Results 131 to 140 of about 8,657 (242)
Null Mutation of the Murine ATP7B (Wilson Disease) Gene Results in Intracellular Copper Accumulation and Late-Onset Hepatic Nodular Transformation [PDF]
Olesia Buiakova +9 more
openalex +1 more source
Lack of evidence for ribosomal frameshifting in ATP7B mRNA decoding
G. Loughran +4 more
semanticscholar +1 more source
Functional Effects of N-Metal Binding Domain Deletion and Specific Mutations on the ATP7B (Wilson Disease) Copper ATPase [PDF]
Rajendra Pilankatta +2 more
openalex +1 more source
Pathogenicity of intronic and synonymous variants of ATP7B in Wilson's disease.
Wan-Qing Xu +3 more
semanticscholar +1 more source
Repurposing melatonin's therapeutic potential in Wilson disease: Addressing copper overload and redox imbalance. [PDF]
Pandey R +17 more
europepmc +1 more source
Functional nano-nucleic acid platform promotes copper-induced gastric cancer cell death. [PDF]
Zhang H, Ding B, Kou Q.
europepmc +1 more source

