Hereditary Xanthinuria Latest Advances

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

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

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

Journal: PLoS biology

Published: January 24, 2025

Characterisation and evaluation of predisposing factors for the development of xanthinuria in dogs with leishmaniosis under allopurinol therapy.

Journal: Parasites & vectors

Published: December 20, 2024

Analysis of a family with hypouricemia due to type Ⅰ xanthinuria

Journal: Zhonghua yi xue za zhi

Published: November 13, 2024

Pseudogenization of the Slc23a4 gene is necessary for the survival of Xdh-deficient mice.

Journal: Scientific reports

Published: September 18, 2024

Hereditary Xanthinuria Latest Advances

Find the Latest Research About Hereditary Xanthinuria

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.

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.

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

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

Characterisation and evaluation of predisposing factors for the development of xanthinuria in dogs with leishmaniosis under allopurinol therapy.

Characterisation and evaluation of predisposing factors for the development of xanthinuria in dogs with leishmaniosis under allopurinol therapy.

Analysis of a family with hypouricemia due to type Ⅰ xanthinuria

Analysis of a family with hypouricemia due to type Ⅰ xanthinuria

Pseudogenization of the Slc23a4 gene is necessary for the survival of Xdh-deficient mice.

Pseudogenization of the Slc23a4 gene is necessary for the survival of Xdh-deficient mice.