Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Anemia and HMOX1[original query] |
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| Polymorphism in the HMOX1 gene is associated with high levels of fetal hemoglobin in Brazilian patients with sickle cell anemia. Hemoglobin 2013 37 (4): 315-24. Gil Gislene P, Ananina Galina, Oliveira Mariana B, Costa Fernando F, Silva Márcio J, Santos Magnun N N, Bezerra Marcos A C, Hatzlhofer Betânia L D, Araujo Aderson S, Melo Mônica |
| Implication of HMOX1 and CCR5 genotypes on clinical phenotype of Egyptian patients with sickle cell anemia. Annals of hematology 2019 Apr . Bakr Salwa, Khorshied Mervat, Talha Noha, Jaffer Karim Yahia, Soliman Nohair, Eid Khaled, El-Ghamrawy Mo |
| Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients. Hematology, transfusion and cell therapy 2020 May . Chinedu Okeke, Tonassé Wouitchékpo Vincent, Albuquerque Dulcinéia Martins, Domingos Igor de Farias, Araújo Aderson da Silva, Bezerra Marcos André Cavalcanti, Sonati Maria de Fátima, Santos Magnun Nueldo Nunes D |
| Significance of heme oxygenase-1(HMOX1) gene on fetal hemoglobin induction in sickle cell anemia patients. Scientific reports 2020 10 10 (1): 18506. Hariharan Priya, Chavan Vrushali, Nadkarni Ani |
| Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
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