Pouladi, Mahmoud A., Graham, Rona K., Karasinska, Joanna M., Xie, Yuanyun, Santos, Rachelle Dar, Petersén, Åsa, ...
Huntington disease is a neurodegenerative disorder caused by an expanded CAG repeat in the Huntington disease gene. The symptomatic phase of the disease is defined by the onset of motor symptoms....
Bode, Felix J., Stephan, Michael, Suhling, Hendrik, Pabst, Reinhard, Straub, Rainer H., Raber, Kerstin A., ...
Recent clinical studies have highlighted that female sex hormones represent potential neuroprotective mediators against damage caused by acute and chronic brain diseases. This evidence has been...
Björkqvist, Maria, Petersén, Åsa, Bacos, Karl, Isaacs, Jeremy, Norlén, Per, Gil, Joana, ...
Huntington's disease (HD) is characterised by a triad of motor, psychiatric, and cognitive symptoms. While many of these symptoms are likely to be related to central nervous system pathology, others...
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy (2006)
Gawlik, Kinga I., Li, Jia-Yi, Petersén, Åsa, Durbeej, Madeleine
Absence of laminin α2 chain leads to a severe form of congenital muscular dystrophy (MDC1A) associated with peripheral neuropathy. Hence, future therapies should be aimed at alleviating both muscle...
Björkqvist, Maria, Petersén, Åsa, Bacos, Karl, Isaacs, Jeremy, Norlén, Per, Gil, Joana, ...
Huntington's disease (HD) is characterized by a triad of motor, psychiatric and cognitive symptoms. Although many of these symptoms are likely to be related to central nervous system pathology,...
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy (2006)
Gawlik, Kinga I., Li, Jia-Yi, Petersén, Åsa, Durbeej, Madeleine
Absence of laminin α2 chain leads to a severe form of congenital muscular dystrophy (MDC1A) associated with peripheral neuropathy. Hence, future therapies should be aimed at alleviating both muscle...
Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice (2005)
Petersén, Åsa, Stewénius, Ylva, Björkqvist, Maria, Gisselsson, David
Abstract Background Huntington's disease (HD) is a hereditary neurodegenerative disorder caused by a CAG repeat expansion in the HD gene. The huntingtin protein expressed from HD has an unknown...
Björkqvist, Maria, Fex, Malin, Renström, Erik, Wierup, Nils, Petersén, Åsa, Gil, Joana, ...
Diabetes frequently develops in Huntington's disease (HD) patients and in transgenic mouse models of HD such as the R6/2 mouse. The underlying mechanisms have not been clarified. Elucidating the...
Orexin loss in Huntington's disease (2005)
Petersén, Åsa, Gil, Joana, Björkqvist, Maria, Tanila, Heikki, Araújo, Inês M., ...
Huntington's disease (HD) is a devastating neurodegenerative disorder caused by an expanded CAG repeat in the gene encoding huntingtin, a protein of unknown function. Mutant huntingtin forms...
Asialoerythropoetin is not effective in the R6/2 line of Huntington's disease mice (2004)
Gil, Joana MAC, Leist, Marcel, Popovic, Natalija, Brundin, Patrik, Petersén, Åsa
Abstract Background Huntington's disease (HD) is a hereditary neurodegenerative disorder caused by an expanded CAG repeat in the HD gene. Both excitotoxicity and oxidative stress have been proposed...
Asialoerythropoetin is not effective in the R6/2 line of Huntington's disease mice (2004)
Gil, Joana MAC, Leist, Marcel, Popovic, Natalija, Brundin, Patrik, Petersén, Åsa
Background: Huntington's disease (HD) is a hereditary neurodegenerative disorder caused by an expanded CAG repeat in the HD gene. Both excitotoxicity and oxidative stress have been proposed to play...
Orexin loss in Huntington's disease (2004)
Petersén, Åsa, Gil, Joana, Maat-Schieman, Marion LC, Björkqvist, Maria, Tanila, Heikki, Araújo, Ines M, ...
Huntington's disease is a devastating neurodegenerative disorder caused by an expanded CAG repeat in the gene encoding huntingtin, a protein of unknown function. Mutant huntingtin forms intracellular...
Orexin loss in Huntington's disease (2004)
Petersén, Åsa, Gil, Joana, Maat-Schieman, Marion LC, Björkqvist, Maria, Tanila, Heikki, Araújo, Ines M, ...
Huntington's disease is a devastating neurodegenerative disorder caused by an expanded CAG repeat in the gene encoding huntingtin, a protein of unknown function. Mutant huntingtin forms intracellular...
Effects of dopamine and excitotoxicity in experimental models of Huntington's disease (2001)
Huntington's disease (HD) is a hereditary neurodegenerative disorder caused by an expansion of a CAG repeat in the HD gene, that leads to dysfunction and death of striatal neurons. The pathogenetic...
Effects of dopamine and excitotoxicity in experimental models of Huntington's disease (2001)
Huntington\\\'s disease (HD) is a hereditary neurodegenerative disorder caused by an expansion of a CAG repeat in the HD gene, that leads to dysfunction and death of striatal neurons. The...
Petersén, Åsa, Larsen, Kristin E., Behr, Gerald G., Romero, Norma, Przedborski, Serge, Brundin, Patrik, ...
Huntington’s disease (HD) is caused by an expanded CAG repeat in exon 1 of the gene coding for the huntingtin protein. The cellular pathway by which this mutation induces HD remains unknown,...
Hansson, Oskar, Petersén, Åsa, Leist, Marcel, Nicotera, Pierluigi, Castilho, Roger F., Brundin, Patrik
Huntingtons disease (HD) is a hereditary neurodegenerative disorder presenting with chorea, dementia, and extensive striatal neuronal death. The mechanism through which the widely expressed mutant...
Asialoerythropoetin is not effective in the R6/2 line of Huntington's disease mice
Gil, Joana MAC, Leist, Marcel, Popovic, Natalija, Brundin, Patrik, Petersén, Åsa
Euploidy in somatic cells from R6/2 transgenic Huntington's disease mice
Petersén, Åsa, Stewénius, Ylva, Björkqvist, Maria, Gisselsson, David