402 results on '"Ellonen, Pekka"'
Search Results
2. Distinct molecular profiles and shared drug vulnerabilities in pancreatic metastases of renal cell carcinoma
3. The phylodynamics of SARS-CoV-2 during 2020 in Finland.
4. Molecular features encoded in the ctDNA reveal heterogeneity and predict outcome in high-risk aggressive B-cell lymphoma
5. Incidence Trends for SARS-CoV-2 Alpha and Beta Variants, Finland, Spring 2021
6. Somatic mutations in lymphocytes in patients with immune-mediated aplastic anemia
7. Integrated drug profiling and CRISPR screening identify essential pathways for CAR T-cell cytotoxicity
8. The CRCbiome study: a large prospective cohort study examining the role of lifestyle and the gut microbiome in colorectal cancer screening participants
9. Examining the effect of mitochondrial DNA variants on blood pressure in two Finnish cohorts
10. Single-cell functional genomics reveals determinants of sensitivity and resistance to natural killer cells in blood cancers
11. Reproducibility and repeatability of six high-throughput 16S rDNA sequencing protocols for microbiota profiling
12. Author Correction: Clonal hematopoiesis in patients with rheumatoid arthritis
13. Somatic mTOR mutation in clonally expanded T lymphocytes associated with chronic graft versus host disease
14. A novel class of somatic mutations in blood detected preferentially in CD8 + cells
15. TaME-seq: An efficient sequencing approach for characterisation of HPV genomic variability and chromosomal integration
16. Abstract 667: Single-cell functional genomics of natural killer cell evasion by tumor cells
17. Data from Individualized Systems Medicine Strategy to Tailor Treatments for Patients with Chemorefractory Acute Myeloid Leukemia
18. Supplementary Table S2 from Individualized Systems Medicine Strategy to Tailor Treatments for Patients with Chemorefractory Acute Myeloid Leukemia
19. Supplementary Figures, Tables and Methods from Individualized Systems Medicine Strategy to Tailor Treatments for Patients with Chemorefractory Acute Myeloid Leukemia
20. mtDNA Mutagenesis Disrupts Pluripotent Stem Cell Function by Altering Redox Signaling
21. Germline Mutation of RPS20, Encoding a Ribosomal Protein, Causes Predisposition to Hereditary Nonpolyposis Colorectal Carcinoma Without DNA Mismatch Repair Deficiency
22. Clonal hematopoiesis in patients with rheumatoid arthritis
23. Single-Cell Functional Genomics of Natural Killer Cell Interaction with Blood Cancers
24. Somatic Mutations in T Cells in Patients with Hematological Diseases
25. 1006 Single-cell functional genomics of natural killer cell evasion in blood cancers
26. STAT3 mutations indicate the presence of subclinical T-cell clones in a subset of aplastic anemia and myelodysplastic syndrome patients
27. Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations
28. Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia
29. Copy number alterations define outcome in Philadelphia chromosome-positive acute lymphoblastic leukemia
30. Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing
31. Single-cell functional genomics of natural killer cell evasion in blood cancers
32. Evaluating Whole Genome Amplification via Multiply-primed Rolling Circle Amplification for SNP Genotyping of Samples with Low DNA Yield
33. Copy number alterations define outcome in Philadelphia chromosome-positive acute lymphoblastic leukemia
34. sj-pdf-2-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
35. sj-pdf-7-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
36. sj-pdf-1-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
37. sj-pdf-3-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
38. sj-pdf-5-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
39. sj-pdf-6-cep-10.1177_03331024211068065 - Supplemental material for NCOR2 is a novel candidate gene for migraine-epilepsy phenotype
40. No evidence for shared etiology in two demyelinative disorders, MS and PLOSL
41. Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci
42. Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencing
43. Additional file 2 of The CRCbiome study: a large prospective cohort study examining the role of lifestyle and the gut microbiome in colorectal cancer screening participants
44. Corrigendum: Adult-Onset Anti-Citrullinated Peptide Antibody-Negative Destructive Rheumatoid Arthritis Is Characterized by a Disease-Specific CD8+ T Lymphocyte Signature (vol 11, 578848, 2020)
45. Additional file 1 of The CRCbiome study: a large prospective cohort study examining the role of lifestyle and the gut microbiome in colorectal cancer screening participants
46. Additional file 3 of The CRCbiome study: a large prospective cohort study examining the role of lifestyle and the gut microbiome in colorectal cancer screening participants
47. The phylodynamics of SARS-CoV-2 during 2020 in Finland — Disappearance and re-emergence of introduced strains.
48. The rise and fall of Alpha and Beta variants of SARS-CoV2 in Finland in spring of 2021
49. Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity
50. Corrigendum: Adult-Onset Anti-Citrullinated Peptide Antibody-Negative Destructive Rheumatoid Arthritis Is Characterized by a Disease-Specific CD8+ T Lymphocyte Signature
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