All Stories

  1. The role of diet in cancer: the potential of shaping public policy and clinical outcomes in the UK
  2. Effect of MYC and PARP Inhibitors in Ovarian Cancer Using anIn VitroModel
  3. Alterations in Genome Organization in Lymphoma Cell Nuclei due to the Presence of the t(14;18) Translocation
  4. Pan-Cancer Analysis Identifies MNX1 and Associated Antisense Transcripts as Biomarkers for Cancer
  5. Engineered model of t(7;12)(q36;p13) AML recapitulates patient-specific features and gene expression profiles
  6. Alterations to Genome Organisation in Stem Cells, Their Differentiation and Associated Diseases
  7. Chromosomal Rearrangements and Altered Nuclear Organization: Recent Mechanistic Models in Cancer
  8. Preclinical Studies on the Effect of Rucaparib in Ovarian Cancer: Impact of BRCA2 Status
  9. From FISH to Hi-C: The Chromatin Architecture of the Chromosomal Region 7q36.3, Frequently Rearranged in Leukemic Cells, Is Evolutionary Conserved
  10. MLL-Rearranged Acute Leukemia with t(4;11)(q21;q23)—Current Treatment Options. Is There a Role for CAR-T Cell Therapy?
  11. The RS4;11 cell line as a model for leukaemia with t(4;11)(q21;q23): Revised characterisation of cytogenetic features
  12. Deletions of Chromosome 7q Affect Nuclear Organization and HLXB9Gene Expression in Hematological Disorders
  13. Insights into maternal diet for the prevention of childhood leukaemia
  14. Genomic properties of chromosomal bands are linked to evolutionary rearrangements and new centromere formation in primates
  15. Folate deficiency as predisposing factor for childhood leukaemia: a review of the literature
  16. Nuclear Repositioning of the Non-Translocated <b><i>HLXB9</i></b> Allele in the Leukaemia Cell Line GDM-1 Harbouring a t(6;7)(q23;q36)
  17. Paediatric acute myeloid leukaemia with the t(7;12)(q36;p13) rearrangement: a review of the biological and clinical management aspects
  18. Detection of t(7;12)(q36;p13) in paediatric leukaemia using dual colour fluorescence in situ hybridisation
  19. Automated Detection of Fluorescent Probes in Molecular Imaging
  20. HLXB9 Gene Expression, and Nuclear Location during In Vitro Neuronal Differentiation in the SK-N-BE Neuroblastoma Cell Line
  21. A Novel Three-Colour Fluorescence in Situ Hybridization Approach for the Detection of t(7;12)(q36;p13) in Acute Myeloid Leukaemia Reveals New Cryptic Three Way Translocation t(7;12;16)
  22. Interphase Chromosome Behavior in Normal and Diseased Cells
  23. Genomic Imbalances Are Confined to Non-Proliferating Cells in Paediatric Patients with Acute Myeloid Leukaemia and a Normal or Incomplete Karyotype
  24. Fluorescence in situ Hybridization (FISH), Basic Principles and Methodology
  25. Mutations of NFKBIA, encoding IκBα, are a recurrent finding in classical Hodgkin lymphoma but are not a unifying feature of non‐EBV‐associated cases
  26. Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias
  27. The radial arrangement of the human chromosome 7 in the lymphocyte cell nucleus is associated with chromosomal band gene density
  28. Graft versus leukemia effect after haploidentical HSCT in a MLL‐negative infant AML with HLXB9/ETV6 rearrangement
  29. Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98–C6orf80 fusion in a case of acute megakaryoblastic leukemia
  30. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia
  31. Human Chromosome 7: DNA Sequence and Biology
  32. Narrowing and genomic annotation of the commonly deleted region of the 5q− syndrome
  33. Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wlds) mouse
  34. Familial partial monosomy 7 and myelodysplasia
  35. t(7;12)(q36;p13), a new recurrent translocation involvingETV6 in infant leukemia
  36. The Tyrosine Kinase Abl-Related Gene ARG Is Fused toETV6 in an AML-M4Eo Patient With a t(1;12)(q25;p13): Molecular Cloning of Both Reciprocal Transcripts
  37. Delineation of multiple deleted regions in 7q in myeloid disorders
  38. Characterization of the human myeloid leukemia‐derived cell line GF‐D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization
  39. Identification of new partner chromosomes involved in fusions with the ETV6 TEL gene in hematologic malignancies
  40. Identification of new partner chromosomes involved in fusions with theETV6 (TEL) gene in hematologic malignancies
  41. Unbalanced t(3;12) in a case of juvenile myelomonocytic leukemia (JMML) results in partial trisomy of 3q as defined by FISH
  42. Molecular Cytogenetic Analysis of 7q Abnormalities in Acute Leukemia
  43. Detection of the breakpoint cluster region-ABL fusion in chronic myeloid leukemia with variant Philadelphia chromosome translocations by in situ hybridization
  44. Physical mapping of the human T-cell receptor beta gene complex, using yeast artificial chromosomes
  45. Reciprocal translocation t(12;13)(p13;q14) in acute nonlymphoblastic leukemia: Report and cytogenetic analysis of two cases
  46. Double target in situ hybridization applied to the study of numerical aberrations in childhood acute lymphoblastic leukemia
  47. First-trimester human trophoblast is class II major histocompatibility complex mRNA+/antigen−
  48. Establishment and characterization of a new granulocyte-macrophage colony-stimulating factor-dependent and interleukin-3-dependent human acute myeloid leukemia cell line (GF-D8)
  49. Microgranular variant of acute promyelocytic leukemia in children.
  50. Detection of Chromosome Abnormalities in Leukemia Using Fluorescence In Situ Hybridization