OBO ID: DOID:1838

Citations

(6 total)

Term: Menkes disease

Wu, Y., Li, J., Zhai, W., Liu, W., Wu, H., Liu, H., Min, J., Wang, F., Liu, J.X. (2025) Atp7a deficiency induces axonal and myelin developmental defects in zebrafish via ferroptosis. Neurobiology of disease. :107027

Ackerman, C.M., Weber, P.K., Xiao, T., Thai, B., Kuo, T.J., Zhang, E., Pett-Ridge, J., Chang, C.J. (2018) Multimodal LA-ICP-MS and nanoSIMS imaging enables copper mapping within photoreceptor megamitochondria in a zebrafish model of Menkes disease. Metallomics : integrated biometal science. 10(3):474-485

Varga, M., Ralbovszki, D., Balogh, E., Hamar, R., Keszthelyi, M., Tory, K. (2018) Zebrafish Models of Rare Hereditary Pediatric Diseases. Diseases (Basel, Switzerland). 6(2)

Lenartowicz, M., Krzeptowski, W., Lipiński, P., Grzmil, P., Starzyński, R., Pierzchała, O., Møller, L.B. (2015) Mottled Mice and Non-Mammalian Models of Menkes Disease. Frontiers in molecular neuroscience. 8:72

Madsen, E.C., Morcos, P.A., Mendelsohn, B.A., and Gitlin, J.D. (2008) In vivo correction of a Menkes disease model using antisense oligonucleotides. Proceedings of the National Academy of Sciences of the United States of America. 105(10):3909-3914

Mendelsohn, B.A., Yin, C., Johnson, S.L., Wilm, T.P., Solnica-Krezel, L., and Gitlin, J.D. (2006) Atp7a determines a hierarchy of copper metabolism essential for notochord development. Cell Metabolism. 4(2):155-162