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

Marie Westerlund

Showing results (21-30 of 30) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 30 results.
Neuroscience Letters|July 2, 2022
Glucocerebrosidase variant T369M is not a risk factor for Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Sandra Gellhaar, et al.
Molecular and Cellular Neurosciences|September 16, 2008
Lrrk2 and alpha-synuclein are co-regulated in rodent striatumMarie Westerlund, Caroline Ran, Anders Borgkvist, et al.
Parkinson'S Disease|May 26, 2017
Genetic Variations and mRNA Expression of NRF2 in Parkinson's DiseaseCaroline Ran, Karin Wirdefeldt, Lovisa Brodin, et al.
Neuroscience Letters|June 1, 2007
Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's diseaseAndrea Carmine Belin, Behnosh F Björk, Marie Westerlund, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2010
Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's diseaseMarie Westerlund, Homira Behbahani, Sandra Gellhaar, et al.
Neuroscience Letters|June 19, 2012
Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's diseaseAndrea Carmine Belin, Caroline Ran, Anna Anvret, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 27, 2013
Modulation of the endoplasmic reticulum-mitochondria interface in Alzheimer's disease and related modelsLouise Hedskog, Catarina Moreira Pinho, Riccardo Filadi, et al.
Neurobiology of Aging|June 4, 2016
Strong association between glucocerebrosidase mutations and Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Lars Forsgren, et al.
Plos One|April 16, 2011
Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2David Ramonet, João Paulo L Daher, Brian M Lin, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Neuroscience Letters|July 2, 2022
Glucocerebrosidase variant T369M is not a risk factor for Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Sandra Gellhaar, et al.
Molecular and Cellular Neurosciences|September 16, 2008
Lrrk2 and alpha-synuclein are co-regulated in rodent striatumMarie Westerlund, Caroline Ran, Anders Borgkvist, et al.
Parkinson'S Disease|May 26, 2017
Genetic Variations and mRNA Expression of NRF2 in Parkinson's DiseaseCaroline Ran, Karin Wirdefeldt, Lovisa Brodin, et al.
Neuroscience Letters|June 1, 2007
Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's diseaseAndrea Carmine Belin, Behnosh F Björk, Marie Westerlund, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2010
Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's diseaseMarie Westerlund, Homira Behbahani, Sandra Gellhaar, et al.
Neuroscience Letters|June 19, 2012
Association of a protective paraoxonase 1 (PON1) polymorphism in Parkinson's diseaseAndrea Carmine Belin, Caroline Ran, Anna Anvret, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 27, 2013
Modulation of the endoplasmic reticulum-mitochondria interface in Alzheimer's disease and related modelsLouise Hedskog, Catarina Moreira Pinho, Riccardo Filadi, et al.
Neurobiology of Aging|June 4, 2016
Strong association between glucocerebrosidase mutations and Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Lars Forsgren, et al.
Plos One|April 16, 2011
Dopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2David Ramonet, João Paulo L Daher, Brian M Lin, et al.
Human Mutation|November 1, 2012
A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeatsJulie van der Zee, Ilse Gijselinck, Lubina Dillen, et al.
Pageof 3