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pro vyhledávání: '"Anjomani Virmouni, Sara"'
Autor:
Anjomani Virmouni, Sara
Friedreich ataxia (FRDA) is an autosomal recessive neurodegenerative disorder, caused by a GAA repeat expansion mutation within intron 1 of the FXN gene, resulting in reduced level of frataxin protein. Normal individuals have 5 to 40 GAA repeat seque
Externí odkaz:
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582931
Autor:
Koundouros, Nikos, Karali, Evdoxia, Tripp, Aurelien, Valle, Adamo, Inglese, Paolo, Perry, Nicholas J.S., Magee, David J., Anjomani Virmouni, Sara, Elder, George A., Tyson, Adam L., Dória, Maria Luisa, van Weverwijk, Antoinette, Soares, Renata F., Isacke, Clare M., Nicholson, Jeremy K., Glen, Robert C., Takats, Zoltan, Poulogiannis, George
Publikováno v:
In Cell 25 June 2020 181(7):1596-1611
PARK2 Depletion Connects Energy and Oxidative Stress to PI3K/Akt Activation via PTEN S-Nitrosylation
Autor:
Gupta, Amit, Anjomani-Virmouni, Sara, Koundouros, Nikos, Dimitriadi, Maria, Choo-Wing, Rayman, Valle, Adamo, Zheng, Yuxiang, Chiu, Yu-Hsin, Agnihotri, Sameer, Zadeh, Gelareh, Asara, John M., Anastasiou, Dimitrios, Arends, Mark J., Cantley, Lewis C., Poulogiannis, George
Publikováno v:
In Molecular Cell 16 March 2017 65(6):999-1013
Autor:
Crombie, Duncan E., Van Bergen, Nicole, Davidson, Kathryn C., Anjomani Virmouni, Sara, Mckelvie, Penny A., Chrysostomou, Vicki, Conquest, Alison, Corben, Louise A., Pook, Mark A., Kulkarni, Tejal, Trounce, Ian A., Pera, Martin F., Delatycki, Martin B., Pébay, Alice
Publikováno v:
In Biochemistry and Biophysics Reports December 2015 4:141-147
Autor:
Anjomani Virmouni, Sara1, Sandi, Chiranjeevi1, Al-Mahdawi, Sahar1, Pook, Mark A.1 Mark.Pook@brunel.ac.uk
Publikováno v:
PLoS ONE. Sep2014, Vol. 9 Issue 9, p1-13. 13p.
Autor:
Sherzai, Mursal, Valle, Adamo, Perry, Nicholas, Kalef-Ezra, Ester, Al-Mahdawi, Sahar, Pook, Mark, Anjomani Virmouni, Sara
Publikováno v:
Frontiers in Genetics; 6/5/2020, Vol. 11, p1-10, 10p
Publikováno v:
In Epigenetic Biomarkers and Diagnostics 2016:401-415
Autor:
Anjomani Virmouni, Sara, Al-Mahdawi, Sahar, Sandi, Chiranjeevi, Yasaei, Hemad, Giunti, Paola, Slijepcevic, Predrag, Pook, Mark A.
Copyright © The Author(s) 2022. Background: Friedreich ataxia (FRDA) is a progressive inherited neurodegenerative disorder caused by mutation of the FXN gene, resulting in decreased frataxin expression, mitochondrial dysfunction and oxidative stress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::03458ef410f9fe07dbdf1435507ba83c
https://bura.brunel.ac.uk/handle/2438/12968
https://bura.brunel.ac.uk/handle/2438/12968
Akademický článek
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Autor:
Ezzatizadeh, Vahid, Sandi, Chiranjeevi, Sandi, Madhavi, Anjomani-Virmouni, Sara, Al-Mahdawi, Sahar, Pook, Mark A.
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100523 (2014)
PLoS ONE
PLoS ONE
This article has been made available through the Brunel Open Access Publishing Fund. Background: Friedreich ataxia (FRDA), the most common autosomal recessive ataxia disorder, is caused by a dynamic GAA repeat expansion mutation within intron 1 of FX
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::605d7c7318967b4c341e727ebded1397
http://bura.brunel.ac.uk/handle/2438/9859
http://bura.brunel.ac.uk/handle/2438/9859