39 results on '"Thomay, Kathrin"'
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2. Establishing a murine xenograft-model for long-term analysis of factors inducing chromosomal instability in myelodysplastic syndrome: Pitfalls and successes
3. Telomere shortening, TP53 mutations and deletions in chronic lymphocytic leukemia result in increased chromosomal instability and breakpoint clustering in heterochromatic regions
4. Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing
5. A child with Li–Fraumeni syndrome: Modes to inactivate the second allele of TP53 in three different malignancies
6. Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing.
7. Jumping translocations: Short telomeres or pathogenicTP53variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?
8. Routes of Clonal Evolution into Complex Karyotypes in Myelodysplastic Syndrome Patients with 5q Deletion
9. Pulmonary Transplantation of Human Induced Pluripotent Stem Cell–derived Macrophages Ameliorates Pulmonary Alveolar Proteinosis
10. Effect of TP53 contact and conformational mutations on cell survival and erythropoiesis of human hematopoietic stem cells in a long term culture model
11. Octasomy 21 in a patient with secondary AML after CMML: the role of acquired NRAS mutations in triggering aneuploidy
12. Mutational Spectrum of Fanconi Anemia Associated Myeloid Neoplasms
13. Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
14. Clinical and Molecular Heterogeneity of RTEL1 Deficiency
15. Clinical and Molecular Heterogeneity of RTE L1 Deficiency (vol 8, pg 449, 2017)
16. Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic Leukemia
17. Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency
18. Comparison of different methods for telomere length measurement in whole blood and blood cell subsets: Recommendations for telomere length measurement in hematological diseases
19. Clinical and Molecular Heterogeneity of RTEL1 Deficiency
20. Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
21. Telomere Shortening, TP53 Mutations and Deletions in Chronic Lymphocytic Leukemia Result in Increased Chromosomal Instability and Breakpoint Clustering in Heterochromatic Regions
22. Clinical Heterogeneity in RUNX1-Associated Familial Myelodysplastic Syndrome - Report of Two Novel Pedigrees with Childhoodleukemia
23. A common ancestral DNMT3A-mutated preleukemic clone giving rise to AML and MDS in an adolescent girl
24. Jumping translocations: Short telomeres or pathogenic TP53 variants as underlying mechanism in acute myeloid leukemia and myelodysplastic syndrome?
25. Identification of a Cryptic Insertion ins(11;X)(q23;q28q12) Resulting in a KMT2A-FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic Leukemia
26. No Observation of Chromosomal Instability after Transplantation of RPS14- and TP53-Modified Human HSCs in NSG/NSGS Mice
27. Dynamic Telomere Shortening and Chromosomal Instability in Irradiated CD34+ Cells Transduced with TP53 Hotspot Mutations R175H, R248W and R249S
28. Mutational Spectrum of Fanconi Anemia Associated Myeloid Neoplasms.
29. Identification of a Cryptic Insertion ins(11;X) (q23;q28q12) Resulting in a KMT2A - FLNA Fusion in a 13-Month-Old Child with Acute Myelomonocytic Leukemia.
30. A common ancestral DNMT3A-mutated preleukemic clone giving rise to AML and MDS in an adolescent girl.
31. Unbalanced Translocation t(5;17) Resulting In a TP53 Loss As Recurrent Aberration In Myelodysplastic Syndrome With Complex Karyotype
32. Numerical Aberrations Involving The X Chromosome As a New Recurrent Aberration In Patients With Chronic Lymphocytic Leukemia
33. Induction of Chromosomal Instability via Telomere Dysfunction and Epigenetic Alterations in Myeloid Neoplasia
34. No evidence for ITSN1 loss in a patient with mental retardation and complex chromosomal rearrangements of 21q21–21q22
35. Clinical and Molecular Heterogeneity of RTEL1 Deficiency
36. Clinical Heterogeneity in RUNX1-AssociatedFamilial Myelodysplastic Syndrome - Report of Two Novel Pedigrees with Childhoodleukemia
37. Telomere Shortening, TP53Mutations and Deletions in Chronic Lymphocytic Leukemia Result in Increased Chromosomal Instability and Breakpoint Clustering in Heterochromatic Regions
38. Dynamic Telomere Shortening and Chromosomal Instability in Irradiated CD34+ Cells Transduced with TP53Hotspot Mutations R175H, R248W and R249S
39. Unbalanced Translocation t(5;17) Resulting In a TP53 LossAs Recurrent Aberration In Myelodysplastic Syndrome With Complex Karyotype
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