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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 17 (of 17 Records)

Query Trace: Disease and KLF1[original query]
Ten novel mutations in the erythroid transcription factor KLF1 gene associated with increased fetal hemoglobin levels in adults.
Haematologica 2012 Mar 97 (3): 340-3.
Gallienne Alice E, Dréau Hélène M P, Schuh Anna, Old John M, Henderson Shirl
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
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
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
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
Fetal haemoglobin induction in sickle cell disease.
British journal of haematology 2017 11 180 (2): 189-200.
Paikari Alireza, Sheehan Vivien
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
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
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
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
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
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