245 results on '"Oshima, Junko"'
Search Results
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. Werner Protein Recruits DNA Polymerase δ to the Nucleolus
6. Dysfunction of the MDM2/p53 axis is linked to premature aging
7. Positional Cloning of the Werner's Syndrome Gene
8. Woodhouse–Sakati syndrome in an Indian patient with a novel pathogenic variant.
9. Accelerated epigenetic aging and DNA methylation alterations in Berardinelli–Seip congenital lipodystrophy.
10. Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
11. ERCC4 variants identified in a cohort of patients with segmental progeroid syndromes
12. High incidence of BSCL2 intragenic recombinational mutation in Peruvian type 2 Berardinelli–Seip syndrome
13. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects
14. POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome
15. Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus
16. TNF‐α/IFN‐γ synergy amplifies senescence‐associated inflammation and SARS‐CoV‐2 receptor expression via hyper‐activated JAK/STAT1.
17. Werner syndrome in a Lebanese family.
18. Atypical Aicardi-Goutieres syndrome: Is the WRN locus a modifier?
19. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
20. Rapamycin decreases DNA damage accumulation and enhances cell growth of WRN-deficient human fibroblasts
21. Regional genomic instability predisposes to complex dystrophin gene rearrangements
22. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
23. Association between APOE e2/e3/e4 polymorphism and disability severity in a national long-term care survey sample
24. Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference
25. Transfection of Neuroprogenitor Cells with Iron Nanoparticles for Magnetic Resonance Imaging Tracking: Cell Viability, Differentiation, and Intracellular Localization
26. Coronary Artery Disease in a Werner Syndrome-Like Form of Progeria Characterized by Low Levels of Progerin, a Splice Variant of Lamin A
27. Long-Read Sequencing Resolves Complex Structural Variants and Identifies Missing Disease-Causing Variants in Unsolved Cases of Hemophilia
28. Lessons from human progeroid syndromes
29. Leukocyte Telomere Length Is Associated with Disability in Older U.S. Population
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. Health-Protective and Adverse Effects of the Apolipoprotein E ϵ2 Allele in Older Men
33. Accelerated telomere shortening and replicative senescence in human fibroblasts overexpressing mutant and wild-type lamin A
34. Phenomics and lamins: From disease to therapy
35. The Spectrum of WRN Mutations in Werner Syndrome Patients
36. Evidence against DNA polymerase β as a candidate gene for Werner syndrome
37. Phenotypic Heterogeneity in Body Fat Distribution in Patients with Atypical Werner’s Syndrome Due to Heterozygous Arg133Leu Lamin A/C Mutation
38. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair
39. Alterations of chaperone protein expression in presenilin mutant neurons in response to glutamate excitotoxicity
40. Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!
41. What Geriatricians Should Know About the Werner Syndrome
42. Ageing: Dietary protection for genes
43. Cell-to-Cell Variation in Gene Expression for Cultured Human Cells Is Controlled in Trans by Diverse Genes: Implications for the Pathobiology of Aging.
44. No detectable mutations at Werner helicase locus in progeria
45. SOD2 polymorphisms: unmasking the effect of polymorphism on splicing
46. Multisystem Progeroid Syndrome With Lipodystrophy, Cardiomyopathy, and Nephropathy Due to an LMNA p.R349W Variant.
47. Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP Synthesis.
48. Aβ 1–40 enhances the proliferation of human diploid fibroblasts
49. Werner helicase expression in human fetal and adult aortas
50. In Memory of George M. Martin.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.