Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marcel Veltrop"'
Autor:
Marcel Veltrop, Laura van Vliet, Margriet Hulsker, Jill Claassens, Conny Brouwers, Cor Breukel, Jos van der Kaa, Margot M Linssen, Johan T den Dunnen, Sjef Verbeek, Annemieke Aartsma-Rus, Maaike van Putten
Publikováno v:
PLoS ONE, Vol 13, Iss 2, p e0193289 (2018)
Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disease generally caused by reading frame disrupting mutations in the DMD gene resulting in loss of functional dystrophin protein. The reading frame can be restored by antisense oligonucleo
Externí odkaz:
https://doaj.org/article/7d1b65ae6d9a47e096721b71e3330f69
Autor:
Margriet Hulsker, Maaike van Putten, Jill W. C. Claassens, Sjef Verbeek, Marcel Veltrop, Laura van Vliet, Conny Brouwers, Annemieke Aartsma-Rus, Cor Breukel, Johan T. den Dunnen, Margot M. Linssen, Jos van der Kaa
Publikováno v:
PLoS ONE, 13(2)
PLoS ONE, Vol 13, Iss 2, p e0193289 (2018)
PLoS ONE
PLoS ONE, Vol 13, Iss 2, p e0193289 (2018)
PLoS ONE
Duchenne muscular dystrophy (DMD) is a severe muscle-wasting disease generally caused by reading frame disrupting mutations in the DMD gene resulting in loss of functional dystrophin protein. The reading frame can be restored by antisense oligonucleo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830ec5c1091a7efcbc75d0cfe6769d14
http://hdl.handle.net/1887/76847
http://hdl.handle.net/1887/76847
Autor:
Seyed Yahya Anvar, Kristiaan J. van der Gaag, Peter de Knijff, Rolf H. A. M. Vossen, Johan T. den Dunnen, Marcel Veltrop, Henk P. J. Buermans, Jaap van der Heijden, J. Sjef Verbeek, Jeroen F.J. Laros, Cor Breukel, Rick H. de Leeuw
Publikováno v:
Bioinformatics, 30(12), 1651-1659
Motivation: Advances in sequencing technologies and computational algorithms have enabled the study of genomic variants to dissect their functional consequence. Despite this unprecedented progress, current tools fail to reliably detect and characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::252f362c67259a1ea5da9609b56bd22d
https://doi.org/10.1093/bioinformatics/btu068
https://doi.org/10.1093/bioinformatics/btu068
Autor:
Marcel Veltrop, Annemieke Aartsma-Rus
Publikováno v:
Experimental Cell Research, 325(1), 50-55
Rare diseases can be caused by genetic mutations that disrupt normal pre-mRNA splicing. Antisense oligonucleotide treatment to the splicing thus has therapeutic potential for many rare diseases. In this review we will focus on the state of the art on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e249bfa94fe587947835d3d8ff9f1a46
https://doi.org/10.1016/j.yexcr.2014.01.026
https://doi.org/10.1016/j.yexcr.2014.01.026
Autor:
Marcel Veltrop, Sjef Verbeek, Jos van der Kaa, Annemieke Aartsma-Rus, Jill W. C. Claassens, Laura van Vliet
Publikováno v:
PLoS Currents
Duchenne muscular dystrophy (DMD) is a muscle-wasting disease in which muscle is continuously damaged, resulting in loss of muscle tissue and function. Antisense-mediated exon skipping is a promising therapeutic approach for DMD. This method uses seq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff638a247205e1f6efaa89b3e0bb476f
https://doi.org/10.1371/currents.md.cbf1d33001de80923ce674302cad7925
https://doi.org/10.1371/currents.md.cbf1d33001de80923ce674302cad7925
Autor:
Marcel Veltrop, H. Beekhuizen
Publikováno v:
The Journal of infectious diseases. 186(8)
Intravascular infection with Staphylococcus aureus, Staphylococcus epidermidis, or Streptococcus sanguis can initiate fibrin formation on endocardial tissue, causing bacterial endocarditis. The ability of these bacteria to injure intact endothelial c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c2858cf8c8de9d731e469bdfbed4574
https://pubmed.ncbi.nlm.nih.gov/12355366
https://pubmed.ncbi.nlm.nih.gov/12355366