Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 127 Records) |
Query Trace: BCL11A[original query] |
---|
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 |
Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children.
Journal of the National Cancer Institute 2020 9 113 (7): 933-937. Lee Shawn H R, Qian Maoxiang, Yang Wentao, Diedrich Jonathan D, Raetz Elizabeth, Yang Wenjian, Dong Qian, Devidas Meenakshi, Pei Deqing, Yeoh Allen, Cheng Cheng, Pui Ching-Hon, Evans William E, Mullighan Charles G, Hunger Stephen P, Savic Daniel, Relling Mary V, Loh Mignon L, Yang Jun |
Association between BCL11A, HSB1L-MYB, and XmnI ?G-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients. Annals of hematology 2020 Aug . El-Ghamrawy Mona, Yassa Marianne E, Tousson Angie M S, El-Hady Marwa Abd, Mikhaeil Erini, Mohamed Nada B, Khorshied Mervat Mamdo |
Detection of BCL11A and HBS1L-MYB Genotypes in Sickle Cell Anemia. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2020 Oct 36 (4): 705-710. Qadah Talal, Noorwali Abdulwahab, Alzahrani Fatma, Banjar Alaa, Filimban Najlaa, Felimban Ra |
F cell numbers are associated with an X-linked genetic polymorphism and correlate with haematological parameters in patients with sickle cell disease. British journal of haematology 2020 Oct . Urio Florence, Nkya Siana, Rooks Helen, Mgaya Josephine A, Masamu Upendo, Zozimus Sangeda Raphael, Mmbando Bruno P, Brumat Marco, Mselle Ted, Menzel Stephan, Luzzatto Lucio, Makani Jul |
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 |
A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease. Blood advances 2021 07 5 (14): 2839-2851. Rampersaud Evadnie, Kang Guolian, Palmer Lance E, Rashkin Sara R, Wang Shuoguo, Bi Wenjian, Alberts Nicole M, Anghelescu Doralina, Barton Martha, Birch Kirby, Boulos Nidal, Brandow Amanda M, Brooke Russell John, Chang Ti-Cheng, Chen Wenan, Cheng Yong, Ding Juan, Easton John, Hodges Jason R, Kanne Celeste K, Levy Shawn, Mulder Heather, Patel Ashwin P, Puri Latika, Rosencrance Celeste, Rusch Michael, Sapkota Yadav, Sioson Edgar, Sharma Akshay, Tang Xing, Thrasher Andrew, Wang Winfred, Yao Yu, Yasui Yutaka, Yergeau Donald, Hankins Jane S, Sheehan Vivien A, Downing James R, Estepp Jeremie H, Zhang Jinghui, DeBaun Michael, Wu Gang, Weiss Mitchell |
Modulatory effect of single nucleotide polymorphism in Xmn1, BCL11A and HBS1L-MYB loci on foetal haemoglobin levels in ?-thalassemia major and Intermedia patients. JPMA. The Journal of the Pakistan Medical Association 2021 May 71 (5): 1394-1398. Bashir Shabnam, Mahmood Saqib, Mohsin Shahida, Tabassum Iqra, Ghafoor Mahmood, Sajjad Oshe |
Genotypic Diversity among Angolan Children with Sickle Cell Anemia. International journal of environmental research and public health 2021 6 18 (10): . Delgadinho Mariana, Ginete Catarina, Santos Brígida, Miranda Armandina, Brito Migu |
Predictive SNPs for ?-thalassemia/HbE disease severity. Scientific reports 2021 5 11 (1): 10352. Munkongdee Thongperm, Tongsima Sissades, Ngamphiw Chumpol, Wangkumhang Pongsakorn, Peerapittayamongkol Chayanon, Hashim Hafizah Binti, Fucharoen Suthat, Svasti Saovar |
A Pragmatic Scoring Tool to Predict Hydroxyurea Response Among ?-Thalassemia Major Patients in Pakistan. Journal of pediatric hematology/oncology 2021 3 44 (1): e77-e83. Ansari Saqib H, Hussain Zeeshan, Zohaib Muhammad, Parveen Sadia, Kaleem Bushra, Qamar Hina, Adil Omair, Khan Muhammad T, Shamsi Tahir |
Genetic modifiers of fetal hemoglobin affect the course of sickle cell disease in patients treated with hydroxyurea. Haematologica 2021 10 107 (7): 1577-1588. Allard Pierre, Alhaj Nareen, Lobitz Stephan, Cario Holger, Jarisch Andreas, Grosse Regine, Oevermann Lena, Hakimeh Dani, Tagliaferri Laura, Kohne Elisabeth, Kopp-Schneider Annette, Kulozik Andreas E, Kunz Joachim |
Significance of genetic modifiers of hemoglobinopathies leading towards precision medicine. Scientific reports 2021 Oct 11 (1): 20906. Hariharan Priya, Gorivale Manju, Sawant Pratibha, Mehta Pallavi, Nadkarni Ani |
Fetal hemoglobin-boosting haplotypes of BCL11A gene and HBS1L-MYB intergenic region in the prediction of clinical and hematological outcomes in a cohort of children with sickle cell anemia. Journal of human genetics 2022 9 67 (12): 701-709. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Viana Marcos Borato, Luizon Marcelo Rizzat |
Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico. Journal of tropical pediatrics 2022 9 68 (5): . Rizo-de la Torre L C, Borrayo-López F J, Perea-Díaz F J, Aquino E, Venegas M, Hernández-Carbajal C, Espinoza-Mata L L, Ibarra-Cortés |
Effects of Senegal haplotype (Xmn1-rs7412844), alpha-thalassemia (3.7kb HBA1/HBA2 deletion), NPRL3-rs11248850 and BCL11A-rs4671393 variants on sickle cell nephropathy. International journal of biochemistry and molecular biology 2022 5 13 (2): 5-16. Ndour El Hadji Malick, Mnika Khuthala, Guèye Tall Fatou, Seck Moussa, Dème Ly Indou, Nembaware Victoria, Sagna-Bassène Hélène Ange Thérèse, Dione Rokhaya, Ndongo Aliou Abdoulaye, Diop Jean Pascal Demba, Barry Nènè Oumou Kesso, Djité Moustapha, Ndiaye Diallo Rokhaya, Guèye Papa Madièye, Diop Saliou, Diagne Ibrahima, Cissé Aynina, Wonkam Ambroise, Lopez Sall Philomè |
Fetal hemoglobin modulates neurocognitive performance in sickle cell anemia. Current research in translational medicine 2022 3 70 (3): 103335. Heitzer Andrew M, Longoria Jennifer, Rampersaud Evadnie, Rashkin Sara R, Estepp Jeremie H, Okhomina Victoria I, Wang Winfred C, Raches Darcy, Potter Brian, Steinberg Martin H, King Allison A, Kang Guolian, Hankins Jane |
Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2022 3 55 e11920. Campello C P, Lima-Silva M F B, Lima E L S de, Nunes G R S, Silva H A M, Dellalibera E, Britto L R P B de, Lemos C A A, Muniz M T |
Do Genetic Polymorphisms Affect Fetal Hemoglobin (HbF) Levels in Patients With Sickle Cell Anemia Treated With Hydroxyurea? A Systematic Review and Pathway Analysis. Frontiers in pharmacology 2021 12 779497. Sales Rahyssa Rodrigues, Nogueira Bárbara Lisboa, Tosatti Jéssica Abdo Gonçalves, Gomes Karina Braga, Luizon Marcelo Rizzat |
A novel BCL11A polymorphism influences gene expression, therapeutic response and epilepsy risk: A multicenter study. Frontiers in molecular neuroscience 2022 12 15 1010101. Wang Shitao, Cai Xuemei, Liu Shiyong, Zhou Qixin, Wang Ting, Du Sunbing, Wang Dan, Yang Fei, Wu Qian, Han Yanbi |
Frequency of secondary modifiers in Beta Thalassemia intermedia in patients from Northern Punjab. Pakistan journal of medical sciences 2023 9 39 (5): 1517-1520. Fariha Nasreen, Attika Khalid, Lubna Zafar, Suhaib Ahmad, Asma Shai |
Correlations between Multiple SNPs and HbF Levels in ?-Thalassemia Carriers. Clinical laboratory 2023 9 69 (9): . Qin Xu, Ling Huang, Tingting Jin, Yuanyuan Han, Juan Liu, Wenqiu Zhang, Yao Biao, Bangquan An, Shengwen Hua |
Molecular basis of a high Hb A/Hb F?-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with ?-globin gene triplication. PeerJ 2023 5 11 e15308. Chayada Soontornpanawet, Kritsada Singha, Hataichanok Srivorakun, Wanicha Tepakhan, Goonnapa Fucharoen, Supan Fucharo |
Identifying signatures of positive selection in human populations from North Africa. Scientific reports 2023 5 13 (1): 8166. Rocio Caro-Consuegra, Marcel Lucas-Sánchez, David Comas, Elena Bos |
Responses of ?-thalassemia and compound heterozygote of Sickle/?thalassemia of BCL11A Gene Polymorphism in Pakistani Patients. Pakistan journal of medical sciences 2023 11 39 (6): 1788-1792. Nayab Soomro, Mohsin Wahid, Mehreen Mehmood, Syed Hasan Dani |
BCL11A Polymorphism in Egyptian Children with ?-Thalassemia: Relation to Phenotypic Heterogeneity. Journal of pediatric genetics 2023 1 12 (1): 16-22. Salah Nouran Y, Ali Heba G A, Bassiouny Noha, Salem Lamya, Taha Sara I, Youssef Mariam K, Annaka Layla, Barakat Noha |
Detection of Asymptomatic Sickle Cell Hemoglobin Carriers and Fetal Hemoglobin Regulating Genetic Variants in African Descendants from Oaxaca, Mexico. Anemia 2024 5 2024 4940760. María De Los Ángeles Romero-Tlalolini, Sergio Roberto Aguilar-Ruiz, Rafael Baltiérrez-Hoyos, Jaime Vargas-Arzola, Luis Alberto Hernández-Osorio, Verónica Rocío Vásquez-Garzón, Héctor Ulises Bernardino-Hernández, Honorio Torres-Aguil |
Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease. International journal of molecular sciences 2024 5 25 (10): . Veerle Labarque, Emmanuel Chide Okocha, |
Foetal haemoglobin elevation, unfavourable prognosis, and protective role of genetic variants HBG2 rs7482144, HBS1L-MYB rs9399137 and BCL11A rs4671393 in children with ALL. Journal of genetics 2024 5 103 . Francisco Javier Borrayo-LóPez, Bertha Ibarra-Cortés, FranciscoJavier Perea-Díaz, Abril Ixchel MuñOz-Zúñiga, Héctor Montoya-Fuentes, Janeth Margarita Soto-Padilla, Lourdes Del Carmen Rizo-De La Tor |
Genetic Modifiers of Sickle Cell Anemia Phenotype in a Cohort of Angolan Children. Genes 2024 4 15 (4): . Catarina Ginete, Mariana Delgadinho, Brígida Santos, Armandina Miranda, Carina Silva, Paulo Guerreiro, Emile R Chimusa, Miguel Bri |
- Page last reviewed:Feb 1, 2024
- Page last updated:Jun 03, 2024
- Content source: