Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic.

doi:10.1038/ki.1996.423

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Article

Evidence that two phenotypically distinct mouse PKD mutations, bpk and jcpk, are allelic.

Kidney international - 1 Oct 1996

Guay-Woodford L M, Bryda E C, Christine B, Lindsey J R, Collier W R, Avner E D, D'Eustachio P, Flaherty L

Abstract excerpt

Numerous mouse models of polycystic kidney disease (PKD) have been described. All of these diseases are transmitted as single recessive traits and in most, the phenotypic severity is influenced by the genetic background. However, based on their genetic map positions, none of these loci appears to...

Topics

Alleles
Animals
Animals, Newborn
Chromosome Mapping
Crosses, Genetic
Disease Models, Animal
Female
Genetic Complementation Test
Kidney
Male
Mice
Mice, Inbred BALB C
Mutation
Phenotype
Polycystic Kidney Diseases
Recombination, Genetic

Source

Open in PubMed

Identifiers

PMID: 8887273
DOI: 10.1038/ki.1996.423

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8887273-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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