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dc.creatorAnsorena-Artieda, E. (Eduardo)-
dc.creatorGarbayo, E-
dc.creatorLanciego, J.L. (José Luis)-
dc.creatorAymerich-Soler, M.S. (María Soledad)-
dc.creatorBlanco-Prieto, M.J. (María José)-
dc.date.accessioned2011-12-01T09:40:51Z-
dc.date.available2011-12-01T09:40:51Z-
dc.date.issued2010-
dc.identifier.citationAnsorena E, Garbayo E, Lanciego JL, Aymerich MS, Blanco-Prieto MJ. Production of highly pure human glycosylated GDNF in a mammalian cell line. Int J Pharm 2010 Jan 29;385(1-2):6-11.es_ES
dc.identifier.issn1873-3476-
dc.identifier.urihttps://hdl.handle.net/10171/20045-
dc.description.abstractThe administration of glial cell line-derived neurotrophic factor (GDNF) has emerged as a promising strategy for the treatment of several diseases of the nervous system as Parkinson's disease, amyotrophic lateral sclerosis, spinal cord injury and nerve regeneration as well as ocular diseases and drug addictions. A procedure for the purification of human recombinant glycosylated GDNF using a mammalian expression system as the source of the protein is discussed in the present paper. The neurotrophic factor was purified using cation exchange chromatography and gel filtration. A human cell line was chosen as the source of therapeutic protein, since a recombinant protein with a structure and glycosylation pattern equivalent to the native form is desirable for its prospective therapeutic utilization. The activity of the highly pure protein obtained was confirmed with a cell-based bioassay. The purified protein is suitable for its in vivo evaluation in animals and for possible subsequent clinical application.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectTherapeutic proteinses_ES
dc.subjectPurification of proteinses_ES
dc.subjectGlycosylated proteinses_ES
dc.subjectGDNFes_ES
dc.subjectNeurotrophic factorses_ES
dc.subjectParkinson’s diseasees_ES
dc.titleProduction of highly pure human glycosylated GDNF in a mammalian cell linees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.identifier.doihttp://dx.doi.org/10.1016/j.ijpharm.2009.10.015es_ES

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