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Red Cells
Citations 31-40 of 1173 total displayed.
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Past content
(since Jan 1997):
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Retention of Plasmodium falciparum ring-infected erythrocytes in the slow, open microcirculation of the human spleen
- Innocent Safeukui, Jean-Michel Correas, Valentine Brousse, Déborah Hirt, Guillaume Deplaine, Sébastien Mulé, Mickael Lesurtel, Nicolas Goasguen, Alain Sauvanet, Anne Couvelard, Sophie Kerneis, Huot Khun, Inès Vigan-Womas, Catherine Ottone, Thierry Jo Molina, Jean-Marc Tréluyer, Odile Mercereau-Puijalon, Geneviève Milon, Peter H. David, and Pierre A. Buffet
Blood 2008; 112: 2520-2528.
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Histopathology of experimentally induced asthma in a murine model of sickle cell disease
- Sandhya D. Nandedkar, Thomas R. Feroah, William Hutchins, Dorothee Weihrauch, Kameswari S. Konduri, Jingli Wang, Robert C. Strunk, Michael R. DeBaun, Cheryl A. Hillery, and Kirkwood A. Pritchard
Blood 2008; 112: 2529-2538.
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Membrane-bound serine protease matriptase-2 (Tmprss6) is an essential regulator of iron homeostasis
- Alicia R. Folgueras, Fernando Martín de Lara, Alberto M. Pendás, Cecilia Garabaya, Francisco Rodríguez, Aurora Astudillo, Teresa Bernal, Rubén Cabanillas, Carlos López-Otín, and Gloria Velasco
Blood 2008; 112: 2539-2545.
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Stochastic modeling of human RBC alloimmunization: evidence for a distinct population of immunologic responders
- John M. Higgins and Steven R. Sloan
Blood 2008; 112: 2546-2553.
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Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia
- Jason E. Farrar, Michelle Nater, Emi Caywood, Michael A. McDevitt, Jeanne Kowalski, Clifford M. Takemoto, C. Conover Talbot, Jr, Paul Meltzer, Diane Esposito, Alan H. Beggs, Hal E. Schneider, Agnieszka Grabowska, Sarah E. Ball, Edyta Niewiadomska, Colin A. Sieff, Adrianna Vlachos, Eva Atsidaftos, Steven R. Ellis, Jeffrey M. Lipton, Hanna T. Gazda, and Robert J. Arceci
Blood 2008; 112: 1582-1592.
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Defective homing is associated with altered Cdc42 activity in cells from patients with Fanconi anemia group A
- Xiaoling Zhang, Xun Shang, Fukun Guo, Kim Murphy, Michelle Kirby, Patrick Kelly, Lilith Reeves, Franklin O. Smith, David A. Williams, Yi Zheng, and Qishen Pang
Blood 2008; 112: 1683-1686.
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A novel loss-of-function mutation in the proton-coupled folate transporter from a patient with hereditary folate malabsorption reveals that Arg 113 is crucial for function
- Inbal Lasry, Bluma Berman, Rachel Straussberg, Yael Sofer, Hanna Bessler, Mohamad Sharkia, Fabian Glaser, Gerrit Jansen, Stavit Drori, and Yehuda G. Assaraf
Blood 2008; 112: 2055-2061.
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HES1 is a novel interactor of the Fanconi anemia core complex
- Cédric S. Tremblay, Feng F. Huang, Ouassila Habi, Caroline C. Huard, Chantal Godin, Georges Lévesque, and Madeleine Carreau
Blood 2008; 112: 2062-2070.
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Hematopoietic-specific Stat5-null mice display microcytic hypochromic anemia associated with reduced transferrin receptor gene expression
- Bing-Mei Zhu, Sara K. McLaughlin, Risu Na, Jie Liu, Yongzhi Cui, Cyril Martin, Akiko Kimura, Gertraud W. Robinson, Nancy C. Andrews, and Lothar Hennighausen
Blood 2008; 112: 2071-2080.
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Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype
- Belinda K. Singleton, Nicholas M. Burton, Carole Green, R. Leo Brady, and David J. Anstee
Blood 2008; 112: 2081-2088.
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