LOW MOLECULAR WEIGHT HEPARIN(S)
Modulation of cell kinetics and cell cycle status by treating CD34 sup + chronic myeloid leukaemia cells with p53 antisense phosphorothioate oligonucleotides
Effects of interleukin-12 on natural killer cell cytotoxicity and the production of interferon-gamma and tumour necrosis factor-alpha in patients with myelodysplastic syndromes
Scintigraphic evaluation of the haemopoietic bone marrow using a sup 99m Tc-anti-granulocyte antibody : a validation study with sup 52 Fe
Administration of rHuGM-CSF activates monocyte reactive oxygen species secretion and adhesion molecule expression in vivo in patients following high-dose chemotherapy
The effect of continuous G-CSF application in human cyclic neutropenia : a model analysis
Clonal and non-clonal karyotypically abnormal cells in haemophagocytic lymphohistiocytosis
Enhanced Mg sup 2+ -ATPase activity in ghosts from HS erythrocytes and in normal ghosts stripped of membrane skeletal proteins may reflect enhanced aminophospholipid translocase activity
Low plasma heparin cofactor II levels in thalassaemia syndromes are corrected by chronic blood transfusion
Haemoglobin Tunis-Bizerte : a new alpha sub 1 globin 129 Leu-->Pro unstable variant with thalassaemic phenotype
Leukaemic non-Hodgkin's lymphomas with hyperdiploid cells and t(11;14)(q13;q32) : a subtype of mantle cell lymphoma?
Assessment of clonal evolution at Ig/TCR loci in acute lymphoblastic leukaemia by single-strand conformation polymorphism studies and highly resolutive PCR derived methods : implication for a general strategy of minimal residual disease detection
Over-expression and amplification of the CDC2 gene in leukaemia cells
Clinical significance of serum thymidine kinase in adult T-cell leukaemia and acute myeloid leukaemia
Prognostic implications of DNA aneuploidy in 156 untreated multiple myeloma patients
Idiotypic oligonucleotide probes to detect myeloma cells by mRNA in situ hybridization
Der(16)t(1;16)(q11;q11) in myelodysplastic syndromes : a new non-random abnormality characterized by cytogenic and fluorescence in situ hybridization studies
Prognostic relevance of serum thymidine kinase in primary myelodysplastic syndromes : relationship to development of acute myeloid leukaemia
Clonal analysis of haemopoietic cells in essential thrombocythaemia
Characterization of genomic BCR-ABL breakpoints in chronic myeloid leukaemia by PCR
Hemizygous expression of the wild-type p53 allele may confer a selective growth advantage before complete inactivation of the p53 gene in the progression of chronic myelogenous leukaemia
Evidence for a paracrine pathway of B-cell stimulation in hairy cell leukaemia
Analysis of heat-shock protein expression in myeloid leukaemia cells by flow cytometry
Attenuated-dose idarubicin in acute myeloid leukaemia of the elderly : pharmacokinetic study and clinical results
Evidence for a light chain restriction of glycoprotein Ib/IX and IIb/IIIa reactive antibodies in chronic idiopathic thrombocytopenic purpura (ITP)
A low M sub r GTP-binding protein, Rap1, in human platelets : localization, translocation and phosphorylation by cyclic AMP-dependent protein kinase
Fibrin degradation product (FnDP) assays : analysis of standardization issues and target antigens in plasma
A monoclonal antibody (B724) to von Willebrand factor recognizing an epitope within the A1 disulphide loop (Cys509-Cys695) discriminates between type 2A and type 2B von Willebrand disease
Resistance to activated protein C activity of an anti-beta sub 2 -glycoprotein I antibody in the presence of beta sub 2 -glycoprotein I
Acquired hypochromic and microcytic sideroblastic anaemia responsive to pyridoxine with low value of free erythrocyte protoporphyrin : a possible subgroup of idiopathic acquired sideroblastic anaemia (IASA)
Random X chromosome inactivation in a female with a variant of Wiskott-Aldrich syndrome
Successful bone marrow transplantation for idiopathic hypereosinophilic syndrome
Refractory cytopenia with t(1;7), +8 abnormality and dysplastic eosinophils showing intranuclear Charcot-Leyden crystals : a fluorescence in situ hybridization study
Expression of an erythropoietin-like gene in the trout
The fusion of TEL and ABL in human acute lymphoblastic leukaemia is a rare event
Detection of the BCR-ABL gene by reverse transcription/polymerase chain reaction and fluorescence in situ hybridization in a patient with Philadelphia chromosome negative acute lymphoblastic leukaemia
Haemoglobin Dhofar is linked to the codon 29 C --> T (IVS-1 nt -- 3) splice mutation which causes beta sup + thalassaemia
G-CSF and Neutrophil Chemotaxis
G-CSF and Neutrophil Chemotaxis
The Molecular Genetics of Haemostasis and its Inherited Disorders
Bone Marrow Transplantation