23 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. Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
5. Werner syndrome through the lens of tissue and tumour genomics
6. Dietary protection for genes
7. Truncated prelamin A expression in HGPS-like patients: a transcriptional study
8. Genetic diversity is a predictor of mortality in humans
9. Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features
10. Clinical utility gene card for: Werner Syndrome - Update 2014
11. Clinical utility gene card for: Werner syndrome
12. LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining
13. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations
14. Regional genomic instability predisposes to complex dystrophin gene rearrangements
15. The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis
16. SOD2polymorphisms: unmasking the effect of polymorphism on splicing
17. Correction of cellular phenotypes of Hutchinson-Gilford Progeria cells by RNA interference
18. Transfection of Neuroprogenitor Cells with Iron Nanoparticles for Magnetic Resonance Imaging Tracking: Cell Viability, Differentiation, and Intracellular Localization
19. Lessons from human progeroid syndromes
20. The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease
21. An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants
22. The Werner syndrome protein is a DNA helicase
23. Evidence against DNA polymerase ? as a candidate gene for Werner syndrome
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