January, 2010
No. 95 (1)


Review Articles

Anti-CD20 monoclonal antibodies: historical and future perspectives (2386 Online Views)

Sean H. Lim, Stephen A. Beers, Ruth R. French, Peter W.M. Johnson, Martin J. Glennie, Mark S. Cragg



Gene expression factors as predictors of genetic risk and survival in chronic lymphocytic leukemia (478 Online Views)

Dirk Kienle, Axel Benner, Carolin Läufle, Dirk Winkler, Christof Schneider, Andreas Bühler, Thorsten Zenz, Annett Habermann, Ulrich Jäger, Peter Lichter, Riccardo Dalla-Favera, Hartmut Döhner, Stephan Stilgenbauer


Arterial cardiovascular risk factors and venous thrombosis: results from a population-based, prospective study (the HUNT 2) (1048 Online Views)

Petter Quist-Paulsen, Inger Anne Næss, Suzanne C. Cannegieter, Pål R. Romundstad, Sverre C. Christiansen, Frits R. Rosendaal, Jens Hammerstrøm


Thymosin β4 has tumor suppressive effects and its decreased expression results in poor prognosis and decreased survival in multiple myeloma (613 Online Views)

Jo Caers, Dirk Hose, Ine Kuipers, Tomas Jan Bos, Els Van Valckenborgh, Eline Menu, Elke De Bruyne, Hartmut Goldschmidt, Ben Van Camp, Bernard Klein, Karin Vanderkerken


TFG, a target of chromosome translocations in lymphoma and soft tissue tumors, fuses to GPR128 in healthy individuals (828 Online Views)

Andrew Chase, Thomas Ernst, Andreas Fiebig, Andrew Collins, Francis Grand, Philipp Erben, Andreas Reiter, Stefan Schreiber, Nicholas C.P. Cross


Rac1 and Rac2 GTPases are necessary for early erythropoietic expansion in the bone marrow but not in the spleen (649 Online Views)

Theodosia A. Kalfa, Suvarnamala Pushkaran, Xiaoling Zhang, James F. Johnson, Dao Pan, Deidre Daria, Hartmut Geiger, Jose A. Cancelas, David A. Williams, Yi Zheng


Hereditary thrombocytosis caused by MPLSer505Asn is associated with a high thrombotic risk, splenomegaly and progression to bone marrow fibrosis (652 Online Views)

Luciana Teofili, Fiorina Giona, Lorenza Torti, Tonia Cenci, Bianca Maria Ricerca, Carlo Rumi, Vittorio Nunes, Robin Foà, Giuseppe Leone, Maurizio Martini, Luigi Maria Larocca


Combined interphase fluorescence in situ hybridization elucidates the genetic heterogeneity of T-cell acute lymphoblastic leukemia in adults (467 Online Views)

Paolo Gorello, Roberta La Starza, Emanuela Varasano, Sabina Chiaretti, Loredana Elia, Valentina Pierini, Gianluca Barba, Lucia Brandimarte, Barbara Crescenzi, Antonella Vitale, Monica Messina, Sara Grammatico, Marco Mancini, Caterina Matteucci, Antonella Bardi, Anna Guarini, Massimo Fabrizio Martelli, Robin Foà, Cristina Mecucci


Concurrent intensive chemotherapy and imatinib before and after stem cell transplantation in newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia. Final results of the CSTIBES02 trial (966 Online Views)

Josep-Maria Ribera, Albert Oriol, Marcos González, Belén Vidriales, Salut Brunet, Jordi Esteve, Eloy del Potro, Concepción Rivas, Maria-José Moreno, Mar Tormo, Victoria Martín-Reina, Josep Sarrá, Ricardo Parody, Jaime Pérez de Oteyza, Encarna Bureo, Maria-Teresa Bernal


Correlations between BCL6 rearrangement and outcome in patients with diffuse large B-cell lymphoma treated with CHOP or R-CHOP (1183 Online Views)

Jesse Shustik, Guangming Han, Pedro Farinha, Nathalie A. Johnson, Susana Ben Neriah, Joseph M. Connors, Laurie H. Sehn, Douglas E. Horsman, Randy D. Gascoyne, Christian Steidl


Brief Reports

A polymorphism associated with STAT3 expression and response of chronic myeloid leukemia to interferon α (403 Online Views)

Sebastian Kreil, Katherine Waghorn, Thomas Ernst, Andrew Chase, Helen White, Rüdiger Hehlmann, Andreas Reiter, Andreas Hochhaus, Nicholas C.P. Cross


Letters to the Editor

Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia (307 Online Views)

Marina Lanciotti, Stefania Indaco, Sonia Bonanomi, Tiziana Coliva, Elena Mastrodicasa, Gianluca Caridi, Michaela Calvillo, Carlo Dufour


Acute Promyelocytic Leukemia

Disorders of Hemostasis

Premature termination codon mutations in the von Willebrand factor gene are associated with allele-specific and position-dependent mRNA decay (425 Online Views)

Manuela Platè, Stefano Duga, Luciano Baronciani, Silvia La Marca, Valentina Rubini, Pier Mannuccio Mannucci, Augusto B. Federici, Rosanna Asselta