195 results on '"Londono-Vallejo A"'
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2. Nuclear envelope disruption triggers hallmarks of aging in lung alveolar macrophages
3. Induction of telomerase in p21-positive cells counteracts capillaries rarefaction and preserves lung function of aging mice
4. Utilisation de longs ARN non codants vers un diagnostic urinaire du cancer de la prostate
5. The N-Terminal Domain of cGAS Determines Preferential Association with Centromeric DNA and Innate Immune Activation in the Nucleus
6. Genome-wide Control of Heterochromatin Replication by the Telomere Capping Protein TRF2
7. Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations
8. TRF2-Mediated Control of Telomere DNA Topology as a Mechanism for Chromosome-End Protection
9. Telomere regulation during ageing and tumorigenesis of the grey mouse lemur
10. Telomeres, Epigenetics, and Aging
11. Induction of telomerase in p21-positive cells counteracts capillaries rarefaction in aging mice lung
12. Induction of telomerase in p21-positive cells counteracts capillaries rarefaction in aging mice lung
13. Mutant Mice Lacking the p53 C-Terminal Domain Model Telomere Syndromes
14. Telomeres and the nucleus
15. Inherited mutations in the helicase RTEL1 cause telomere dysfunction and Hoyeraal-Hreidarsson syndrome
16. Telomeres and telomerase dance to the rhythm of the cell cycle
17. Overexpression of Nucleolin and Associated Genes in Prostate Cancer
18. Nuclear envelope disruption triggers hallmarks of aging in lung alveolar macrophages
19. Telomerase Prevents Emphysema in Old Mice by Sustaining Subpopulations of Endothelial and AT2 Cells
20. Probing PML Body Function in ALT Cells Reveals Spatiotemporal Requirements for Telomere Recombination
21. Overexpression of Nucleolin and Associated Genes in Prostate Cancer
22. Nuclear envelope disruption triggers hallmarks of aging in lung alveolar macrophages
23. SARS-COV-2 infection causes massive lung-cell senescence
24. Mutations of the RTEL1 Helicase in a Hoyeraal-Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain
25. TRF2 and Apollo Cooperate with Topoisomerase 2α to Protect Human Telomeres from Replicative Damage
26. The telomere/telomerase system in autoimmune and systemic immune-mediated diseases
27. Nuclear Envelope Disruption Triggers Hallmarks of Aging in Lung Alveolar Macrophages
28. Evidence That SARS-CoV-2 Induces Lung Cell Senescence: Potential Impact on COVID-19 Lung Disease
29. Growth defects in mouse telomerase RNA-deficient cells expressing a template-mutated mouse telomerase RNA
30. Telomere instability and cancer
31. Telomere length inheritance and aging
32. Topoisomerase IIIα is required for normal proliferation and telomere stability in alternative lengthening of telomeres
33. Pt-ttpy, a G-quadruplex binding platinum complex, induces telomere dysfunction and G-rich regions DNA damage
34. Telomerase Prevents Emphysema in Old Mice by Sustaining Subpopulations of Endothelial and AT2 Cells
35. The effect of TERC haploinsufficiency on the inheritance of telomere length
36. PD-0822 First evidence of a FLASH sparing effect in human healthy lung samples
37. Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability
38. Pulmonary Alveolar Proteinosis Revealing a Telomerase Disease
39. The structure of long telomeres in chromosomes of the Iberian shrew
40. Human RTEL1 associates with Poldip3 to facilitate responses to replication stress and R-loop resolution
41. Germline mutation of MDM4 , a major p53 regulator, in a familial syndrome of defective telomere maintenance
42. Germline mutation of
43. Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p– syndrome
44. The Pattern of Chromosome-Specific Variations in Telomere Length in Humans Shows Signs of Heritability and Is Maintained through Life
45. Human RTEL1 associates with Poldip3 to facilitate responses to replication stress and R-loop resolution
46. Telomere length heterogeneity and chromosome instability
47. Extracellular signal protein triggering the proteolytic activation of a developmental transcription factor in B. subtilis
48. Mutation of the putative nucleotide binding site of the Bacillus subtilis membrane protein ComFA abolishes the uptake of DNA during transformation
49. Segmental polymorphisms in the proterminal regions of a subset of human chromosomes
50. Telomere maintenance by telomerase and by recombination can coexist in human cells
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