168 results on '"López-Bigas, Núria"'
Search Results
2. Author Correction: Modulating the immune response to SARS-CoV-2 by different nanocarriers delivering an mRNA expressing trimeric RBD of the spike protein: COVARNA Consortium
3. Modulating the immune response to SARS-CoV-2 by different nanocarriers delivering an mRNA expressing trimeric RBD of the spike protein: COVARNA Consortium
4. Implications of noncoding regulatory functions in the development of insulinomas
5. Analyses of non-coding somatic drivers in 2,658 cancer whole genomes.
6. Detection of early seeding of Richter transformation in chronic lymphocytic leukemia
7. Origins of Second Malignancies in Children and Mutational Footprint of Chemotherapy in Normal Tissues
8. Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
9. Assessment of Human SARS CoV-2-Specific T-Cell Responses Elicited In Vitro by New Computationally Designed mRNA Immunogens (COVARNA)
10. Identification of Clonal Hematopoiesis Driver Mutations through In Silico Saturation Mutagenesis
11. The road ahead in genetics and genomics
12. Bayesian Non-parametric Clustering of Single-Cell Mutation Profiles
13. Genomic deletions explain the generation of alternative BRAF isoforms conferring resistance to MAPK inhibitors in melanoma
14. Assessment of Human SARS CoV-2-Specific T-Cell Responses Elicited In Vitro by New Computationally Designed mRNA Immunogens (COVARNA).
15. Abstract 3795: Early seeding of Richter transformation in chronic lymphocytic leukemia
16. Chromatin-Bound IκBα Regulates a Subset of Polycomb Target Genes in Differentiation and Cancer
17. Coordinated repression of cell cycle genes by KDM5A and E2F4 during differentiation
18. Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
19. Jagged1 Is the Pathological Link between Wnt and Notch Pathways in Colorectal Cancer
20. Nucleotide excision repair is impaired by binding of transcription factors to DNA
21. Author Correction: Reduced mutation rate in exons due to differential mismatch repair
22. Mapping of six somatic linker histone H1 variants in human breast cancer cells uncovers specific features of H1.2
23. High p16 expression and heterozygous RB1 loss are biomarkers for CDK4/6 inhibitor resistance in ER+ breast cancer
24. Analyses of non-coding somatic drivers in 2,658cancer whole genomes
25. Loss of E2F compromises mitochondrial function and protects cells from irradiation-induced apoptosis in Drosophila
26. Pervasive lesion segregation shapes cancer genome evolution
27. A partially supervised classification approach to dominant and recessive human disease gene prediction
28. Pervasive lesion segregation shapes cancer genome evolution
29. Highly consistent patterns for inherited human diseases at the molecular level
30. CoGenT++: an extensive and extensible data environment for computational genomics
31. Expansion of the BioCyc collection of pathway/genome databases to 160 genomes
32. Genome-wide identification of genes likely to be involved in human genetic disease
33. Connexin mutations in hearing loss, dermatological and neurological disorders
34. Genomic Data Improves Prognostic Stratification in Adult T-Cell Acute Lymphoblastic Leukemia Patients Enrolled in Measurable Residual Disease-Oriented Trials
35. Differences in the evolutionary history of disease genes affected by dominant or recessive mutations
36. Structural and functional properties of genes involved in human cancer
37. Abstract 3282: Standardization and coordination of variant interpretation knowledgebases improves clinical genome actionability
38. Discovery and characterization of coding and non-coding driver mutations in more than 2,500 whole cancer genomes
39. Reduced mutation rate in exons due to differential mismatch repair
40. Whole-genome landscapes of major melanoma subtypes
41. Pervasive lesion segregation shapes cancer genome evolution
42. OncodriveFML: a general framework to identify coding and non-coding regions with cancer driver mutations
43. 4. Coordinating variant interpretation knowledgebases improves clinical interpretation of genomic variants in cancers
44. An Intronic microRNA Links Rb/E2F and EGFR Signaling
45. Patterns of Clonal Evolution Assessed By Whole Exome Sequencing during Progression from MDS to AML Are Related to Therapy
46. Analysis of Clonal Evolution in Chronic Lymphocytic Leukemia from Inactive to Symptomatic Disease Prior Treatment Using Whole-Exome Sequencing
47. Biological convergence of cancer signatures
48. HDAC7 Is a Repressor of Myeloid Genes Whose Downregulation Is Required for Transdifferentiation of Pre-B Cells into Macrophages
49. Inhibition of Specific NF-κB Activity Contributes to the Tumor Suppressor Function of 14-3-3σ in Breast Cancer
50. mir-11 limits the proapoptotic function of its host gene, dE2f1
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.