Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Gatt, Ariana"'
Autor:
Gatt, Ariana Pia
Mitochondria play critical roles in the generation of cellular energy, apoptosis, calcium buffering, and mitochondrial dysfunction is strongly implicated in common neurodegenerative diseases such as Alzheimer’s and Parkinson’s disease. However, w
Externí odkaz:
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677073
Autor:
Jiang, Xinwa1,2 (AUTHOR) xinwa.jiang.21@ucl.ac.uk, Gatt, Ariana1,2 (AUTHOR) a.gatt@ucl.ac.uk, Lashley, Tammaryn1,2 (AUTHOR) a.gatt@ucl.ac.uk
Publikováno v:
Cells (2073-4409). Jun2023, Vol. 12 Issue 12, p1633. 23p.
Akademický článek
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Publikováno v:
In Neurobiology of Aging April 2019 76:166-180
Autor:
Sidhu, Rahul1,2 (AUTHOR), Gatt, Ariana1,2 (AUTHOR), Fratta, Pietro3 (AUTHOR), Lashley, Tammaryn1,2 (AUTHOR) t.lashley@ucl.ac.uk, Bampton, Alexander1,2 (AUTHOR) alexander.bampton.18@ucl.ac.uk
Publikováno v:
Neuropathology & Applied Neurobiology. Jun2022, Vol. 48 Issue 4, p1-4. 4p.
Autor:
Boyanova, Sevda T., Lloyd-Morris, Ethlyn, Corpe, Christopher, Rahman, Khondaker Miraz, Farag, Doaa B., Page, Lee K., Wang, Hao, Fleckney, Alice L., Gatt, Ariana, Troakes, Claire, Vizcay-Barrena, Gema, Fleck, Roland, Reeves, Suzanne J., Thomas, Sarah A.
Publikováno v:
PLoS ONE; 10/24/2023, Vol. 18 Issue 10, p1-32, 32p
Autor:
Harley, Peter, Kerins, Caoimhe, Gatt, Ariana, Neves, Guilherme, Riccio, Federica, Machado, Carolina Barcellos, Cheesbrough, Aimee, R’Bibo, Lea, Burrone, Juan, Lieberam, Ivo
Publikováno v:
In Cell Reports 26 December 2023 42(12)
Autor:
Cagin, Umut, Duncan, Olivia F., Gatt, Ariana P., Dionne, Marc S., Sweeney, Sean T., Bateman, Joseph M.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2015 Nov 01. 112(44), E6000-E6009.
Externí odkaz:
https://www.jstor.org/stable/26465697
Autor:
Brown, Anna-Leigh, Wilkins, Oscar G., Keuss, Matthew J., Hill, Sarah E., Zanovello, Matteo, Lee, Weaverly Colleen, Bampton, Alexander, Lee, Flora C. Y., Masino, Laura, Qi, Yue A., Bryce-Smith, Sam, Gatt, Ariana, Hallegger, Martina, Fagegaltier, Delphine, Phatnani, Hemali, Kwan, Justin, Sareen, Dhruv, Broach, James R., Simmons, Zachary, Arcila-Londono, Ximena, Lee, Edward B., Van Deerlin, Vivianna M., Shneider, Neil A., Fraenkel, Ernest, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Berry, James D., Malaspina, Andrea, Fratta, Pietro, Cox, Gregory A., Thompson, Leslie M., Finkbeiner, Steve, Dardiotis, Efthimios, Miller, Timothy M., Chandran, Siddharthan, Pal, Suvankar, Hornstein, Eran, MacGowan, Daniel J., Heiman-Patterson, Terry, Hammell, Molly G., Patsopoulos, Nikolaos. A., Butovsky, Oleg, Dubnau, Joshua, Nath, Avindra, Bowser, Robert, Harms, Matthew, Aronica, Eleonora, Poss, Mary, Phillips-Cremins, Jennifer, Crary, John, Atassi, Nazem, Lange, Dale J., Adams, Darius J., Stefanis, Leonidas, Gotkine, Marc, Baloh, Robert H., Babu, Suma, Raj, Towfique, Paganoni, Sabrina, Shalem, Ophir, Smith, Colin, Zhang, Bin, Harris, Brent, Broce, Iris, Drory, Vivian, Ravits, John, McMillan, Corey, Menon, Vilas, Wu, Lani, Altschuler, Steven, Lerner, Yossef, Sattler, Rita, Van Keuren-Jensen, Kendall, Rozenblatt-Rosen, Orit, Lindblad-Toh, Kerstin, Nicholson, Katharine, Gregersen, Peter, Lee, Jeong-Ho, Kokos, Sulev, Muljo, Stephen, Newcombe, Jia, Gustavsson, Emil K., Seddighi, Sahba, Reyes, Joel F., Coon, Steven L., Ramos, Daniel, Schiavo, Giampietro, Fisher, Elizabeth M. C., Secrier, Maria, Lashley, Tammaryn, Ule, Jernej, Buratti, Emanuele, Humphrey, Jack, Ward, Michael E.
Publikováno v:
Nature, 603(7899), 131-137. Nature Publishing Group
Nature, vol 603, iss 7899
NYGC ALS Consortium 2022, ' TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A ', Nature, vol. 603, no. 7899, pp. 131-137 . https://doi.org/10.1038/s41586-022-04436-3
Nature, 603(7899), 131-+. NATURE PORTFOLIO
Nature, vol 603, iss 7899
NYGC ALS Consortium 2022, ' TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A ', Nature, vol. 603, no. 7899, pp. 131-137 . https://doi.org/10.1038/s41586-022-04436-3
Nature, 603(7899), 131-+. NATURE PORTFOLIO
Variants of UNC13A, a critical gene for synapse function, increase the risk of amyotrophic lateral sclerosis and frontotemporal dementia1–3, two related neurodegenerative diseases defined by mislocalization of the RNA-binding protein TDP-434,5. Her
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a25848cce9d1ba10e3d3a48fd3e242
Akademický článek
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