Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Hutton

Showing results (181-190 of 239) with videos related to

Pageof 24
Sort By:
American Journal of Medical Genetics|June 5, 1998
Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonismJ Hardy, J Pérez-Tur, M Baker, et al.
Neurobiology of Disease|April 28, 2000
Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenesK Duff, H Knight, L M Refolo, et al.
FEBS Letters|April 1, 1999
Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylationR Dayanandan, M Van Slegtenhorst, T G Mack, et al.
Neurodegeneration : a Journal for Neurodegenerative Disorders, Neuroprotection, and Neuroregeneration|September 1, 1996
A further presenilin 1 mutation in the exon 8 cluster in familial Alzheimer's diseaseJ Perez-Tur, R Croxton, K Wright, et al.
Dementia and Geriatric Cognitive Disorders|February 15, 2002
Corticobasal degeneration and frontotemporal dementia presentations in a kindred with nonspecific histopathologyB F Boeve, D M Maraganore, J E Parisi, et al.
Nature Medicine|September 30, 1999
Alzheimer disease PS-1 exon 9 deletion definedG Prihar, A Verkkoniem, J Perez-Tur, et al.
FEBS Letters|October 2, 1998
TNF-alpha converting enzyme (TACE) is inhibited by TIMP-3A Amour, P M Slocombe, A Webster, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2000
Research goals in progressive supranuclear palsy. First International Brainstorming Conference on PSPI Litvan, D W Dickson, J A Buttner-Ennever, et al.
Brain : a Journal of Neurology|March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factorN C Fox, A M Kennedy, R J Harvey, et al.
Journal of Neurochemistry|January 26, 2000
Frontal lobe dysfunction in progressive supranuclear palsy: evidence for oxidative stress and mitochondrial impairmentD S Albers, S J Augood, L C Park, et al.
Pageof 24

Showing results (181-190 of 239) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics|June 5, 1998
Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonismJ Hardy, J Pérez-Tur, M Baker, et al.
Neurobiology of Disease|April 28, 2000
Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenesK Duff, H Knight, L M Refolo, et al.
FEBS Letters|April 1, 1999
Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylationR Dayanandan, M Van Slegtenhorst, T G Mack, et al.
Neurodegeneration : a Journal for Neurodegenerative Disorders, Neuroprotection, and Neuroregeneration|September 1, 1996
A further presenilin 1 mutation in the exon 8 cluster in familial Alzheimer's diseaseJ Perez-Tur, R Croxton, K Wright, et al.
Dementia and Geriatric Cognitive Disorders|February 15, 2002
Corticobasal degeneration and frontotemporal dementia presentations in a kindred with nonspecific histopathologyB F Boeve, D M Maraganore, J E Parisi, et al.
Nature Medicine|September 30, 1999
Alzheimer disease PS-1 exon 9 deletion definedG Prihar, A Verkkoniem, J Perez-Tur, et al.
FEBS Letters|October 2, 1998
TNF-alpha converting enzyme (TACE) is inhibited by TIMP-3A Amour, P M Slocombe, A Webster, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 1, 2000
Research goals in progressive supranuclear palsy. First International Brainstorming Conference on PSPI Litvan, D W Dickson, J A Buttner-Ennever, et al.
Brain : a Journal of Neurology|March 1, 1997
Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factorN C Fox, A M Kennedy, R J Harvey, et al.
Journal of Neurochemistry|January 26, 2000
Frontal lobe dysfunction in progressive supranuclear palsy: evidence for oxidative stress and mitochondrial impairmentD S Albers, S J Augood, L C Park, et al.
Pageof 24