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Kidney

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Related literature

Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome.
Kidney
A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum disease.
Kidney
Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis.
Kidney
Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.
Kidney
Evaluation of clinicopathologic characteristics and the BRAF V600E mutation in Erdheim-Chester disease among Chinese adults.
Kidney
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.
Kidney
In vivo genotoxicity of a novel heterocyclic amine, aminobenzoazepinoquinolinone-derivative (ABAQ), produced by the Maillard reaction between glucose and l-tryptophan.
Kidney
Evaluating the weak in vivo micronucleus response of a genotoxic carcinogen, aristolochic acids.
Kidney
A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus.
Kidney
Kinetic modeling of Nav1.7 provides insight into erythromelalgia-associated F1449V mutation.
Kidney

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