Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Thalassemia and KLF1[original query] |
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| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 ?-thalassemia patients. Hemoglobin 2015 39 (1): 24-9. Zaker-Kandjani Behzad, Namdar-Aligoodarzi Pegah, Azarkeivan Azita, Najmabadi Hossein, Banan Meh |
| 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 |
| KFL1 Gene Variants in ?-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 |
| Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran. Journal of pediatric hematology/oncology 2018 2 40 (3): 192-195. Hamid Mohammad, Ershadi Oskouei Sanaz, Shariati Gholamreza, Babaei Esmaeil, Galehdari Hamid, Saberi Alihossein, Sedaghat Alire |
| Analysis of the Genotypes in a Chinese Population with Increased Hb A and Low Hematological Indices. Hemoglobin 2018 10 42 (3): 154-158. Jiang Fan, Chen Gui-Lan, Li Jian, Zhou Jian-Ying, Liao Can, Li Dong-Z |
| KLF1 gene and borderline hemoglobin A in Saudi population. Archives of medical science : AMS 2018 1 14 (1): 230-236. Borgio J Francis, AbdulAzeez Sayed, Al-Muslami Ahmed M, Naserullah Zaki A, Al-Jarrash Sana, Al-Suliman Ahmed M, Al-Madan Mohammed S, Al-Ali Amein |
| Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia. Annals of hematology 2019 9 98 (12): 2673-2681. Nicolau Marta, Vargas Sofia, Silva Marisa, Coelho Andreia, Ferreira Emanuel, Mendonça Joana, Vieira Luís, Kjöllerström Paula, Maia Raquel, Silva Rita, Dias Alexandra, Ferreira Teresa, Morais Anabela, Soares Isabel Mota, Lavinha João, Faustino Pau |
| Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-?-Thalassemia Disease without ?-Thalassemia. Mediterranean journal of hematology and infectious diseases 2019 11 (1): e2019038. Phanrahan Paramee, Yamsri Supawadee, Teawtrakul Nattiya, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
| A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as ?-Thalassemia Intermedia Due to a KLF1 Gene Mutation. Hemoglobin 2019 6 43 (2): 140-144. Yang Kun, Ren Quan, Wu Yi, Zhou Yali, Yin Xiaol |
| Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with ?-Thalassemia Intermedia. Hemoglobin 2019 2 43 (1): 12-17. Tamaddoni Ahmad, Khabaz Astaneh Sahar, Tabaripour Reza, Akhavan-Niaki Hal |
| A novel SNP rs11759328 on Rho GTPase-activating protein 18 gene is associated with the expression of Hb F in hemoglobin E-related disorders. Annals of hematology 2019 11 99 (1): 23-29. Jomoui Wittaya, Tepakhan Wanicha, Yamsri Supawadee, Srivorakun Hataichanok, Fucharoen Goonnapa, Fucharoen Sup |
| Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous ?-Thalassemia 3.5?kb Deletions. Hemoglobin 2020 Sep 1-6. Tepakhan Wanicha, Kanjanaopas Sataron, Srewaradachpisal Kornt |
| Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA in ?-thalassaemia carriers. Archives of medical science : AMS 2021 8 17 (4): 1064-1074. Cyrus Cyril, Vatte Chittibabu, Chathoth Shahanas, Sayed Abdul Azeez, Borgio J Francis, Alrubaish Mohammed Abdullah, Alfalah Rawan, Alsaikhan Jana, Al Ali Amein |
| Borderline HbA levels: Dilemma in diagnosis of beta-thalassemia carriers. Mutation research. Reviews in mutation research 2021 12 788 108387. Colaco Stacy, Nadkarni Ani |
| Identification and Functional Analysis of Known and New Mutations in the Transcription Factor KLF1 Linked with ?-Thalassemia-like Phenotypes. Biology 2023 4 12 (4): . Rosa Catapano, Raffaele Sessa, Silvia Trombetti, Elena Cesaro, Filippo Russo, Paola Izzo, Alexandros Makis, Michela Gros |
| Whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia. Hematology (Amsterdam, Netherlands) 2023 3 28 (1): 2187155. Hantaweepant Chattree, Suktitipat Bhoom, Pithukpakorn Manop, Chinthammitr Yingyong, Limwongse Chanin, Tansiri Nawaporn, Sawatnatee Surasak, Takpradit Chayamon, Rotchanapanya Wannaphorn, Pongudom Saranya, Charoenprasert Kanyaporn, Paiboonsukwong Kittiphong, Thamprasert Wichuda, Nolwachai Narumol, Rattanasawat Wanlapa, Sae-Aeng Busakorn, Khorwanichakij Nisachon, Saetow Putchong, Saengboon Supawee, Kamjornpreecha Krittichat, Pholmoo Wikanda, Dujjawan Boonyanuch, Siritanaratkul Noppad |
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