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]

open access: bronze, 1999
Olesia Buiakova   +9 more
openalex   +1 more source

Lack of evidence for ribosomal frameshifting in ATP7B mRNA decoding

open access: yesMolecules and Cells, 2022
G. Loughran   +4 more
semanticscholar   +1 more source

Pathogenicity of intronic and synonymous variants of ATP7B in Wilson's disease.

open access: yesJournal of Molecular Diagnostics, 2022
Wan-Qing Xu   +3 more
semanticscholar   +1 more source

ATP7B genotype and chronic liver disease treatment outcomes in Wilson disease: worse survival with loss of function variants.

open access: yesClinical Gastroenterology and Hepatology, 2022
J. Nayagam   +7 more
semanticscholar   +1 more source

Repurposing melatonin's therapeutic potential in Wilson disease: Addressing copper overload and redox imbalance. [PDF]

open access: yesRedox Biol
Pandey R   +17 more
europepmc   +1 more source

P-coumaric acid regulates exon 12 splicing of the ATP7B gene by modulating hnRNP A1 protein expressions

open access: diamond
Ying‐Ju Lin   +10 more
openalex   +2 more sources

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