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Brief Reports
Citations 131-140 of 1234 total displayed.
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Past content
(since Jul 1999):
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Cellular microRNA expression correlates with susceptibility of monocytes/macrophages to HIV-1 infection
- Xu Wang, Li Ye, Wei Hou, Yu Zhou, Yan-Jian Wang, David S. Metzger, and Wen-Zhe Ho
Blood 2009; 113: 671-674.
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R93W mutation in Orai1 causes impaired calcium influx in platelets
- Wolfgang Bergmeier, Masatsugu Oh-hora, Christie-Ann McCarl, R. Claire Roden, Paul F. Bray, and Stefan Feske
Blood 2009; 113: 675-678.
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Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor XIII: a novel form of acquired factor XIII deficiency
- Éva Ajzner, Ágota Schlammadinger, Adrienne Kerényi, Zsuzsanna Bereczky, Éva Katona, Gizella Haramura, Zoltán Boda, and László Muszbek
Blood 2009; 113: 723-725.
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Thyroid function following hematopoietic cell transplantation in children: 30 years' experience
- Jean E. Sanders, Paul A. Hoffmeister, Ann E. Woolfrey, Paul A. Carpenter, Barry E. Storer, Rainer F. Storb, and Frederick R. Appelbaum
Blood 2009; 113: 306-308.
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Mutation of the β1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly
- Shinji Kunishima, Ryoji Kobayashi, Tomohiko J. Itoh, Motohiro Hamaguchi, and Hidehiko Saito
Blood 2009; 113: 458-461.
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A high-mobility, low-cost phenotype defines human effector-memory CD8+ T cells
- Gabriela Zenhaeusern, Patrick Gubser, Petra Eisele, Olivier Gasser, Andrea Steinhuber, Andrej Trampuz, Christoph Handschin, Andrew D. Luster, and Christoph Hess
Blood 2009; 113: 95-99.
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AT-101 induces apoptosis in CLL B cells and overcomes stromal cell–mediated Mcl-1 induction and drug resistance
- Kumudha Balakrishnan, Jan A. Burger, William G. Wierda, and Varsha Gandhi
Blood 2009; 113: 149-153.
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Characteristics and outcome of chronic myeloid leukemia patients with F317L BCR-ABL kinase domain mutation after therapy with tyrosine kinase inhibitors
- Elias Jabbour, Hagop M. Kantarjian, Dan Jones, Neeli Reddy, Susan O'Brien, Guillermo Garcia-Manero, Jan Burger, and Jorge Cortes
Blood 2008; 112: 4839-4842.
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Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
- Veronique Frémeaux-Bacchi, Elizabeth C. Miller, M. Kathryn Liszewski, Lisa Strain, Jacques Blouin, Alison L. Brown, Nadeem Moghal, Bernard S. Kaplan, Robert A. Weiss, Karl Lhotta, Gaurav Kapur, Tej Mattoo, Hubert Nivet, William Wong, Sophie Gie, Bruno Hurault de Ligny, Michel Fischbach, Ritu Gupta, Richard Hauhart, Vincent Meunier, Chantal Loirat, Marie-Agnès Dragon-Durey, Wolf H. Fridman, Bert J. C. Janssen, Timothy H. J. Goodship, and John P. Atkinson
Blood 2008; 112: 4948-4952.
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BCR-ABL fusion transcript types and levels and their interaction with secondary genetic changes in determining the phenotype of Philadelphia chromosome–positive leukemias
- Dan Jones, Rajyalakshmi Luthra, Jorge Cortes, Deborah Thomas, Susan O'Brien, Carlos Bueso-Ramos, Seema Hai, Farhad Ravandi, Marcos de Lima, Hagop Kantarjian, and Jeffrey L. Jorgensen
Blood 2008; 112: 5190-5192.
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