Results 131 to 140 of about 6,030 (184)

Cuproptosis in Ischemic Stroke: Molecular Mechanisms and Therapeutic Potential. [PDF]

Molecules
Han X, Zhang W, An H, Zhang J, Tian J, Wang Y.   +5 more
europepmc   +1 more source

Wilson's Disease Coexisting with Narcolepsy Type 1: Evidence for a Multifactorial Cause of Excessive Daytime Sleepiness from a Case Report. [PDF]

Neurol Ther
Xu Z, Wang Y, Xu C, Hou Z, Yang W.
europepmc   +1 more source

Preclinical pharmacology and toxicology study of an AAV8-tATP7B vector for Wilson's disease. [PDF]

Clin Mol Hepatol
Wang Z, Wang M, Wu M, Ye L, Lou T, Sun X, Zhao W, Liu F, Ren T, Li W, Fan JG.   +10 more
europepmc   +1 more source

Copper Metabolism-Related Cell Death in Kidney Diseases: Molecular Mechanisms, Disease-Specific Evidence, and Translational Implications. [PDF]

Int J Mol Sci
Shao W, Wang Q, Liu Y, Li L, Li X, Wang X, Cheng F.   +6 more
europepmc   +1 more source

Glutaredoxin 1 promotes intestinal epithelial cell copper toxicity in inflammatory bowel disease. [PDF]

Redox Biol
Zhang T, Zhang X, Cai H, Yu M, Liu Q, Song X, Lin B, Xu L, Li L, Shen Z, Yu C, Zhang J.   +11 more
europepmc   +1 more source

Precision Diagnosis of Wilson Disease Using a MultiGene Panel: Insights From a Prospective Cohort Study. [PDF]

Neurol Genet
Lin J, Wang YL, Qu Y, Dong S, Fang Y, Chen R, Ding Y, Lin W, Chen J, Cai N, Wang N, Chen WJ, Lin Y, Wang Z.   +13 more
europepmc   +1 more source

A broad-spectrum inhibitor of copper-exporting P_1B-type ATPases. [PDF]

Proc Natl Acad Sci U S A
Shanbhag VC, Anakpeba-Dinguyella S, Gudekar N, Conrad K, Azubuogu C, Probst C, Ralle M, Mediavilla MG, Cricco JA, Garza NM, Gohil VM, Peck S, Kumar S, Natarajan A, Horadigala-Gamage MA, Meloni G, Singh K, Petris MJ.   +17 more
europepmc   +1 more source

Multiscale computational genomics in Wilson disease: from atomic dynamics to clinical prediction. [PDF]

Front Genet
Luan M, Xue Q, Cao Y, Cheng G, Huo X.
europepmc   +1 more source

Case Report: Long-standing multisystem Wilson's disease in a pregnant woman with prolonged chelation discontinuation. [PDF]

Front Med (Lausanne)
Li S, Zhang X, Zhu Y, Hao Y, Zhao L.
europepmc   +1 more source

Clinical Exome Sequencing in Unexplained Hyperferritinemia Reveals Digenic and Oligogenic Inheritance Beyond Iron Homeostasis. [PDF]

Liver Int
Morel P, Silva Rodriguez M, Benmouffek C, Goksen B, Chéry C, Haghnejad V, Bensenane M, Feillet F, Guéant JL, Namour F, Bronowicki JP, Oussalah A.   +11 more
europepmc   +1 more source