Hereditary Xanthinuria Latest Advances

Paralogous guanine deaminases acquired from bacteria by horizontal gene transfer promote purine homeostasis in Caenorhabditis elegans.

Journal: bioRxiv : the preprint server for biology

Published: August 01, 2026

Genetic Insights into Persistent Hypouricemia in Adults: Novel Findings from an Adult Nephrogenetic Clinic.

Journal: Kidney diseases (Basel, Switzerland)

Published: March 10, 2026

Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics.

Journal: Metabolites

Published: February 09, 2026

The hitchhiker's guide to feline xanthinuria.

Journal: Journal of feline medicine and surgery

Published: February 05, 2026

EXPRESS: The Hitchhiker's Guide to Feline Xanthinuria.

Journal: Journal of feline medicine and surgery

Published: February 05, 2026

Chronic kidney disease and reduced renal COX2 expression in xanthinuria: a case-control study.

Journal: BMC nephrology

Published: January 20, 2026

A nonsense mutation in the Mocos gene induces xanthinuria, obstructive nephropathy, and anemia in rats.

Journal: Experimental animals

Published: December 03, 2025

Management of urinary stones by experts in stone disease (ESD 2025).

Journal: Archivio italiano di urologia, andrologia : organo ufficiale [di] Societa italiana di ecografia urologica e nefrologica

Published: June 19, 2025

A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency.

Journal: European journal of pediatrics

Published: June 17, 2025

Long-standing myalgia and hypouricemia in a young woman : Case report and review of the literature

Journal: Zeitschrift fur Rheumatologie

Published: June 10, 2025

Clinical and genetic analysis of MOCOS gene-related hypouricemia.

Journal: Frontiers in genetics

Published: May 30, 2025

XDH-1 inactivation causes xanthine stone formation in C. elegans which is inhibited by SULP-4-mediated anion exchange in the excretory cell.

Journal: bioRxiv : the preprint server for biology

Published: February 20, 2025

Hereditary Xanthinuria Latest Advances

Find the Latest Research About Hereditary Xanthinuria

Paralogous guanine deaminases acquired from bacteria by horizontal gene transfer promote purine homeostasis in Caenorhabditis elegans.

Paralogous guanine deaminases acquired from bacteria by horizontal gene transfer promote purine homeostasis in Caenorhabditis elegans.

Genetic Insights into Persistent Hypouricemia in Adults: Novel Findings from an Adult Nephrogenetic Clinic.

Genetic Insights into Persistent Hypouricemia in Adults: Novel Findings from an Adult Nephrogenetic Clinic.

Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics.

Identification of Primary Hyperoxaluria Type III by Gas Chromatography/Mass Spectrometry-Based Urine Metabolomics.

The hitchhiker's guide to feline xanthinuria.

The hitchhiker's guide to feline xanthinuria.

EXPRESS: The Hitchhiker's Guide to Feline Xanthinuria.

EXPRESS: The Hitchhiker's Guide to Feline Xanthinuria.

Chronic kidney disease and reduced renal COX2 expression in xanthinuria: a case-control study.

Chronic kidney disease and reduced renal COX2 expression in xanthinuria: a case-control study.

A nonsense mutation in the Mocos gene induces xanthinuria, obstructive nephropathy, and anemia in rats.

A nonsense mutation in the Mocos gene induces xanthinuria, obstructive nephropathy, and anemia in rats.

Management of urinary stones by experts in stone disease (ESD 2025).

Management of urinary stones by experts in stone disease (ESD 2025).

A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency.

A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiency.

Long-standing myalgia and hypouricemia in a young woman : Case report and review of the literature

Long-standing myalgia and hypouricemia in a young woman : Case report and review of the literature

Clinical and genetic analysis of MOCOS gene-related hypouricemia.

Clinical and genetic analysis of MOCOS gene-related hypouricemia.

XDH-1 inactivation causes xanthine stone formation in C. elegans which is inhibited by SULP-4-mediated anion exchange in the excretory cell.

XDH-1 inactivation causes xanthine stone formation in C. elegans which is inhibited by SULP-4-mediated anion exchange in the excretory cell.