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pro vyhledávání: '"BOEC"'
Akademický článek
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Autor:
Cristina Olgasi, Chiara Borsotti, Simone Merlin, Thorsten Bergmann, Patrick Bittorf, Adeolu Badi Adewoye, Nicholas Wragg, Kelcey Patterson, Andrea Calabria, Fabrizio Benedicenti, Alessia Cucci, Alessandra Borchiellini, Berardino Pollio, Eugenio Montini, Delfina M. Mazzuca, Martin Zierau, Alexandra Stolzing, Philip.M. Toleikis, Joris Braspenning, Antonia Follenzi
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss , Pp 551-566 (2021)
Hemophilia A (HA) is a rare bleeding disorder caused by deficiency/dysfunction of the FVIII protein. As current therapies based on frequent FVIII infusions are not a definitive cure, long-term expression of FVIII in endothelial cells through lentivir
Externí odkaz:
https://doaj.org/article/7a58ac952d7247cb827b394f9103e931
Publikováno v:
Kafkas Universitesi Veteriner Fakültesi Dergisi, Vol 27, Iss 2, Pp 151-158 (2021)
Oviduct is an important tubular organ fostering critical physiological processes such as transport of gametes and embryos, capacitation, fertilization, early embryo development, and maturation of gametes. The aim of the present study was to evaluate
Externí odkaz:
https://doaj.org/article/d3880919010b4bf999ec7aad8ae669ec
Akademický článek
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Autor:
Strietman, Elsa
Publikováno v:
Modern Language Review. Jan2006, Vol. 101 Issue 1, p300-302. 3p.
Akademický článek
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Autor:
Masashi, Noda, Kohei, Tatsumi, Hideto, Matsui, Yasunori, Matsunari, Takeshi, Sato, Yasushi, Fukuoka, Akitsu, Hotta, Teruo, Okano, Kimihiko, Kichikawa, Mitsuhiko, Sugimoto, Midori, Shima, Kenji, Nishio
Publikováno v:
Regenerative Therapy
Introduction Gene therapy have recently attracted much attention as a curative therapeutic option for inherited single gene disorders such as hemophilia. Hemophilia is a hereditary bleeding disorder caused by the deficiency of clotting activity of fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2785e299495ddad51d8a41a5a213594
https://pubmed.ncbi.nlm.nih.gov/34584911
https://pubmed.ncbi.nlm.nih.gov/34584911
Autor:
Berardino Pollio, Kelcey Patterson, Joris Braspenning, Alessandra Borchiellini, Alexandra Stolzing, Philip M. Toleikis, Simone Merlin, Alessia Cucci, Martin Zierau, Eugenio Montini, Andrea Calabria, Delfina M. Mazzuca, Chiara Borsotti, Thorsten Bergmann, Adeolu Badi Adewoye, Fabrizio Benedicenti, Cristina Olgasi, Nicholas M. Wragg, Antonia Follenzi, Patrick Bittorf
Publikováno v:
Molecular Therapy-Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss, Pp 551-566 (2021)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss, Pp 551-566 (2021)
Molecular Therapy. Methods & Clinical Development
Hemophilia A (HA) is a rare bleeding disorder caused by deficiency/dysfunction of the FVIII protein. As current therapies based on frequent FVIII infusions are not a definitive cure, long-term expression of FVIII in endothelial cells through lentivir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2ff8cd4584a8b2d9e58d1ea9112e85b
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Lidia R. Bons, Kirsten Lodder, Hans-Marc J. Siebelink, Kondababu Kurakula, Jolien W. Roos-Hesselink, Vera van de Pol, Marco C. DeRuiter, Marie-José Goumans, Gonzalo Sanchez-Duffhues
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 13, p 3251 (2019)
International Journal of Molecular Sciences, 20(13):3251. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences
Volume 20
Issue 13
International Journal of Molecular Sciences, 20(13). MDPI
van de Pol, V, Bons, L R, Lodder, K, Kurakula, K B, Sanchez-Duffhues, G, Siebelink, H M J, Roos-Hesselink, J W, Deruiter, M C & Goumans, M J 2019, ' Endothelial colony forming cells as an autologous model to study endothelial dysfunction in patients with a bicuspid aortic valve ', International Journal of Molecular Sciences, vol. 20, no. 13, 3251 . https://doi.org/10.3390/ijms20133251
International Journal of Molecular Sciences, 20(13):3251. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences
Volume 20
Issue 13
International Journal of Molecular Sciences, 20(13). MDPI
van de Pol, V, Bons, L R, Lodder, K, Kurakula, K B, Sanchez-Duffhues, G, Siebelink, H M J, Roos-Hesselink, J W, Deruiter, M C & Goumans, M J 2019, ' Endothelial colony forming cells as an autologous model to study endothelial dysfunction in patients with a bicuspid aortic valve ', International Journal of Molecular Sciences, vol. 20, no. 13, 3251 . https://doi.org/10.3390/ijms20133251
Bicuspid aortic valve (BAV), the most common congenital heart defect, is associated with an increased prevalence of aortic dilation, aortic rupture and aortic valve calcification. Endothelial cells (ECs) play a major role in vessel wall integrity. Li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7de2053e929bc148af13f29d8ce55e6
https://doi.org/10.3390/ijms20133251
https://doi.org/10.3390/ijms20133251