Renin Gene Polymorphisms in Bangladeshi Hypertensive Population
Author:
Publisher
Ivyspring International Publisher
Subject
General Medicine
Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Mutational analyses of mitochondrial ATP6 gene reveal a possible association with abnormal levels of lactic acid and ammonia in Bangladeshi children with autism spectrum disorder: A case-control study;Human Gene;2024-12
2. Genetic analyses of truncated variant rs200185429 in ZNT8 encoding SLC30A8 gene with respect to prediabetes and type 2 diabetes in Bangladeshi population;Endocrine and Metabolic Science;2024-09
3. Genetic and epigenetic analyses of IFN-γ gene proximal promoter region underlying positive correlation between persistently high anti-SARS-CoV-2 IgG and IFN-γ among COVID-19 vaccinated Bangladeshi adults;Vaccine;2024-08
4. Mutational landscape of mitochondrial cytochrome b and its flanking tRNA genes associated with increased mitochondrial DNA copy number and disease risk in children with autism;Gene Reports;2024-06
5. Endocrinological, immunological and metabolic features of patients with Fabry disease under therapy;Journal of Pediatric Endocrinology and Metabolism;2023-05-31
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