Differential Gene Expression Profiling of Dystrophic Dog Muscle after MuStem Cell Transplantation
BACKGROUND: Several adult stem cell populations exhibit myogenic regenerative potential, thus representing attractive candidates
Early interaction of adeno-associated virus serotype 8 vector with the host immune system following intramuscular delivery results in weak but detectable lymphocyte and dendritic cell transduction
Following in vivo recombinant adeno-associated virus (rAAV)-based gene transfer, adaptive immune responses specific to the
Efficient central nervous system AAVrh10-mediated intrathecal gene transfer in adult and neonate rats
Intracerebral administration of recombinant adeno-associated vector (AAV) has been performed in several clinical trials. However,
Hepatic lentiviral gene transfer prevents the long-term onset of hepatic tumours of glycogen storage disease type 1a in mice
Glycogen storage disease type 1a (GSD1a) is a rare disease due to the deficiency in
Human neonatal hepatocyte transplantation induces long-term rescue of unconjugated hyperbilirubinemia in the Gunn rat
Crigler-Najjar type 1 disease is a rare inherited metabolic disease characterized by high levels of
Interplay of thermal and covalent gelation of silanized hydroxypropyl methyl cellulose gels
Silanized hydroxypropyl methyl cellulose (Si-HPMC) is a biocompatible polysaccharide that forms a covalently crosslinked hydrogel