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Hematopoiesis and Stem Cells
Citations 371-380 of 2602 total displayed.
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Past content
(since Jan 1997):
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Hypoxic stress underlies defects in erythroblast islands in the Rb-null mouse
- Benjamin T. Spike, Benjamin C. Dibling, and Kay F. Macleod
Blood 2007; 110: 2173-2181.
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A novel erythrocytosis-associated PHD2 mutation suggests the location of a HIF binding groove
- Melanie J. Percy, Paul W. Furlow, Philip A. Beer, Terence R. J. Lappin, Mary Frances McMullin, and Frank S. Lee
Blood 2007; 110: 2193-2196.
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X-linked clonality testing: interpretation and limitations
- George L. Chen and Josef T. Prchal
Blood 2007; 110: 1411-1419.
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Activation of mitogen-activated protein kinase kinase (MEK)/extracellular signal–regulated kinase (ERK) signaling pathway is involved in myeloid lineage commitment
- Chia-Lin Hsu, Kazu Kikuchi, and Motonari Kondo
Blood 2007; 110: 1420-1428.
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Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita
- Blanche P. Alter, Gabriela M. Baerlocher, Sharon A. Savage, Stephen J. Chanock, Babette B. Weksler, Judith P. Willner, June A. Peters, Neelam Giri, and Peter M. Lansdorp
Blood 2007; 110: 1439-1447.
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The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA
- Karthik A. Ganapathi, Karyn M. Austin, Chung-Sheng Lee, Anusha Dias, Maggie M. Malsch, Robin Reed, and Akiko Shimamura
Blood 2007; 110: 1458-1465.
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The SOCS box of suppressor of cytokine signaling-3 contributes to the control of G-CSF responsiveness in vivo
- Kristy Boyle, Paul Egan, Steven Rakar, Tracy A. Willson, Ian P. Wicks, Donald Metcalf, Douglas J. Hilton, Nicos A. Nicola, Warren S. Alexander, Andrew W. Roberts, and Lorraine Robb
Blood 2007; 110: 1466-1474.
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Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia
- Daniel C. Link, Ghada Kunter, Yumi Kasai, Yu Zhao, Tracie Miner, Michael D. McLellan, Rhonda E. Ries, Deepak Kapur, Rakesh Nagarajan, David C. Dale, Audrey Anna Bolyard, Laurence A. Boxer, Karl Welte, Cornelia Zeidler, Jean Donadieu, Christine Bellanné-Chantelot, James W. Vardiman, Michael A. Caligiuri, Clara D. Bloomfield, John F. DiPersio, Michael H. Tomasson, Timothy A. Graubert, Peter Westervelt, Mark Watson, William Shannon, Jack Baty, Elaine R. Mardis, Richard K. Wilson, and Timothy J. Ley
Blood 2007; 110: 1648-1655.
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Mutations in the SBDS gene in acquired aplastic anemia
- Rodrigo T. Calado, Solomon A. Graf, Keisha L. Wilkerson, Sachiko Kajigaya, Philip J. Ancliff, Yigal Dror, Stephen J. Chanock, Peter M. Lansdorp, and Neal S. Young
Blood 2007; 110: 1141-1146.
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The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption
- Rongbao Zhao, Sang Hee Min, Andong Qiu, Antoinette Sakaris, Gary L. Goldberg, Claudio Sandoval, J. Jeffrey Malatack, David S. Rosenblatt, and I. David Goldman
Blood 2007; 110: 1147-1152.
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