Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: KLF1[original query] |
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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 |
Krüppel-like factor 1 mutations and expression of hemoglobins F and A2 in homozygous hemoglobin E syndrome. Annals of hematology 2015 Jul 94 (7): 1093-8. Tepakhan Wanicha, Yamsri Supawadee, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder. Blood cells, molecules & diseases 2016 Jul 59 85-91. Tepakhan Wanicha, Yamsri Supawadee, Sanchaisuriya Kanokwan, Fucharoen Goonnapa, Xu Xiangmin, Fucharoen Sup |
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 |
Fetal haemoglobin induction in sickle cell disease. British journal of haematology 2017 11 180 (2): 189-200. Paikari Alireza, Sheehan Vivien |
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 |
Clinical and genetic features of congenital dyserythropoietic anemia (CDA). European journal of haematology 2018 6 101 (3): 368-378. Moreno-Carralero María-Isabel, Horta-Herrera Saul, Morado-Arias Marta, Ricard-Andrés María-Pilar, Lemes-Castellano Angelina, Abio-Calvete Mariola, Cedena-Romero María-Teresa, González-Fernández Fernando-Ataulfo, Llorente-González Laura, Periago-Peralta Adela-María, de-la-Iglesia-Íñigo Silvia, Méndez Manuel, Morán-Jiménez María-Jo |
Survey and evaluation of mutations in the human KLF1 transcription unit. Scientific reports 2018 4 8 (1): 6587. Gnanapragasam Merlin Nithya, Crispino John D, Ali Abdullah M, Weinberg Rona, Hoffman Ronald, Raza Azra, Bieker James |
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 |
Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data. Transfusion 2018 12 59 (2): 768-778. Schoeman Elizna M, Roulis Eileen V, Perry Maree A, Flower Robert L, Hyland Catherine |
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 |
Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. BMC medical genetics 2020 Jun 21 (1): 125. Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul |
Molecular and biochemical study of glutaric aciduria type 1 in 49 Russian families: nine novel mutations in the GCDH gene. Metabolic brain disease 2020 4 35 (6): 1009-1016. Kurkina Marina V, Mihaylova Svetlana V, Baydakova Galina V, Saifullina Elena V, Korostelev Sergey A, Pyankov Denis V, Kanivets Ilya V, Yunin Maksim A, Pechatnikova Natalya L, Zakharova Ekaterina |
An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype. Transfusion 2021 9 61 (10): E73-E74. Floch Aline, Vege Sunitha, Burgos Anna, Kuchma Sharon, Bell Mollie, Lomas-Francis Christine, Westhoff Connie |
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 |
Krüppel-like factor 1 (KLF1) gene single nucleotide polymorphisms in sickle cell disease and its association with disease-related morbidities. Annals of hematology 2021 Jan . Kumar Ravindra, Yadav Rajiv, Mishra Sweta, Singh M P S S, Gwal Anil, Bharti Praveen K, Rajasubramaniam Shanmug |
A stepwise haematological screening and whole-exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A from a cohort of 47336 individuals. International journal of laboratory hematology 2022 9 45 (1): 90-95. Lou Jiwu, Ye Yuhua, Sun Manna, Zhao Ying, Fu Youqing, Liu Yanh |
Whole-exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes. British journal of haematology 2022 7 198 (6): 1051-1064. Songdej Duantida, Kadegasem Praguywan, Tangbubpha Noppawan, Sasanakul Werasak, Deelertthaweesap Bhurichaya, Chuansumrit Ampaiwan, Sirachainan Nongnu |
Identification of Lutheran Blood Groups and Genetic Variants within KLF1 among Thai Blood Donors. Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2023 9 50 (4): 313-320. Kamphon Intharanut, Piyathida Khumsuk, Oytip Nathala |
In silico genotyping of blood group alleles using WGS data: a comparative study of the Orang Asli in Peninsular Malaysia. Journal of genetics 2023 9 102 . Mercy Rophina, Teh Lay Kek, Sridhar Sivasubbu, Vinod Scaria, Mohd Zaki Sall |
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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- Page last updated:Apr 22, 2024
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