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Hematology Volume 21, 2016 - Issue 7
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Hemoglobinopathy

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Leila ChaouchUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, TunisiaCorrespondence[email protected]
,
Imen MoumniUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
,
Houyem OuraginiUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
,
Imen DarragiUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
,
Miniar KalaiUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
,
Dorra ChaouachiUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
,
Imen BoudriguaUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
,
Raouf HafsiaUniversité de Tunis El Manar, Hopital Aziza Othmena, d'Hématologie Clinique, Tunisia
&
Salem AbbesUniversité de Tunis El Manar, Institut Pasteur de Tunis, Laboratoire d'Hématologie Moléculaire et Cellulaire, Tunisia
 show all
Pages 425-429 | Published online: 22 Jan 2016

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Gloria Pokuaa Manu, Catherine Segbefia, Benoit Banga N’guessan, Shadrack Asiedu Coffie & George Obeng Adjei. (2022) Association Between Selected Single Nucleotide Polymorphisms in Globin and Related Genes and Response to Hydroxyurea Therapy in Ghanaian Children with Sickle Cell Disease. Pharmacogenomics and Personalized Medicine 15, pages 205-214.
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Ahmet Genc, Deniz Tastemir Korkmaz, Suleyman Bayram & Eyyup Rencuzogullari. (2020) The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey. Hemoglobin 44:4, pages 231-239.
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Articles from other publishers (12)

Justin K. Kirkham, Jeremie H. Estepp, Mitch J. Weiss & Sara R. Rashkin. (2023) Genetic Variation and Sickle Cell Disease Severity. JAMA Network Open 6:10, pages e2337484.
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Poonam Tripathi, Sarita Agarwal, Kausik Mandal, Anshul Gupta & Aditya Narayan Sarangi. (2023) Impact of Genetic Polymorphisms in Modifier Genes in Determining Fetal Hemoglobin Levels in Beta-Thalassemia. Thalassemia Reports 13:1, pages 85-112.
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L C Rizo-de la Torre, F J Borrayo-López, F J Perea-Díaz, E Aquino, M Venegas, C Hernández-Carbajal, L L Espinoza-Mata & B Ibarra-Cortés. (2022) Fetal hemoglobin regulating genetic variants identified in homozygous (HbSS) and heterozygous (HbSA) subjects from South Mexico. Journal of Tropical Pediatrics 68:5.
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Siti Nur Nabeela A’ifah Mohammad, Salfarina Iberahim, Wan Suriana Wan Ab Rahman, Mohd Nazri Hassan, Hisham Atan Edinur, Maryam Azlan & Zefarina Zulkafli. (2022) Single Nucleotide Polymorphisms in XMN1-HBG2, HBS1L-MYB, and BCL11A and Their Relation to High Fetal Hemoglobin Levels That Alleviate Anemia. Diagnostics 12:6, pages 1374.
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YousefSaeed Mohammad Abu Za'ror, SitiNor Assyuhada Mat Ghani, NurSalwani Bakar, Zefarina Zulkafli & Maryam Azlan. (2022) Detection of BCL11A, HMIP, and XmnI polymorphisms among anemic pregnant women in hospital Universiti Sains Malaysia. Journal of Applied Hematology 13:4, pages 183.
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C.P. Campello, M.F.B. Lima-Silva, E.L.S. de Lima, G.R.S. Nunes, H.A.M. Silva, E. Dellalibera, L.R.P.B. de Britto, C.A.A. Lemos & M.T.C. Muniz. (2022) Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review. Brazilian Journal of Medical and Biological Research 55.
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Charles T. Quinn, Omar Niss, Min Dong, Amanda Pfeiffer, Jennifer Korpik, Mary Reynaud, Holly Bonar, Theodosia A. Kalfa, Luke R. Smart, Punam Malik, Russell E. Ware, Alexander A. Vinks & Patrick T. McGann. (2021) Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics‐guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia. British Journal of Haematology 194:3, pages 617-625.
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Ylenia Barbanera, Francesco Arcioni, Hovirag Lancioni, Roberta La Starza, Irene Cardinali, Caterina Matteucci, Valeria Nofrini, Antonella Roetto, Antonio Piga, Paola Grammatico, Maurizio Caniglia, Cristina Mecucci & Paolo Gorello. (2020) Comprehensive analysis of mitochondrial and nuclear DNA variations in patients affected by hemoglobinopathies: A pilot study. PLOS ONE 15:10, pages e0240632.
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Talal Qadah, Abdulwahab Noorwali, Fatma Alzahrani, Alaa Banjar, Najlaa Filimban & Raed Felimban. (2020) Detection of BCL11A and HBS1L-MYB Genotypes in Sickle Cell Anemia. Indian Journal of Hematology and Blood Transfusion 36:4, pages 705-710.
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Li Hu, Ling Huang, Yuanyuan Han, Tingting Jin, Juan Liu, Minmin Jiang, Xingmei Liu, Yuanyuan Li, Wenping Han, Bangquan An & Shengwen Huang. (2020) Association of polymorphisms in the HBG1‐HBD intergenic region with HbF levels . Journal of Clinical Laboratory Analysis 34:6.
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Jiawei Yin, Xiaoli Xie, Yufu Ye, Lijuan Wang & Fengyuan Che. (2019) BCL11A: a potential diagnostic biomarker and therapeutic target in human diseases. Bioscience Reports 39:11.
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Raffaella Colombatti & Laura Sainati. (2016) Management of Children With Sickle Cell Disease in Europe: Current Situation and Future Perspectives. EMJ Hematology, pages 129-135.
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