Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Margarida, Viola"'
Autor:
Maarten P. Bebelman, Caitrin Crudden, Bart Snieder, Evangelia Thanou, Catharina J.M. Langedijk, Margarida Viola, Steven Eleonora, Urszula Baginska, Olaf Cotugno, Jan Paul M. Bebelman, Monique A.J. van Eijndhoven, Leontien Bosch, Ka Wan Li, Martine J. Smit, Guillaume van Niel, August B. Smit, Frederik J. Verweij, D. Michiel Pegtel
Dysregulated extracellular vesicle (EV) release has been implicated in various pathologies, including cancer, neurodegenerative disease and osteoarthritis. Despite clear therapeutic potential, drug screening for EV release modulators has yielded limi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f564ca74c198c33f77f318f016ad3a26
https://doi.org/10.1101/2023.02.23.529257
https://doi.org/10.1101/2023.02.23.529257
The transverse aortic constriction heart failure animal model: a systematic review and meta-analysis
Autor:
Marissa Bastemeijer, Judith J. de Haan, Joost P.G. Sluijter, Gerard Pasterkamp, Kimberley E. Wever, Lena Bosch, Saskia C.A. de Jager, Margarida Viola, Jennifer J. van der Burg, Erik van der Worp, Clémene Odille, Marian Wesseling, Hamid el Azzouzi
Publikováno v:
Heart Failure Reviews
Heart Failure Reviews, 26, 1515-1524
Heart Failure Reviews, 26, 6, pp. 1515-1524
Heart Failure Reviews, 26, 1515-1524
Heart Failure Reviews, 26, 6, pp. 1515-1524
The transverse aortic constriction (TAC) model is frequently used to study adverse cardiac remodeling upon pressure overload. We set out to define the most important characteristics that define the degree of cardiac remodeling in this model. A system
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55c1d905a1425cdb714207416af55ab9
http://europepmc.org/articles/PMC8510918
http://europepmc.org/articles/PMC8510918
Autor:
Ana Cláudia Santos, João Serra, António J. Ribeiro, Joana Sequeira, Margarida Viola, Raquel Seiça, Francisco Veiga
Publikováno v:
Journal of Controlled Release. 286:301-314
The convenience of subcutaneous (SC) administration and the increasing interest in monoclonal antibody (mAb)-based therapies for chronic diseases, hint their potential for SC delivery in a near future. In addition, there is a common interest among pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1af0d18a9bece1a6b4bf60ccf7b72085
https://doi.org/10.1016/j.jconrel.2018.08.001
https://doi.org/10.1016/j.jconrel.2018.08.001
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 7831, p 7831 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 7831, p 7831 (2021)
After myocardial infarction (MI), a strong inflammatory response takes place in the heart to remove the dead tissue resulting from ischemic injury. A growing body of evidence suggests that timely resolution of this inflammatory process may aid in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07213bd9039039a7e4c8e1ab1f1bb04f
https://doi.org/10.3390/ijms22157831
https://doi.org/10.3390/ijms22157831
Autor:
Charles A, Steward, Jolien, Roovers, Marie-Marthe, Suner, Jose M, Gonzalez, Barbara, Uszczynska-Ratajczak, Dmitri, Pervouchine, Stephen, Fitzgerald, Margarida, Viola, Hannah, Stamberger, Fadi F, Hamdan, Berten, Ceulemans, Patricia, Leroy, Caroline, Nava, Anne, Lepine, Electra, Tapanari, Don, Keiller, Stephen, Abbs, Alba, Sanchis-Juan, Detelina, Grozeva, Anthony S, Rogers, Mark, Diekhans, Roderic, Guigó, Robert, Petryszak, Berge A, Minassian, Gianpiero, Cavalleri, Dimitrios, Vitsios, Slavé, Petrovski, Jennifer, Harrow, Paul, Flicek, F, Lucy Raymond, Nicholas J, Lench, Peter De, Jonghe, Jonathan M, Mudge, Sarah, Weckhuysen, Sanjay M, Sisodiya, Adam, Frankish
Publikováno v:
NPJ Genomic Medicine
The developmental and epileptic encephalopathies (DEE) are a group of rare, severe neurodevelopmental disorders, where even the most thorough sequencing studies leave 60–65% of patients without a molecular diagnosis. Here, we explore the incomplete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed837732110def8ffe866152d0c3c556
https://pubmed.ncbi.nlm.nih.gov/31814998
https://pubmed.ncbi.nlm.nih.gov/31814998
Autor:
Stephen Abbs, Caroline Nava, Sanjay M. Sisodiya, Jyoti S. Choudhary, Dimitrios Vitsios, Dmitri D. Pervouchine, Electra Tapanari, Fadi F. Hamdan, Hannah Stamberger, Berten Ceulemans, Detelina Grozeva, Jennifer Harrow, Patricia Leroy, Marie Marthe Suner, Charles A. Steward, Gianpiero L. Cavalleri, Margarida Viola, Anne Fabienne Lepine, José M. González, Mark Diekhans, Barbara Uszczynska-Ratajczak, Paul Flicek, Nicholas Lench, F. Lucy Raymond, Adam Frankish, Robert Petryszak, Stephen Fitzgerald, Sarah Weckhuysen, Alba Sanchis-Juan, James C. Wright, Peter De Jonghe, Roderic Guigó, Anthony Rogers, Slavé Petrovski, Don Keiller, Jonathan M. Mudge, Jolien Roovers, Berge A. Minassian
The early infantile epileptic encephalopathies (EIEE) are a group of rare, severe neurodevelopmental disorders, where even the most thorough sequencing studies leave 60-65% of patients without a molecular diagnosis. Here, we explore the incompletenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b19da24628aeae9fad19e53f09c9ec01
Autor:
Stephen Abbs, Dimitrios Vitsios, Dmitri D. Pervouchine, Paul Flicek, Hannah Stamberger, Roderic Guigó, Barbara Uszczynska-Ratajczak, F. Lucy Raymond, Margarida Viola, Jennifer Harrow, Adam Frankish, Robert Petryszak, Sarah Weckhuysen, Alba Sanchis-Juan, Caroline Nava, Electra Tapanari, José M. González, Anthony Rogers, Slavé Petrovski, Anne Fabienne Lepine, Patricia Leroy, Detelina Grozeva, Marie Marthe Suner, Mark Diekhans, Gianpiero L. Cavalleri, Don Keiller, Berten Ceulemans, Nicholas Lench, Jonathan M. Mudge, Jolien Roovers, Stephen Fitzgerald, Berge A. Minassian, Charles A. Steward, Peter De Jonghe, Sanjay M. Sisodiya, Fadi F. Hamdan
Publikováno v:
Npj genomic medicine
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-11 (2019)
Recercat. Dipósit de la Recerca de Catalunya
instname
npj Genomic Medicine, Vol 4, Iss 1, Pp 1-11 (2019)
Recercat. Dipósit de la Recerca de Catalunya
instname
The developmental and epileptic encephalopathies (DEE) are a group of rare, severe neurodevelopmental disorders, where even the most thorough sequencing studies leave 60–65% of patients without a molecular diagnosis. Here, we explore the incomplete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::719086b39714e946b1cc05f5c5d1f337
https://hdl.handle.net/10067/1650780151162165141
https://hdl.handle.net/10067/1650780151162165141