Marialena Chrysanthou

ORCID: 0000-0003-4847-0813
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About
Contact & Profiles
Research Areas
  • Renal cell carcinoma treatment
  • Renal and related cancers
  • Advanced Glycation End Products research
  • Biochemical effects in animals
  • Alzheimer's disease research and treatments
  • Genetic and Kidney Cyst Diseases
  • Natural Antidiabetic Agents Studies
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Pediatric Urology and Nephrology Studies

Wageningen University & Research
2022-2024

Radboud University Nijmegen
2023

Radboud University Medical Center
2023

Radboud Institute for Molecular Life Sciences
2023

Advanced glycation end-products (AGEs) are products of a non-enzymatic reaction between amino acids and reducing sugars. Glycated human serum albumin (HSA) increases in diabetics as consequence elevated blood glucose levels glycating metabolites like methylglyoxal (MGO). The impact different types on the immunomodulatory properties HSA is poorly understood studied here. was glycated with D-glucose, MGO, or glyoxylic acid (CML). Glycation-related biochemical changes were characterized using...

10.3390/biom14121492 article EN cc-by Biomolecules 2024-11-23

Congenital anomalies of the kidney and urinary tract (CAKUT) are predominant cause for chronic disease below age 30 years. Many monogenic forms have been discovered due to comprehensive genetic testing like exome sequencing. However, disease-causing variants in known disease-associated genes only explain a proportion cases. Here, we aim unravel underlying molecular mechanisms syndromic CAKUT three unrelated multiplex families with presumed autosomal recessive inheritance. Exome sequencing...

10.1016/j.kint.2023.11.032 article EN cc-by Kidney International 2023-12-26

Abstract Background Congenital anomalies of the kidney and urinary tract (CAKUT) are predominant cause for chronic disease below 30 years age. Many monogenic forms have been discovered mainly due to comprehensive genetic testing like exome sequencing (ES). However, disease-causing variants in known disease-associated genes still only explain a proportion cases. Aim this study was unravel underlying molecular mechanism syndromic CAKUT two multiplex families with presumed autosomal recessive...

10.1101/2023.03.21.23287206 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2023-03-22
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