HuGE Literature Finder
Records 1-27
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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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Genetic Modifiers of Fetal Haemoglobin (HbF) and Phenotypic Severity in ?-Thalassemia Patients.
Current molecular medicine 2018 Oct . Razak S A A, Murad N A A, Masra F, Chong D L S, Abdullah N, Jalil N, Alauddin H, Sabudin R Z A R, Ithnin A, Alias H, Khai L C, Aziz N A, Muda Z, Ibrahim H, Jamal R, Latif Z |
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The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease.
International journal of laboratory hematology 2018 Sep . Al-Allawi Nasir, Qadir Shatha M A, Puehringer Helene, Chui David H K, Farrell John J, Oberkanins Christi |
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Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with ?-Thalassemia and Sickle Cell Disease.
Hemoglobin 2018 Mar 42 (2): 103-107. Listì Florinda, Sclafani Serena, Agrigento Veronica, Barone Rita, Maggio Aurelio, D'Alcamo Ele |
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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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Genetic Variants at BCL11A and HBS1L-MYB loci Influence Hb F Levels in Chinese Zhuang ?-Thalassemia Intermedia Patients.
Hemoglobin 2016 Nov 40 (6): 405-410. Lai Yunli, Chen Yun, Chen Biyan, Zheng Haiyang, Yi Sheng, Li Guojian, Wei Hongwei, He Sheng, Zheng Chengua |
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A Multi-Locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese ?-Thalassemia Carriers.
Hemoglobin 2016 Oct 1-12. Chan Nelson C N, Lau Kin-Mang, Cheng Kelvin C K, Chan Natalie P H, Ng Margaret H |
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Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci.
British journal of haematology 2016 Feb . Leonardo Flávia C, Brugnerotto Ana F, Domingos Igor F, Fertrin Kleber Y, de Albuquerque Dulcinéia M, Bezerra Marcos A C, Araújo Aderson S, Saad Sara T O, Costa Fernando F, Menzel Stephan, Conran Nicola, Thein Swee L |
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Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin.
Blood cells, molecules & diseases 2015 Apr 54 (4): 315-20. Pereira Clara, Relvas Luís, Bento Celeste, Abade Augusto, Ribeiro M Letícia, Manco Licín |
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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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Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.
BMC medical genetics 2015 16 4. Mtatiro Siana N, Mgaya Josephine, Singh Tarjinder, Mariki Harvest, Rooks Helen, Soka Deogratius, Mmbando Bruno, Thein Swee Lay, Barrett Jeffrey C, Makani Julie, Cox Sharon E, Menzel Steph |
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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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Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.
PloS one 2014 9 (3): e92506. Wonkam Ambroise, Ngo Bitoungui Valentina J, Vorster Anna A, Ramesar Raj, Cooper Richard S, Tayo Bamidele, Lettre Guillaume, Ngogang Jean |
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Utility of the multivariate approach in predicting ?-thalassemia intermedia or ?-thalassemia major types In Iranian patients.
Hemoglobin 2013 37 (5): 413-22. Banan Mehdi, Bayat Hadi, Namdar-Aligoodarzi Pegah, Azarkeivan Azita, Kamali Koorosh, Daneshmand Parvaneh, Zaker-Kandjani Behzad, Najmabadi Hosse |
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Genetic modifiers of ?-thalassemia and clinical severity as assessed by age at first transfusion.
Haematologica 2012 Jul 97 (7): 989-93. Danjou Fabrice, Anni Franco, Perseu Lucia, Satta Stefania, Dessì Carlo, Lai Maria Eliana, Fortina Paolo, Devoto Marcella, Galanello Ren |
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Influence of BCL11A, HBS1L-MYB, HBBP1 single nucleotide polymorphisms and the HBG2 XmnI polymorphism On Hb F levels.
Hemoglobin 2012 36 (6): 592-9. Roy Papai, Bhattacharya Gargi, Mandal Amrita, Dasgupta Uma B, Banerjee Debasis, Chandra Sarmila, Das Manikanch |
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Influences of genetic variation on fetal hemoglobin.
Pediatric hematology and oncology 2011 Nov 28 (8): 708-17. He Yunyan, Lin Weixiong, Luo Jianmi |
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Variants in genetic modifiers of ?-thalassemia can help to predict the major or intermedia type of the disease.
Haematologica 2011 Nov 96 (11): 1712-4. Badens Catherine, Joly Philippe, Agouti Imane, Thuret Isabelle, Gonnet Katia, Fattoum Synda, Francina Alain, Simeoni Marie-Claude, Loundou Anderson, Pissard Ser |
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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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The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients.
Blood cells, molecules & diseases 2010 Aug 45 (2): 124-7. Nguyen Thi Khanh Tien, Joly Philippe, Bardel Claire, Moulsma Mustapha, Bonello-Palot Nathalie, Francina Ala |
A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.
Human genetics 2010 Mar 127 (3): 303-14. Nuinoon Manit, Makarasara Wattanan, Mushiroda Taisei, Setianingsih Iswari, Wahidiyat Pustika Amalia, Sripichai Orapan, Kumasaka Natsuhiko, Takahashi Atsushi, Svasti Saovaros, Munkongdee Thongperm, Mahasirimongkol Surakameth, Peerapittayamongkol Chayanon, Viprakasit Vip, Kamatani Naoyuki, Winichagoon Pranee, Kubo Michiaki, Nakamura Yusuke, Fucharoen Suth |
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A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E.
Human genetics 2009 Nov . Nuinoon M, Makarasara W, Mushiroda T, Setianingsih I, Wahidiyat PA, Sripichai O, Kumasaka N, Takahashi A, Svasti S, Munkongdee T, Mahasirimongkol S, Peerapittayamongkol C, Viprakasit V, Kamatani N, Winichagoon P, Kubo M, Nakamura Y, Fucharoen S |
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Amelioration of Sardinian beta0 thalassemia by genetic modifiers.
Blood 2009 Oct 114 (18): 3935-7. Galanello Renzo, Sanna Serena, Perseu Lucia, Sollaino Maria Carla, Satta Stefania, Lai Maria Eliana, Barella Susanna, Uda Manuela, Usala Gianluca, Abecasis Goncalo R, Cao Anton |
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Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patients.
PloS one 2009 4 (1): e4218. Creary Lisa E, Ulug Pinar, Menzel Stephan, McKenzie Colin A, Hanchard Neil A, Taylor Veronica, Farrall Martin, Forrester Terrence E, Thein Swee L |
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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 |
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Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis.
Blood cells, molecules & diseases 0 53 (1-2): 11-5. Pakdee Naruwat, Yamsri Supawadee, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Pissard Serge, Fucharoen Sup |
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- Page last updated:Apr 06, 2020
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