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

Chris Kay

Showing results (21-30 of 41) with videos related to

Pageof 5
Sort By:
Plos Computational Biology|August 15, 2015
Curation of the Mammalian Palmitoylome Indicates a Pivotal Role for Palmitoylation in Diseases and Disorders of the Nervous System and CancersShaun S Sanders, Dale D O Martin, Stefanie L Butland, et al.
European Journal of Human Genetics : EJHG|March 7, 2013
Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypesFiona K Baine, Chris Kay, Maria E Ketelaar, et al.
Genetics in Medicine Open|December 13, 2024
Ascertainment of uninterrupted CAG repeat length and disease-modifying variants in fragment-based genetic testing for Huntington DiseaseHailey Findlay Black, Chris Kay, Jessica Dawson, et al.
Plos One|June 1, 2012
Low levels of human HIP14 are sufficient to rescue neuropathological, behavioural, and enzymatic defects due to loss of murine HIP14 in Hip14-/- miceFiona B Young, Sonia Franciosi, Amanda Spreeuw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Frequency of the loss of CAA interruption in the HTT CAG tract and implications for Huntington disease in the reduced penetrance rangeHailey Findlay Black, Galen E B Wright, Jennifer A Collins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 15, 2020
Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle EastFerdinando Squitieri, Tommaso Mazza, Sabrina Maffi, et al.
European Journal of Medical Genetics|December 3, 2014
A new mutation for Huntington disease following maternal transmission of an intermediate alleleAlicia Semaka, Chris Kay, René D M Belfroid, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 24, 2015
Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European AncestryChris Kay, Jennifer A Collins, Niels H Skotte, et al.
Nature Reviews. Disease Primers|May 19, 2016
Huntington diseaseGillian P Bates, Ray Dorsey, James F Gusella, et al.
European Journal of Human Genetics : EJHG|December 22, 2016
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin AmericaChris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Plos Computational Biology|August 15, 2015
Curation of the Mammalian Palmitoylome Indicates a Pivotal Role for Palmitoylation in Diseases and Disorders of the Nervous System and CancersShaun S Sanders, Dale D O Martin, Stefanie L Butland, et al.
European Journal of Human Genetics : EJHG|March 7, 2013
Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypesFiona K Baine, Chris Kay, Maria E Ketelaar, et al.
Genetics in Medicine Open|December 13, 2024
Ascertainment of uninterrupted CAG repeat length and disease-modifying variants in fragment-based genetic testing for Huntington DiseaseHailey Findlay Black, Chris Kay, Jessica Dawson, et al.
Plos One|June 1, 2012
Low levels of human HIP14 are sufficient to rescue neuropathological, behavioural, and enzymatic defects due to loss of murine HIP14 in Hip14-/- miceFiona B Young, Sonia Franciosi, Amanda Spreeuw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 4, 2020
Frequency of the loss of CAA interruption in the HTT CAG tract and implications for Huntington disease in the reduced penetrance rangeHailey Findlay Black, Galen E B Wright, Jennifer A Collins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 15, 2020
Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle EastFerdinando Squitieri, Tommaso Mazza, Sabrina Maffi, et al.
European Journal of Medical Genetics|December 3, 2014
A new mutation for Huntington disease following maternal transmission of an intermediate alleleAlicia Semaka, Chris Kay, René D M Belfroid, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 24, 2015
Huntingtin Haplotypes Provide Prioritized Target Panels for Allele-specific Silencing in Huntington Disease Patients of European AncestryChris Kay, Jennifer A Collins, Niels H Skotte, et al.
Nature Reviews. Disease Primers|May 19, 2016
Huntington diseaseGillian P Bates, Ray Dorsey, James F Gusella, et al.
European Journal of Human Genetics : EJHG|December 22, 2016
The targetable A1 Huntington disease haplotype has distinct Amerindian and European origins in Latin AmericaChris Kay, Indira Tirado-Hurtado, Mario Cornejo-Olivas, et al.
Pageof 5