Julien Rossignol and Kyle D Fink are equal contributors.International audienceINTRODUCTION: Huntington's disease (HD) is an autosomal dominant disorder caused by an expanded CAG repeat (greater than 38) on the short arm of chromosome 4, resulting in loss and dysfunction of neurons in the neostriatum and cortex, leading to cognitive decline, motor dysfunction, and death, typically occurring 15 to 20 years after the onset of motor symptoms. Although an effective treatment for HD has remained elusive, current studies using transplants of bone-marrow-derived mesenchymal stem cells provides considerable promise. This study further investigates the efficacy of these transplants with a focus on comparing how passage number of these cells may affec...
Summary: Huntington disease (HD) is an inherited, progressive neurological disorder characterized by...
Implantation of human multipotent stromal cells from bone marrow (hMSCs) into the dentate gyrus of t...
Huntington Disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG trinucle...
Julien Rossignol and Kyle D Fink are equal contributors.International audienceINTRODUCTION: Huntingt...
IntroductionHuntington's disease (HD) is an autosomal dominant disorder caused by an expanded CAG re...
neuropathology in the R6/2 mouse model of Huntington’s disease following transplantation of senchyma...
Summary: Huntington's disease (HD) is an inherited neurodegenerative disorder with no disease-modify...
Huntington's disease (HD) is a genetic neurodegenerative disorder characterized by neuronal loss and...
International audienceIntroductionHuntington's disease (HD) is an autosomal dominant disorder caused...
We investigated the therapeutic potential of human bone marrow-derived mesenchymal stem cells (hBM-M...
IntroductionHuntington's disease (HD) is an autosomal dominant disorder caused by an expanded CAG re...
Huntington's disease (HD) is a fatal degenerative autosomal dominant neuropsychiatric disease that c...
Huntington's disease (HD) is an inherited neurodegenerative disorder with no disease-modifying treat...
Huntington's disease (HD) is a fatal autosomal-dominant neurodegenerative disease caused by a trinuc...
Background: Cell therapy is a potential therapeutic approach for several neurodegenetative disease, ...
Summary: Huntington disease (HD) is an inherited, progressive neurological disorder characterized by...
Implantation of human multipotent stromal cells from bone marrow (hMSCs) into the dentate gyrus of t...
Huntington Disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG trinucle...
Julien Rossignol and Kyle D Fink are equal contributors.International audienceINTRODUCTION: Huntingt...
IntroductionHuntington's disease (HD) is an autosomal dominant disorder caused by an expanded CAG re...
neuropathology in the R6/2 mouse model of Huntington’s disease following transplantation of senchyma...
Summary: Huntington's disease (HD) is an inherited neurodegenerative disorder with no disease-modify...
Huntington's disease (HD) is a genetic neurodegenerative disorder characterized by neuronal loss and...
International audienceIntroductionHuntington's disease (HD) is an autosomal dominant disorder caused...
We investigated the therapeutic potential of human bone marrow-derived mesenchymal stem cells (hBM-M...
IntroductionHuntington's disease (HD) is an autosomal dominant disorder caused by an expanded CAG re...
Huntington's disease (HD) is a fatal degenerative autosomal dominant neuropsychiatric disease that c...
Huntington's disease (HD) is an inherited neurodegenerative disorder with no disease-modifying treat...
Huntington's disease (HD) is a fatal autosomal-dominant neurodegenerative disease caused by a trinuc...
Background: Cell therapy is a potential therapeutic approach for several neurodegenetative disease, ...
Summary: Huntington disease (HD) is an inherited, progressive neurological disorder characterized by...
Implantation of human multipotent stromal cells from bone marrow (hMSCs) into the dentate gyrus of t...
Huntington Disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG trinucle...