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Down syndrome childhood acute lymphoblastic leukemia has a unique spectrum of sentinel cytogenetic lesions that influences treatment outcome: a report from the Children's Oncology Group
Hydroxyurea in essential thrombocythemia: rate and clinical relevance of responses by European LeukemiaNet criteria
Obesity is associated with an increased risk of monoclonal gammopathy of undetermined significance among black and white women
Diffuse large B-cell lymphomas with CDKN2A deletion have a distinct gene expression signature and a poor prognosis under R-CHOP treatment: a GELA study
XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission
Issue Archive
August 19 2010
Table of Contents
Inside blood
Plenary paper
PLENARY PAPER
Genomewide DNA methylation analysis reveals novel targets for drug development in mantle cell lymphoma
Violetta V. Leshchenko,Pei-Yu Kuo,Rita Shaknovich,David T. Yang,Tobias Gellen,Adam Petrich,Yiting Yu,Yvonne Remache,Marc A. Weniger,Sarwish Rafiq,K. Stephen Suh,Andre Goy,Wyndham Wilson,Amit Verma,Ira Braunschweig,Natarajan Muthusamy,Brad S. Kahl,John C. Byrd,Adrian Wiestner,Ari Melnick,Samir Parekh
Review Article
Clinical Trials and Observations
Down syndrome childhood acute lymphoblastic leukemia has a unique spectrum of sentinel cytogenetic lesions that influences treatment outcome: a report from the Children's Oncology Group
Clinical Trials & Observations
Kelly W. Maloney,William L. Carroll,Andrew J. Carroll,Meenakshi Devidas,Michael J. Borowitz,Paul L. Martin,Jeanette Pullen,James A. Whitlock,Cheryl L. Willman,Naomi J. Winick,Bruce M. Camitta,Stephen P. Hunger
Hydroxyurea in essential thrombocythemia: rate and clinical relevance of responses by European LeukemiaNet criteria
Clinical Trials & Observations
Alessandra Carobbio,Guido Finazzi,Elisabetta Antonioli,Alessandro M. Vannucchi,Giovanni Barosi,Marco Ruggeri,Francesco Rodeghiero,Federica Delaini,Alessandro Rambaldi,Tiziano Barbui
Obesity is associated with an increased risk of monoclonal gammopathy of undetermined significance among black and white women
Brief Report
Ola Landgren,S. Vincent Rajkumar,Ruth M. Pfeiffer,Robert A. Kyle,Jerry A. Katzmann,Angela Dispenzieri,Qiuyin Cai,Lynn R. Goldin,Neil E. Caporaso,Joseph F. Fraumeni,William J. Blot,Lisa B. Signorello
Diffuse large B-cell lymphomas with CDKN2A deletion have a distinct gene expression signature and a poor prognosis under R-CHOP treatment: a GELA study
Clinical Trials & Observations
Fabrice Jardin,Jean-Philippe Jais,Thierry-Jo Molina,Françoise Parmentier,Jean-Michel Picquenot,Philippe Ruminy,Hervé Tilly,Christian Bastard,Gilles-André Salles,Pierre Feugier,Catherine Thieblemont,Christian Gisselbrecht,Aurelien de Reynies,Bertrand Coiffier,Corinne Haioun,Karen Leroy
Hematopoiesis and Stem Cells
Immunobiology
XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
Brief Report
Rebecca A. Marsh,Lisa Madden,Brenda J. Kitchen,Rajen Mody,Brad McClimon,Michael B. Jordan,Jack J. Bleesing,Kejian Zhang,Alexandra H. Filipovich
Interferon-γ and tumor necrosis factor-α induce an immunoinhibitory molecule, B7-H1, via nuclear factor-κB activation in blasts in myelodysplastic syndromes
Asaka Kondo,Taishi Yamashita,Hideto Tamura,Wanhong Zhao,Takashi Tsuji,Masumi Shimizu,Eiji Shinya,Hidemi Takahashi,Koji Tamada,Lieping Chen,Kazuo Dan,Kiyoyuki Ogata
Lymphoid Neoplasia
MicroRNA expression in Sézary syndrome: identification, function, and diagnostic potential
Erica Ballabio,Tracey Mitchell,Marloes S. van Kester,Stephen Taylor,Heather M. Dunlop,Jianxiang Chi,Isabella Tosi,Maarten H. Vermeer,Daniela Tramonti,Nigel J. Saunders,Jacqueline Boultwood,James S. Wainscoat,Francesco Pezzella,Sean J. Whittaker,Cornelius P. Tensen,Christian S. R. Hatton,Charles H. Lawrie
Myeloid Neoplasia
Pediatric mastocytosis–associated KIT extracellular domain mutations exhibit different functional and signaling properties compared with KIT-phosphotransferase domain mutations
Ying Yang,Sébastien Létard,Laurence Borge,Amandine Chaix,Katia Hanssens,Sophie Lopez,Marina Vita,Pascal Finetti,Daniel Birnbaum,François Bertucci,Sophie Gomez,Paulo de Sepulveda,Patrice Dubreuil
Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission
Brief Report
Olivier Nibourel,Olivier Kosmider,Meyling Cheok,Nicolas Boissel,Aline Renneville,Nathalie Philippe,Hervé Dombret,François Dreyfus,Bruno Quesnel,Sandrine Geffroy,Samuel Quentin,Catherine Roche-Lestienne,Jean-Michel Cayuela,Christophe Roumier,Pierre Fenaux,William Vainchenker,Olivier A. Bernard,Jean Soulier,Michaëla Fontenay,Claude Preudhomme
Phagocytes, Granulocytes, and Myelopoiesis
Platelets and Thrombopoiesis
Transplantation
Vascular Biology
CD99 and CD99L2 act at the same site as, but independently of, PECAM-1 during leukocyte diapedesis
M. Gabriele Bixel,Hang Li,Bjoern Petri,Alexander G. Khandoga,Andrej Khandoga,Alexander Zarbock,Karen Wolburg-Buchholz,Hartwig Wolburg,Lydia Sorokin,Dagmar Zeuschner,Sigrid Maerz,Stefan Butz,Fritz Krombach,Dietmar Vestweber
Correspondence
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Cover Image
Cover Image
Three-dimensional reconstruction of the open canalicular system (blue) and dense tubular system (yellow) in nonstimulated human platelet. Electron tomography reveals close association and a highly intertwined nature of both membrane complexes. See the article by van Nispen tot Pannerden et al on page 1147.
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