Zobrazeno 1 - 10
of 301
pro vyhledávání: '"Sander J H, van Deventer"'
Autor:
Jason G. van Genderen, Malon Van den Hof, Claudia G. de Boer, Hans P. G. Jansen, Sander J. H. van Deventer, Sotirios Tsimikas, Joseph L. Witztum, John J. P. Kastelein, Dasja Pajkrt
Publikováno v:
Viruses, Vol 13, Iss 10, p 2067 (2021)
HIV is an independent risk factor of cardiovascular disease (CVD); therefore, perinatally HIV-infected (PHIV) children potentially have a greater CVD risk at older age. Lipoprotein(a) (Lp(a)) is an established risk factor for CVD in the general popul
Externí odkaz:
https://doaj.org/article/e7fc141841c847bf85d41fbf0d24e115
Publikováno v:
Nature Biotechnology. 39:266-269
Autor:
Sotirios Tsimikas, Claudia G. de Boer, John J.P. Kastelein, Sander J. H. van Deventer, Hans Jansen, Jason G. van Genderen, Dasja Pajkrt, Malon Van den Hof, Joseph L. Witztum
Publikováno v:
Viruses, vol 13, iss 10
Viruses
Viruses, 13(10). MDPI
Viruses, Vol 13, Iss 2067, p 2067 (2021)
Viruses, 13(10):2067. Multidisciplinary Digital Publishing Institute (MDPI)
Volume 13
Issue 10
Viruses
Viruses, 13(10). MDPI
Viruses, Vol 13, Iss 2067, p 2067 (2021)
Viruses, 13(10):2067. Multidisciplinary Digital Publishing Institute (MDPI)
Volume 13
Issue 10
HIV is an independent risk factor of cardiovascular disease (CVD)
therefore, perinatally HIV-infected (PHIV) children potentially have a greater CVD risk at older age. Lipoprotein(a) (Lp(a)) is an established risk factor for CVD in the general p
therefore, perinatally HIV-infected (PHIV) children potentially have a greater CVD risk at older age. Lipoprotein(a) (Lp(a)) is an established risk factor for CVD in the general p
Autor:
Jeannette Hübener-Schmid, Jiri Klima, Sonay Keskin, Huu Phuc Nguyen, Pavlina Konstantinova, Janice Stricker-Shaver, Eva Haas, Marina Sogorb-Gonzalez, Stefan Juhas, Lodewijk J.A. Toonen, Melvin M. Evers, Jana Juhasova, Sander J. H. van Deventer, Zdenka Ellederova, Jan Motlik, Raygene Martier
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 343-358 (2019)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Spinocerebellar ataxia type 3 (SCA3) or Machado-Joseph disease (MJD) is a progressiveneurodegenerative disorder caused by a CAG expansion in the ATXN3 gene. The expanded CAGrepeat is translated into a prolonged polyglutamine repeat in the ataxin-3 pr
Autor:
Cynthia Brouwers, Pavlina Konstantinova, Amber L. Southwell, Hailey Findlay Black, Michael R. Hayden, Lisa M. Anderson, Nicholas S. Caron, Melvin M. Evers, Xiang Zhu, Seunghyun Ko, Louisa Dal Cengio, Yuanyun Xie, Sander J. H. van Deventer
Publikováno v:
Nucleic Acids Research
Huntington disease (HD) is a fatal neurodegenerative disease caused by a pathogenic expansion of a CAG repeat in the huntingtin (HTT) gene. There are no disease-modifying therapies for HD. Artificial microRNAs targeting HTT transcripts for degradatio
Autor:
Christian F. Meyer, Bart A. Nijmeijer, Valerie Ferreira, Martin de Haan, Margit H. Lampen, Anna Majowicz, Marco Tangelder, Lisa Spronck, Harald Petry, Sander J. H. van Deventer
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Currently, individuals with pre-existing neutralizing antibodies (NABs) against adeno-associated virus (AAV) above titer of 5 are excluded from systemic AAV-based clinical trials. In this study we explored the impact of pre-existing anti-AAV5 NABs on
Autor:
Astrid Vallès, Sander J. H. van Deventer, Cynthia Brouwers, Marina Sogorb-Gonzalez, Raygene Martier, Sonay Keskin, Melvin M. Evers, Pavlina Konstantinova, Josse A. Depla
Publikováno v:
Molecular therapy. Methods & clinical development, 15, 275-284. Nature Publishing Group
Molecular Therapy-Methods and Clinical Development, 15, 275-284. CELL PRESS
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 275-284 (2019)
Molecular Therapy-Methods and Clinical Development, 15, 275-284. CELL PRESS
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 15, Iss, Pp 275-284 (2019)
Huntington disease (HD) is a fatal neurodegenerative genetic disorder, thought to reflect a toxic gain of function in huntingtin (Htt) protein. Adeno-associated viral vector serotype 5 (AAV5)- microRNA targeting huntingtin (miHTT) is a HD gene-therap
Autor:
Carlos Vendrell-Tornero, Astrid Vallès, Seyda Acar-Broekmans, Roman Liscak, Cynthia Brouwers, Lieke Paerels, Pavlina Konstantinova, Melvin M. Evers, Jan Motlik, Marina Sogorb-Gonzalez, Jiri Klima, Harald Petry, Bas Blits, Anouk Stam, Roberta Pintauro, Zdenek Starek, Michal Crha, Dušan Urgošík, Valentina Fodale, Bozena Bohuslavova, Alberto Bresciani, Zdenka Ellederova, Sander J. H. van Deventer
Publikováno v:
Science Translational Medicine. 13
Huntingtin (HTT)-lowering therapies hold promise to slow down neurodegeneration in Huntington's disease (HD). Here, we assessed the translatability and long-term durability of recombinant adeno-associated viral vector serotype 5 expressing a microRNA
Autor:
Pavlina Konstantinova, Martin de Haan, Anouk Stam, Astrid Vallès, Carlos Vendrell-Tornero, Rienk Nieuwland, Sander J. H. van Deventer, Elisabeth A. Spronck, Sonay Keskin, Melvin M. Evers, Jolanda Snapper, Jana Miniarikova, Marina Sogorb-Gonzalez
Publikováno v:
Brain Communications
Brain Communications, 3(2). Oxford University Press
Brain Communications, 3(2). Oxford University Press
The preclinical development of microRNA-based gene therapies for inherited neurodegenerative diseases is accompanied by translational challenges. Due to the inaccessibility of the brain to periodically evaluate therapy effects, accessible and reliabl