1,896 results on '"Schlegelberger, Brigitte"'
Search Results
2. Recurrent DNMT3B rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
3. Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)
4. An artificial intelligence-assisted clinical framework to facilitate diagnostics and translational discovery in hematologic neoplasia
5. Cytogenetics and genomics in CML and other myeloproliferative neoplasms
6. Publisher Correction: Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker
7. European standard clinical practice – Key issues for the medical care of individuals with familial leukemia
8. MiR-129-5p exerts Wnt signaling-dependent tumor-suppressive functions in hepatocellular carcinoma by directly targeting hepatoma-derived growth factor HDGF
9. OnkoRiskNET: a multicenter, interdisciplinary, telemedicine-based model to improve care for patients with a genetic tumor risk syndrome
10. Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker
11. Guiding the global evolution of cytogenetic testing for hematologic malignancies
12. Classification of fluorescent R-Band metaphase chromosomes using a convolutional neural network is precise and fast in generating karyograms of hematologic neoplastic cells
13. Knockout of the HMG domain of the porcine SRY gene causes sex reversal in gene-edited pigs
14. Cytogenetics in Haematology
15. Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
16. Review of guidelines for the identification and clinical care of patients with genetic predisposition for hematological malignancies
17. Altered enhancer-promoter interaction leads to MNX1expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)
18. Germline variants drive myelodysplastic syndrome in young adults
19. Students’ attitudes towards somatic genome editing versus genome editing of the germline using an example of familial leukemia
20. Somatic variant profiling in chronic phase pediatric chronic myeloid leukemia
21. IDH1/2 mutations in acute myeloid leukemia patients and risk of coronary artery disease and cardiac dysfunction—a retrospective propensity score analysis
22. Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
23. Risk of tumor lysis syndrome in patients with acute myeloid leukemia treated with venetoclax-containing regimens without dose ramp-up
24. High-risk additional chromosomal abnormalities at low blast counts herald death by CML
25. Wnt status-dependent oncogenic role of BCL9 and BCL9L in hepatocellular carcinoma
26. Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia
27. Treatment and outcome of IG-MYC+ neoplasms with precursor B-cell phenotype in childhood and adolescence
28. Altered NFE2 activity predisposes to leukemic transformation and myelosarcoma with AML-specific aberrations
29. Altered enhancer-promoter interaction leads toMNX1expression in pediatric acute myeloid leukemia with t(7;12)(q36;p13)
30. Somatic variant profiling in chronic phase pediatric chronic myeloid leukemia
31. Measurable residual disease monitoring by NGS before allogeneic hematopoietic cell transplantation in AML
32. 12q14 microdeletion syndrome: A family with short stature and Silver-Russell syndrome (SRS)-like phenotype and review of the literature
33. Homozygous frame shift variant in ATP7B exon 1 leads to bypass of nonsense-mediated mRNA decay and to a protein capable of copper export
34. A tandem duplication of BRCA1 exons 1–19 through DHX8 exon 2 in four families with hereditary breast and ovarian cancer syndrome
35. Clonal Dominance of Hematopoietic Stem Cells Triggered by Retroviral Gene Marking
36. Induction of Aneuploidy by Increasing Chromosomal Instability during Dedifferentiation of Hepatocellular Carcinoma
37. S120: MNX1-ACTIVATING ENHANCER HIJACKING EVENTS IN ACUTE MYELOID LEUKEMIA WITH DELETIONS ON CHROMOSOME 7Q
38. P322: DECIPHERING THE UNDERLYING MOLECULAR COMPLEXITY OF THE IKZF1PLUS SIGNATURE
39. Impact of Molecular Genetics on Outcome in Myelofibrosis Patients after Allogeneic Stem Cell Transplantation
40. The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants
41. P3 - SPECTRUM OF CLINICAL PHENOTYPES AND SOMATIC VARIANTS IN RUNX1-ASSOCIATED FAMILIAL PLATELET DISORDER WITH PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES
42. P2 - VARIANT PROFILING IN PEDIATRIC CHRONIC MYELOID LEUKEMIA
43. OC 19 - FUNCTIONAL ANALYSES OF RUNX1 VARIANTS IN THE CONTEXT OF FAMILIAL PLATELET DISORDER WIT PREDISPOSITION TO HEMATOLOGIC MALIGNANCIES
44. Front-line imatinib treatment in children and adolescents with chronic myeloid leukemia: results from a phase III trial
45. MLL is Fused to CBP, a Histone Acetyltransferase, in Therapy-Related Acute Myeloid Leukemia with a t(11;16)(q23;p13.3)
46. Functional characterization of novel or yet uncharacterized ATP7B missense variants detected in patients with clinical Wilson's disease
47. Genetic susceptibility in children, adolescents, and young adults diagnosed with soft-tissue sarcomas
48. Parallel deletion and duplication at 7q11.23 in a silent carrier for two reciprocal syndromic disorders
49. A Novel Alu Element Insertion in ATM Induces Exon Skipping in Suspected HBOC Patients
50. Rare and potentially fatal ‐ Cytogenetically cryptic TNIP1::PDGFRB and PCM1::FGFR1 fusion leading to myeloid/lymphoid neoplasms with eosinophilia in children
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