Article

Sulfate handling in proximal renal tubular defects

2026-02-27

Abstract excerpt

<title>Abstract</title> <p> Background Renal tubular disease causes loss of electrolytes and other molecules. One of these electrolytes is sulfate, which is reabsorbed by dedicated transporters (NaS1, encoded by <italic>SLC13A1</italic> gene). Still, sulfate is rarely measured in clinical practice, although it is essential for development and functioning of several organ systems. The importance of adequate su...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 7dbee6ee-8897-5e4f-9b6a-c3153d9e140f
DOI: 10.21203/rs.3.rs-8907668/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Sulfate handling in proximal renal tubular defectsDOI 10.21203/rs.3.rs-8907668/v1Read

[Electrolyte disorders as a hallmark of monogenetic diseases].Semantic proximity Read

A Focus on the Proximal Tubule Dysfunction in Dent Disease Type 1.Semantic proximity Read

Biallelic variants in the SLC13A1 sulfate transporter gene cause hyposulfatemia with a mild spondylo‐epi‐metaphyseal dysplasiaSemantic proximity Read

A Focus on the Metabolic Dysfunction of Proximal Tubule Cells in Dent Disease Type 1Semantic proximity Read

Genetics and pathophysiology of mammalian sulfate biology.Semantic proximity Read

From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.Semantic proximity Read

Renal urate handling: clinical relevance of recent advances.Semantic proximity Read

Inherited and acquired disorders of magnesium homeostasis.Semantic proximity Read

Cystinuria: mechanisms and management.Semantic proximity Read

Chloride channels in renal disease.Semantic proximity Read

Cystinuria: an inborn cause of urolithiasis.Semantic proximity Read

Update on cystinuria.Semantic proximity Read