<p>Lentiviral gene transfer of PA28γ and S5a, in control and HD model striatal neurons. (A) Schematic experimental outline of gene transfer and differentiation of striatal neurons followed by exposure to HD model experimental toxins. HD model striatal cells were gene engineered with PA28γ, S5a. After verification of expression for the transferred genes, cells were grown in medium containing 1μg/ml of doxycyclin for 48h before toxin treatment. After 24 h incubation in the toxic environment, medium was collected for the MTS assay and cells were harvested for proteasome activity determination. (B) Semiquantitative Western blot of the huntingtin showing a slight decrease of protein levels by lenti-viral transduction of PA28γ gene into HD model ...
<p>Young (3 week old) and old (15 month old) rats were injected with a lentiviral vector encoding th...
Huntington's disease (HD) is a neurodegenerative disease with currently only symptomatic treatment. ...
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by an expanded CAG repeat in ...
<p>Proteasome activities following lentiviral gene transfer of PA28γ and S5a, in control and HD mode...
<p>Experimental exposure of PA28γ (A–D) or S5a (E–G) overexpressing control and HD model striatal ne...
<p>Proteasome activities following lentiviral gene transfer of PA28γ and S5a, in control and HD fibr...
A lentiviral vector expressing a mutant huntingtin protein (htt171-82Q) was used to generate a chron...
A lentiviral vector expressing a mutant huntingtin protein (htt171-82Q) was used to generate a chron...
Huntington’s disease (HD) is a neurodegenerative disorder characterized by a triad of motor, cogniti...
Cultures of striatal neurons expressing the reporter gene GFP, were transduced with a lentiviral vec...
A new strategy based on lentiviral-mediated delivery of mutant huntingtin (htt) was used to create a...
Defective handling of proteins is a central feature of major neurodegenerative diseases. The discove...
Huntington's disease (HD) is neurologically characterized by involuntary movements, associated w...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by the expansion...
() Dose-dependent toxicity of DA (24 h treatment) assessed in striatal neurons (21 DIV) using the LD...
<p>Young (3 week old) and old (15 month old) rats were injected with a lentiviral vector encoding th...
Huntington's disease (HD) is a neurodegenerative disease with currently only symptomatic treatment. ...
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by an expanded CAG repeat in ...
<p>Proteasome activities following lentiviral gene transfer of PA28γ and S5a, in control and HD mode...
<p>Experimental exposure of PA28γ (A–D) or S5a (E–G) overexpressing control and HD model striatal ne...
<p>Proteasome activities following lentiviral gene transfer of PA28γ and S5a, in control and HD fibr...
A lentiviral vector expressing a mutant huntingtin protein (htt171-82Q) was used to generate a chron...
A lentiviral vector expressing a mutant huntingtin protein (htt171-82Q) was used to generate a chron...
Huntington’s disease (HD) is a neurodegenerative disorder characterized by a triad of motor, cogniti...
Cultures of striatal neurons expressing the reporter gene GFP, were transduced with a lentiviral vec...
A new strategy based on lentiviral-mediated delivery of mutant huntingtin (htt) was used to create a...
Defective handling of proteins is a central feature of major neurodegenerative diseases. The discove...
Huntington's disease (HD) is neurologically characterized by involuntary movements, associated w...
Huntington’s disease (HD) is an autosomal dominant neurodegenerative disease caused by the expansion...
() Dose-dependent toxicity of DA (24 h treatment) assessed in striatal neurons (21 DIV) using the LD...
<p>Young (3 week old) and old (15 month old) rats were injected with a lentiviral vector encoding th...
Huntington's disease (HD) is a neurodegenerative disease with currently only symptomatic treatment. ...
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by an expanded CAG repeat in ...