399 results on '"Grossmann, V"'
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2. Prognostic impact and landscape of NOTCH1 mutations in chronic lymphocytic leukemia (CLL): a study on 852 patients
3. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
4. DIGITAL TWINNING IN THE OCEAN – CHALLENGES IN MULTIMODAL SENSING AND MULTISCALE FUSION BASED ON FAITHFUL VISUAL MODELS
5. Fusion von Tauchroboter- und Satellitenmessungen über unterschiedliche Skalen, Messmodelle und spektrale Abtastungen
6. Growth and characterization of II–VI semiconductor lasers
7. Stratifizierung des kardiovaskulären Risikos bei Patienten mit Typ-2-Diabetes
8. Overview of the Tycho Catalogue
9. The role of different genetic subtypes of CEBPA mutated AML
10. SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients
11. Monitoring of residual disease by next-generation deep-sequencing of RUNX1 mutations can identify acute myeloid leukemia patients with resistant disease
12. Prognostic impact and landscape of NOTCH1 mutations in chronic lymphocytic leukemia (CLL): a study on 852 patients
13. Age, JAK2V617F and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis
14. Acute erythroid leukemia (AEL) can be separated into distinct prognostic subsets based on cytogenetic and molecular genetic characteristics
15. High incidence of RAS signalling pathway mutations in MLL-rearranged acute myeloid leukemia
16. Landmark analysis of DNMT3A mutations in hematological malignancies
17. GATA2 mutations are frequent in intermediate-risk karyotype AML with biallelic CEBPA mutations and are associated with favorable prognosis
18. ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome
19. Landscape of TET2 mutations in acute myeloid leukemia
20. Deletion of the tumor-suppressor gene NF1 occurs in 5% of myeloid malignancies and is accompanied by a mutation in the remaining allele in half of the cases
21. The NPM1 wild-type OCI-AML2 and the NPM1-mutated OCI-AML3 cell lines carry DNMT3A mutations
22. The Interlaboratory RObustness of Next-generation sequencing (IRON) study: a deep sequencing investigation of TET2, CBL and KRAS mutations by an international consortium involving 10 laboratories
23. Targeted next-generation sequencing detects point mutations, insertions, deletions and balanced chromosomal rearrangements as well as identifies novel leukemia-specific fusion genes in a single procedure
24. A deep-sequencing study of chronic myeloid leukemia patients in blast crisis (BC-CML) detects mutations in 76.9% of cases
25. STAT3 mutations are highly specific for large granular lymphocytic leukemia
26. Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance
27. Methylation analysis of the proximal, distal and core promoter of CEBPA revealed high differences in frequencies but no impact on prognosis: V999
28. Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis
29. Chronic myelomonocytic leukemia (CMML) is characterized by frequent alterations in TET2, RUNX1, CBL, and RAS: A next-generation deep-sequencing study reveals a characteristic pattern of molecular mutations in 72.8% of patients: V758
30. COMPUTER ASSISTED OPERATION OF ASDEX UPGRADE REFLECTOMETRY DIAGNOSTIC
31. The role of the RAS pathway in iAMP21-ALL
32. Overview of the Tycho Catalogue
33. New developments for the control and data acquisition system of the reflectometry on ASDEX-Upgrade
34. Influence of driving conditions on the stability of ZnSe-based cw-laser diodes
35. Generation of misfit dislocations due to thermally induced strain – a study by temperature-dependent HRXRD
36. Förderung der natürlichen Geburt und Senkung der Kaiserschnittrate: Ergebnisse einer Interventionsstudie
37. Homoepitaxial laser diodes grown on conducting and insulating ZnSe substrates
38. Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
39. Comparison of HapMap and 1000 genomes reference panels in a large-scale genome-wide association study
40. Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study
41. A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
42. BRCC3 mutations in myeloid neoplasms
43. THE EFFECT OF SOME CARDIOVASCULAR DRUGS ON THE EXPERIMENTAL MYOCARDIAL INFARCT IN RATS
44. QUANTITATIVE EVALUATION OF EMG DURING THE DEVELOPMENT OF TETANUS TOXIN INTOXICATION OF RABBITS AND ITS POSSIBLE RELATION TO THE EFFECTS OF MYORELAXANT DRUGS
45. A CONTRIBUTION TO THE EFFECTS OF PROTECTIVE DRUGS
46. Veränderungen des Dolsinmetabolismus im Laufe der Irradiationskrankheit bei Ratten
47. High power T-Bars with narrow in-plane far-field angle
48. Landscape of genetic lesions in 944 patients with myelodysplastic syndromes
49. Advances in Microwave Reflectometry on ASDEX Upgrade
50. Routine Density Profiles with High Spatial and Temporal Resolutions from the FM-Broadband Reflectometry System in ASDEX Upgrade
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