Zobrazeno 1 - 10
of 424
pro vyhledávání: '"Mitochondria/genetics"'
Autor:
Vawter, Marquis, Morgan, Linda, Akil, Huda, Watson, Stanley, Myers, Richard, Lee, Francis, Schatzberg, Alan, Bunney, William, Hjelm, Brooke, Manojlovic, Zarko, Jin, Yuxin, Rollins, Brandi
Publikováno v:
In Biological Psychiatry 1 May 2021 89(9) Supplement:S5-S5
Autor:
Whelan, J., Giraud, E.
Publikováno v:
In Brenner’s Encyclopedia of Genetics Edition: Second Edition. 2013:433-435
Mitochondria are organelles found in eukaryotic cells that are defined by an outer and an inner membrane. They have specialized roles in energy production and carry out additional functions ranging from the biosynthesis of various molecules to initia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::332fb543f6c019f1ab756364c1ae98f0
https://doi.org/10.1016/b978-0-12-374984-0.00634-3
https://doi.org/10.1016/b978-0-12-374984-0.00634-3
Akademický článek
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Autor:
Kate N. O’Neill, Emily Aubrey, Laura D. Howe, Evie Stergiakouli, Santiago Rodriguez, Patricia M. Kearney, Linda M. O’Keeffe
Publikováno v:
O'Neill, K N, Aubrey, E, Howe, L D, Stergiakouli, E, Rodriguez, S, Kearney, P M & O'Keeffe, L M 2023, ' Mitochondrial DNA haplogroups and trajectories of cardiometabolic risk factors during childhood and adolescence : A prospective cohort study ', PLoS ONE, vol. 18, no. 4, e0284226 . https://doi.org/10.1371/journal.pone.0284226
Background Mitochondria are organelles responsible for converting glucose into energy. Mitochondrial DNA is exclusively maternally inherited. The role of mitochondrial DNA haplogroups in the aetiology of cardiometabolic disease risk is not well under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::988819509493c47fabe65f1b609206f9
https://hdl.handle.net/1983/2304c2f8-0814-4855-8895-d513001e82cb
https://hdl.handle.net/1983/2304c2f8-0814-4855-8895-d513001e82cb
Autor:
Sibelle T. Vilaça, Francesco Maroso, Paulo Lara, Benoit de Thoisy, Damien Chevallier, Larissa Souza Arantes, Fabricio R. Santos, Giorgio Bertorelle, Camila J. Mazzoni
This dataset contains ddRAD data used in our sea turtles genomics research on hybridization in Brazil. In this paper, we analyzed hybridization patterns, population structure and relatedness between southwest Atlantic population with a focus on Brazi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8f1336fbe82f91c0c4cc61aeb3d8fcb
https://doi.org/10.1101/2022.10.10.511144
https://doi.org/10.1101/2022.10.10.511144
Autor:
Sophia Millington‐Ward, Naomi Chadderton, Laura K. Finnegan, Iris J.M. Post, Matthew Carrigan, Tom Gardiner, Elisa Peixoto, Daniel Maloney, Marian M. Humphries, Alan Stitt, Thierry Léveillard, Pete Humphries, Paul F. Kenna, Arpad Palfi, G. Jane Farrar
Publikováno v:
Clinical and Translational Medicine
Millington-Ward, S, Chadderton, N, Finnegan, L K, Post, I J M, Carrigan, M, Gardiner, T, Peixoto, E, Maloney, D, Humphries, M M, Stitt, A, Léveillard, T, Humphries, P, Kenna, P F, Palfi, A & Farrar, G J 2022, ' AAV-mediated gene therapy improving mitochondrial function provides benefit in age-related macular degeneration models ', Clinical and Translational Medicine, vol. 12, no. 8, e952 . https://doi.org/10.1002/ctm2.952
Millington-Ward, S, Chadderton, N, Finnegan, L K, Post, I J M, Carrigan, M, Gardiner, T, Peixoto, E, Maloney, D, Humphries, M M, Stitt, A, Léveillard, T, Humphries, P, Kenna, P F, Palfi, A & Farrar, G J 2022, ' AAV-mediated gene therapy improving mitochondrial function provides benefit in age-related macular degeneration models ', Clinical and Translational Medicine, vol. 12, no. 8, e952 . https://doi.org/10.1002/ctm2.952
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de0ba68887019dfd9054574032d5da9b
Autor:
Lee, R.G., Balasubramaniam, S., Stentenbach, M., Kralj, T., McCubbin, T., Padman, B., Smith, J., Riley, L.G., Priyadarshi, A., Peng, L.Y., Nuske, M.R., Webster, R., Peacock, K., Roberts, P., Stark, Z., Lemire, G., Ito, Y.A., Boycott, K.M., Geraghty, M.T., Klinken, J.B., Ferdinandusse, S., Zhou, Y., Walsh, R., Marcellin, E., Thorburn, D.R., Rosciolli, T., Fletcher, J., Rackham, O., Vaz, F.M., Reid, G.E., Filipovska, A., Care4Rare Canada Consortium
Publikováno v:
Human Molecular Genetics, 31(21), 3597-3612. OXFORD UNIV PRESS
Human molecular genetics, 31(21), 3597-3612. Oxford University Press
Human molecular genetics, 31(21), 3597-3612. Oxford University Press
Mitochondrial diseases are a group of inherited diseases with highly varied and complex clinical presentations. Here, we report four individuals, including two siblings, affected by a progressive mitochondrial encephalopathy with biallelic variants i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19e79bac1d14fa395f9b21de73859fd0
https://pubmed.ncbi.nlm.nih.gov/36563328
https://pubmed.ncbi.nlm.nih.gov/36563328
Publikováno v:
Ji, J & Day, A 2020, ' Construction of a highly error-prone DNA polymerase for developing organelle mutation systems ', Nucleic Acids Res, vol. 48, no. 21, DOI: gkaa929, pp. 11868-11879 . https://doi.org/10.1093/nar/gkaa929
Nucleic Acids Research
Nucleic Acids Research
A novel family of DNA polymerases replicates organelle genomes in a wide distribution of taxa encompassing plants and protozoans. Making error-prone mutator versions of gamma DNA polymerases revolutionised our understanding of animal mitochondrial ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf2dfc0f7a24dd32b9eaaa993c0d7130
http://www.narbreakthrough.com/2020/11/03/construction-of-a-highly-error-prone-dna-polymerase-for-developing-organelle-mutation-systems/
http://www.narbreakthrough.com/2020/11/03/construction-of-a-highly-error-prone-dna-polymerase-for-developing-organelle-mutation-systems/