International audienceHuntingtin (htt) is a multi-domain protein of 350 kDa that is mutated in Huntington's disease (HD) but whose function is yet to be fully understood. This absence of information is due in part to the difficulty of manipulating large DNA fragments by using conventional molecular cloning techniques. Consequently, few studies have addressed the cellular function(s) of full-length htt and its dysfunction(s) associated with the disease
<div><p>Huntington’s disease (HD) is a devastating neurological disorder that is caused by an expans...
Huntington's disease (HD) is an autosomal dominant, fatal neurodegenerative disorder characterized b...
Huntington Disease (HD) is a dominant, lethal neurodegenerative disorder caused by the abnormal expa...
International audienceHuntingtin (htt) is a multi-domain protein of 350 kDa that is mutated in Hunti...
Presentation abstract: The pathogenic Huntington's disease (HD) mutation causes polyglutamine (polyQ...
Huntington disease (HD) is an autosomal-dominant neurodegenerative disorder caused by the pathogenic...
Huntington's disease is a dreadful, incurable disorder. It springs from the autosomal dominant mutat...
ABSTRACT: The pathogenic Huntington’s disease (HD) mutation causes polyglutamine (polyQ) tract expa...
Huntington's disease (HD) is a fatal genetic neurodegenerative disorder caused by a CAG repeat expan...
Huntington’s disease (HD) is a progressive neurological disorder caused by a mutation in the hunting...
Huntington disease is an inherited neurodegenerative disorder that is caused by expanded CAG trinucl...
Background The underlying mutation of the neurodegenerative disorder Huntington's disease (HD) is an...
Huntington’s disease is a rare neurodegenerative and autosomal dominant disorder. HD is caused by a ...
<div><p>Huntingtin (Htt) is a 350 kD intracellular protein, ubiquitously expressed and mainly locali...
Huntington’s Disease (HD) is a hereditary neurodegenerative disease; the cause of which is due to a ...
<div><p>Huntington’s disease (HD) is a devastating neurological disorder that is caused by an expans...
Huntington's disease (HD) is an autosomal dominant, fatal neurodegenerative disorder characterized b...
Huntington Disease (HD) is a dominant, lethal neurodegenerative disorder caused by the abnormal expa...
International audienceHuntingtin (htt) is a multi-domain protein of 350 kDa that is mutated in Hunti...
Presentation abstract: The pathogenic Huntington's disease (HD) mutation causes polyglutamine (polyQ...
Huntington disease (HD) is an autosomal-dominant neurodegenerative disorder caused by the pathogenic...
Huntington's disease is a dreadful, incurable disorder. It springs from the autosomal dominant mutat...
ABSTRACT: The pathogenic Huntington’s disease (HD) mutation causes polyglutamine (polyQ) tract expa...
Huntington's disease (HD) is a fatal genetic neurodegenerative disorder caused by a CAG repeat expan...
Huntington’s disease (HD) is a progressive neurological disorder caused by a mutation in the hunting...
Huntington disease is an inherited neurodegenerative disorder that is caused by expanded CAG trinucl...
Background The underlying mutation of the neurodegenerative disorder Huntington's disease (HD) is an...
Huntington’s disease is a rare neurodegenerative and autosomal dominant disorder. HD is caused by a ...
<div><p>Huntingtin (Htt) is a 350 kD intracellular protein, ubiquitously expressed and mainly locali...
Huntington’s Disease (HD) is a hereditary neurodegenerative disease; the cause of which is due to a ...
<div><p>Huntington’s disease (HD) is a devastating neurological disorder that is caused by an expans...
Huntington's disease (HD) is an autosomal dominant, fatal neurodegenerative disorder characterized b...
Huntington Disease (HD) is a dominant, lethal neurodegenerative disorder caused by the abnormal expa...