Background Many publications report the prevalence of chronic kidney disease (CKD) in the
general population. Comparisons across studies are hampered as CKD prevalence …

MYH9 related diseases are caused by mutations in the MYH9 gene and constitute a rare
group of genetic entities. Its inheritance follows an autosomal dominant pattern. The MYH9 …

Several common KCNQ1 gene polymorphisms have been associated with the risk of type 2
diabetes (T2DM) and diabetic nephropathy. This effect is explained by the role of the kcnq1 …

The kidney lost a lot of protein in the urine when you have nephrotic syndrome (NS). Clinical
manifestations mostly common in NS include massive proteinuria, hypoalbuminemia …

Single‐nucleotide polymorphisms (SNPs) in MYH9-APOL1 gene regions have been
reported to be associated with diabetic kidney disease (DKD) in the American population …

Background/Aims: This study explored the correlation between hypertension and non-
muscle myosin heavy chain 9 (MYH9) gene polymorphisms in Chinese chronic kidney …

Chronic kidney disease (CKD) has shown an increasing prevalence in the last century. CKD
encompasses a poor prognosis related to a remarkable number of comorbidities, and many …

A total of 569 individuals aged 55–85 and Caucasian were genotyped for SNP rs10927887
in the K a renal chloride channel gene (CLCNKA). The following variables were significantly …

非肌肉肌球蛋白IIA (non-muscle myosin IIA, NM IIA) 由非肌肉肌球蛋白重链9 (Non-muscle
myosin heavy chain 9, MYH9) 基因编码, 是非肌肉肌球蛋白II 的家族成员, 在多种细胞中表达 …

Introduction Certain polymorphisms in the non-muscle myosin IIA (MYH9) and
apolipoprotein L1 (APOL1) genes have been associated to chronic kidney disease (CKD) in …