Zobrazeno 1 - 10
of 270
pro vyhledávání: '"Ferrari-Bardile"'
Publikováno v:
In Trends in Molecular Medicine October 2023 29(10):802-816
Autor:
Radulescu CI; Agency for Science, Technology and Research (A*STAR), Translational Laboratory in Genetic Medicine (TLGM), Singapore, 138648, Singapore.; UK Dementia Research Institute (DRI), Department of Brain Sciences, Imperial College London, Hammersmith Hospital Campus, Du Cane Road, London, W12 0NN, UK., Ferrari Bardile C; Agency for Science, Technology and Research (A*STAR), Translational Laboratory in Genetic Medicine (TLGM), Singapore, 138648, Singapore.; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, 950 West 28th Avenue, Vancouver, V5Z 4H4, Canada., Garcia-Miralles M; Agency for Science, Technology and Research (A*STAR), Translational Laboratory in Genetic Medicine (TLGM), Singapore, 138648, Singapore., Sidik H; Agency for Science, Technology and Research (A*STAR), Translational Laboratory in Genetic Medicine (TLGM), Singapore, 138648, Singapore., Yusof NABM; Agency for Science, Technology and Research (A*STAR), Translational Laboratory in Genetic Medicine (TLGM), Singapore, 138648, Singapore., Pouladi MA; Agency for Science, Technology and Research (A*STAR), Translational Laboratory in Genetic Medicine (TLGM), Singapore, 138648, Singapore. mahmoud.pouladi@ubc.ca.; Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics, Djavad Mowafaghian Centre for Brain Health, British Columbia Children's Hospital Research Institute, University of British Columbia, 950 West 28th Avenue, Vancouver, V5Z 4H4, Canada. mahmoud.pouladi@ubc.ca.
Publikováno v:
Molecular neurobiology [Mol Neurobiol] 2024 Jul; Vol. 61 (7), pp. 4278-4288. Date of Electronic Publication: 2023 Dec 11.
Autor:
Oguz K. Ozgoren, Glen Lester Sequiera, Costanza Ferrari Bardile, Sophia C. Gjervan, Areesha Salman, Anna Lehman, Stuart E. Turvey, Colin J.D. Ross, Sylvia Stockler, Mahmoud A. Pouladi
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103174- (2023)
Hypomyelinating Leukodystrophy 22 (HLD22) is caused by a stoploss mutation in CLDN11. To study the molecular mechanisms underlying HLD22, human induced pluripotent stem cells (hiPSCs) were generated from patient fibroblasts carrying the stop-loss mut
Externí odkaz:
https://doaj.org/article/da28363744664b88907f8eb810119337
Autor:
Oronzo Catalano, Giulia Bendotti, Teresa L. Aloi, Alberto Ferrari Bardile, Mirella Memmi, Patrick Gambelli, Daniela Zanaboni, Alessandra Gualco, Emanuela Cattaneo, Antonio Mazza, Mauro Frascaroli, Esmeralda Eshja, Riccardo Bellazzi, Paolo Poggi, Giovanni Forni, Maria Teresa La Rovere
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 2 (2023)
Background Atherosclerosis vulnerability regression has been evidenced mostly in randomized clinical trials with intensive lipid‐lowering therapy. We aimed to demonstrate vulnerability regression in real life, with a comprehensive quantitative meth
Externí odkaz:
https://doaj.org/article/40f95a60d3784b2ca6dc93ece95aea6d
Autor:
Oronzo Catalano, Giulia Bendotti, Alessia Mori, Maria De Salvo, Marialuisa Falconi, Teresa L. Aloi, Valentina Tibollo, Riccardo Bellazzi, Alberto Ferrari Bardile, Stefano Montagna, Clara Pesarin, Paolo Poggi, Roberto F. E. Pedretti, Silvia G. Priori
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract MRI can assess plaque composition and has demonstrated an association between some atherosclerotic risk factors (RF) and markers of plaque vulnerability in naive patients. We aimed at investigating this association in medically treated asymp
Externí odkaz:
https://doaj.org/article/37793f767bc749dcb79ec4c2159076e6
Akademický článek
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Autor:
Ferrari Bardile, Costanza1,2,3 (AUTHOR), Sidik, Harwin1 (AUTHOR), Quek, Reynard1 (AUTHOR), Yusof, Nur Amirah Binte Mohammad1 (AUTHOR), Garcia-Miralles, Marta1 (AUTHOR), Pouladi, Mahmoud A.1,2,3 (AUTHOR) map@pouladilab.org
Publikováno v:
Journal of Huntington's Disease. 2021, Vol. 10 Issue 3, p377-384. 8p.
Autor:
Carola I. Radulescu, Marta Garcia-Miralles, Harwin Sidik, Costanza Ferrari Bardile, Nur Amirah Binte Mohammad Yusof, Hae Ung Lee, Eliza Xin Pei Ho, Collins Wenhan Chu, Emma Layton, Donovan Low, Paola Florez De Sessions, Sven Pettersson, Florent Ginhoux, Mahmoud A. Pouladi
Publikováno v:
Neurobiology of Disease, Vol 127, Iss , Pp 65-75 (2019)
Structural and molecular myelination deficits represent early pathological features of Huntington disease (HD). Recent evidence from germ-free (GF) animals suggests a role for microbiota-gut-brain bidirectional communication in the regulation of myel
Externí odkaz:
https://doaj.org/article/57a94a7b970649ec909b982d493a2399
Autor:
Carola I. Radulescu, Marta Garcia-Miralles, Harwin Sidik, Costanza Ferrari Bardile, Nur Amirah Binte Mohammad Yusof, Hae Ung Lee, Eliza Xin Pei Ho, Collins Wenhan Chu, Emma Layton, Donovan Low, Paola Florez De Sessions, Sven Pettersson, Florent Ginhoux, Mahmoud A. Pouladi
Publikováno v:
Neurobiology of Disease, Vol 135, Iss , Pp 104744- (2020)
Structural and molecular myelination deficits represent early pathological features of Huntington disease (HD). Recent evidence from germ-free (GF) animals suggests a role for microbiota-gut-brain bidirectional communication in the regulation of myel
Externí odkaz:
https://doaj.org/article/7120aaec36004d4c8dc6c5ba2b8ffd5c
Autor:
Bachetti, Tiziana, Ferrari Bardile, Alberto, Aloi, Teresa Lucia, Colombo, Barbara, Assi, Emma, Savino, Giuseppina, Vercelli, Andrea, Colombo, Roberto, Corti, Angelo
Publikováno v:
In International Journal of Cardiology 1 June 2017 236:438-443