Julien Baruteau

Great Ormond Street Institute of Child Health, University College London

Affiliated withUniversity College London Great Ormond Street Hospital for Children NHS Foundation Trust National Institute of Health Research Great Ormond Street Biomedical Research Centre

Research Area

Biology

Biography

Julien Baruteau has not added Biography.
If you are Julien Baruteau and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2024

Other Publications

Article	Year
Transcatheter closure of patent ductus arteriosus: past, present and future. Archives of cardiovascular diseases\| PubMed ID: 24560920	2014
Perinatal systemic gene delivery using adeno-associated viral vectors. Frontiers in molecular neuroscience\| PubMed ID: 25452713	2014
Expanding the phenotype in argininosuccinic aciduria: need for new therapies. Journal of inherited metabolic disease\| PubMed ID: 28251416	2017
Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects. Journal of inherited metabolic disease\| PubMed ID: 28567541	2017
Age-Related Seroprevalence of Antibodies Against AAV-LK03 in a UK Population Cohort. Human gene therapy\| PubMed ID: 30027761	2019
Ascending Vaginal Infection Using Bioluminescent Bacteria Evokes Intrauterine Inflammation, Preterm Birth, and Neonatal Brain Injury in Pregnant Mice. The American journal of pathology\| PubMed ID: 30036519	2018
Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice. Molecular therapy. Nucleic acids\| PubMed ID: 30081233	2018
Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer. Nature communications\| PubMed ID: 30158522	2018
Fetal gene therapy for neurodegenerative lysosomal storage diseases. Journal of inherited metabolic disease\| PubMed ID: 30715735	2019
Liver neoplasms in methylmalonic aciduria: An emerging complication. Journal of inherited metabolic disease\| PubMed ID: 31260114	2019
Urea Cycle Related Amino Acids Measured in Dried Bloodspots Enable Long-Term In Vivo Monitoring and Therapeutic Adjustment. Metabolites\| PubMed ID: 31718089	2019
Generation of light-producing somatic-transgenic mice using adeno-associated virus vectors. Scientific reports\| PubMed ID: 32034258	2020
Cervical Gene Delivery of the Antimicrobial Peptide, Human β-Defensin (HBD)-3, in a Mouse Model of Ascending Infection-Related Preterm Birth. Frontiers in immunology\| PubMed ID: 32117260	2020
Clinical and Molecular Features of Early Infantile Niemann Pick Type C Disease. International journal of molecular sciences\| PubMed ID: 32709131	2020
Novel therapies for mucopolysaccharidosis type III. Journal of inherited metabolic disease\| PubMed ID: 32944950	2021
cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing. Nature genetics\| PubMed ID: 33230297	2020
Gene therapy for inherited metabolic diseases. Journal of mother and child\| PubMed ID: 33554501	2020
Disentangling molecular and clinical stratification patterns in beta-galactosidase deficiency. Journal of medical genetics\| PubMed ID: 33737400	2022
Clinical applications for exosomes: Are we there yet? British journal of pharmacology\| PubMed ID: 33751579	2021
The exosome journey: from biogenesis to uptake and intracellular signalling. Cell communication and signaling : CCS\| PubMed ID: 33892745	2021
Gene Therapy for Lysosomal Storage Disorders: Ongoing Studies and Clinical Development. Biomolecules\| PubMed ID: 33924076	2021
Gene therapy restores dopamine transporter expression and ameliorates pathology in iPSC and mouse models of infantile parkinsonism. Science translational medicine\| PubMed ID: 34011628	2021
ASL expression in ALDH1A1 neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype. Human genetics\| PubMed ID: 34417872	2021
Safety and efficacy of an engineered hepatotropic AAV gene therapy for ornithine transcarbamylase deficiency in cynomolgus monkeys. Molecular therapy. Methods & clinical development\| PubMed ID: 34703837	2021
Modelling urea cycle disorders using iPSCs. NPJ Regenerative medicine\| PubMed ID: 36163209	2022
Inherited and acquired vitamin B12 deficiencies: Which administration route to choose for supplementation? Frontiers in pharmacology\| PubMed ID: 36249776	2022
Three-Country Snapshot of Ornithine Transcarbamylase Deficiency. Life (Basel, Switzerland)\| PubMed ID: 36362876	2022
Assessment of Pre-Clinical Liver Models Based on Their Ability to Predict the Liver-Tropism of Adeno-Associated Virus Vectors. Human gene therapy\| PubMed ID: 36927149	2023
Natural history of epilepsy in argininosuccinic aciduria provides new insights into pathophysiology: A retrospective international study. Epilepsia\| PubMed ID: 36994644	2023
Gene therapy for urea cycle defects: An update from historical perspectives to future prospects. Journal of inherited metabolic disease\| PubMed ID: 37026568	2024
Recapitulation of Skewed X-Inactivation in Female Ornithine Transcarbamylase-Deficient Primary Human Hepatocytes in the FRG Mouse: A Novel System for Developing Epigenetic Therapies. Human gene therapy\| PubMed ID: 37350098	2023
Prolonged respiratory failure responds to conventional therapy in isolated homocysteine remethylation defects. JIMD reports\| PubMed ID: 37404677	2023
The incidence of movement disorder increases with age and contrasts with subtle and limited neuroimaging abnormalities in argininosuccinic aciduria. Journal of inherited metabolic disease\| PubMed ID: 38044746	2023
Liver transplantation in ornithine transcarbamylase deficiency: A retrospective multicentre cohort study. Molecular genetics and metabolism reports\| PubMed ID: 38053940	2023
Liver-directed gene therapy for inherited metabolic diseases. Journal of inherited metabolic disease\| PubMed ID: 38171926	2024
mRNA therapy corrects defective glutathione metabolism and restores ureagenesis in preclinical argininosuccinic aciduria. Science translational medicine\| PubMed ID: 38198573	2024
Mission possible: Gene therapy for inherited metabolic diseases. Journal of inherited metabolic disease\| PubMed ID: 38221761	2024
Generation of induced pluripotent stem cells (UCLi024-A) from a patient with argininosuccinate lyase deficiency carrying a homozygous c.437G > A (p.Arg146Gln) mutation. Stem cell research\| PubMed ID: 38422816	2024
precision-cut liver slices model disease phenotype and monitor therapeutic response for liver monogenic diseases. F1000Research\| PubMed ID: 38618017	2023
Asymptomatic pediatric presentation of S-adenosylhomocysteine hydrolase deficiency. JIMD reports\| PubMed ID: 39512434	2024