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au.\*:("FABRY, Mary E")

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Antisickling property of fetal hemoglobin enhances nitric oxide bioavailability and ameliorates organ oxidative stress in transgenic-knockout sickle miceDASGUPTA, Trisha; FABRY, Mary E; KAUL, Dhananjay K et al.American journal of physiology. Regulatory, integrative and comparative physiology. 2010, Vol 67, Num 2, issn 0363-6119, R394-R402Article

The panoply of animal models for sickle cell anaemiaNAGEL, Ronald L; FABRY, Mary E.British journal of haematology. 2001, Vol 112, Num 1, pp 19-25, issn 0007-1048Article

Direct intracellular measurement of deoxygenated hemoglobin S solubilityFABRY, Mary E; DESROSIERS, Laurephile; SUZUKA, Sandra M et al.Blood. 2001, Vol 98, Num 3, pp 883-884, issn 0006-4971Article

Arginine therapy of transgenic-knockout sickle mice improves microvascular function by reducing non-nitric oxide vasodilators, hemolysis, and oxidative stressKAUL, Dhananjay K; XIAOQIN ZHANG; DASGUPTA, Trisha et al.American journal of physiology. Heart and circulatory physiology. 2008, Vol 64, Num 1, issn 0363-6135, H39-H47Article

The paradox of hemoglobin SC diseaseNAGEL, Ronald L; FABRY, Mary E; STEINBERG, Martin H et al.Blood reviews. 2003, Vol 17, Num 3, pp 167-178, issn 0268-960X, 12 p.Article

Second generation knockout sickle mice : the effect of HbFFABRY, Mary E; SUZUKA, Sandra M; WEINBERG, Rona S et al.Blood. 2001, Vol 97, Num 2, pp 410-418, issn 0006-4971Article

Arginine supplementation of sickle transgenic mice reduces red cell density and Gardos channel activityROMERO, José R; SUZUKA, Sandra M; NAGEL, Ronald L et al.Blood. 2002, Vol 99, Num 4, pp 1103-1108, issn 0006-4971Article

Correction of sickle cell disease in transgenic mouse models by gene therapyPAWLIUK, Robert; WESTERMAN, Karen A; HUMPHRIES, R. Keith et al.Science (Washington, D.C.). 2001, Vol 294, Num 5550, pp 2368-2371, issn 0036-8075Article

Antisickling fetal hemoglobin reduces hypoxia-inducible factor-1α expression in normoxic sickle mice: microvascular implicationsKAUL, Dhananjay K; FABRY, Mary E; SUZUKA, Sandra M et al.American journal of physiology. Heart and circulatory physiology. 2013, Vol 73, Num 1, issn 0363-6135, H42-H50Article

Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1 BNOLAN, Vikki G; QIANLI MA; NAGEL, Ronald L et al.American journal of hematology. 2007, Vol 82, Num 3, pp 179-184, issn 0361-8609, 6 p.Article

Expression of a human β-globin transgene in erythroid cells derived from retrovirally transduced transplantable human fetal liver and cord blood cellsNICOLINI, Franck E; IMREN, Suzan; OH, Ii-Hoan et al.Blood. 2002, Vol 100, Num 4, pp 1257-1264, issn 0006-4971, 8 p.Article

Genetic endothelial systems biology of sickle stroke risk. CommentaryFABRY, Mary E; CHANG MILBAUER, Liming; YANG, Ruey-Bing et al.Blood. 2008, Vol 111, Num 7, issn 0006-4971, 3310, 3872-3879 [9 p.]Article

Murine glutathione S-transferase Al-1 in sickle transgenic miceGINZBURG, Yelena Z; ANDORFER, John H; RYBICKI, Anne C et al.American journal of hematology. 2007, Vol 82, Num 10, pp 911-915, issn 0361-8609, 5 p.Article

Inhibition of TNF-α-induced sickle RBC retention in retina by a VLA-4 antagonistLUTTY, Gerard A; TAOMOTO, Makoto; JINGTAI CAO et al.Investigative ophthalmology & visual science. 2001, Vol 42, Num 6, pp 1349-1355, issn 0146-0404Article

Velocity measurements of normal and sickle red blood cells in the rat retinal and choroidal vasculaturesWAJER, Stephen D; TAOMOTO, Makoto; MCLEOD, D. Scott et al.Microvascular research (Print). 2000, Vol 60, Num 3, pp 281-293, issn 0026-2862Article

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