Diabetic nephropathy is a serious diabetic complication. Elevated blood glucose is a major cause of cerebral palsy, but diabetic nephropathy is a complex multi-site disease. Family studies have shown that inherited factors also increase the risk of disease. For the past ten years, genome-wide association studies (GWAS) have posed a danger to strong BCS to identify genetic studies. In recent years, more people have become participants in GWAS, which leads to an increase in statistical power to identify a large genetic risk. In addition, studies across the exome and genome sequence aim to identify rare genetic risk factors for renal failure.
| Mualliflar | Pulatova Sh.H, Shodiqulova G.Z, Kenjaev M.L |
|---|---|
| Jurnal | Klinik fanlar yilnomasi |
| Nashr sanasi | 2026-05-02 |
| Jild | 3 |
| Son | 1/1 |
| Til | O‘zbek |
diabetic kidney disease, renal failure, GWAS, genome sequencing, exome sequencing, epigenetics, whole epigenomic association study, EWAS, диабетическая болезнь почек, почечная недостаточность, GWAS, секвенирование генома, секвенирование экзома, эпигенетика, исследование всей эпигеномной ассоциации, EWAS, diabetik buyrak kasalligi, buyrak yetishmovchiligi, GWAS, genomni ketma-ketlashtirish, ekzomni ketma-ketlashtirish, epigenetika, butun epigenom assotsiatsiyasini tadqiq qilish, EWAS
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