HuGE Literature Finder
Records 1-20
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Detection of BCL11A and HBS1L-MYB Genotypes in Sickle Cell Anemia.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2020 Oct 36 (4): 705-710. Qadah Talal, Noorwali Abdulwahab, Alzahrani Fatma, Banjar Alaa, Filimban Najlaa, Felimban Ra |
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Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia.
Annals of hematology 2020 May . Sales Rahyssa Rodrigues, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Luizon Marcelo Rizzatti, Viana Marcos Bora |
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Combined and differential effects of alpha-thalassemia and HbF-quantitative trait loci in Senegalese hydroxyurea-free children with sickle cell anemia.
Pediatric blood & cancer 2019 Jul e27934. Gueye Tall Fatou, Martin Cyril, Ndour El Hadji Malick, Renoux Céline, Ly Indou Déme, Connes Philippe, Gueye Papa Madieye, Diallo Rokhaya Ndiaye, Diagne Ibrahima, Diop Pape Amadou, Cissé Aynina, Lopez Sall Philomène, Joly Philip |
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Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia.
Journal of clinical laboratory analysis 2017 Mar . Mikobi Tite Minga, Tshilobo Lukusa Prosper, Aloni Michel Ntetani, Lumaka Aimé Zola, Kaba Didine Kinkodi, Devriendt Koenraad, Matthijs Gert, Mbuyi Muamba Jean Marie, Race Valér |
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The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil.
Blood cells, molecules & diseases 2016 Nov 62 32-37. Friedrisch João Ricardo, Sheehan Vivien, Flanagan Jonathan M, Baldan Alessandro, Summarell Carly C Ginter, Bittar Christina Matzembacher, Friedrisch Bruno Kras, Wilke Ianaê Indiara, Ribeiro Camila Blos, Daudt Liane Esteves, da Rocha Silla Lucia Maria |
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APOL1, Alpha thalassemia, and BCL11A variants as a genetic risk profile for progression of chronic kidney disease in sickle cell anemia.
Haematologica 2016 Sep . Saraf Santosh L, Shah Binal N, Zhang Xu, Han Jin, Tayo Bamidele O, Abbasi Taimur, Ostrower Adam, Guzman Elizabeth, Molokie Robert E, Gowhari Michel, Hassan Johara, Jain Shivi, Cooper Richard S, Machado Roberto F, Lash James P, Gordeuk Victor |
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A Candidate Trans-acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia: -ANTXR1 Variants and HbF.
American journal of hematology 2016 Aug . Vathipadiekal Vinod, Farrell John J, Wang Shuai, Edward Heather L, Shappell Heather, Al-Rubaish A M, Al-Muhanna Fahad, Naserullah Z, Alsuliman A, Qutub Hatem Othman, Simkin Irene, Farrer Lindsay A, Jiang Zhihua, Luo Hong-Yuan, Huang Shengwen, Mostoslavsky Gustavo, Murphy George, Patra Pradeep K, Chui David H K, Alsultan Abdulrahman, Al-Ali Amein K, Sebastiani Paola, Steinberg Martin |
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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Hematology (Amsterdam, Netherlands) 2016 Aug 21 (7): 425-9. Chaouch Leila, Moumni Imen, Ouragini Houyem, Darragi Imen, Kalai Miniar, Chaouachi Dorra, Boudrigua Imen, Hafsia Raouf, Abbes Sal |
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Rs 11886868 and rs 4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients.
Hematology (Amsterdam, Netherlands) 2015 Jun . Chaouch Leila, Moumni Imen, Ouragini Houyem, Darragi Imen, Kalai Miniar, Chaouachi Dorra, Boudrigua Imen, Hafsia Raouf, Abbes Sal |
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BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.
Blood cells, molecules & diseases 2015 Mar 54 (3): 224-30. Sebastiani P, Farrell J J, Alsultan A, Wang S, Edward H L, Shappell H, Bae H, Milton J N, Baldwin C T, Al-Rubaish A M, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra P K, Farrer L A, Ngo D, Vathipadiekal V, Chui D H K, Al-Ali A K, Steinberg M |
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Genetic variant in the BCL11A (rs1427407), but not HBS1-MYB (rs6934903) loci associate with fetal hemoglobin levels in Indian sickle cell disease patients.
Blood cells, molecules & diseases 2015 Jan 54 (1): 4-8. Bhanushali Aparna A, Patra P K, Nair D, Verma H, Das B |
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Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania.
American journal of hematology 2015 Jan 90 (1): E1-4. Mtatiro Siana Nkya, Makani Julie, Mmbando Bruno, Thein Swee Lay, Menzel Stephan, Cox Sharon |
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DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.
Blood cells, molecules & diseases 2014 Dec 53 (4): 176-9. Cardoso Greice Lemos, Diniz Isabela Guerreiro, Silva Aylla Núbia Lima Martins da, Cunha Daniele Almeida, Silva Junior Josivaldo Soares da, Uchôa Camila Tavares Carvalho, Santos Sidney Emanuel Batista dos, Trindade Saide Maria Sarmento, Cardoso Maria do Socorro de Oliveira, Guerreiro João Fari |
The genetics of hemoglobin A2 regulation in sickle cell anemia.
American journal of hematology 2014 Nov 89 (11): 1019-23. Griffin Paula J, Sebastiani Paola, Edward Heather, Baldwin Clinton T, Gladwin Mark T, Gordeuk Victor R, Chui David H K, Steinberg Martin |
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Prediction of fetal hemoglobin in sickle cell anemia using an ensemble of genetic risk prediction models.
Circulation. Cardiovascular genetics 2014 Apr 7 (2): 110-5. Milton Jacqueline N, Gordeuk Victor R, Taylor James G, Gladwin Mark T, Steinberg Martin H, Sebastiani Pao |
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Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
American journal of hematology 2013 Jul 88 (7): 571-6. Sheehan Vivien A, Luo Zhaoyu, Flanagan Jonathan M, Howard Thad A, Thompson Bruce W, Wang Winfred C, Kutlar Abdullah, Ware Russell E, |
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Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia.
Blood 2011 Nov 118 (18): 4985-91. Ware Russell E, Despotovic Jenny M, Mortier Nicole A, Flanagan Jonathan M, He Jin, Smeltzer Matthew P, Kimble Amy C, Aygun Banu, Wu Song, Howard Thad, Sparreboom Al |
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Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia.
Blood 2011 Jan 117 (4): 1390-2. Makani Julie, Menzel Stephan, Nkya Siana, Cox Sharon E, Drasar Emma, Soka Deogratius, Komba Albert N, Mgaya Josephine, Rooks Helen, Vasavda Nisha, Fegan Gregory, Newton Charles R, Farrall Martin, Thein Swee L |
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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Blood 2010 Mar 115 (9): 1815-22. Solovieff Nadia, Milton Jacqueline N, Hartley Stephen W, Sherva Richard, Sebastiani Paola, Dworkis Daniel A, Klings Elizabeth S, Farrer Lindsay A, Garrett Melanie E, Ashley-Koch Allison, Telen Marilyn J, Fucharoen Supan, Ha Shau Yin, Li Chi-Kong, Chui David H K, Baldwin Clinton T, Steinberg Martin |
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Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proceedings of the National Academy of Sciences of the United States of America 2008 Feb 105 (5): 1620-5. Uda Manuela, Galanello Renzo, Sanna Serena, Lettre Guillaume, Sankaran Vijay G, Chen Weimin, Usala Gianluca, Busonero Fabio, Maschio Andrea, Albai Giuseppe, Piras Maria Grazia, Sestu Natascia, Lai Sandra, Dei Mariano, Mulas Antonella, Crisponi Laura, Naitza Silvia, Asunis Isadora, Deiana Manila, Nagaraja Ramaiah, Perseu Lucia, Satta Stefania, Cipollina Maria Dolores, Sollaino Carla, Moi Paolo, Hirschhorn Joel N, Orkin Stuart H, Abecasis Gonçalo R, Schlessinger David, Cao Anton |
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- Page last updated:Nov 27, 2020
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