Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Elisa Cabiscol"'
Autor:
Arabela Sanz-Alcázar, Marta Portillo-Carrasquer, Fabien Delaspre, Maria Pazos-Gil, Jordi Tamarit, Joaquim Ros, Elisa Cabiscol
Publikováno v:
Redox Biology, Vol 76, Iss , Pp 103339- (2024)
Friedreich ataxia (FA) is a rare neurodegenerative disease caused by decreased levels of the mitochondrial protein frataxin. Frataxin has been related in iron homeostasis, energy metabolism, and oxidative stress. Ferroptosis has recently been shown t
Externí odkaz:
https://doaj.org/article/9b59a3a421f5404c971987defaf49e32
Autor:
Isabel C. Lopez‐Mejia, Jordi Pijuan, Raúl Navaridas, Maria Santacana, Sònia Gatius, Ana Velasco, Gerard Castellà, Anaïs Panosa, Elisa Cabiscol, Miquel Pinyol, Laura Coll, Núria Bonifaci, Laura Plata Peña, August Vidal, Alberto Villanueva, Eloi Gari, David Llobet‐Navàs, Lluis Fajas, Xavier Matias‐Guiu, Andrée Yeramian
Publikováno v:
Molecular Oncology, Vol 17, Iss 1, Pp 98-118 (2023)
Uterine serous carcinoma (USC) is an aggressive form of endometrial cancer (EC), characterized by its high propensity for metastases. In fact, while endometrioid endometrial carcinoma (EEC), which accounts for 85% of EC, presents a good prognosis, US
Externí odkaz:
https://doaj.org/article/f663469d36c74406919fb1ffb516ab40
Autor:
Rocio Gomez-Pastor, Eileen T. Burchfiel, Daniel W. Neef, Alex M. Jaeger, Elisa Cabiscol, Spencer U. McKinstry, Argenia Doss, Alejandro Aballay, Donald C. Lo, Sergey S. Akimov, Christopher A. Ross, Cagla Eroglu, Dennis J. Thiele
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-17 (2017)
Huntington’s disease (HD) is caused by misfolding of mutant Htt protein. The authors find that in HD models, the decreased expression of heat shock transcription factor 1 that usually protects against protein misfolding, is in part caused by elevat
Externí odkaz:
https://doaj.org/article/10e213fe581949ff9cd3a516b23f2861
Publikováno v:
Redox Biology, Vol 24, Iss , Pp - (2019)
Yeast Sir2 is an NAD-dependent histone deacetylase related to oxidative stress and aging. In a previous study, we showed that Sir2 is regulated by S-glutathionylation of key cysteine residues located at the catalytic domain. Mutation of these residue
Externí odkaz:
https://doaj.org/article/27669eff2f104bbe8b09dfa6e40c882c
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 24, p 9574 (2020)
Hcm1 is a member of the forkhead transcription factor family involved in segregation, spindle pole dynamics, and budding in Saccharomyces cerevisiae. Our group described the role of Hcm1 in mitochondrial biogenesis and stress resistance, and in the c
Externí odkaz:
https://doaj.org/article/9f2285723f274ebfb07ef8d63edfde4a
Autor:
Arabela Sanz-Alcázar, Elena Britti, Fabien Delaspre, Marta Medina-Carbonero, Maria Pazos-Gil, Jordi Tamarit, Joaquim Ros, Elisa Cabiscol
Friedreich ataxia (FA) is a rare, recessive neuro-cardiodegenerative disease caused by deficiency of the mitochondrial protein frataxin. Mitochondrial dysfunction, a reduction in the activity of iron-sulfur enzymes, iron accumulation, and increased o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11690086071ba22b0e8bd95fbb1cadd7
https://doi.org/10.1101/2023.02.01.526688
https://doi.org/10.1101/2023.02.01.526688
Autor:
null Isabel C. Lopez‐Mejia, null Jordi Pijuan, null Raúl Navaridas, null Maria Santacana, null Sònia Gatius, null Ana Velasco, null Gerard Castellà, null Anaïs Panosa, null Elisa Cabiscol, null Miquel Pinyol, null Laura Coll, null Núria Bonifaci, null Laura Plata Peña, null August Vidal, null Alberto Villanueva, null Eloi Gari, null David Llobet‐Navàs, null Lluis Fajas, null Xavier Matias‐Guiu, null Andrée Yeramian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f022c0b74452dd6eba65d4ddb92e8b86
https://doi.org/10.1002/1878-0261.13346/v2/response1
https://doi.org/10.1002/1878-0261.13346/v2/response1
Autor:
Marta Medina-Carbonero, Arabela Sanz-Alcázar, Elena Britti, Fabien Delaspre, Elisa Cabiscol, Joaquim Ros, Jordi Tamarit
Publikováno v:
Cellular and Molecular Life Sciences
Repositorio Abierto de la UdL
Universitad de Lleida
Repositorio Abierto de la UdL
Universitad de Lleida
Friedreich Ataxia (FA) is a rare neuro-cardiodegenerative disease caused by mutations in the frataxin (FXN) gene. The most prevalent mutation is a GAA expansion in the first intron of the gene causing decreased frataxin expression. Some patients pres
Biochemical alterations precede neurobehavioral deficits in a novel mouse model of Friedreich ataxia
Autor:
Jordi Tamarit, Elisa Cabiscol, Fabien Delaspre, Joaquim Ros, A. Sanz-Alcázar, Elena Britti, Marta Medina-Carbonero
Friedreich Ataxia (FA) is a rare neuro-cardiodegenerative disease, caused by partial deficiency of frataxin, a mitochondrial protein. This deficiency is caused by the presence of a GAA triplet expansion in the first intron of the frataxin gene or, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87c33d7c95cefa57ac0babc0f5ef0a87
https://doi.org/10.1101/2021.04.05.438486
https://doi.org/10.1101/2021.04.05.438486
Autor:
Arabela Sanz-Alcázar, Joaquim Ros, Fabien Delaspre, Jordi Tamarit, Elisa Cabiscol, Elena Britti, Marta Medina-Carbonero
Publikováno v:
IUBMB lifeREFERENCES. 73(3)
Friedreich Ataxia is a neuro-cardiodegenerative disease caused by the deficiency of frataxin, a mitochondrial protein. Many evidences indicate that frataxin deficiency causes an unbalance of iron homeostasis. Nevertheless, in the last decade many res