<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Calvo AC</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Amyotrophic lateral sclerosis (ALS) is one of the most devastating neurodegenerative diseases. Neurotrophic factors have been widely tested to counteract neurodegenerative conditions, despite their unspecific neuronal access. The non-toxic C-terminal fragment of the tetanus toxin (TTC) heavy chain has been studied not only as a carrier molecule to the CNS but also as a neuroprotective agent. Because the neurotrophic effects of BDNF have been demonstrated in vitro and in vivo, the question addressed in this work is whether a fusion molecule of BDNF-TTC may have a synergistic effect and enhance the neuroprotective properties of TTC alone in a mouse model of ALS.&lt;h4>Methods&lt;/h4>Recombinant plasmid constructs (pCMV-TTC and pCMV-BDNF-TTC) were injected into the quadriceps fem</pubmed_abstract><journal>Orphanet journal of rare diseases</journal><pagination>10</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3072305</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lack of a synergistic effect of a non-viral ALS gene therapy based on BDNF and a TTC fusion molecule.</pubmed_title><pmcid>PMC3072305</pmcid><pubmed_authors>Moreno-Igoa M</pubmed_authors><pubmed_authors>Munoz MJ</pubmed_authors><pubmed_authors>Mancuso R</pubmed_authors><pubmed_authors>Calvo AC</pubmed_authors><pubmed_authors>Navarro X</pubmed_authors><pubmed_authors>Penas C</pubmed_authors><pubmed_authors>Manzano R</pubmed_authors><pubmed_authors>Osta R</pubmed_authors><pubmed_authors>Olivan S</pubmed_authors><pubmed_authors>Zaragoza P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lack of a synergistic effect of a non-viral ALS gene therapy based on BDNF and a TTC fusion molecule.</name><description>&lt;h4>Background&lt;/h4>Amyotrophic lateral sclerosis (ALS) is one of the most devastating neurodegenerative diseases. Neurotrophic factors have been widely tested to counteract neurodegenerative conditions, despite their unspecific neuronal access. The non-toxic C-terminal fragment of the tetanus toxin (TTC) heavy chain has been studied not only as a carrier molecule to the CNS but also as a neuroprotective agent. Because the neurotrophic effects of BDNF have been demonstrated in vitro and in vivo, the question addressed in this work is whether a fusion molecule of BDNF-TTC may have a synergistic effect and enhance the neuroprotective properties of TTC alone in a mouse model of ALS.&lt;h4>Methods&lt;/h4>Recombinant plasmid constructs (pCMV-TTC and pCMV-BDNF-TTC) were injected into the quadriceps fem</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Mar</publication><modification>2025-04-20T02:20:31.11Z</modification><creation>2021-02-20T00:53:54Z</creation></dates><accession>S-EPMC3072305</accession><cross_references><pubmed>21418619</pubmed><doi>10.1186/1750-1172-6-10</doi></cross_references></HashMap>