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 (21-30 of 240) with videos related to

Pageof 24
Sort By:
Plos One|February 14, 2008
Genome-wide prediction of functional gene-gene interactions inferred from patterns of genetic differentiation in mice and menZoltán Bochdanovits, David Sondervan, Sophie Perillous, et al.
Molecular Genetics and Metabolism|March 27, 2002
The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetesOmer T Njajou, Norbert Vaessen, Ben Oostra, et al.
Journal of Child Neurology|October 18, 2007
Benign hereditary chorea: clinical, neuroimaging, and genetic findingsMuhammad Mahajnah, Dov Inbar, Adam Steinmetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 16, 2011
Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's diseaseLonneke M L de Lau, Dagmar Verbaan, Johan Marinus, et al.
European Journal of Human Genetics : EJHG|June 6, 2013
Accurate prediction of a minimal region around a genetic association signal that contains the causal variantZoltán Bochdanovits, Javier Simón-Sánchez, Marianne Jonker, et al.
Biochimica Et Biophysica Acta|August 2, 2002
Characterization of ZNF333, a novel double KRAB domain containing zinc finger gene on human chromosome 19p13.1Yong Tian, Guido J Breedveld, Shangzhi Huang, et al.
Dementia and Geriatric Cognitive Disorders|June 5, 2004
Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17John C van Swieten, Sonia M Rosso, Esther van Herpen, et al.
Science Advances|August 25, 2020
Deep learning-based cell composition analysis from tissue expression profilesKevin Menden, Mohamed Marouf, Sergio Oller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2003
Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli): a community-based case-control studyFusun Duzcan, Mehmet Zencir, Fatma Ozdemir, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotypeEsther Brusse, Inge de Koning, Anneke Maat-Kievit, et al.
Pageof 24

Showing results (21-30 of 240) with videos related to

Sort By:
Pageof 24
Plos One|February 14, 2008
Genome-wide prediction of functional gene-gene interactions inferred from patterns of genetic differentiation in mice and menZoltán Bochdanovits, David Sondervan, Sophie Perillous, et al.
Molecular Genetics and Metabolism|March 27, 2002
The hemochromatosis N144H mutation of SLC11A3 gene in patients with type 2 diabetesOmer T Njajou, Norbert Vaessen, Ben Oostra, et al.
Journal of Child Neurology|October 18, 2007
Benign hereditary chorea: clinical, neuroimaging, and genetic findingsMuhammad Mahajnah, Dov Inbar, Adam Steinmetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 16, 2011
Catechol-O-methyltransferase Val158Met and the risk of dyskinesias in Parkinson's diseaseLonneke M L de Lau, Dagmar Verbaan, Johan Marinus, et al.
European Journal of Human Genetics : EJHG|June 6, 2013
Accurate prediction of a minimal region around a genetic association signal that contains the causal variantZoltán Bochdanovits, Javier Simón-Sánchez, Marianne Jonker, et al.
Biochimica Et Biophysica Acta|August 2, 2002
Characterization of ZNF333, a novel double KRAB domain containing zinc finger gene on human chromosome 19p13.1Yong Tian, Guido J Breedveld, Shangzhi Huang, et al.
Dementia and Geriatric Cognitive Disorders|June 5, 2004
Phenotypic variation in frontotemporal dementia and parkinsonism linked to chromosome 17John C van Swieten, Sonia M Rosso, Esther van Herpen, et al.
Science Advances|August 25, 2020
Deep learning-based cell composition analysis from tissue expression profilesKevin Menden, Mohamed Marouf, Sergio Oller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2003
Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli): a community-based case-control studyFusun Duzcan, Mehmet Zencir, Fatma Ozdemir, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotypeEsther Brusse, Inge de Koning, Anneke Maat-Kievit, et al.
Pageof 24