Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Mary E. Fabry"'
Autor:
Mary E. Fabry, Ronald L. Nagel
Publikováno v:
Genetically Abnormal Red Cells ISBN: 9780429263989
Genetically Abnormal Red Cells
Genetically Abnormal Red Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a570d2b734900aa4288f94f499e96e47
https://doi.org/10.1201/9780429263989-2
https://doi.org/10.1201/9780429263989-2
Autor:
Mary E. Fabry, Ronald L. Nagel
Publikováno v:
Genetically Abnormal Red Cells ISBN: 9780429263989
Genetically Abnormal Red Cells
Genetically Abnormal Red Cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63396d901b9b1677908a26d60141682d
https://doi.org/10.1201/9780429263989-1
https://doi.org/10.1201/9780429263989-1
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 304:H42-H50
Chronic inflammation is a salient feature of sickle cell disease (SCD) and transgenic-knockout sickle (BERK) mice. Inflammation is implicated in the activation of hypoxia-inducible factor-1α (HIF-1α) under normoxic conditions. We hypothesize that,
Autor:
Eric E, Bouhassira, Henny H, Billett, Mary E, Fabry, Rhoda E, Hirsch, Rajagopal, Krishnamoorthy
Publikováno v:
American journal of hematology. 91(9)
Autor:
Jens C. Krause, Eric P. Skaar, Amanda L. McCoy, Gleb Pishchany, James E. Crowe, Mary E. Fabry, Victor J. Torres
Publikováno v:
Cell Host & Microbe. 8(6):544-550
SummaryIron is required for bacterial proliferation, and Staphylococcus aureus steals this metal from host hemoglobin during invasive infections. This process involves hemoglobin binding to the cell wall of S. aureus, heme extraction, passage through
Autor:
Yelena Ginzburg, Leni von Bonsdorff, Mary E. Fabry, Eric E. Bouhassira, Charles B. Hall, William Breuer, Z. Ioav Cabantchik, Huihui Li, Anne C Rybicki, Sandra M. Suzuka
Publikováno v:
Nature Medicine. 16:177-182
Individuals with beta-thalassemia develop progressive systemic iron overload, resulting in high morbidity and mortality. These complications are caused by labile plasma iron, which is taken up by parenchymal cells in a dysregulated manner; in contras
Publikováno v:
Blood Cells, Molecules, and Diseases. 41:60-66
Red blood cells with abnormal hemoglobins (Hb) are frequently associated with increased hemoglobin autoxidation, accumulation of iron in membranes, increased membrane damage and a shorter red cell life span. The mechanisms for many of these changes h
Autor:
A. Seetharama Acharya, Mary E. Fabry, Eric E. Bouhasirra, Ronald L. Nagel, Muthuchidambaran Prabhakaran, Raouf Alami, Steven Fiering, Sonati Srinivasulu
Publikováno v:
The Protein Journal. 26:523-532
Recombinant α-Savaria globin (αS49R) was assembled with βS chains by the alloplex intermediate pathway to generate tetrameric rHbS-Sarvaria (α 2 S49R β 2 E6V ) that exhibited normal O2 affinity and co-operatively at pH 7.4. Allosteric effectors,
Autor:
Rhoda Elison Hirsch, Arnaud Besse, Mary E. Fabry, Eric E. Bouhassira, Qiuying Chen, Ronald L. Nagel, Sandra M. Suzuka
Publikováno v:
Blood Cells, Molecules, and Diseases. 33:303-307
Hemoglobin E (HbE, beta26 Glu-->Lys) is the most common abnormal Hb variant in the world, and found in greatest frequency in Southeast (SE) Asia. In the United States, HbE is the third most prevalent variant (after HbS and HbC); and its now increasin
Autor:
Suzan Imren, Mary E. Fabry, Karen A. Westerman, Robert Pawliuk, Patrick Tang, Patricia M. Rosten, Ronald L. Nagel, Philippe Leboulch, Connie J. Eaves, R. Keith Humphries
Publikováno v:
Journal of Clinical Investigation. 114:953-962