Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Bartter Syndromes and Other Salt-Losing Tubulopathies

21 Jun 2006

Abstract excerpt

Genetic studies into rare inborn errors of renal tubular sodium handling in man have brought many interesting, sometimes surprising insights into how we can maintain our bodies' electrolytes and fluids homeostasis. The cloning and identification of sodium transporting genes and proteins like NHE3, NKCC2, ROMK, CLCNKB, NCC, and EnaC has considerably improved our understanding of renal salt handling. Subsequently,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Electrolyte and hormonal disorders
Share to Ion Transport and Channel Regulation

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 16785747
DOI: 10.1159/000094001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bartter Syndromes and Other Salt-Losing TubulopathiesPMID 16785747Read ↗

Molecular pathophysiology of Bartter's and Gitelman's syndromes.Semantic proximity Read ↗

Bartter's and Gitelman's syndromes: from gene to clinic.Semantic proximity Read ↗

Bartter and Gitelman syndromes: Questions of class.Semantic proximity Read ↗

WNK kinases and the kidney.Semantic proximity Read ↗

WNK Kinases, Renal Ion Transport and HypertensionSemantic proximity Read ↗

Future considerations based on the information from Barrter's and Gitelman's syndromes.Semantic proximity Read ↗

Role of WNK kinases in regulating tubular salt and potassium transport and in the development of hypertension.Semantic proximity Read ↗

The Molecular Genetics of Gordon Syndrome.Semantic proximity Read ↗

Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance.Semantic proximity Read ↗

WNK kinases and renal sodium transport in health and disease: an integrated view.Semantic proximity Read ↗

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.Semantic proximity Read ↗

Straightening out the renal tubule: advances in the molecular basis of the inherited tubulopathies.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.