Non-dialyzable uremic toxins and renal tubular cell damage in CKD patients: a systems biology approach

Notably, WNT1/11, AGT, FGF4/17/22, LMX1B, GATA4, and CXCL12 emerged as promising targets for further exploration in renal tubular pathology related to non-dialyzable uremic toxins. Understanding the molecular players and pathways linked to renal tubular dysfunction opens avenues for novel therapeutic interventions and improved clinical management of chronic kidney disease and its complications.

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Publication Details

Journal
European journal of medical research
Published
2024-08-09
DOI
https://doi.org/10.1186/s40001-024-01951-z
Citations
4
Primary Topic
Dialysis and Renal Disease Management
Type
article
Field-Weighted Citation Impact
1.36
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article

Non-dialyzable uremic toxins and renal tubular cell damage in CKD patients: a systems biology approach

Pejman Shadpour, Akram Nakhaei, Roya Asadi
4 citations
European journal of medical research
Dialysis and Renal Disease Management
1.36
article

Non-dialyzable uremic toxins and renal tubular cell damage in CKD patients: a systems biology approach

Pejman Shadpour, Akram Nakhaei, Roya Asadi
article en
4 citations

Abstract

Notably, WNT1/11, AGT, FGF4/17/22, LMX1B, GATA4, and CXCL12 emerged as promising targets for further exploration in renal tubular pathology related to non-dialyzable uremic toxins. Understanding the molecular players and pathways linked to renal tubular dysfunction opens avenues for novel therapeutic interventions and improved clinical management of chronic kidney disease and its complications.

European journal of medical researchVol. 29(1)
University of Science and Culture (IR), Mazandaran University of Science and Technology (IR), Iran University of Medical Sciences (IR), Hasheminejad Kidney Center (IR)
Zero hunger
Openalex Percentile: Top 17%
Dialysis and Renal Disease Management
1.36
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Non-dialyzable uremic toxins and renal tubular cell damage in CKD patients: a systems biology approach — Pejman Shadpour, Akram Nakhaei, et al. · European journal of medical research (2024) | TGRS Research Map | TGRS