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Advanced therapies for hemophilia: reality or fantasy?

dc.contributor.authorLiras, Antonio
dc.date.accessioned2023-06-20T03:53:27Z
dc.date.available2023-06-20T03:53:27Z
dc.date.issued2012-06
dc.description.abstractThe article is about the future therapeutic products based on advanced therapies such as gene and cell therapy and tissue engineering or induced pluripotent stem cell technology may offer innumerable potential clinical applicationsfor the treatment of several monogenic disorders including hemophilia.
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipRoyal Foundation "Victoria Eugenia" of Haemophilia
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/30733
dc.identifier.doi10.1586/EHM.12.25
dc.identifier.issn1747-4086, 1747-4094(ESSN)
dc.identifier.officialurlhttp://informahealthcare.com/toc/err/6/5
dc.identifier.relatedurlhttp://informahealthcare.com/journal/err
dc.identifier.urihttps://hdl.handle.net/20.500.14352/44623
dc.issue.number3
dc.journal.titleExpert review of hematology
dc.language.isoeng
dc.page.final247
dc.page.initial245
dc.publisherinforma healthcare
dc.rights.accessRightsrestricted access
dc.subject.cdu616.151.5
dc.subject.keywordAdvanced therapies
dc.subject.keywordCell therapy
dc.subject.keywordGene therapy
dc.subject.keywordHemophilia
dc.subject.ucmFarmacología (Medicina)
dc.subject.ucmHematología
dc.subject.unesco3205.04 Hematología
dc.titleAdvanced therapies for hemophilia: reality or fantasy?
dc.typejournal article
dc.volume.number5
dcterms.references1 Tirino V, Papaccio G. A new, most likely unusual approach is crucial and upcoming for the use of stem cells in regenerative medicine. Front. Physiol. 2, 1–2 (2012). 2 Liras A. Future research and therapeutic applications of human stem cells: general,regulatory, and bioethical aspects. J. Transl.Med. 8, 131 (2010). 3 Liras A. Induced human pluripotent stem cells and advanced therapies:future perspectives for the treatment ofhaemophilia? Thromb. Res. 128(1), 8–13 (2011). 4 Vandendriessche T, Chuah MK. Clinical progress in gene therapy: sustained partial correction of the bleeding disorder in patients suffering from severe hemophilia B. Hum. Gene Ther. 23(1), 4–6 (2012). 5 Liras A. Gene therapy for haemophilia: the end of a ‘royal pathology’ in the third millennium? Haemophilia 7(5), 441–445 (2001). 6 Li H, Haurigot V, Doyon Y et al. In vivo genome editing restores haemostasis in a mouse model of haemophilia. Nature 475(7355), 217–221 (2011). 7 Olmedillas S, García-Arranz M, Vega L,García-Gómez I, García-Olmo D, Liras A. Non-viral gene transfer to human adiposederived stem cells for FIX secretion. Presented at: 4th National Congress of Spanish Society of Gene and Cellular Therapy. Zaragoza, Spain, 21–23 September 2011. 8 Nathwani AC, Tuddenham EG, Rangarajan S et al. Adenovirus-associated virus vectormediated gene transfer in hemophilia B. N. Engl. J. Med. 365(25), 2357–2365 (2011). 9 Mannucci PM, Tuddenham EG. The hemophilias – from royal genes to gene therapy. N. Engl. J. Med. 344(23),1773–1779 (2001). 10 Liras A, Olmedillas S. Gene therapy for haemophilia. Yes, but with non-viral vectors? Haemophilia 15(3), 811–816 (2009). 11 Ponder KP. Merry christmas for patients with hemophilia B. N. Engl. J. Med. 365(25), 2424–2425 (2011). Website 101 European Medicines Agency. Advanced therapies. www.ema.europa.eu/ema/index.jsp?curl=pages/special_topics/general/general_content_000504.jsp&mid=WC0b01ac058050f347
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