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

Peter Heutink

Showing results (141-150 of 240) with videos related to

Pageof 24
Sort By:
Neuron|February 22, 2024
Harnessing diversity to study Alzheimer's disease: A new iPSC resource from the NIH CARD and ADNILaurel A Screven, Caroline B Pantazis, Katherine M Andersh, et al.
Scientific Data|November 1, 2017
Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous systemMargherita Francescatto, Marina Lizio, Ingrid Philippens, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
Annals of Neurology|October 8, 2016
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson'sGanqiang Liu, Brendon Boot, Joseph J Locascio, et al.
NPJ Parkinson'S Disease|October 22, 2024
Direct and indirect regulation of β-glucocerebrosidase by the transcription factors USF2 and ONECUT2Kathi Ging, Lukas Frick, Johannes Schlachetzki, et al.
Brain : a Journal of Neurology|July 24, 2003
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based studySonia M Rosso, Laura Donker Kaat, Timo Baks, et al.
Brain : a Journal of Neurology|March 14, 2013
Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathySietske H Kevelam, Marianna Bugiani, Gajja S Salomons, et al.
Scientific Data|December 1, 2023
A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypesKevin Menden, Margherita Francescatto, Tenzin Nyima, et al.
Behavior Genetics|October 16, 2008
A Functional polymorphism under positive evolutionary selection in ADRB2 is associated with human intelligence with opposite effects in the young and the elderlyZoltán Bochdanovits, Florencia M Gosso, Linda van den Berg, et al.
Human Molecular Genetics|September 24, 2013
Genetic comorbidities in Parkinson's diseaseMike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Pageof 24

Showing results (141-150 of 240) with videos related to

Sort By:
Pageof 24
Neuron|February 22, 2024
Harnessing diversity to study Alzheimer's disease: A new iPSC resource from the NIH CARD and ADNILaurel A Screven, Caroline B Pantazis, Katherine M Andersh, et al.
Scientific Data|November 1, 2017
Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous systemMargherita Francescatto, Marina Lizio, Ingrid Philippens, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
Annals of Neurology|October 8, 2016
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson'sGanqiang Liu, Brendon Boot, Joseph J Locascio, et al.
NPJ Parkinson'S Disease|October 22, 2024
Direct and indirect regulation of β-glucocerebrosidase by the transcription factors USF2 and ONECUT2Kathi Ging, Lukas Frick, Johannes Schlachetzki, et al.
Brain : a Journal of Neurology|July 24, 2003
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based studySonia M Rosso, Laura Donker Kaat, Timo Baks, et al.
Brain : a Journal of Neurology|March 14, 2013
Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathySietske H Kevelam, Marianna Bugiani, Gajja S Salomons, et al.
Scientific Data|December 1, 2023
A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypesKevin Menden, Margherita Francescatto, Tenzin Nyima, et al.
Behavior Genetics|October 16, 2008
A Functional polymorphism under positive evolutionary selection in ADRB2 is associated with human intelligence with opposite effects in the young and the elderlyZoltán Bochdanovits, Florencia M Gosso, Linda van den Berg, et al.
Human Molecular Genetics|September 24, 2013
Genetic comorbidities in Parkinson's diseaseMike A Nalls, Mohamad Saad, Alastair J Noyce, et al.
Pageof 24