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

Lesley Jones

Showing results (101-110 of 138) with videos related to

Pageof 14
Sort By:
American Journal of Human Genetics|June 27, 2020
Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier EffectsKyung-Hee Kim, Eun Pyo Hong, Jun Wan Shin, et al.
Scientific Reports|March 22, 2017
Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's diseaseDavina J Hensman Moss, Michael D Flower, Kitty K Lo, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2006
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaLyudmila Georgieva, Valentina Moskvina, Tim Peirce, et al.
Human Genetics|May 22, 2003
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's diseaseDenise Harold, Timothy Peirce, Valentina Moskvina, et al.
Research Square|November 23, 2022
Large libraries of single-chain trimer peptide-MHCs enable rapid antigen-specific CD8+ T cell discovery and analysisJames Heath, William Chour, Jongchan Choi, et al.
Brain Communications|March 7, 2024
Modification of Huntington's disease by short tandem repeatsEun Pyo Hong, Eliana Marisa Ramos, N Ahmad Aziz, et al.
NAR Genomics and Bioinformatics|December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencingAlysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Annals of Neurology|April 5, 2016
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesConceição Bettencourt, Davina Hensman-Moss, Michael Flower, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 19, 2003
Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset ADAmanda J Myers, Helen Marshall, Peter Holmans, et al.
Human Molecular Genetics|March 7, 2003
Transgenic rat model of Huntington's diseaseStephan von Hörsten, Ina Schmitt, Huu Phuc Nguyen, et al.
Pageof 14

Showing results (101-110 of 138) with videos related to

Sort By:
Pageof 14
American Journal of Human Genetics|June 27, 2020
Genetic and Functional Analyses Point to FAN1 as the Source of Multiple Huntington Disease Modifier EffectsKyung-Hee Kim, Eun Pyo Hong, Jun Wan Shin, et al.
Scientific Reports|March 22, 2017
Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's diseaseDavina J Hensman Moss, Michael D Flower, Kitty K Lo, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 8, 2006
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaLyudmila Georgieva, Valentina Moskvina, Tim Peirce, et al.
Human Genetics|May 22, 2003
Sequence variation in the CHAT locus shows no association with late-onset Alzheimer's diseaseDenise Harold, Timothy Peirce, Valentina Moskvina, et al.
Research Square|November 23, 2022
Large libraries of single-chain trimer peptide-MHCs enable rapid antigen-specific CD8+ T cell discovery and analysisJames Heath, William Chour, Jongchan Choi, et al.
Brain Communications|March 7, 2024
Modification of Huntington's disease by short tandem repeatsEun Pyo Hong, Eliana Marisa Ramos, N Ahmad Aziz, et al.
NAR Genomics and Bioinformatics|December 8, 2022
Repeat Detector: versatile sizing of expanded tandem repeats and identification of interrupted alleles from targeted DNA sequencingAlysha S Taylor, Dinis Barros, Nastassia Gobet, et al.
Annals of Neurology|April 5, 2016
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesConceição Bettencourt, Davina Hensman-Moss, Michael Flower, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 19, 2003
Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset ADAmanda J Myers, Helen Marshall, Peter Holmans, et al.
Human Molecular Genetics|March 7, 2003
Transgenic rat model of Huntington's diseaseStephan von Hörsten, Ina Schmitt, Huu Phuc Nguyen, et al.
Pageof 14