Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Pain and HBB[original query] |
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DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America 2008 Aug 105 (33): 11869-74. Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart |
Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1. American journal of hematology 2011 1 86 (2): 220-3. Dworkis Daniel A, Klings Elizabeth S, Solovieff Nadia, Li Guihua, Milton Jacqueline N, Hartley Stephen W, Melista Efthymia, Parente Jason, Sebastiani Paola, Steinberg Martin H, Baldwin Clinton |
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia. British journal of haematology 2013 Oct 163 (2): 268-76. Bean Christopher J, Boulet Sheree L, Yang Genyan, Payne Amanda B, Ghaji Nafisa, Pyle Meredith E, Hooper W Craig, Bhatnagar Pallav, Keefer Jeffrey, Barron-Casella Emily A, Casella James F, Debaun Michael |
Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia. Translational research : the journal of laboratory and clinical medicine 2015 Jun 165 (6): 696-703. Bhanushali Aparna A, Patra Pradip K, Pradhan Smarnika, Khanka Suraj S, Singh Sujata, Das Bibhu |
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