Urea Cycle Disorders (UCD) Latest Advances

Corrected Version: Sodium Benzoate, A Metabolite of Cinnamon and A Food Additive, Improves Cognitive Functions in Mice After Controlled Cortical Impact Injury.

Journal: Journal of clinical & experimental immunology

Published: June 01, 2026

RNA-LNP-mediated in vivo prime editing corrects disease phenotypes in a mouse model of citrullinemia type I.

Journal: Science translational medicine

Published: May 13, 2026

Therapeutic potential of three-dimensional hepatocyte-like cells from human adipose-derived mesenchymal stem cells in urea cycle disorders.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: April 28, 2026

Fatal Late-Onset Ornithine Transcarbamylase Deficiency in an Adolescent: A Case Report.

Journal: Cureus

Published: April 25, 2026

An amperometric l-citrulline biosensor.

Journal: Bioelectrochemistry (Amsterdam, Netherlands)

Published: April 17, 2026

Letter to the editor: Newborn screening for low blood citrulline leads to diagnosis of ornithine aminotransferase deficiency.

Journal: Molecular genetics and metabolism

Published: April 03, 2026

Metabolic mimicry of perioral myoclonia with absences: A signature of thalamocortical instability in childhood-onset ornithine transcarbamylase deficiency.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: April 03, 2026

Pegzilarginase in Arginase 1 Deficiency: Clinical and Biochemical Effects of Treatment Initiation, Discontinuation and Re-Initiation.

Journal: Children (Basel, Switzerland)

Published: April 02, 2026

Extracellular Vesicles Delivered a Functional ARG1 Enzyme and Restored Its Activity in a Mouse Model of ARG1-D Resulting in Improved Lifespan.

Journal: International journal of molecular sciences

Published: April 01, 2026

Synthesis and preliminary enzymatic evaluation of polyol-based 4-phenylbutyrate derivatives.

Journal: Bioorganic & medicinal chemistry letters

Published: March 31, 2026

Sudden Acute Liver Failure in Citrullinemia type 1: An Argument for Earlier Liver Transplantation?

Journal: The Journal of pediatrics

Published: March 31, 2026

Implications of the FDA's new plausible mechanism framework for the development of a personalized in vivo prime editing platform.

Journal: American journal of human genetics

Published: March 24, 2026

Urea Cycle Disorders (UCD) Latest Advances

Find the Latest Research About Urea Cycle Disorders (UCD)

Corrected Version: Sodium Benzoate, A Metabolite of Cinnamon and A Food Additive, Improves Cognitive Functions in Mice After Controlled Cortical Impact Injury.

Corrected Version: Sodium Benzoate, A Metabolite of Cinnamon and A Food Additive, Improves Cognitive Functions in Mice After Controlled Cortical Impact Injury.

RNA-LNP-mediated in vivo prime editing corrects disease phenotypes in a mouse model of citrullinemia type I.

RNA-LNP-mediated in vivo prime editing corrects disease phenotypes in a mouse model of citrullinemia type I.

Therapeutic potential of three-dimensional hepatocyte-like cells from human adipose-derived mesenchymal stem cells in urea cycle disorders.

Therapeutic potential of three-dimensional hepatocyte-like cells from human adipose-derived mesenchymal stem cells in urea cycle disorders.

Fatal Late-Onset Ornithine Transcarbamylase Deficiency in an Adolescent: A Case Report.

Fatal Late-Onset Ornithine Transcarbamylase Deficiency in an Adolescent: A Case Report.

An amperometric l-citrulline biosensor.

An amperometric l-citrulline biosensor.

Letter to the editor: Newborn screening for low blood citrulline leads to diagnosis of ornithine aminotransferase deficiency.

Letter to the editor: Newborn screening for low blood citrulline leads to diagnosis of ornithine aminotransferase deficiency.

Metabolic mimicry of perioral myoclonia with absences: A signature of thalamocortical instability in childhood-onset ornithine transcarbamylase deficiency.

Metabolic mimicry of perioral myoclonia with absences: A signature of thalamocortical instability in childhood-onset ornithine transcarbamylase deficiency.

Pegzilarginase in Arginase 1 Deficiency: Clinical and Biochemical Effects of Treatment Initiation, Discontinuation and Re-Initiation.

Pegzilarginase in Arginase 1 Deficiency: Clinical and Biochemical Effects of Treatment Initiation, Discontinuation and Re-Initiation.

Extracellular Vesicles Delivered a Functional ARG1 Enzyme and Restored Its Activity in a Mouse Model of ARG1-D Resulting in Improved Lifespan.

Extracellular Vesicles Delivered a Functional ARG1 Enzyme and Restored Its Activity in a Mouse Model of ARG1-D Resulting in Improved Lifespan.

Synthesis and preliminary enzymatic evaluation of polyol-based 4-phenylbutyrate derivatives.

Synthesis and preliminary enzymatic evaluation of polyol-based 4-phenylbutyrate derivatives.

Sudden Acute Liver Failure in Citrullinemia type 1: An Argument for Earlier Liver Transplantation?

Sudden Acute Liver Failure in Citrullinemia type 1: An Argument for Earlier Liver Transplantation?

Implications of the FDA's new plausible mechanism framework for the development of a personalized in vivo prime editing platform.

Implications of the FDA's new plausible mechanism framework for the development of a personalized in vivo prime editing platform.