1,810 results on '"Kakita, Akiyoshi"'
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2. Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans
3. A novel PET probe to selectively image heat shock protein 90α/β isoforms in the brain
4. Polygenic effects on the risk of Alzheimer’s disease in the Japanese population
5. The cycad genotoxin methylazoxymethanol, linked to Guam ALS/PDC, induces transcriptional mutagenesis
6. Missense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis
7. Recent advances in liquid biopsy of central nervous system lymphomas: case presentations and review of the literature
8. Stage-dependent immunity orchestrates AQP4 antibody-guided NMOSD pathology: a role for netting neutrophils with resident memory T cells in situ
9. Reliable detection of genetic alterations in cyst fluid DNA for the diagnosis of brain tumors
10. Multi-omics analyses of choroid plexus carcinoma cell lines reveal potential targetable pathways and alterations
11. Usefulness and limitations of intraoperative pathological diagnosis using frozen sections for spinal cord tumors
12. Indications for a brain biopsy in neurological diseases of unknown etiology: The role of magnetic resonance imaging findings and liquid biopsy in yielding definitive pathological diagnoses
13. Imaging α-synuclein pathologies in animal models and patients with Parkinson’s and related diseases
14. Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation
15. Identification of schizophrenia symptom-related gene modules by postmortem brain transcriptome analysis
16. An integrated genetic analysis of epileptogenic brain malformed lesions
17. Pharmacological evaluation of E2730, a novel selective uncompetitive GAT1 inhibitor, on epileptiform activities in resected brain tissues from human focal cortical dysplasia ex vivo
18. Human early-onset dementia caused by DAP12 deficiency reveals a unique signature of dysregulated microglia
19. Ethnicity-dependent effect of rs1799971 polymorphism on OPRM1 expression in the postmortem brain and responsiveness to antipsychotics
20. Epilepsy surgery without lipoma removal for temporal lobe epilepsy associated with lipoma in the Sylvian fissure
21. Elevated ratio of C-type lectin-like receptor 2 level and platelet count (C2PAC) aids in the diagnosis of post-operative venous thromboembolism in IDH-wildtype gliomas
22. Elevation of EGR1/zif268, a Neural Activity Marker, in the Auditory Cortex of Patients with Schizophrenia and its Animal Model
23. EGF Downregulates Presynaptic Maturation and Suppresses Synapse Formation In Vitro and In Vivo
24. Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient
25. Spinal intradural pseudocyst formation in central nervous system superficial siderosis.
26. Deep learning-based diagnosis of temporal lobe epilepsy associated with hippocampal sclerosis: An MRI study
27. In Vivo Assessment of Astrocyte Reactivity in Patients with Progressive Supranuclear Palsy
28. Availability of individual proteins for quantitative analysis in postmortem brains preserved in two different brain banks
29. Successful Multimodal Treatment of Intracranial Growing Teratoma Syndrome with Malignant Features
30. Reactive astrocytes contribute to epileptogenesis in patients with cavernous angioma
31. Alzheimer's Aβ assembly binds sodium pump and blocks endothelial NOS activity via ROS-PKC pathway in brain vascular endothelial cells
32. Structure-based classification of tauopathies
33. Publisher Correction: Human early-onset dementia caused by DAP12 deficiency reveals a unique signature of dysregulated microglia
34. Predicting BRAF V600E mutation in glioblastoma: utility of radiographic features
35. Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy
36. Proteomic profile differentiating between mesial temporal lobe epilepsy with and without hippocampal sclerosis
37. Topoisomerase IIβ immunoreactivity (IR) co-localizes with neuronal marker-IR but not glial fibrillary acidic protein-IR in GLI3-positive medulloblastomas: an immunohistochemical analysis of 124 medulloblastomas from the Japan Children’s Cancer Group
38. ALDH4A1 expression levels are elevated in postmortem brains of patients with schizophrenia and are associated with genetic variants in enzymes related to proline metabolism
39. Skull diploë is rich in aquaporin-4
40. Genome-wide association analysis identifies PLA2G4C as a susceptibility locus for Multiple System Atrophy
41. Marked alteration of phosphoinositide signaling‐associated molecules in postmortem prefrontal cortex with bipolar disorder
42. Tau filaments from amyotrophic lateral sclerosis/parkinsonism-dementia complex adopt the CTE fold
43. 10141-GMC-13 MULTIREGIONAL GENOMIC ANALYSIS: A NOVEL APPROACH FOR DETECTING PATHOGENIC DRIVER MUTATION ASSOCIATED WITH MALIGNANT PROGRESSION IN NEUROCUTANEOUS MELANOSIS
44. A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features
45. Age-related demethylation of the TDP-43 autoregulatory region in the human motor cortex
46. Correction to: A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features
47. Cytosolic dsDNA of mitochondrial origin induces cytotoxicity and neurodegeneration in cellular and zebrafish models of Parkinson’s disease
48. Human and mouse single-nucleus transcriptomics reveal TREM2-dependent and TREM2-independent cellular responses in Alzheimer’s disease
49. Na, K-ATPase α3 is a death target of Alzheimer patient amyloid-β assembly
50. Pathological alterations of chondroitin sulfate moiety in postmortem hippocampus of patients with schizophrenia
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