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Hemoglobin|December 10, 2008
Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-->Leu, CAT>CTT]Erin Dainer, Richard Shell, Randy Miller, et al.American Journal of Hematology|April 23, 2013
Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypesVivien A Sheehan, Zhaoyu Luo, Jonathan M Flanagan, et al.Blood|March 24, 2005
Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosisClinton Baldwin, Vikki G Nolan, Diego F Wyszynski, et al.British Journal of Pharmacology|November 13, 2015
Endothelin-1 contributes to the progression of renal injury in sickle cell disease via reactive oxygen speciesJ Brett Heimlich, Joshua S Speed, Paul M O'Connor, et al.Blood Cells, Molecules & Diseases|September 28, 2011
The proinflammatory cytokine GM-CSF downregulates fetal hemoglobin expression by attenuating the cAMP-dependent pathway in sickle cell diseaseTohru Ikuta, Adekunle D Adekile, Diana R Gutsaeva, et al.Cytokine|November 11, 2009
Plasma interleukin-1beta concentration is associated with stroke in sickle cell diseaseKwaku Asare, Beatrice E Gee, Jonathan K Stiles, et al.Haematologica|December 7, 2007
Missense mutation of the last nucleotide of exon 1 (G->C) of beta globin gene not only leads to undetectable mutant peptide and transcript but also interferes with the expression of wild alleleNeeraj Agarwal, Ferdane Kutlar, Mariluz P Mojica-Henshaw, et al.British Journal of Haematology|January 11, 2005
Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemiaVikki G Nolan, Clinton Baldwin, Qianli Ma, et al.HCA Healthcare Journal of Medicine|July 10, 2023
Utilization of Patient-Controlled Analgesia Reduces Length of Stay of Sickle Cell Crisis HospitalizationsBrett M Prestia, Talha Ramzan, Catherine Waldron, et al.Journal of the American Society of Nephrology : JASN|March 29, 2017
Long-Term Endothelin-A Receptor Antagonism Provides Robust Renal Protection in Humanized Sickle Cell Disease MiceMalgorzata Kasztan, Brandon M Fox, Joshua S Speed, et al.Pageof 12