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

Genotype–Phenotype Correlations with TRPC6-Associated Podocytopathy

7 Jan 2025

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Celiac Disease Research and Management
Share to Chronic Lymphocytic Leukemia Research
Share to Renal Diseases and Glomerulopathies

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 39774909
DOI: 10.1681/asn.0000000598

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotype–Phenotype Correlations with TRPC6-Associated PodocytopathyPMID 39774909Read ↗

Natural History and Clinicopathological Associations of TRPC6-Associated PodocytopathySemantic proximity Read ↗

A novel TRPC6mutation in a family with podocytopathy and clinical variabilitySemantic proximity Read ↗

TRPC channel modulation in podocytes-inching toward novel treatments for glomerular disease.Semantic proximity Read ↗

A Novel TRPC6 Mutation Causes Autosomal Dominant FSGSSemantic proximity Read ↗

Genotype/phenotype correlations in Gaucher's disease.Semantic proximity Read ↗

Genotype-phenotype correlation and risk stratification in a cohort of 123 hereditary stomatocytosis patients.Semantic proximity Read ↗

TRPC Channels in Proteinuric Kidney DiseasesSemantic proximity Read ↗

Genotype-phenotype correlations in FTDP-17: does form follow function?Semantic proximity Read ↗

Phenotype–genotype correlations for clinical variants caused by CYLD mutationsSemantic proximity Read ↗

Unexpected role of TRPC6 channel in familial nephrotic syndrome: does it have clinical implications?Semantic proximity Read ↗

Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patientsSemantic proximity Read ↗

TRPC6 channels and their binding partners in podocytes: role in glomerular filtration and pathophysiology.Semantic proximity Read ↗

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