423 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. Werner syndrome RECQ helicase participates in and directs maintenance of the protein complexes of constitutive heterochromatin in proliferating human cells
4. Maternal histone methyltransferases antagonistically regulate monoallelic expression inC. elegans
5. 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
6. Accelerated epigenetic aging in Werner syndrome
7. Caspase 5 depletion is linked to hyper-inflammatory response and progeroid syndrome
8. Insights into aging from progeroid syndrome epigenetics
9. Key elements of cellular senescence involve transcriptional repression of mitotic and DNA repair genes through the p53-p16/RB-E2F-DREAM complex
10. 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
11. Werner Protein Recruits DNA Polymerase δ to the Nucleolus
12. The Biological Basis of Aging
13. List of Contributors
14. Dysfunction of the MDM2/p53 axis is linked to premature aging
15. Accelerated epigenetic aging and DNA methylation alterations in Berardinelli–Seip congenital lipodystrophy
16. In Memory of George M. Martin
17. Rapid emergence of transcriptional heterogeneity upon molecular stress predisposes cells to two distinct states of senescence
18. Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia
19. Positional Cloning of the Werner's Syndrome Gene
20. Woodhouse–Sakati syndrome in an Indian patient with a novel pathogenic variant.
21. List of Contributors
22. Werner Syndrome as a Model of Human Aging
23. Key Elements of Cellular Senescence Involve Transcriptional Repression of Mitotic and DNA Repair Genes Through the p53-p16/pRB-E2F-DREAM Complex
24. Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
25. TNF‐α/IFN‐γ synergy amplifies senescence‐associated inflammation and SARS‐CoV‐2 receptor expression via hyper‐activated JAK/STAT1
26. Oxidative Stress Induced Senescence Gives Rise to Transcriptionally Distinct Physiological States
27. Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases
28. ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes
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. DNA methylation signatures in Blood DNA of Hutchinson–Gilford Progeria syndrome
32. Werner syndrome in a Lebanese family
33. 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）
34. (1) Overall Summary of the Meeting
35. POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome
36. A Novel Homozygous WRN Mutation Identified in a Middle Aged Man With Diabetes Mellitus Complicated By Multiple Features of Accelerated Aging
37. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
38. Atypical Aicardi-Goutieres syndrome: Is the WRN locus a modifier?
39. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
40. Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts
41. Regional genomic instability predisposes to complex dystrophin gene rearrangements
42. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
43. Association between APOE e2/e3/e4 polymorphism and disability severity in a national long-term care survey sample
44. Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now PursueAntigeroid Syndromes!
45. The Biological Basis of Aging
46. Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference
47. Transfection of Neuroprogenitor Cells with Iron Nanoparticles for Magnetic Resonance Imaging Tracking: Cell Viability, Differentiation, and Intracellular Localization
48. LMNA Mutations in Progeroid Syndromes
49. Coronary Artery Disease in a Werner Syndrome-Like Form of Progeria Characterized by Low Levels of Progerin, a Splice Variant of Lamin A
50. 15 - The Biological Basis of Aging: Implications for Medical Genetics
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