Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: CYB5R3[original query] |
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Evaluation of polymorphisms in the sulfonamide detoxification genes NAT2, CYB5A, and CYB5R3 in patients with sulfonamide hypersensitivity. Pharmacogenetics and genomics 2012 Oct 22 (10): 733-40. Sacco James C, Abouraya Mahmoud, Motsinger-Reif Alison, Yale Steven H, McCarty Catherine A, Trepanier Lauren |
Polymorphisms in the carcinogen detoxification genes CYB5A and CYB5R3 and breast cancer risk in African American women. Cancer causes & control : CCC 2014 Nov 25 (11): 1513-21. Blanke Kristina L, Sacco James C, Millikan Robert C, Olshan Andrew F, Luo Jingchun, Trepanier Lauren |
A single-nucleotide polymorphism in the canine cytochrome b reductase (CYB5R3) gene is associated with sulfonamide hypersensitivity and is overrepresented in Doberman Pinschers. Journal of veterinary pharmacology and therapeutics 2018 1 41 (3): 402-408. Reinhart J M, Ekena J, Cioffi A C, Trepanier L |
The CYB5R3 and G6PD A alleles modify severity of anemia in malaria and sickle cell disease. American journal of hematology 2020 7 95 (11): 1269-1279. Gordeuk Victor R, Shah Binal N, Zhang Xu, Thuma Philip E, Zulu Stenford, Moono Rodgers, Reading N Scott, Song Jihyun, Zhang Yingze, Nouraie Mehdi, Campbell Andrew, Minniti Caterina P, Rana Sohail R, Darbari Deepika S, Kato Gregory J, Niu Mei, Castro Oswaldo L, Machado Roberto, Gladwin Mark T, Prchal Josef |
Differences in the genotype frequencies of genes related to blood pressure regulation - a comparative study between South-West Europe and Peri-equatorial Africa. African health sciences 2022 3 21 (4): 1669-1676. Aguiar Laura, Semente Ildegário, Ferreira Joana, Carvalho Andreia, Silva Alda P, Caroça Cristina, Caria Helena, Damasceno Albertino, Laires Maria J, Sardinha Luís, Monteiro Cristina, Mascarenhas Mário R, Faustino Paula, Inácio Ângela, Bicho Manu |
Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia. Molecular biology reports 2022 1 49 (3): 2141-2147. Deorukhkar Anuradha, Kulkarni Anuja, Kedar Prabhak |
Identification of High-Risk Single Nucleotide Polymorphisms in the Human CYB5R3 Gene Responsible for Recessive Congenital Methemoglobinemia: A Computational Approach. Molecular syndromology 2023 10 14 (5): 375-393. Emna Bouatrous, Sonia Nouira, Samia Menif, Houyem Ouragi |
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- Page last updated:Apr 16, 2024
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