Zobrazeno 1 - 10
of 880
pro vyhledávání: '"TMRM, tetramethylrhodamine methyl ester"'
Autor:
Lounas, Amel1 (AUTHOR), Lebrun, Ariane1 (AUTHOR), Laflamme, Isabelle1 (AUTHOR), Vernoux, Nathalie2 (AUTHOR), Savage, Julie2 (AUTHOR), Tremblay, Marie-Ève2,3 (AUTHOR), Germain, Marc4 (AUTHOR), Richard, François J.1 (AUTHOR) francois.richard@fsaa.ulaval.ca
Publikováno v:
Scientific Reports. 9/13/2022, Vol. 12 Issue 1, p1-10. 10p.
Publikováno v:
Molecular Metabolism
Molecular Metabolism, Vol 6, Iss 8, Pp 797-808 (2017)
Molecular Metabolism, Vol 6, Iss 8, Pp 797-808 (2017)
Objective Brown adipocytes (BAs) are endowed with a high metabolic capacity for energy expenditure due to their high mitochondria content. While mitochondrial pH is dynamically regulated in response to stimulation and, in return, affects various meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dc978cdf69b23cde7364b16b4949fd1
http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100775204
http://t2r2.star.titech.ac.jp/cgi-bin/publicationinfo.cgi?q_publication_content_number=CTT100775204
Publikováno v:
The Journal of Investigative Dermatology
Reelfs, O, Abbate, V, Hider, R C & Pourzand, C 2016, ' A powerful mitochondria-targeted iron chelator affords high photoprotection against solar ultraviolet A radiation ', Journal Of Investigative Dermatology, vol. 136, no. 8, pp. 1692-1700 . https://doi.org/10.1016/j.jid.2016.03.041
Reelfs, O, Abbate, V, Hider, R C & Pourzand, C 2016, ' A powerful mitochondria-targeted iron chelator affords high photoprotection against solar ultraviolet A radiation ', Journal Of Investigative Dermatology, vol. 136, no. 8, pp. 1692-1700 . https://doi.org/10.1016/j.jid.2016.03.041
Mitochondria are the principal destination for labile iron, making these organelles particularly susceptible to oxidative damage on exposure to ultraviolet A (UVA, 320-400 nm), the oxidizing component of sunlight. The labile iron-mediated oxidative d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8a70599c168b6182c9f11c45b8b9f253
Autor:
Li Feng, Youping Li, Hong-Sheng Li, Jia-Bi Zhang, Yanni Zhou, Lu Li, Dan Long, Shengfu Li, Xuelu Chen
Publikováno v:
Redox Biology
Redox Biology, Vol 25, Iss, Pp-(2019)
Redox Biology, Vol 25, Iss, Pp-(2019)
The transcription factor hypoxia inducible factor-1α (HIF-1α) mediates adaptive responses to oxidative stress by nuclear translocation and regulation of gene expression. Mitochondrial changes are critical for the adaptive response to oxidative stre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a886e678fab1cdbd21eb362879cc744e
http://europepmc.org/articles/PMC6859547
http://europepmc.org/articles/PMC6859547
Autor:
Emma R, Wilson, Umaiyal, Kugathasan, Andrey Y, Abramov, Alex J, Clark, David L H, Bennett, Mary M, Reilly, Linda, Greensmith, Bernadett, Kalmar
Publikováno v:
Neurobiology of Disease
Hereditary sensory neuropathy type 1 (HSN-1) is a peripheral neuropathy most frequently caused by mutations in the SPTLC1 or SPTLC2 genes, which code for two subunits of the enzyme serine palmitoyltransferase (SPT). SPT catalyzes the first step of de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22e274073f526b75eb0e51d71303ab1c
https://pubmed.ncbi.nlm.nih.gov/29778900
https://pubmed.ncbi.nlm.nih.gov/29778900
Autor:
Sonia Levi, Valeria Tiranti, Sabrina Dusi, Michela Guaraldo, Barbara Garavaglia, Vania Broccoli, Paolo Santambrogio, Luisa Ida Rotundo
Publikováno v:
Neurobiology of Disease
Neurobiology of Disease, Vol 81, Iss, Pp 144-153 (2015)
Neurobiology of Disease, Vol 81, Iss, Pp 144-153 (2015)
Pantothenate kinase-associated neurodegeneration is an early onset autosomal recessive movement disorder caused by mutation of the pantothenate kinase-2 gene, which encodes a mitochondrial enzyme involved in coenzyme A synthesis. The disorder is char
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47111460d6c550971554646d7eadd0e6
Autor:
Markéta Tesařová, Alena Pecinová, Jan Janota, Jiří Zeman, Tomáš Mráček, Petr Pecina, Hana Houšťková, Hana Hansikova, Hana Nůsková, Josef Houštěk
Publikováno v:
BBA Clinical
Background Mitochondrial diseases belong to the most severe inherited metabolic disorders affecting pediatric population. Despite detailed knowledge of mtDNA mutations and progress in identification of affected nuclear genes, diagnostics of a substan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64188a06064bf7f4a9b62d4a832cdab1
Autor:
Joerg Stetefeld, Joanna Rzeszowska-Wolny, Mayur V. Jain, Artur Cieślar-Pobuda, Wiem Chaabane, Saeid Ghavami, Marek J. Łos, Mohamed El-Gazzah, Mehrdad Rafat
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 16, Iss 9, Pp 679-693 (2014)
Neoplasia (New York, N.Y.)
Neoplasia (New York, N.Y.)
The human gyrovirus derived protein Apoptin (HGV-Apoptin) a homologue of the chicken anemia virus Apoptin (CAV-Apoptin), a protein with high cancer cells selective toxicity, triggers apoptosis selectively in cancer cells. In this paper, we show that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ff91e1764b6bc1727600d6c646b3f55
https://doi.org/10.1016/j.neo.2014.08.001
https://doi.org/10.1016/j.neo.2014.08.001
Autor:
Clarke, Benjamin E.1,2 (AUTHOR) ben.clarke@crick.ac.uk, Ziff, Oliver J.1,2,3 (AUTHOR) oliver.ziff@crick.ac.uk, Tyzack, Giulia1,2 (AUTHOR), Howe, Marija Petrić1,2 (AUTHOR), Wang, Yiran1,2 (AUTHOR), Klein, Pierre1,2 (AUTHOR), Smith, Claudia A.4 (AUTHOR), Hall, Cameron A.4 (AUTHOR), Helmy, Adel4 (AUTHOR), Howell, Michael2 (AUTHOR), Kelly, Gavin2 (AUTHOR), Patani, Rickie1,2,3 (AUTHOR) rickie.patani@ucl.ac.uk
Publikováno v:
Molecular Neurodegeneration. 11/26/2024, Vol. 19 Issue 1, p1-24. 24p.
Autor:
Meng, Linghui1,2 (AUTHOR), Hao, Dingqian1,2 (AUTHOR), Liu, Yuan1,3 (AUTHOR), Yu, Peng1,2 (AUTHOR), Luo, Jinfeng1,2 (AUTHOR), Li, Chunhao1,2 (AUTHOR), Jiang, Tianjiao1,2 (AUTHOR), Yu, JinZhuang1,2 (AUTHOR), Zhang, Qian1,2 (AUTHOR), Liu, Shengyang1,2 (AUTHOR) 454415082@qq.com, Shi, Li1,2 (AUTHOR) shili126@sina.com
Publikováno v:
Journal of Translational Medicine. 11/16/2024, Vol. 22 Issue 1, p1-18. 18p.