosis using human pluripotent stem cell-derived alveolar organoids
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Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ
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Enhanced osteoclastogenesis in patients with MSMD due to impaired response to IFN-γ
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Unique reticular hyperkeratotic eruptions seen in a patient with Darier's disease and attention deficit hyperactivity disorder
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Bone marrow-derived inducible microglia-like cells ameliorate motor function and survival in a mouse model of amyotrophic lateral sclerosis.
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Paraneoplastic Pemphigus Mimicking Toxic Epidermal Necrolysis Associated with Follicular Lymphoma: Possible Pathological Role of CD8 T Cells.
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MicroRNA profiling in adults with high-functioning autism spectrum disorder
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Optimal conditions for graft survival and reinnervation of denervated muscles after embryonic motoneuron transplantation into peripheral nerves undergoing Wallerian degeneration
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Persistent elevation of lysophosphatidylcholine promotes radiation brain necrosis with microglial recruitment by P2RX4 activation
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Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
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Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
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Genetic screening for malignant hyperthermia and comparison of clinical symptoms in Japan
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Role of Dopamine D2 Receptor/Fatty Acid-Binding Protein 3 Signaling in Nicotine-Induced Addiction
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Serum neurofilament light chain in chronic inflammatory demyelinating polyneuropathy
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Lack of impact of the ALDH2 rs671 variant on breast cancer development in Japanese BRCA1/2‐mutation carriers
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Phosphorylation of Npas4 by MAPK Regulates Reward-Related Gene Expression and Behaviors
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Development of Highly Selective PET Tau Probes without Off-Target Binding (オフターゲット結合を示さない高選択的PETタウプローブの開発)
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The Protective Effect of Amber Extract on Neurodegenerative Diseases
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Collective fusion activity determines neurotropism of an en bloc transmitted enveloped virus
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Differentiation of Hypertrophic Chondrocytes from Human iPSCs for the In Vitro Modeling of Chondrodysplasias
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MAGI-2 orchestrates the localization of backbone proteins in the slit diaphragm of podocytes
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Human recombinant erythropoietin improves motor function in rats with spinal cord compression-induced cervical myelopathy
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A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
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Morphea in a Crohn's disease patient undergoing ustekinumab treatment
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Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease
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Concepts of Regeneration for Spinal Diseases in 2021
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Suppression of Systemic Lupus Erythematosus in NZBWF1 mice infected with Hymenolepis microstoma
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A VCP modulator, KUS121, as a promising therapeutic agent for post-traumatic osteoarthritis
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Autism-associated mutation in Hevin/Sparcl1 induces endoplasmic reticulum stress through structural instability
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Reduced Cholinergic Activity in the Hippocampus of Hippocampal Cholinergic Neurostimulating Peptide Precursor Protein Knockout Mice
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Lionheart LincRNA alleviates cardiac systolic dysfunction under pressure overload
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The association of thyroglobulin single nucleotide polymorphism with miniature dachshunds-specific inflammatory colorectal polyps and its involvement in interleukin-6 amplifier induced chronic inflammation
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Investigation of the mechanisms of taxane-induced peripheral neuropathy focusing on Schwann cell and search for novel therapies by drug repositioning
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Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
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Reproductive and Developmental Toxicity, and Neurotoxicity of a Tropomyosin-Related Kinase A Inhibitor, ASP7962, in Rats
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Site-directed mutagenesis study of host and viral proteins : single nucleotide variants of human TBK1 and functional sites of ebolavirus VP35
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Severe neurodevelopmental disorder caused by an MEF2C nonsense mutation
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Diagnosis and Characterization of Endoscopic Findings in XIAP Deficiency
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iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome
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miR-142 induces accumulation of reactive oxygen species (ROS) by inhibiting pexophagy in aged bone marrow mesenchymal stem cells
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Distinctive roles of syntaxin binding protein 4 and its action target, TP63, in lung squamous cell carcinoma: a theranostic study for the precision medicine
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Clinical and genetic investigation of 136 Japanese patients with congenital hypothyroidism
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SMN promotes mitochondrial metabolic maturation during myogenesis by regulating the MYOD-miRNA axis
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Activation of the pentose phosphate pathway in macrophages is crucial for granuloma formation in sarcoidosis
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Sarcomatoid mesothelioma diagnosed in a patient with mesothelioma in situ: a case report on morphologic differences after 9-month interval with details analysis of cytology in early-stage mesothelioma
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Prognostic stratification for IDH-wild-type lower-grade astrocytoma by Sanger sequencing and copy-number alteration analysis with MLPA
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Neuromelanin‐Sensitive Magnetic Resonance Imaging Using DANTE Pulse