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

Molecular analysis of aquaporin genes 1 to 4 in patients with Menière's disease.

Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology - 1 Jan 2010

Candreia Claudia, Schmuziger Nicolas, Gürtler Nicolas

Abstract excerpt

BACKGROUND: Menière's Disease (MD) is an episodic cochleovestibular dysfunction of unknown etiology, still lacking a specific test and therapy. The proposed theories on the pathophysiology include genetic factors and factors relating to inner ear homeostasis. Various aquaporins (AQP), water chann...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Aquaporin 1
Share to Aquaporin 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Aquaporin 4

Share to Meniere Disease

Share to Mutation

Share to Polymorphism, Single Nucleotide

Share to Sequence Analysis, RNA

Source

Identifiers

PMID: 21063116
DOI: 10.1159/000322346

Genes

AQP1
AQP3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21063116-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular analysis of aquaporin genes 1 to 4 in patients with Menière's disease.PMID 21063116Read ↗

Ménière's Disease: Molecular Analysis of Aquaporins 2, 3 and Potassium Channel KCNE1 Genes in Brazilian Patients.Semantic proximity Read ↗

The genomic landscape of Ménière's disease: a path to endolymphatic hydropsSemantic proximity Read ↗

A replication study on proposed candidate genes in Ménière's disease, and a review of the current status of genetic studies.Semantic proximity Read ↗

D184E mutation in aquaporin-4 gene impairs water permeability and links to deafness.Semantic proximity Read ↗

Gly460Trp alpha-adducin mutation as a possible mechanism leading to endolymphatic hydrops in Ménière's syndrome.Semantic proximity Read ↗

Ménière's disease is associated with single nucleotide polymorphisms in the human potassium channel genes, KCNE1 and KCNE3.Semantic proximity Read ↗

[Research advancement in related genes of Ménière's disease].Semantic proximity Read ↗

Polymorphisms in genes encoding aquaporins 4 and 5 and estrogen receptor α in patients with Ménière's disease and sudden sensorineural hearing loss.Semantic proximity Read ↗

Genetic analysis of aquaporin-4 in neuromyelitis optica.Semantic proximity Read ↗

Familial Ménière's disease in five generations.Semantic proximity Read ↗

Genetic investigations of Meniere's disease.Semantic proximity Read ↗

Polymorphic analysis of the heat-shock protein 70 gene (HSPA1A) in Ménière's disease.Semantic proximity Read ↗

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