Publications by authors named "Shi-Lu Cao"

Article Synopsis
  • Diabetic nephropathy (DN) is a major contributor to end-stage renal disease, with unclear mechanisms hindering effective diagnosis and treatment.* -
  • The study used nanopore-based transcriptome sequencing on blood samples from patients with slow (DNSP) and rapid (DNRP) progression of DN, identifying thousands of novel transcripts and genes.* -
  • Key findings revealed that specific pathways related to oxidative stress, lipid metabolism, and cell death processes are differentially expressed in slow versus fast progressing DN, offering insights for future research.*
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To evaluate whether platelet-to-albumin ratio (PAR) can predict diabetic nephropathy (DN) in type 2 diabetes mellitus (T2DM). A total of 140 patients with T2DM and 40 healthy individuals were enrolled retrospectively. T2DM patients were divided into three groups based on the urinary albumin-to-creatinine ratio, PAR was compared and receiver operating characteristic curve was constructed to evaluate the predictive value of PAR in DN in T2DM.

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Objectives: Cyclin-dependent kinase 5 (Cdk5) activity is specifically active in neurogenesis, and Cdk5 and neocortical neurons migration related biomarker are expressed in Cos-7 cells. However, the function of Cdk5 on the transformation of immortalized Cos-7 cells into neuronal-like cells is not clear.

Methods: Cdk5 kinase activity was measured by [γ-P] ATP and p81 phosphocellulose pads based method.

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Diabetic nephropathy (DN) is one of the leading causes of chronic kidney disease (CKD), during which hyperglycemia is composed of the major force for the deterioration to end-stage renal disease (ESRD). However, the underlying mechanism triggering the effect of hyperglycemia on DN is not very clear and the clinically available drug for hyperglycemia-induced DN is in need of urgent development. Here, we found that high glucose (HG) increased the activity of cyclin-dependent kinase 5 (CDK5) dependent on P35/25 and which upregulated the oxidative stress and apoptosis of mouse podocytes (MPC-5).

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