Cargando…
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
INTRODUCTION: Mutations affecting genes involved in oxidative and signaling pathways may be associated with kidney disease in sickle cell anemia. We determined the allele and genotype frequencies of some polymorphisms in the promoter regions of the Heme Oxygenase-1 (HMOX1) [rs2071746 (A > T) and...
Autores principales: | 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 dos |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Hematologia e Hemoterapia
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8211626/ https://www.ncbi.nlm.nih.gov/pubmed/32461055 http://dx.doi.org/10.1016/j.htct.2020.01.009 |
Ejemplares similares
-
Endothelial Barrier Integrity Is Disrupted In Vitro by Heme and by Serum From Sickle Cell Disease Patients
por: Santaterra, Vanessa Araujo Gomes, et al.
Publicado: (2020) -
The CCR5Δ32 Polymorphism in Brazilian Patients with Sickle Cell Disease
por: Lopes, Mariana Pezzute, et al.
Publicado: (2014) -
Haptoglobin Gene Polymorphism in Patients with Sickle Cell Anemia: Findings from a Nigerian Cohort Study
por: Olatunya, Oladele Simeon, et al.
Publicado: (2020) -
Haptoglobin: an emerging candidate for phenotypic modulation of sickle cell anemia?()
por: Santos, Magnun Nueldo Nunes dos
Publicado: (2015) -
Investigating alpha-globin structural variants: a retrospective review of 135,000 Brazilian individuals
por: Kimura, Elza Miyuki, et al.
Publicado: (2015)