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PD-L1 expression on neoplastic or stromal cells is respectively a poor or good prognostic factor for adult T-cell leukemia/lymphoma
Integrating clinical features and genetic lesions in the risk assessment of patients with chronic myelomonocytic leukemia
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia
Issue Archive
Table of Contents
BLOOD FLASHBACK
INSIDE BLOOD COMMENTARIES
REVIEW ARTICLE
Treatment recommendations from the Eighth International Workshop on Waldenström’s Macroglobulinemia
Véronique Leblond,Efstathios Kastritis,Ranjana Advani,Stephen M. Ansell,Christian Buske,Jorge J. Castillo,Ramón García-Sanz,Morie Gertz,Eva Kimby,Charalampia Kyriakou,Giampaolo Merlini,Monique C. Minnema,Pierre Morel,Enrica Morra,Mathias Rummel,Ashutosh Wechalekar,Christopher J. Patterson,Steven P. Treon,Meletios A. Dimopoulos
CLINICAL TRIALS AND OBSERVATIONS
HEMATOPOIESIS AND STEM CELLS
IMMUNOBIOLOGY
IL-10+ regulatory B cells are enriched in cord blood and may protect against cGVHD after cord blood transplantation
Anushruti Sarvaria,Rafet Basar,Rohtesh S. Mehta,Hila Shaim,Muharrem Muftuoglu,Ahmad Khoder,Takuye Sekine,Elif Gokdemir,Kayo Kondo,David Marin,May Daher,Amin M. Alousi,Abdullah Alsuliman,Enli Liu,Betul Oran,Amanda Olson,Roy B. Jones,Uday Popat,Chitra Hosing,Richard Champlin,Elizabeth J. Shpall,Katayoun Rezvani
LYMPHOID NEOPLASIA
The genetics of nodal marginal zone lymphoma
Valeria Spina,Hossein Khiabanian,Monica Messina,Sara Monti,Luciano Cascione,Alessio Bruscaggin,Elisa Spaccarotella,Antony B. Holmes,Luca Arcaini,Marco Lucioni,Fabrizio Tabbò,Sakellarios Zairis,Fary Diop,Michaela Cerri,Sabina Chiaretti,Roberto Marasca,Maurilio Ponzoni,Silvia Deaglio,Antonio Ramponi,Enrico Tiacci,Laura Pasqualucci,Marco Paulli,Brunangelo Falini,Giorgio Inghirami,Francesco Bertoni,Robin Foà,Raul Rabadan,Gianluca Gaidano,Davide Rossi
PD-L1 expression on neoplastic or stromal cells is respectively a poor or good prognostic factor for adult T-cell leukemia/lymphoma
Clinical Trials & Observations
Hiroaki Miyoshi,Junichi Kiyasu,Takeharu Kato,Noriaki Yoshida,Joji Shimono,Shintaro Yokoyama,Hiroaki Taniguchi,Yuya Sasaki,Daisuke Kurita,Keisuke Kawamoto,Koji Kato,Yoshitaka Imaizumi,Masao Seto,Koichi Ohshima
Venetoclax responses of pediatric ALL xenografts reveal sensitivity of MLL-rearranged leukemia
Seong Lin Khaw,Santi Suryani,Kathryn Evans,Jennifer Richmond,Alissa Robbins,Raushan T. Kurmasheva,Catherine A. Billups,Stephen W. Erickson,Yuelong Guo,Peter J. Houghton,Malcolm A. Smith,Hernan Carol,Andrew W. Roberts,David C. S. Huang,Richard B. Lock
Targeting Epstein-Barr virus–transformed B lymphoblastoid cells using antibodies with T-cell receptor–like specificities
Junyun Lai,Wei Jian Tan,Chien Tei Too,Joanna Ai Ling Choo,Lan Hiong Wong,Fatimah Bte Mustafa,Nalini Srinivasan,Angeline Pei Chiew Lim,Youjia Zhong,Nicholas R. J. Gascoigne,Brendon J. Hanson,Soh Ha Chan,Jianzhu Chen,Paul A. MacAry
MYELOID NEOPLASIA
Integrating clinical features and genetic lesions in the risk assessment of patients with chronic myelomonocytic leukemia
Clinical Trials & Observations
Chiara Elena,Anna Gallì,Esperanza Such,Manja Meggendorfer,Ulrich Germing,Ettore Rizzo,Jose Cervera,Elisabetta Molteni,Annette Fasan,Esther Schuler,Ilaria Ambaglio,Maria Lopez-Pavia,Silvia Zibellini,Andrea Kuendgen,Erica Travaglino,Reyes Sancho-Tello,Silvia Catricalà,Ana I. Vicente,Torsten Haferlach,Claudia Haferlach,Guillermo F. Sanz,Luca Malcovati,Mario Cazzola
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia
Brief Report
Katarina Kapralova,Monika Horvathova,Christian Pecquet,Jana Fialova Kucerova,Dagmar Pospisilova,Emilie Leroy,Barbora Kralova,Jelena D. Milosevic Feenstra,Fiorella Schischlik,Robert Kralovics,Stefan N. Constantinescu,Vladimir Divoky
TRANSPLANTATION
LETTERS TO BLOOD
BLOOD WORK
ERRATA
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Cover Image
Cover Image
Erythroid hyperplasia detected by immunohistochemical staining for glycophorin C (brown) in bone marrow biopsy from a patient with hereditary erythrocytosis and megakaryocytic atypia caused by coinheritance of 2 weakly activating JAK2 mutations. See the article by Kapralova et al on page 1418.
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