HuGE Literature Finder
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| Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous ß-Thalassemia 3.5?kb Deletions. Hemoglobin 2020 Sep 1-6. Tepakhan Wanicha, Kanjanaopas Sataron, Srewaradachpisal Kornt |
| Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-ß-Thalassemia Disease without a-Thalassemia. Mediterranean journal of hematology and infectious diseases 2019 11 (1): e2019038. Phanrahan Paramee, Yamsri Supawadee, Teawtrakul Nattiya, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
| KFL1 Gene Variants in a-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese Population. Hemoglobin 2018 Sep 1-5. Jiang Fan, Qu Yan-Xia, Chen Gui-Lan, Li Jian, Zhou Jian-Ying, Zuo Lian-Dong, Liao Can, Li Dong-Z |
| Molecular Understanding of Non-Transfusion-Dependent Thalassemia Associated with Hemoglobin E-ß-Thalassemia in Northeast Thailand. Acta haematologica 2016 Oct 136 (4): 233-239. Yamsri Supawadee, Pakdee Naruwat, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
| Changes in hematological parameters in a-thalassemia individuals co-inherited with erythroid Krüppel-like factor mutations. Clinical genetics 2015 Jul 88 (1): 56-61. Yu L-H, Liu D, Cai R, Shang X, Zhang X-H, Ma X-X, Yan S-H, Fang P, Zheng C-G, Wei X-F, Liu Y-H, Zhou T-B, Xu X |
| 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 |
| Mutation screening of the Krüppel-like factor 1 gene using single-strand conformational polymorphism in a cohort of Iranian ß-thalassemia patients. Hemoglobin 2015 39 (1): 24-9. Zaker-Kandjani Behzad, Namdar-Aligoodarzi Pegah, Azarkeivan Azita, Najmabadi Hossein, Banan Meh |
| KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of ß-thalassemia. Blood 2014 Jul 124 (5): 803-11. Liu Dun, Zhang Xinhua, Yu Lihua, Cai Ren, Ma Xiaoxia, Zheng Chengguang, Zhou Yuqiu, Liu Qiji, Wei Xiaofeng, Lin Li, Yan Tizhen, Huang Jiwei, Mohandas Narla, An Xiuli, Xu Xiangm |
| Genomic variation in the MAP3K5 gene is associated with ß-thalassemia disease severity and hydroxyurea treatment efficacy. Pharmacogenomics 2013 Apr 14 (5): 469-83. Tafrali Christina, Paizi Arsinoi, Borg Joseph, Radmilovic Milena, Bartsakoulia Marina, Giannopoulou Emily, Giannakopoulou Olga, Stojiljkovic-Petrovic Maja, Zukic Branka, Poulas Konstantinos, Stavrou Eleana F, Lambropoulou Polyxeni, Kourakli Alexandra, Felice Alexander E, Papachatzopoulou Adamantia, Philipsen Sjaak, Pavlovic Sonja, Georgitsi Marianthi, Patrinos George |
| KLF1 gene mutations in Chinese adults with increased fetal hemoglobin. Hemoglobin 2013 37 (5): 501-6. Wang Ting, He Yi, Zhou Jian-Ying, Xie Xing-Mei, Li Jian, Li Ru, Liao Can, Li Dong-Z |
| KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in ß-hemoglobinopathy patients. Pharmacogenomics 2012 Oct 13 (13): 1487-500. Borg Joseph, Phylactides Marios, Bartsakoulia Marina, Tafrali Christina, Lederer Carsten, Felice Alexander E, Papachatzopoulou Adamantia, Kourakli Alexandra, Stavrou Eleana F, Christou Soteroula, Hou Jun, Karkabouna Sophia, Lappa-Manakou Christina, Ozgur Zeliha, van Ijcken Wilfred, von Lindern Marieke, Grosveld Frank G, Georgitsi Marianthi, Kleanthous Marina, Philipsen Sjaak, Patrinos George |
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- Page last updated:Jan 12, 2022
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