458 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. Accelerated epigenetic aging in Werner syndrome
4. 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
5. Werner syndrome RECQ helicase participates in and directs maintenance of the protein complexes of constitutive heterochromatin in proliferating human cells
6. Maternal histone methyltransferases antagonistically regulate monoallelic expression inC. elegans
7. RECQ helicase disease and related progeroid syndromes: RECQ2018 meeting
8. Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome
9. Insights into aging from progeroid syndrome epigenetics
10. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions
11. Werner Protein Recruits DNA Polymerase δ to the Nucleolus
12. The Biological Basis of Aging
13. List of Contributors
14. Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complex
15. 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
16. Positional Cloning of the Werner's Syndrome Gene
17. List of Contributors
18. Werner Syndrome as a Model of Human Aging
19. Accelerated epigenetic aging and DNA methylation alterations in Berardinelli–Seip congenital lipodystrophy
20. In Memory of George M. Martin
21. Dysfunction of the MDM2/p53 axis is linked to premature aging
22. Rapid emergence of transcriptional heterogeneity upon molecular stress predisposes cells to two distinct states of senescence
23. Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia
24. Key Elements of Cellular Senescence Involve Transcriptional Repression of Mitotic and DNA Repair Genes Through the p53-p16/pRB-E2F-DREAM Complex
25. Woodhouse–Sakati syndrome in an Indian patient with a novel pathogenic variant.
26. ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes
27. Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
28. Functional deficit associated with a missense Werner syndrome mutation
29. High incidence of BSCL2 intragenic recombinational mutation in Peruvian type 2 Berardinelli–Seip syndrome
30. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
31. TNF‐α/IFN‐γ synergy amplifies senescence‐associated inflammation and SARS‐CoV‐2 receptor expression via hyper‐activated JAK/STAT1
32. Oxidative Stress Induced Senescence Gives Rise to Transcriptionally Distinct Physiological States
33. Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases
34. DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome
35. Werner syndrome in a Lebanese family
36. 日本環境教育学会第32回年次大会（北九州・オンライン）報告（2）
37. (1) Overall Summary of the Meeting
38. POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome
39. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
40. Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in mice
41. Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A
42. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
43. Atypical Aicardi-Goutieres syndrome: Is the WRN locus a modifier?
44. Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts
45. Regional genomic instability predisposes to complex dystrophin gene rearrangements
46. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
47. A Novel Homozygous WRN Mutation Identified in a Middle Aged Man With Diabetes Mellitus Complicated By Multiple Features of Accelerated Aging
48. Association between APOE e2/e3/e4 polymorphism and disability severity in a national long-term care survey sample
49. The Biological Basis of Aging
50. Phenomics and lamins: From disease to therapy
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