232 results on '"Oshima, Junko"'
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2. Rapid emergence of transcriptional heterogeneity upon molecular stress predisposes cells to two distinct states of senescence
3. SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome—the Myhre syndrome
4. Accelerated epigenetic aging in Werner syndrome
5. Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome
6. Insights into aging from progeroid syndrome epigenetics
7. Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complex
8. Renal dysfunction, malignant neoplasms, atherosclerotic cardiovascular diseases, and sarcopenia as key outcomes observed in a three-year follow-up study using the Werner Syndrome Registry
9. Werner Protein Recruits DNA Polymerase δ to the Nucleolus
10. Dysfunction of the MDM2/p53 axis is linked to premature aging
11. Accelerated epigenetic aging and DNA methylation alterations in Berardinelli–Seip congenital lipodystrophy
12. Rapid emergence of transcriptional heterogeneity upon molecular stress predisposes cells to two distinct states of senescence
13. Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia
14. Positional Cloning of the Werner's Syndrome Gene
15. Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
16. TNF‐α/IFN‐γ synergy amplifies senescence‐associated inflammation and SARS‐CoV‐2 receptor expression via hyper‐activated JAK/STAT1
17. Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases
18. DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome
19. A Novel Homozygous WRN Mutation Identified in a Middle Aged Man With Diabetes Mellitus Complicated By Multiple Features of Accelerated Aging
20. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
21. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
22. Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts
23. Regional genomic instability predisposes to complex dystrophin gene rearrangements
24. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
25. Association between APOE e2/e3/e4 polymorphism and disability severity in a national long-term care survey sample
26. Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference
27. Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an LMNA p.R349W Variant
28. A Case Report of Werner’s Syndrome With a Novel Mutation From India
29. Lessons from human progeroid syndromes
30. Cigarette Smoke Induces Cellular Senescence via Wernerʼs Syndrome Protein Down-regulation
31. An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants
32. Toward Structuralizing for Educational Capability of Tourism
33. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes
34. Evidence against DNA polymerase β as a candidate gene for Werner syndrome
35. Phenotypic Heterogeneity in Body Fat Distribution in Patients with Atypical Werner’s Syndrome Due to Heterozygous Arg133Leu Lamin A/C Mutation
36. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair
37. Epigenetic signatures of Werner syndrome occur early in life and are distinct from normal epigenetic aging processes
38. Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C
39. Ageing: Dietary protection for genes
40. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures
41. SOD2 polymorphisms: unmasking the effect of polymorphism on splicing
42. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
43. ラーニング・ポートフォリオを用いた教育実践報告 : ふりかえりシートを最大限に生かす試み
44. Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies
45. Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients
46. Ethnic-specific WRN mutations in South Asian Werner syndrome patients: potential founder effect in patients with Indian or Pakistani ancestry
47. Practical Studies on Developing Local Skills to Solve Community-based Problems with Forest Tourism (1) : A Case Study of Initiatives in Yambaru Area, Okinawa
48. Werner syndrome through the lens of tissue and tumour genomics
49. Dietary protection for genes
50. Werner syndrome protein limits MYC-induced cellular senescence
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