270 results on '"Kamino, Kouzin"'
Search Results
2. Mitochondrial ALDH2 Deficiency as an Oxidative Stress
3. The SIGMAR1 gene is associated with a risk of schizophrenia and activation of the prefrontal cortex
4. No association between the PCM1 gene and schizophrenia: A multi-center case-control study and a meta-analysis
5. The chitinase 3-like 1 gene and schizophrenia: Evidence from a multi-center case–control study and meta-analysis
6. A functional polymorphism in the disrupted-in schizophrenia 1 gene is associated with chronic fatigue syndrome
7. Association study of the G72 gene with schizophrenia in a Japanese population: A multicenter study
8. Cell-Type-Specific and Regulated Expression of a Human γ 1 Heavy-Chain Immunoglobulin Gene in Transgenic Mice
9. Aphidicolin-Resistant Human Cell Lines Resistant to UV and Bleomycin
10. Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non-APOE-ε4 carriers
11. Genetic deficiency of a mitochondrial aldehyde dehydrogenase increases serum lipid peroxides in community-dwelling females
12. A novel alternative splice variant of nicastrin and its implication in Alzheimer disease
13. The [tau] protein of oral epithelium increases in Alzheimer's disease
14. Functional genetic variation at the NRGN gene and schizophrenia: Evidence from a gene-based case–control study and gene expression analysis
15. Lymphocyte-specific protein tyrosine kinase is a novel risk gene for Alzheimer disease
16. The DYRK1A gene, encoded in chromosome 21 Down syndrome critical region, bridges between β-amyloid production and tau phosphorylation in Alzheimer disease
17. Linkage and haplotype analysis of familial early-onset Alzheimer disease in Japanese population
18. Albumin gene encoding free fatty acid and β-amyloid transporter is genetically associated with Alzheimer disease
19. Toll-like receptor 3 mediated hyperphosphorylation of tau in human SH-SY5Y neuroblastoma cells
20. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus
21. Evidence against DNA polymerase β as a candidate gene for Werner syndrome
22. Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2–p22
23. Promoter polymorphism in fibroblast growth factor 1 gene increases risk of definite Alzheimer’s disease
24. TAFI polymorphisms at amino acids 147 and 325 are not risk factors for cerebral infarction
25. Increased incidence of dementia with Lewy bodies in patients carrying the ϵ4-allele of apolipoprotein E
26. Aluminum alters cell viability and axonal transport system in Alzheimerʼs disease pathogenic mutation-bearing cells
27. C677T polymorphism of methylenetetrahydrofolate reductase gene affects plasma homocysteine level and is a genetic factor of late-onset Alzheimerʼs disease
28. PROGRESS TOWARD THE IDENTIFICATION OF THE CHROMOSOME 10q LOCUS FOR LATE ONSET ALZHEIMERʼS DISEASE
29. Deficiency in a mitochondrial aldehyde dehydrogenase increases vulnerability to oxidative stress in PC12 cells
30. Dinucleotide repeat polymorphism at the D8S1055
31. Gene dose effect of the APOE-ϵ4 allele on plasma HDL cholesterol level in patients with Alzheimer’s disease
32. Mutational screening of APP gene in patients with early-onset Alzheimer disease utilizing mismatched PCR-RFLP
33. Deficiency in Mitochondrial Aldehyde Dehydrogenase Increases the Risk for Late-Onset Alzheimer's Disease in the Japanese Population
34. Two dinucleotide repeat polymorphisms at the D8S1442 and D8S1443 loci
35. Identification of a single base polymorphism in intron 2 of the c-fos gene and its detection by mismatched PCR-RFLP
36. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers
37. A genome-wide association study of late-onset Alzheimer’s disease in a Japanese population
38. Association between CAG repeat length in the PPP2R2B gene and Alzheimer disease in the Japanese population
39. SORL1 is genetically associated with Alzheimer disease in a Japanese population
40. Decrease of dynamin 2 levels in late-onset Alzheimer’s disease alters Aβ metabolism
41. How to diagnose the 22q11.2 deletion syndrome in patients with schizophrenia: a case report
42. TheAKT1gene is associated with attention and brain morphology in schizophrenia
43. TheKCNH2gene is associated with neurocognition and the risk of schizophrenia
44. Association study ofKIBRAgene with memory performance in a Japanese population
45. AKT1 GENE IS ASSOCIATED WITH ATTENTION AND BRAIN MORPHOLOGY IN PATIENTS WITH SCHIZOPHRENIA
46. KIBRA Genetic Polymorphism Influences Episodic Memory in Alzheimer’s Disease, but Does Not Show Association with Disease in a Japanese Cohort
47. Promoter variant in the Chitinase 3-like 1 gene is associated with risk for schizophrenia and personality trait
48. Mutational screening of APP gene in patients with early-onset Alzheimer disease utilizing mismatched PCR-RFLP
49. Regulation of Notch Signaling by Dynamic Changes in the Precision of S3 Cleavage of Notch-1
50. Peripheral ethanolamine plasmalogen deficiency: a logical causative factor in Alzheimer's disease and dementia
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