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Red Cells
Citations 121-130 of 1173 total displayed.
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Past content
(since Jan 1997):
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Point mutations involved in red cell stomatocytosis convert the electroneutral anion exchanger 1 to a nonselective cation conductance
- Hélène Guizouarn, Sonia Martial, Nicole Gabillat, and Franck Borgese
Blood 2007; 110: 2158-2165.
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Platelet activation in patients with sickle disease, hemolysis-associated pulmonary hypertension, and nitric oxide scavenging by cell-free hemoglobin
- José Villagra, Sruti Shiva, Lori A. Hunter, Roberto F. Machado, Mark T. Gladwin, and Gregory J. Kato
Blood 2007; 110: 2166-2172.
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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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Iron transferrin regulates hepcidin synthesis in primary hepatocyte culture through hemojuvelin and BMP2/4
- Lan Lin, Erika V. Valore, Elizabeta Nemeth, Julia B. Goodnough, Victoria Gabayan, and Tomas Ganz
Blood 2007; 110: 2182-2189.
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Factor H–mediated cell surface protection from complement is critical for the survival of PNH erythrocytes
- Viviana P. Ferreira and Michael K. Pangburn
Blood 2007; 110: 2190-2192.
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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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Nonhemolytic antigen loss from red blood cells requires cooperative binding of multiple antibodies recognizing different epitopes
- James C. Zimring, Chantel M. Cadwell, Traci E. Chadwick, Steven L. Spitalnik, David A. Schirmer, Tao Wu, Charles A. Parkos, and Christopher D. Hillyer
Blood 2007; 110: 2201-2208.
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Deficient CD4+ CD25+ FOXP3+ T regulatory cells in acquired aplastic anemia
- Elena E. Solomou, Katayoun Rezvani, Stephan Mielke, Daniela Malide, Keyvan Keyvanfar, Valeria Visconte, Sachiko Kajigaya, A. John Barrett, and Neal S. Young
Blood 2007; 110: 1603-1606.
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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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Effects of age-dependent membrane transport changes on the homeostasis of senescent human red blood cells
- Virgilio L. Lew, Nuala Daw, Zipora Etzion, Teresa Tiffert, Adaeze Muoma, Laura Vanagas, and Robert M. Bookchin
Blood 2007; 110: 1334-1342.
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