HuGE Literature Finder
Records 1-30
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The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese ß-thalassemia patients.
Blood cells, molecules & diseases 2020 Apr 84 102442. Yang Kun, Wu Yi, Ma Yanni, Xiao Jian, Zhou Yali, Yin Xiaol |
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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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An enhancer haplotype may influence BCL11A expression levels and the response to hydroxyurea in ?-thalassemia patients.
Pharmacogenomics 2017 Jun . Maroofi Nahal, Azarkeivan Azita, Banihashemi Soosan, Mohammadparast Saeid, Aghajanirefah Ali, Banan Meh |
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Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi ?-Thalassemia Patients.
BioMed research international 2017 2017 1972429. Cyrus Cyril, Vatte Chittibabu, Borgio J Francis, Al-Rubaish Abdullah, Chathoth Shahanas, Nasserullah Zaki A, Jarrash Sana Al, Sulaiman Ahmed, Qutub Hatem, Alsaleem Hassan, Alzahrani Alhusain J, Steinberg Martin H, Ali Amein K |
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The association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang ß-thalassemia intermedia patients.
Blood cells, molecules & diseases 2017 03 63 52-57. Lai Yunli, Zhou Lin, Yi Sheng, Chen Yun, Tang Yanqing, Yi Shang, Yang Ze, Wei Hongwei, Zheng Chenguang, He She |
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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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Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-?-Thalassemia in Northeast Thailand.
Acta haematologica 2016 Oct 136 (4): 233-239. Yamsri Supawadee, Pakdee Naruwat, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
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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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Modifying effect of XmnI, BCL11A, and HBS1L-MYB on clinical appearances: A study on ß-thalassemia and hemoglobin E/ß-thalassemia patients in Indonesia.
Hematology/oncology and stem cell therapy 2016 Jun 9 (2): 55-63. Rujito Lantip, Basalamah Muhammad, Siswandari Wahyu, Setyono Joko, Wulandari Gondo, Mulatsih Sri, Sofro Abdul Salam M, Sadewa Ahmad Hamim, Sutaryo Sutar |
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The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals.
Hemoglobin 2016 Jun 40 (3): 198-201. Keyhani Elaheh, Jafari Vesiehsari Mahjoobeh, Talebi Kakroodi Setareh, Darabi Elham, Zamani Fahimeh, Karimlou Masoud, Kamali Koorosh, Neishabury Mary |
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A genetic score for the prediction of beta-thalassemia severity.
Haematologica 2015 Apr 100 (4): 452-7. Danjou Fabrice, Francavilla Marcella, Anni Franco, Satta Stefania, Demartis Franca-Rosa, Perseu Lucia, Manca Matteo, Sollaino Maria Carla, Manunza Laura, Mereu Elisabetta, Marceddu Giuseppe, Pissard Serge, Joly Philippe, Thuret Isabelle, Origa Raffaella, Borg Joseph, Forni Gian Luca, Piga Antonio, Lai Maria Eliana, Badens Catherine, Moi Paolo, Galanello Ren |
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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 Modifiers in ß-Thalassemia Intermedia: A Study on 102 Iraqi Arab Patients.
Genetic testing and molecular biomarkers 2015 Mar . Al-Allawi Nasir A S, Puehringer Helene, Raheem Ruzaiqah A, Oberkanins Christi |
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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 Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.
Hemoglobin 2015 39 (3): 156-61. Muszlak Mathias, Pissard Serge, Badens Catherine, Chamouine Abdourahim, Maillard Olivier, Thuret Isabel |
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The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background.
Blood cells, molecules & diseases 2013 Aug 51 (2): 80-4. Neishabury Maryam, Zamani Fahimeh, Keyhani Elahe, Azarkeivan Azita, Abedini Seyedeh Sedigheh, Eslami Masumeh Sadat, Kakroodi Setareh Talebi, Vesiehsari Mahjoobeh Jafari, Najmabadi Hosse |
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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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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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[Correlation between hemoglobin F levels and single nucleotide polymorphism at BCL11A gene rs11886868 locus in ?-thalassemia patients].
Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 2012 Jun 20 (3): 650-3. Chen Qun-Rong, Sun Shun-Chang, Peng Yun-Sheng, Wang Qing, Mo Bao-M |
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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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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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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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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:Mar 05, 2021
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