Neutrophil extracellular traps delivering lactylated S100a9 aggravate neuronal cuproptosis by regulating Ttr/Commd1/Atp7b axis after traumatic brain injury. [PDF]
Xu J +16 more
europepmc +1 more source
Recent advances in research on high-frequency mutations in the ATP7B gene associated with Wilson disease in the Chinese population: from genetic evolution to precision medicine. [PDF]
Xuan Q +5 more
europepmc +1 more source
A Novel Homozygous <i>ATP7B</i> Splice-Site Variant Causes Late-Onset Hepatic Wilson Disease. [PDF]
Alkhateb O, Rockey DC, Barada K.
europepmc +1 more source
An incidental heterozygous ATP7B nonsense variant leading to a diagnostic pitfall for Wilson disease: a pediatric case report. [PDF]
Xu Z, Tang J.
europepmc +1 more source
Copper, cuproptosis, and cancer: biology concepts of a novel cell death. [PDF]
Eshraghi R +9 more
europepmc +1 more source
ATP7B analysis of a Wilson disease family
Tatsumi, Yasuaki +9 more
openaire +2 more sources
Prognosis of pediatric hepatic Wilson disease with ATP7B loss of function variants. [PDF]
Mishra AK +6 more
europepmc +1 more source
Hepatic methanethiol oxidase (MTO) activity of mice requires adequate dietary supply of copper. [PDF]
Krafczyk N +8 more
europepmc +1 more source
Referral-spectrum Effect in Hypercupriuric Referrals for Suspected Wilson Disease: Diagnostic Implications for Ceruloplasmin and 24-hour Urinary Copper Excretion. [PDF]
Zhang Y +14 more
europepmc +1 more source
Adipose-derived mesenchymal stem cell exosomes ameliorate copper metabolism dysregulation and reduce cuproptosis caused by liver IRI. [PDF]
Cao L +7 more
europepmc +1 more source

