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BRITISH JOURNAL OF HAEMATOLOGY (PRINT)
Rivista
Codice:
E025360
ISSN:
0007-1048
Dati Generali
Dati Generali
Pubblicazioni (71)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
18F-fluorodeoxyglucose positron emission tomography/computed tomography in the evaluation of early response in a primary hepatic lymphoma
Articolo
A NEW BETA-THALASSEMIA FRAMESHIFT MUTATION DETECTED BY PCR AFTER SELECTIVE HYBRIDIZATION TO IMMOBILIZED OLIGONUCLEOTIDES
Articolo
A Sardinian founder mutation in glycoprotein Ib platelet subunit beta(GP1BB) that impacts thrombocytopenia
Articolo
A beta-thalassemia phenotype not linked to the beta-globin cluster in an italian family
Articolo
A novel silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF.
Articolo
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemia.
Articolo
Assessment of metabolic activity by PET-CT with F-18-FDG in patients with T-cell lymphoma
Articolo
Assessment of metabolic activity by PET-CT with F-18-FDG in patients with T-cell lymphoma
Articolo
Assessment of metabolic activity by PET-CT with F-18-FDG in patients with T-cell lymphoma.
Articolo
Ataluren improves myelopoiesis and neutrophil chemotaxis by restoring ribosome biogenesis and reducing p53 levels in Shwachman-Diamond syndrome cells
Articolo
Balance of TGF-Beta1 and PDGF-BB is associated with kidney allograft rejection
Articolo
Beta+45 G --> C: a novel silent beta-thalassaemia mutation, the first in the Kozak sequence
Articolo
Beta-thalassaemia-87 C > G: relationship of the Hb F modulation and polymorphisms in compound heterozygous patients
Articolo
CTLA-4 expressed by chemoresistant, as well as untreated, myeloid leukaemia cells can be targeted with ligands to induce apoptosis.
Articolo
Cardiac complications and diabetes in thalassaemia major: A large historical multicentre study
Articolo
Chemotherapy after PD-1 inhibitors in relapsed/refractory Hodgkin lymphoma: Outcomes and clonal evolution dynamics
Articolo
Cholelithiasis and Gilbert's syndrome in homozygous beta thalassaemia
Articolo
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts (RAEB).
Articolo
Clinical proof of concept for a safe and effective NF-kappa B-targeting strategy in multiple myeloma
Articolo
Clinical significance ofTFR2andEPORexpression in bone marrow cells in myelodysplastic syndromes
Articolo
Deguelin, A PI3K/AKT inhibitor, enhances chemosensitivity of leukaemia cells with an active PI3K/AKT pathway,
Articolo
Detection of serine 473 phosphorylated Akt in acute myeloid leukaemia blasts by flow cytometry,
Articolo
Different switching patterns of beta-thalassaemic mutations at the proximal and distal CACCC box of the human HBB (beta-globin) gene
Articolo
Endothelin-1 receptor blockade as new possible therapeutic approach in multiple myeloma
Articolo
Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markers
Articolo
Fetal hemoglobin expression in the compound heterozygous state for nondeletional HPFH and beta-thalassemia
Abstract
Fetal hemoglobin expression in the compound heterozygous state for nondeletional HPFH and beta-thalassemia
Abstract
Flow cytometry detection of serotonin content and release in resting and activated platelets.
Articolo
Genetic polymorphism of the major regulatory element HS-40 upstream of the human alpha-globin gene cluster.
Articolo
Glucose 6-phosphate dehydrogenase deficiency red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia
Articolo
HEPATIC ERYTHROPOIETIN ENHANCED PRODUCTION IN ANEPHRIC RATS WITH HYPERPLASIA OF KUPFFER CELLS
Articolo
HIV-1 matrix protein p17 enhances the proliferative activity of natural killer cells and increases their ability to secrete proinflammatory cytokines.
Articolo
Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala > Pro and Hb Caserta alpha2 26 Ala > Thr) in a single HBA2 gene
Articolo
In reply to Schafer et al: new evidence on the role of endothelin-1 axis as a potential therapeutic target in multiple myeloma
Articolo
In vivo anti-myeloma activity and modulation of gene expression profile induced by valproic acid, a histone deacetylase inhibitor.
Articolo
In vivo metabolic studies of glucose, ATP and 2,3-DPG in alpha-thalassemia intermedia, Heterozygous beta-thalassemic and normal erythrocytes: 13C and 31P MRS studies
Articolo
Induction of therapeutic levels of HbF in genome-edited primary beta(0)39-thalassaemia haematopoietic stem and progenitor cells
Articolo
Infant ALL patients carrying t(4;11) have a different genotypic profile than older ALL children
Abstract
Influence of age, sex and ethnicity on platelet count in five Italian geographic isolates: mild thrombocytopenia may be physiological
Articolo
Influence of age, sex and ethnicity on platelet count in five Italian geographic isolates: mild thrombocytopenia may be physiological.
Articolo
Italian external and multicentric validation of the MD Anderson Cancer Center nomogram and prognostic index for chronic lymphocytic leukaemia patients: analysis of 1502 cases
Articolo
KINETICS OF ERYTHROID AND MYELOID STEM CELLS IN POST HYPOXIA POLYCYTHEMIA
Articolo
Mesenchymal stromal cells primed with Paclitaxel attract and kill leukaemia cells, inhibit angiogenesis and improve survival of leukaemia-bearing mice
Articolo
Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.
Articolo
Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity correlation genotype-phenotype description of a new variant (G6PD Neapolis).
Articolo
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)
Articolo
Myeloperoxidase gene expression in non-infant pro-B acute lymphoblastic leukaemia with or without ALL1/AF4 transcript
Articolo
Novel 2'-substituted, 3'-deoxy-phosphatidyl-myo-inositol analogues reduce drug resistance in human leukaemia cell lines with an activated phosphoinositide 3-kinase/Akt pathway,
Articolo
Phosphoinositide 3-kinase/Akt inhibition increases arsenic trioxide-induced apoptosis of acute promyelocytic and T-cell leukaemias,
Articolo
Promoter mutations producing mild beta-thalassaemia in the Italian population
Articolo
Reduced IL-33 plasma levels in multiple myeloma patients are associated with more advanced stage of disease.
Articolo
Reduced IL-33 plasma levels in multiple myeloma patients are associated with more advanced stage of disease.
Articolo
Regulation of the human HBA genes by KLF4 in erythroid cell lines
Articolo
Regulation of the human HBA genes by KLF4 in erythroid cell lines.
Articolo
Response to different treatments in chronic myelogenous leukemia (CML) according to risk assessment at diagnosis: survival advantage with interferon alfa therapy.
Abstract
SDS with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability
Articolo
Severe erythrocyte adenylate kinase deficiency due to homozygous A -> G substitution at codon 164 of human AK1 gene associated with chronic haemolytic anaemia
Articolo
Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
Articolo
Spectrin Cosenza: a novel Beta chain variant associated with Sp AlphaI/74 hereditary elliptocytosis
Articolo
Spectrin Cosenza: a novel beta chain variant associated with Sp alphaI/74 Hereditary Elliptocytosis
Articolo
Temsirolimus, an mTOR inhibitor, in combination with lower-dose clofarabine as salvage therapy for older patients with acute myeloid leukaemia: results of a phase II GIMEMA study (AML-1107)
Articolo
Thalassaemia-like carriers not linked to the beta-globin gene cluster.
Articolo
The C-T substitution in the distal CACCC box of the ?-globin gene promoter is a common cause of silent ? thalassaemia in the Italian population
Articolo
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassemia in the italian population
Articolo
The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta-thalassemia in the italian population
Articolo
The DNA-binding drugs mithramycin and chromomycin are powerful inducers of erythroid differentiation of human K562 cells
Articolo
The Germinal centre-derived lymphomas seen through their cellular microenvironment
Articolo
The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLF.
Articolo
The long-acting anti-C5 ravulizumab results in C3 binding to PNH red cells similar to its parental molecule eculizumab
Articolo
The safety and effectiveness of deferiprone in a large-scale, 3-year study in italian patients
Articolo
Transcript profiling of human dendritic cells maturation-induced under defined culture conditions: comparison of the effects of tumour necrosis factor alpha, soluble CD40 ligand trimer and interferon gamma.
Articolo
No Results Found
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