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Article

Genetic studies: a key to understanding pathogenesis in PKD.

Nephrology news & issues - 1 Dec 2006

Harris Peter C

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Share to Disease Progression
Share to Genetic Heterogeneity
Share to Genetic Linkage
Share to Membrane Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polycystic Kidney, Autosomal Dominant

Share to Polycystic Kidney, Autosomal Recessive

Share to Receptors, Cell Surface

Share to TRPP Cation Channels

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Identifiers

PMID: 17168054

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic studies: a key to understanding pathogenesis in PKD.PMID 17168054Read ↗

Genotype-phenotype correlation in 11 Romanian PKU families.Semantic proximity Read ↗

Human gene mutations. Gene symbol: PKD1. Disease: Polycystic kidney disease.Semantic proximity Read ↗

Haplotype distribution and molecular defects of PKU in Italy.Semantic proximity Read ↗

Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts.Semantic proximity Read ↗

Association of PKD1 sequence variants with pathophysiology of ADPKD in Indian patientsSemantic proximity Read ↗

Forensic Autopsy Reveals Novel Pathogenic Variant of PKD1 Associated With Polycystic Kidney Disease.Semantic proximity Read ↗

The genetic defect of PNH.Semantic proximity Read ↗

The long walk toward the PKD1 gene. The European PKD1 Consortium.Semantic proximity Read ↗

Genetics meets pathology - an increasingly important relationship.Semantic proximity Read ↗

The PKD2 gene: structure, interactions, mutations, and inactivation.Semantic proximity Read ↗

In this issue: defined patient populations are required to establish genetic pathogenesis.Semantic proximity Read ↗

Genetic Diagnosis of Rare Diseases: Past and Present.Semantic proximity Read ↗

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