27 results on '"Göhring, G"'
Search Results
2. Epidemiological, genetic, and clinical characterization by age of newly diagnosed acute myeloid leukemia based on an academic population-based registry study (AMLSG BiO)
3. Increased megakaryocytic proliferation, pro-platelet deposition and expression of fibrosis-associated factors in children with chronic myeloid leukaemia with bone marrow fibrosis
4. Acute myeloid leukemia derived from lympho-myeloid clonal hematopoiesis
5. Validation of the revised IPSS at transplant in patients with myelodysplastic syndrome/transformed acute myelogenous leukemia receiving allogeneic stem cell transplantation: a retrospective analysis of the EBMT chronic malignancies working party
6. Enantiomer-specific and paracrine leukemogenicity of mutant IDH metabolite 2-hydroxyglutarate
7. Frequency and prognostic impact of casein kinase 1A1 mutations in MDS patients with deletion of chromosome 5q
8. Prognostic implications and molecular associations of NADH dehydrogenase subunit 4 (ND4) mutations in acute myeloid leukemia
9. Low frequency of calreticulin mutations in MDS patients
10. Prognostic effect of calreticulin mutations in patients with myelofibrosis after allogeneic hematopoietic stem cell transplantation
11. The clinical relevance of minor paroxysmal nocturnal hemoglobinuria clones in refractory cytopenia of childhood: a prospective study by EWOG-MDS
12. Marrow fibrosis predicts early fatal marrow failure in patients with myelodysplastic syndromes
13. Chromosomal aberrations in congenital bone marrow failure disorders—an early indicator for leukemogenesis?
14. Analysis of NUP98/NSD1 translocations in adult AML and MDS patients
15. Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML)
16. SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications
17. Long-term transfusion independence in del(5q) MDS patients who discontinue lenalidomide
18. Systemic mastocytosis (SM) with associated BCR-ABL-positive myelogenous leukaemia (SM-AHNMD): evidence that mast cells do not belong to the leukaemic clone
19. Global increase in DNA methylation in patients with myelodysplastic syndrome
20. P816: TRANSIENT MONOSOMY 7 IN SAMD9/9L SYNDROMES: IS IT SAFE TO WATCH AND WAIT?
21. Minimal Residual Disease-based Treatment is Adequate for Relapse-prone Childhood Acute Lymphoblastic Leukemia with an intrachromosomal amplification of chromosome 21: The experience of the ALL-BFM 2000 trial.
22. Chromosomal Instability and Telomere Shortening in Long-Term Culture of Hematopoietic Stem Cells: Insights from a Cell Culture Model of RPS14 Haploinsufficiency.
23. Prenatal diagnosis of an epignathus associated with a 49,XXXXY karyotype--a case report.
24. Generation of two iPSC clones (MHHi021-A and MHHi021-B) from a patient with hypertrophic cardiomyopathy with p.Arg723Gly mutation in the MYH7 gene.
25. Generation of two human ISG15 knockout iPSC clones using CRISPR/Cas9 editing.
26. 150 INFLUENCE OF TP53 MUTATIONS ON HEMATOPOIESIS IN MYELODYSPLASTIC SYNDROMES (MDS) AND ACUTE MYELOID LEUKEMIAS (AML).
27. Phosphoinositide Phospholipase C{beta}1 (PI-PLC{beta}1) Gene in Myelodysplastic Syndromes and Cytogenetically Normal Acute Myeloid Leukemia: Not a Deletion, but Increased PI-PLC{beta}1 Expression Is an Independent Prognostic Factor.
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