British Journal of Haematology
Sequential fluorescence in situ hybridization for the quantification of minimal residual disease in recipient cells after sex-mismatched allogeneic stem cell transplantation
The natural history of a solitary plasmacytoma
The value of allogeneic bone marrow transplant in patients with acute myeloid leukaemia at differing risk of relapse: results of the UK MRC AML 10 trial
Superior effect of 9-cis retinoic acid (RA) compared with all-trans RA and 13-cis RA on the inhibition of clonogenic cellgrowth and the induction of apoptosis in OCI/AML-2 subclones: is the p53 pathway involved?
Minimal residual disease quantification in patients with acute myeloid leukaemia and inv(16)/CBFB-MYH11 gene fusion
Simultaneous induction of matrix metalloproteinase-9 and interleukin 8 by all-trans retinoic acid in human PL-21 and NB4 myeloid leukaemia cells
Distinct genetic patterns can be identified in acute monoblastic and acute monocytic leukaemia (FAB AML M5a and M5b): a study of 124 patients
SAB — a promising new treatment to improve remission rates in AML in the elderly?
Assessment of caspase activity as a possible prognostic factor in acute myeloid leukaemia
Diabetes insipidus as first manifestation of acute myeloid leukaemia with EVI-1-positive, 3q21q26 syndrome and T cell-line antigen expression: what is the EVI-1 gene role?
Persistent aplasia after chemotherapy for acute myeloid leukaemia treated with stem cell transplantation from a matched unrelated donor after dose-reduced conditioning
Failure of a new protocol to improve treatment results in paediatric lymphoblastic leukaemia: lessons from the UK Medical Research Council trials UKALL X and UKALL XI
Immunodeficiency-related lymphoproliferative disorders: prospective data from the United Kingdom Children's Cancer Study Group Registry
DNA microarray analysis of T cell-type lymphoproliferative disease of granular lymphocytes
Reliability of lymphoma classification in bone marrow trephines
Association between xenobiotic gene polymorphisms and non-Hodgkin's lymphoma risk
Expression of cutaneous lymphocyte antigen is associated with a poor outcome of nasal-type natural killer-cell lymphoma
CD95 (Fas) expression is regulated by sequestration in the Golgi complex in B-cell lymphoma
β2-microglobulin as a negative growth regulator of myeloma cells
Adenovirus transduction to effect CD40 signalling improves the immune stimulatory activity of myeloma cells
A molecular study of the t(4;14) in multiple myeloma
The anti-apoptotic genes Bcl-XL and Bcl-2 are over-expressed and contribute to chemoresistance of non-proliferating leukaemic CD34+ cells
Phosphatidylinositol 3-kinases are involved in the all-trans retinoic acid-induced upregulation of CD38 antigen on human haematopoietic cells
Long-term follow up with conventional cytogenetics and band 13q14 interphase/metaphase in situ hybridization monitoring in monoclonal gammopathies of undetermined significance
JH probe real-time quantitative polymerase chain reaction assay for Bcl-2/IgH rearrangements
Philadelphia chromosome-positive mature B-cell (Burkitt cell) leukaemia
The relative role of peripheral blood and bone marrow for monitoring molecular evidence of disease in follicular lymphoma by quantitative real-time polymerase chain reaction
Spontaneous remission of low-grade B-cell non-Hodgkin's lymphoma following withdrawal of methotrexate in a patient with rheumatoid arthritis: case report and review of the literature
Possible role of Marcks in the cellular modulation of monocytic tissue factor-initiated hypercoagulation
Acquired activated protein C resistance is associated with the co-existence of anti-prothrombin antibodies and lupus anticoagulant activity in patients with systemic lupus erythematosus
Effect of Helicobacter pylori eradication on platelet recovery in Japanese patients with chronic idiopathic thrombocytopenic purpura and secondary autoimmune thrombocytopenic purpura
A Tyr346→Cys substitution in the interdomain acidic region a1 of factor VIII in an individual with factor VIII:C assay discrepancy
Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia
The role of strain gauge plethysmography in the assessment of patients with suspected deep vein thrombosis
Protein C inhibitor (plasminogen activator inhibitor-3) and the risk of venous thrombosis
Prothrombin A19911G and G20210A polymorphisms' role in thrombosis
Protein C/S ratio, an accurate and simple tool to identify carriers of a protein C gene mutation
Erythroid 5-aminolevulinate synthase, ferrochelatase and DMT1 expression in erythroid progenitors: differential pathways for erythropoietin and iron-dependent regulation
Transforming growth factor-β1 causes transcriptional activation of CD34 and preserves haematopoietic stem/progenitor cell activity
MyD88 is involved in the signalling pathway for Taxol-induced apoptosis and TNF-α expression in human myelomonocytic cells
Protein kinase C-ζ overexpression induces erythroid phenotype in the monocytic leukaemia cell line U937
Induction and characterization of cutaneous lymphocyte antigen on natural killer cells
The membrane characteristics of Plasmodium falciparum-infected and -uninfected heterozygous α0thalassaemic erythrocytes
The β-globin C→G mutation at 6 bp 3′ to the termination codon causes β-thalassaemia by decreasing the mRNA level
The frequency of bleeding complications in patients with haematological malignancy following the introduction of a stringent prophylactic platelet transfusion policy
Prognostic significance of risk group stratification in elderly patients with acute myeloid leukaemia
Myeloid/natural killer cell precursor acute leukaemia with minor bcr/abl mRNA transcript