Unveiling Immune System Perturbations in Early Development Through Zebrafish Models of NADHX Repair Deficiency
Fuente:
Wiley Open Access
Saved in:
| Main Authors: | Myrto Patraskaki, Najmesadat Seyedkatouli, Lisa Schlicker, Marc O. Warmoes, Maria Lorena Cordero‐Maldonado, Ursula Heins‐Marroquin, Carole L. Linster |
|---|---|
| Format: | Artículo Open Access |
| Published: |
Wiley
2026
|
| Subjects: | |
| Online Access: | |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
Impaired Proteostasis is Linked to Neurological Pathology in a Zebrafish NGLY1 Deficiency Model
by: Aviv Mesika, et al.
Published: (2025)
by: Aviv Mesika, et al.
Published: (2025)
Impact of Early Intervention on the Developmental and Ocular Outcome of Patients With Cobalamin C Deficiency Identified Through Newborn Screening
by: Anna T. Reischl‐Hajiabadi, et al.
Published: (2026)
by: Anna T. Reischl‐Hajiabadi, et al.
Published: (2026)
Allopurinol Treatment Improves Cognitive Skills, Adaptive Behavior, and Biochemical Markers in Young Patients With Adenylosuccinate Lyase Deficiency
by: Bérangère Rousselot‐Pailley, et al.
Published: (2025)
by: Bérangère Rousselot‐Pailley, et al.
Published: (2025)
Long‐Term Follow‐Up of Patients With Transaldolase Deficiency
by: Marco Scaglione, et al.
Published: (2026)
by: Marco Scaglione, et al.
Published: (2026)
Current Understanding of Pathogenic Mechanisms and Disease Models of Citrin Deficiency
by: Denis Lacabanne, et al.
Published: (2025)
by: Denis Lacabanne, et al.
Published: (2025)
CLPB Deficiency, a Mitochondrial Chaperonopathy With Neutropenia and Neurological Presentation
by: D. Mróz, et al.
Published: (2025)
by: D. Mróz, et al.
Published: (2025)
Deficient glycan extension and endoplasmic reticulum stresses in ALG3‐CDG
by: Earnest J. P. Daniel, et al.
Published: (2024)
by: Earnest J. P. Daniel, et al.
Published: (2024)
MRPS Genes Causing Leukoencephalopathy With Profound Cerebral Folate Deficiency in Adults
by: Daniele Mandia, et al.
Published: (2026)
by: Daniele Mandia, et al.
Published: (2026)
Effectiveness of Pyridoxal‐5′‐Phosphate in PNPO Deficiency: A Systematic Review
by: Nina N. Stolwijk, et al.
Published: (2025)
by: Nina N. Stolwijk, et al.
Published: (2025)
Aldolase B Deficient Mice Are Characterized by Hepatic Nucleotide Sugar Abnormalities
by: Amée M. Buziau, et al.
Published: (2024)
by: Amée M. Buziau, et al.
Published: (2024)
Myo‐Inositol Deficiency, Structural Brain Changes, and Cerebral Perfusion Alterations in Classic Galactosemia: Preliminary Insights From a Multiparametric MRI Study
by: Eva Niess, et al.
Published: (2025)
by: Eva Niess, et al.
Published: (2025)
Positive Clinical, Neuropsychological, and Metabolic Impact of Liver Transplantation in Patients With Argininosuccinate Lyase Deficiency
by: Barbara Siri, et al.
Published: (2025)
by: Barbara Siri, et al.
Published: (2025)
Multimodal Noninvasive Biomarker Characterization of Structural and Functional Alterations in ADSS1 ‐Deficient Myopathy
by: Merve Koç Yekedüz, et al.
Published: (2026)
by: Merve Koç Yekedüz, et al.
Published: (2026)
Tyrosine Hydroxylase Deficiency Impairs TH Axonal Transport, Brain Function, and Neuronal Plasticity
by: Tie‐Jun Sten Shi, et al.
Published: (2026)
by: Tie‐Jun Sten Shi, et al.
Published: (2026)
Identification of Cepharanthine as a Potential Therapy of Acid Sphingomyelinase Deficiency by Reducing Cellular Sphingosylphosphorylcholine
by: Mengni Yi, et al.
Published: (2025)
by: Mengni Yi, et al.
Published: (2025)
Elamipretide Improves Mitochondrial Function in Mitochondrial Trifunctional Protein‐Deficient Mice and Human Fibroblasts
by: Eduardo Vieira Neto, et al.
Published: (2026)
by: Eduardo Vieira Neto, et al.
Published: (2026)
Clinical Characteristics of Arginase 1 Deficiency: Natural History Insights From International Clinical Trials
by: Mattias Rudebeck, et al.
Published: (2026)
by: Mattias Rudebeck, et al.
Published: (2026)
Increased Survival in Patients With Molybdenum Cofactor Deficiency Type A Treated With Cyclic Pyranopterin Monophosphate
by: Guenter Schwarz, et al.
Published: (2025)
by: Guenter Schwarz, et al.
Published: (2025)
Dietary Shift Leads to Venous Thrombosis‐Induced Congestive Liver Failure in CBS ‐Deficient Mice
by: Hyung‐Ok Lee, et al.
Published: (2025)
by: Hyung‐Ok Lee, et al.
Published: (2025)
Correction to “Multimodal Noninvasive Biomarker Characterization of Structural and Functional Alterations in ADSS1 ‐Deficient Myopathy”
Published: (2026)
Published: (2026)
Lipid Metabolism Alterations in Hereditary Inorganic Pyrophosphate Deficiency Syndromes: A Narrative Review of Insights and Controversies
by: Robbe Derudder, et al.
Published: (2025)
by: Robbe Derudder, et al.
Published: (2025)
Exploring Outcome Measures for Mitochondrial Myopathies; Insights From a Longitudinal Study on TK2 Deficiency
by: Paloma Martín‐Jimenez, et al.
Published: (2026)
by: Paloma Martín‐Jimenez, et al.
Published: (2026)
Correlation of Plasma and Urine 2,8‐Dihydroxyadenine and Adenine and Clinical Characteristics in Individuals With Adenine Phosphoribosyltransferase Deficiency
by: Unnur A. Thorsteinsdottir, et al.
Published: (2025)
by: Unnur A. Thorsteinsdottir, et al.
Published: (2025)
Liver‐Directed Gene Therapy Mitigates Early Nephropathy in Murine Glycogen Storage Disease Type Ia
by: Cheol Lee, et al.
Published: (2025)
by: Cheol Lee, et al.
Published: (2025)
Pathophysiology of the Neutropenia of GSDIb and G6PC3 Deficiency: Origin, Metabolism and Elimination of 1,5‐Anhydroglucitol
by: Maria Veiga‐da‐Cunha, et al.
Published: (2025)
by: Maria Veiga‐da‐Cunha, et al.
Published: (2025)
Phosphoribosylformylglycinamidine Synthase ( PFAS ) Deficiency: Clinical, Genetic and Metabolic Characterisation of a Novel Defect in Purine de Novo Synthesis
by: Marie Zikanova, et al.
Published: (2025)
by: Marie Zikanova, et al.
Published: (2025)
iPSC ‐Derived Liver Organoids as a Tool to Study Medium Chain Acyl‐ CoA Dehydrogenase Deficiency
by: Ligia A. Kiyuna, et al.
Published: (2025)
by: Ligia A. Kiyuna, et al.
Published: (2025)
Setting the Stage for Treatment of Aminoacyl‐ tRNA Synthetase ( ARS )1‐Deficiencies: Phenotypic Characterization and a Review of Treatment Effects
by: Eva M. M. Hoytema van Konijnenburg, et al.
Published: (2025)
by: Eva M. M. Hoytema van Konijnenburg, et al.
Published: (2025)
Valine Restriction Extends Survival in a Drosophila Model of Short‐Chain Enoyl‐CoA Hydratase 1 (ECHS1) Deficiency
by: Sarah Mele, et al.
Published: (2024)
by: Sarah Mele, et al.
Published: (2024)
From Neonatal Encephalopathy to Adult Survival: Revisiting the Natural History of D‐Bifunctional Protein Deficiency in a Multicentre International Case Series
by: U. Diaz‐Moreno, et al.
Published: (2025)
by: U. Diaz‐Moreno, et al.
Published: (2025)
Plasma Metabolomics, Lipidomics, and Acylcarnitines Are Associated With Vision and Genotype but Not With Dietary Intake in Long‐Chain 3‐Hydroxyacyl‐CoA Dehydrogenase Deficiency (LCHADD)
by: Hak Chung, et al.
Published: (2025)
by: Hak Chung, et al.
Published: (2025)
Cluster of Severe Arginase 1 Deficiency in the Comoros: Clinical, Neuroimaging, and Molecular Features in 17 Patients From Mayotte Compared With 10 From Paris
by: Aurélie De Bruyne, et al.
Published: (2026)
by: Aurélie De Bruyne, et al.
Published: (2026)
A Meta‐Analysis to Unveil the Diagnostic Gaps in Anderson–Fabry Disease in Women
by: L. Lenzini, et al.
Published: (2026)
by: L. Lenzini, et al.
Published: (2026)
Brain Age in Adult Patients With Early‐Treated Phenylketonuria
by: Laura Winiger, et al.
Published: (2026)
by: Laura Winiger, et al.
Published: (2026)
Quantitative MRI Biomarkers for Early Muscle Involvement in Late Onset Pompe Disease
by: Michele G. Croce, et al.
Published: (2026)
by: Michele G. Croce, et al.
Published: (2026)
Human glyoxylate metabolism revisited: New insights pointing to multi‐organ involvement with implications for siRNA‐based therapies in primary hyperoxaluria
by: Ronald J. A. Wanders, et al.
Published: (2024)
by: Ronald J. A. Wanders, et al.
Published: (2024)
Early diagnosis and treatment by newborn screening (NBS) or family history is associated with improved visual outcomes for long‐chain 3‐hydroxyacylCoA dehydrogenase deficiency (LCHADD) chorioretinopathy
by: Melanie B. Gillingham, et al.
Published: (2024)
by: Melanie B. Gillingham, et al.
Published: (2024)
Molecular Profile of Mucopolysaccharidosis Type I Patients in Brazil
by: Carlos Robson Costa Cruz, et al.
Published: (2026)
by: Carlos Robson Costa Cruz, et al.
Published: (2026)
Executive and adaptive function impacts long‐term outcomes for adults with maple syrup urine disease
by: Jessica I. Gold, et al.
Published: (2024)
by: Jessica I. Gold, et al.
Published: (2024)
Speech, Language and Non‐verbal Communication in CLN2 and CLN3 Batten Disease
by: Lottie D. Morison, et al.
Published: (2025)
by: Lottie D. Morison, et al.
Published: (2025)
Similar Items
-
Impaired Proteostasis is Linked to Neurological Pathology in a Zebrafish NGLY1 Deficiency Model
by: Aviv Mesika, et al.
Published: (2025) -
Impact of Early Intervention on the Developmental and Ocular Outcome of Patients With Cobalamin C Deficiency Identified Through Newborn Screening
by: Anna T. Reischl‐Hajiabadi, et al.
Published: (2026) -
Allopurinol Treatment Improves Cognitive Skills, Adaptive Behavior, and Biochemical Markers in Young Patients With Adenylosuccinate Lyase Deficiency
by: Bérangère Rousselot‐Pailley, et al.
Published: (2025) -
Long‐Term Follow‐Up of Patients With Transaldolase Deficiency
by: Marco Scaglione, et al.
Published: (2026) -
Current Understanding of Pathogenic Mechanisms and Disease Models of Citrin Deficiency
by: Denis Lacabanne, et al.
Published: (2025)