Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder. However, little information is available concerning the way each patient learns about the existence of Huntington's disease in his family and the way he transmits the information to his descendants. This study aims to ...
Huntington's disease is due to the mutation of the IT15 gene coding for Huntingtin protein (Htt). This mutation leads to the expression of an abnormal repeat of polyglutamines in the N-terminal region of Htt. The pathophysiology of Huntington's disease remains to be elucidated. Various mechani...
Huntington's disease is due to the mutation of the IT15 gene coding for Huntingtin protein (Htt). This mutation leads to the expression of an abnormal repeat of polyglutamines in the N-terminal region of Htt. The pathophysiology of Huntington's disease remains to be elucidated. Various ...
Maladie de Huntington (caractérisation du rle neuroprotecteur de la voie de signalisation induite par IGF-1)Earth's coregeostrophic flowsmagnetoconvectionrotationTaylor's conditionThe variational lower bound v>0.39 pi(2) determined by Ivers (1984) for the ...
Pasquier, FCabaret, MPetit, H
In 1872, George Huntington was the first to describe a genetic disease combining three types of disorder symptoms viz: motor, cognitive鈥揺volving to cortical dementia and psychiatric. The purpose of this paper is to provide a selective review of the major issues and findings concerning suicide ...
Iconography : Physiopathologie de la maladie de Huntington : état des connaissancesdoi:10.1016/j.neurol.2008.03.006Huntington's disease is due to the mutation of the gene coding for Huntingtin protein (Htt). This mutation leads to the expression of an abnormal repeat of polyglutamines in ...
Étude des mécanismes moléculaires responsables des interactions aberrantes de la Huntingtine dans la maladie de HuntingtonHtt is a molecular interactions platform involved in critical cellular functions. The affinity of many Htt partners seems i...
Being a very cost-effective and label-free monitoring method, its potential as an alternative to cell viability assays was evaluated. Three simple morphology feature extraction and comparison algorithms were developed and implemented for analysis ...
Maladie de Huntington: données actuelles sur la prise en charge thérapeutique des troubles psychiatriquesCare managementClinical caseDegenerationGenetic diseaseHuntington's diseaseNeurological diseasePsychiatric disordersHuntington's disease is a neurodegenerative genetic, autosomal dominant disease. George ...