Lisa Gianesello

Via Giustiniani 2
Padova, 35128, Italy

Last Updated: 09/26/2026

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Found 23 publications

Human parietal epithelial cells as Trojan horses in albumin overload.

Human parietal epithelial cells as Trojan horses in albumin overload.

Journal: Scientific reports

Published: March 18, 2024

Human parietal epithelial cells (PECs) and proteinuria in lupus nephritis: a role for ClC-5, megalin, and cubilin?

Human parietal epithelial cells (PECs) and proteinuria in lupus nephritis: a role for ClC-5, megalin, and cubilin?

Journal: Journal of nephrology

Published: January 24, 2023

Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?

Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?

Journal: International journal of molecular sciences

Published: November 23, 2022

Rare genetic tubulopathies Gitelman's and Bartter's syndromes and their naturally occurring protection from COVID-19.

Rare genetic tubulopathies Gitelman's and Bartter's syndromes and their naturally occurring protection from COVID-19.

Journal: Minerva medica

Published: April 06, 2022

The Lesson Learned from the New c.2547-1G > T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect.

The Lesson Learned from the New c.2547-1G > T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect.

Journal: Thrombosis and haemostasis

Published: February 21, 2022

Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: OCRL Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Journal: Genes

Published: September 01, 2021

ACE2 and SARS-CoV-2 Infection Risk: Insights From Patients With Two Rare Genetic Tubulopathies, Gitelman's and Bartter's Syndromes.

ACE2 and SARS-CoV-2 Infection Risk: Insights From Patients With Two Rare Genetic Tubulopathies, Gitelman's and Bartter's Syndromes.

Journal: Frontiers in medicine

Published: December 29, 2020

Letter: ACE2, Rho kinase inhibition and the potential role of vitamin D against COVID-19.

Letter: ACE2, Rho kinase inhibition and the potential role of vitamin D against COVID-19.

Journal: Alimentary pharmacology & therapeutics

Published: July 14, 2020

Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon.

Genetics and phenotypic heterogeneity of Dent disease: the dark side of the moon.

Journal: Human genetics

Published: June 24, 2020

Downregulation of megalin, cubilin, ClC-5 and podocin in Fabry nephropathy: potential implications in the decreased effectiveness of enzyme replacement therapy.

Downregulation of megalin, cubilin, ClC-5 and podocin in Fabry nephropathy: potential implications in the decreased effectiveness of enzyme replacement therapy.

Journal: Journal of nephrology

Published: June 22, 2020

From protein uptake to Dent disease: An overview of the CLCN5 gene.

From protein uptake to Dent disease: An overview of the CLCN5 gene.

Journal: Gene

Published: February 14, 2020

CLCN5 5'UTR isoforms in human kidneys: differential expression analysis between controls and patients with glomerulonephritis.

CLCN5 5'UTR isoforms in human kidneys: differential expression analysis between controls and patients with glomerulonephritis.

Journal: Journal of investigative medicine : the official publication of the American Federation for Clinical Research

Published: January 03, 2020

Showing 1-12 of 23

Last Updated: 09/26/2026