392 results on '"Jerez, Andres"'
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2. Influence of TP53 gene mutations and their allelic status in myelodysplastic syndromes with isolated 5q deletion
3. Desperation among university students during SARS-COV-2 virus quarantine/Desesperanza en universitarios durante la cuarentena ante el virus SARS-COV-2
4. Outcomes of patients with chronic myelomonocytic leukaemia treated with non-curative therapies: a retrospective cohort study
5. Representaciones sociales del conflicto armado en Colombia en adolescentes de la provincia de Soto Norte, Santander/Social Representations of the Armed Conflict in Colombia in Adolescents of the Province of Soto Norte, Santander
6. Sucesos vitales estresantes, ansiedad y depresión en estudiantes de una universidad privada de Bucaramanga /Stressful life events, anxiety and depression in students of a private university in Bucaramanga /Eventos de vida estressantes, ansiedade e depressão em alunos de uma universidade particular em Bucaramanga
7. Desesperanza en universitarios durante la cuarentena ante el virus SARS-COV-2
8. Validation of the Artificial Intelligence Prognostic Scoring System for Myelodysplastic Syndromes in chronic myelomonocytic leukaemia: A novel approach for improved risk stratification
9. Myeloid Malignancies with Chromosome 5q Deletions Acquire a Dependency on an Intrachromosomal NF-κB Gene Network
10. Spectral Image Fusion for Increasing the Spatio-Spectral Resolution Through Side Information
11. Intermediate coupling fixed point study in the overscreened regime of generalized multichannel SU(N) Kondo models
12. Transition from a strong-coupling fixed point to an intermediate-coupling fixed point in a single-channel SU(N) Kondo model: role of the filling and two-stage screening
13. X-ray Dichroism in Noncetrosymmetric crystals
14. X-ray dichroism and orbital anapoles
15. Machine Learning Improves Risk Stratification in Myelodysplastic Neoplasms: An Analysis of the Spanish Group of Myelodysplastic Syndromes
16. Solution of the Multichannel Coqblin-Schrieffer Impurity Model and Application to Multi-Level systems
17. Chiral Liquids in 1-d: A New Class of NFL-Fixed Points
18. Chiral Non-Fermi Liquids in 1-d
19. Fermi and Non-Fermi behavior in the anisotropic Multichannel Kondo Model -- Bethe Ansatz solution
20. P703: THE AIPSS-MDS MACHINE LEARNING MODEL PREDICTS OVERALL SURVIVAL AND LEUKEMIC TRANSFORMATION IN CMML: AN ANALYSIS OF THE SPANISH REGISTRY OF MDS
21. P720: A BONE MARROW MICROENVIRONMENTAL CELL SIGNATURE SCORING SYSTEM INDEPENDENTLY PREDICTED SURVIVAL AND DRUG RESISTANCE IN CHRONIC MYELOMONOCYTIC LEUKAEMIA PATIENTS
22. Erythroleukemia shares biological features and outcome with myelodysplastic syndromes with excess blasts: a rationale for its inclusion into future classifications of myelodysplastic syndromes
23. A three‐gene leukaemic stem cell signature score is robustly prognostic in chronic myelomonocytic leukaemia
24. Deep Unrolled Single Snapshot Phase Retrieval via Non-Convex Formulation and Phase Mask Design
25. Plan Prospectivo de Tennis and Sports Academy 2023-2026
26. Supervised Machine Learning Improves Risk Stratification in Newly Diagnosed Myelodysplastic Syndromes: An Analysis of the Spanish Group of Myelodysplastic Syndromes
27. A Three Gene Leukemic Stem Cell Signature Score Is Robustly Prognostic in Chronic Myelomonocytic Leukemia
28. ERCC6L2 in Early-Onset Adult Myelodysplastic Syndrome without Pre-Existing Disorder
29. Deep sequencing of the T-cell receptor repertoire in CD8+ T-large granular lymphocyte leukemia identifies signature landscapes
30. STAT3 mutations indicate the presence of subclinical T-cell clones in a subset of aplastic anemia and myelodysplastic syndrome patients
31. Patterns of missplicing due to somatic U2AF1 mutations in myeloid neoplasms
32. Targeting IRAK1 as a Therapeutic Approach for Myelodysplastic Syndrome
33. Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia
34. TP53 Allelic State in Myelodysplastic Syndromes with 5q Deletion
35. Phase 2 study of the lenalidomide and azacitidine combination in patients with higher-risk myelodysplastic syndromes
36. SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes
37. STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia
38. Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis
39. Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
40. Representaciones sociales del conflicto armado en Colombia en adolescentes de la provincia de Soto Norte, Santander.
41. The role of bone marrow biopsy and FDG-PET/CT in identifying bone marrow infiltration in the initial diagnosis of high grade non-Hodgkin B-cell lymphoma and Hodgkin lymphoma. accuracy in a multicenter series of 372 patients
42. CIBERBULLYING DURANTE LA PANDEMIA POR LA COVID-19: UN ESTUDIO EN ADOLESCENTES DE SANTANDER, COLOMBIA.
43. Treatment Patterns and Overall Survival in Patients with Intermediate-Risk MDS: A Retrospective Analysis in the Spanish MDS Registry
44. Germline and Somatic Variants Co-Ocurrence Profile in Early Onset Adult Myelodysplastic Syndromes without a Preexisting Disorder
45. NOTCH1 Mutation in CLL Enhances Cell Cycle G1/S Transition through Specific Cyclin Overexpression: Preclinical Ground for CDK4/6 Targeted Inhibition
46. Overactivation of the NLRP3 Inflammasome in Chronic Myelomonocytic Leukemia KRAS Mutated Patients Can be Detected By the Apoptosis-Associated Speck-like Protein (ASC) and Reverted By IL1β Inhibitors
47. Deep Unrolled Phase Retrieval Approach from Coded Diffraction Patterns
48. Object Classification using Deep Neural Networks from Coded Diffraction Patterns
49. Clinical and Genomic-Based Decision Support System to Define the Optimal Timing of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Myelodysplastic Syndromes (MDS)
50. Clinical Impact of the New Bone Marrow Blasts Cutoff Defined By the International Classification Consortium (ICC) in Myeloid Neoplasms with Mutated TP53 gene
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