{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Rogujski P"],"funding":["European Social Fund","European Regional Development Fund in the Operational Program","National Science Center","National Center for Research and Development"],"pagination":["10580"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11477205"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["25(19)"],"pubmed_abstract":["Glial cell dysfunction results in myelin loss and leads to subsequent motor and cognitive deficits throughout the demyelinating disease course.Therefore, in various therapeutic approaches, significant attention has been directed toward glial-restricted progenitor (GRP) transplantation for myelin repair and remyelination, and numerous studies using exogenous GRP injection in rodent models of hypomyelinating diseases have been performed. Previously, we proposed the transplantation of canine glial-restricted progenitors (cGRPs) into the double-mutant immunodeficient, demyelinated neonatal shiverer mice (shiverer/Rag2<sup>-/-</sup>). The results of our previous study revealed the myelination of axons within the corpus callosum of transplanted animals; however, the extent of myelination and lif"],"journal":["International journal of molecular sciences"],"pubmed_title":["Multisite Injections of Canine Glial-Restricted Progenitors Promote Brain Myelination and Extend the Survival of Dysmyelinated Mice."],"pmcid":["PMC11477205"],"funding_grant_id":["SONATA project 2017/26/D/NZ3/00721","\"Innovative Economy\" for 2007-2013","project POWR.03.02.00-00-I028/17-00","STRATEGMED I project \"GRP&ALS\""],"pubmed_authors":["Stanaszek L","Lukomska B","Gewartowska M","Fiedorowicz M","Frontczak-Baniewicz M","Sanford J","Walczak P","Janowski M","Rogujski P"],"additional_accession":[]},"is_claimable":false,"name":"Multisite Injections of Canine Glial-Restricted Progenitors Promote Brain Myelination and Extend the Survival of Dysmyelinated Mice.","description":"Glial cell dysfunction results in myelin loss and leads to subsequent motor and cognitive deficits throughout the demyelinating disease course.Therefore, in various therapeutic approaches, significant attention has been directed toward glial-restricted progenitor (GRP) transplantation for myelin repair and remyelination, and numerous studies using exogenous GRP injection in rodent models of hypomyelinating diseases have been performed. Previously, we proposed the transplantation of canine glial-restricted progenitors (cGRPs) into the double-mutant immunodeficient, demyelinated neonatal shiverer mice (shiverer/Rag2<sup>-/-</sup>). The results of our previous study revealed the myelination of axons within the corpus callosum of transplanted animals; however, the extent of myelination and lif","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Oct","modification":"2025-04-04T07:40:44.019Z","creation":"2025-04-04T07:40:44.019Z"},"accession":"S-EPMC11477205","cross_references":{"pubmed":["39408910"],"doi":["10.3390/ijms251910580"]}}