Pitfalls in the Diagnosis of Wilson Disease., PMID:40504409
Metabolic dysfunction-associated steatotic liver disease in patients and mouse with Wilson's disease., PMID:40499780
C5a/C5aR pathway blocking promoted CuS-mediated cancer therapy effect by inhibiting cuproptosis resistance., PMID:40484643
Role and mechanisms of cuproptosis in the pathogenesis of Wilson's disease (Review)., PMID:40476570
Prevalence of common autosomal recessive and X-linked conditions in pregnant women in Vietnam: a cross-sectional study., PMID:40447697
Molecular genetic analysis of pulmonary benign metastasizing leiomyoma and intravenous leiomyomatosis: a comparative study using whole exome sequencing., PMID:40434516
MiR-133a-5p Facilitates Cuproptosis in Hepatocellular Carcinoma Through Targeting of ATP7B., PMID:40433054
Some Properties of the C. elegans Multicopper Oxidase F21D5.3, an Ortholog of Human Ceruloplasmin., PMID:40429919
Genome-Wide Association Studies and Candidate Genes for Egg Production Traits in Layers from an F2 Crossbred Population Produced Using Two Divergently Selected Chicken Breeds, Russian White and Cornish White., PMID:40428405
Changes in the FXR-cistrome and alterations in bile acid physiology in Wilson disease., PMID:40408300
Nisin Self-assembles to Interfere with Cellular Endocytosis for Ribosome-Mediated Anti-inflammatory Efficiency., PMID:40403150
A single-cell transcriptomic atlas of immune cells in Wilson disease identifies copper-specific immune regulation., PMID:40384935
Copper's new role in cancer: how cuproptosis-related genes could revolutionize glioma treatment., PMID:40355831
Current Management of Neurological Wilson's Disease., PMID:40351566
How Cells Die in Psoriasis?, PMID:40332377
ATPase copper transporting beta attenuates malignant features with high expression as an indicator of favorable prognosis in breast cancer., PMID:40316883
Oxidized-LDL aggravates renal injury via tubular cuproptosis., PMID:40306349
Asymptomatic Wilson's Disease Diagnosed during the Course of Ulcerative Colitis: A Case Report and Review., PMID:40276013
Application of a Core Care Nursing Outcomes Classification System for Liver Transplantation Patients: A Retrospective Case Study., PMID:40262188
From severe aplastic anemia with TERT variant to Wilson disease - associations or not., PMID:40257477
Intrathecal Baclofen Therapy Improves Refractory Status Dystonicus in Neuro-hepatic Wilson's Disease: A Case Report., PMID:40255925
[Clinical application of next-generation sequencing in early screening of neonatal diseases]., PMID:40241361
[Analysis of clinical phenotype and ATP7B variants characteristics of 337 patients with hepatolenticular degeneration in Anhui province]., PMID:40222831
Physiological and Histological Responses of Awassi Lambs to High Dietary Organic Copper Supplementation., PMID:40218459
Isolated neurological symptoms of Wilson's disease manifesting as focal epileptic seizures without hepatic involvement: Insights from a case report., PMID:40215409
Induction of Cuproptosis by Dichloromethane Extract From Patrinia scabiosaefolia Fisch on K562 Cells., PMID:40177825
Unmasking the Duo: Wilson's Disease in the Context of Lupus and Existing Hepatitis E Coinfection., PMID:40161035
Challenges and Recent Advances in Diagnosing Wilson Disease., PMID:40160676
Case report: Co-occurrence of Wilson's and Alexander's diseases revealed by genetic analysis., PMID:40144630
Practical and Multidisciplinary Review on Wilson Disease: The Portuguese Perspective., PMID:40143934
Hepatic microtubule destabilization facilitates liver fibrosis in the mouse model of Wilson disease., PMID:40140071
Epigallocatechin Gallate Promotes Cuproptosis via the MTF1/ATP7B Axis in Hepatocellular Carcinoma., PMID:40136640
Engineering Dual-Responsive Nanoplatform Achieves Copper Metabolism Disruption and Glutathione Consumption to Provoke Cuproptosis/Ferroptosis/Apoptosis for Cancer Therapy., PMID:40134095
A self-accelerating 'copper bomb' strategy activated innate and adaptive immune response against triple-negative breast cancer., PMID:40130080
Evaluation of efficacy and safety of AAV8-ΔC4ATP7B gene therapy in a mutant mouse model of Wilson's disease., PMID:40104154
Blocking copper transporter protein-dependent drug efflux with albumin-encapsulated Pt(IV) for synergistically enhanced chemo-immunotherapy., PMID:40102840
Clinical, biochemical and cell biological characterization of KIDAR syndrome associated with a novel AP1B1 variant., PMID:40101690
Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results., PMID:40088892
Integrated bulk and single-cell transcriptomic analysis unveiled a novel cuproptosis-related lipid metabolism gene molecular pattern and a risk index for predicting prognosis and antitumor drug sensitivity in breast cancer., PMID:40085377
Hepatic progenitor cells reprogrammed from mouse fibroblasts repopulate hepatocytes in Wilson's disease mice., PMID:40069754
Elevated COMMD1 Contributes to Cardiomyocyte Copper Efflux in Chronic Myocardial Ischemia: Insights From Rhesus Monkey., PMID:40032621
N,N'-bis(2-mercaptoethyl)isophthalamide (NBMI) as a novel chelator for Wilson's disease., PMID:40032031
Synergistic effects of lead and copper co-exposure on promoting oxidative stress and apoptosis in the neuronal cells., PMID:40010429
Effects of Dietary Copper Sources and Levels on Liver Copper Metabolism and the Expression of Transporters in Growing Pigs., PMID:40003008
The Importance of Genetic Testing: A Case Report of Wilson's Disease in Two Siblings of a Three-Sibling Family., PMID:39996228
Pathogenicity analysis of ATP7B in pediatric patients with Wilson's disease and functional verification of alternative splice variants., PMID:39978457
Exploring a novel model for newborn genetic screening in Ningxia, northern China: A retrospective observational study., PMID:39969324
Kidney stones in patients with Wilson's disease at a tertiary hospital in Northeastern Brazil., PMID:39956877
Spectrum and classification of ATP7B variants with clinical correlation in children with Wilson disease., PMID:39933775