Results 221 to 230 of about 8,657 (242)
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Copper-transporting ATPases ATP7A and ATP7B: cousins, not twins

Journal of Bioenergetics and Biomembranes, 2007
Copper plays an essential role in human physiology and is indispensable for normal growth and development. Enzymes that are involved in connective tissue formation, neurotransmitter biosynthesis, iron transport, and others essential physiological processes require copper as a cofactor to mediate their reactions. The biosynthetic incorporation of copper
Rachel, Linz, Svetlana, Lutsenko
openaire   +2 more sources

Age and Sex but Not ATP7B Genotype Effectively Influence the Clinical Phenotype of Wilson Disease

Hepatology, 2019
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variation in clinical presentations, the most common ones being liver disease and neuropsychiatric disturbances. This study investigated the clinical presentation
P. Ferenci   +17 more
semanticscholar   +1 more source

Pseudo‐Wilsonian Crisis in a ATP7B Heterozygote

Liver Transplantation, 2021
Mohammad Qasim Khan   +4 more
openaire   +2 more sources

Intracellular Copper Transport and ATP7B, the Wilson’s Disease Protein

2002
Copper is an essential trace metal for all living organisms because this metal serves as a cofactor for activating numerous enzymes critical for homeostasis. However, when copper exceeds the cellular needs, it is toxic through the production of highly reactive hydroxyl radicals that have deleterious effects on cellular components, including ...
Kunihiko Terada, Toshihiro Sugiyama
openaire   +1 more source

Genomic Variations in ATP7B Gene in Indian Patients with Wilson Disease

Indian Journal of Pediatrics, 2022
A. Nagral   +10 more
semanticscholar   +1 more source

ATP7B Function

2019
Hannah Pierson, Svetlana Lutsenko
openaire   +1 more source

Identification of ATP7B

2019
Peter C. Bull   +2 more
openaire   +1 more source

ATP7B Knockout in einer intestinalen Zelllinie

Zeitschrift für Gastroenterologie, 2019
S Guttmann, H Schmidt
openaire   +1 more source

Mutational analysis of exon 8 and exon 14 of ATP7B gene in Bangladeshi children with Wilson disease

Indian Journal of Gastroenterology, 2022
Ruhina Tasmeen   +9 more
semanticscholar   +1 more source

ATP7B and Alzheimer Disease

2019
Rosanna Squitti   +3 more
openaire   +1 more source

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