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

Andrew J Sharp

Showing results (31-40 of 85) with videos related to

Pageof 9
Sort By:
European Journal of Human Genetics : EJHG|September 19, 2013
Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2Christine Tyson, Andrew J Sharp, Monica Hrynchak, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 6, 2015
Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC ExposureCorey T Watson, Henrietta Szutorisz, Paras Garg, et al.
Behavioural Brain Research|November 5, 2010
The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndromeArnaud Duchon, Stéphanie Pothion, Véronique Brault, et al.
Epigenetics|July 18, 2015
Placental expression profile of imprinted genes impacts birth weightMaya A Kappil, Benjamin B Green, David A Armstrong, et al.
Nature Communications|December 3, 2024
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK BiobankCeline A Manigbas, Bharati Jadhav, Paras Garg, et al.
Plos One|August 18, 2009
Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencingSergey I Nikolaev, Christian Iseli, Andrew J Sharp, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 9, 2024
A Population-Wide Exploration of the THAP11 CAG Repeat Size and Structure in the 100,000 Genomes Project and UK BiobankChris Clarkson, Zhongbo Chen, Clarissa Rocca, et al.
Nucleic Acids Research|April 10, 2016
Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humansJavier Quilez, Audrey Guilmatre, Paras Garg, et al.
Plos Genetics|June 14, 2012
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse modelMatthieu Raveau, Jacques M Lignon, Valérie Nalesso, et al.
Genome Medicine|January 26, 2016
Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's diseaseCorey T Watson, Panos Roussos, Paras Garg, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
European Journal of Human Genetics : EJHG|September 19, 2013
Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2Christine Tyson, Andrew J Sharp, Monica Hrynchak, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|June 6, 2015
Genome-Wide DNA Methylation Profiling Reveals Epigenetic Changes in the Rat Nucleus Accumbens Associated With Cross-Generational Effects of Adolescent THC ExposureCorey T Watson, Henrietta Szutorisz, Paras Garg, et al.
Behavioural Brain Research|November 5, 2010
The telomeric part of the human chromosome 21 from Cstb to Prmt2 is not necessary for the locomotor and short-term memory deficits observed in the Tc1 mouse model of Down syndromeArnaud Duchon, Stéphanie Pothion, Véronique Brault, et al.
Epigenetics|July 18, 2015
Placental expression profile of imprinted genes impacts birth weightMaya A Kappil, Benjamin B Green, David A Armstrong, et al.
Nature Communications|December 3, 2024
A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK BiobankCeline A Manigbas, Bharati Jadhav, Paras Garg, et al.
Plos One|August 18, 2009
Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencingSergey I Nikolaev, Christian Iseli, Andrew J Sharp, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 9, 2024
A Population-Wide Exploration of the THAP11 CAG Repeat Size and Structure in the 100,000 Genomes Project and UK BiobankChris Clarkson, Zhongbo Chen, Clarissa Rocca, et al.
Nucleic Acids Research|April 10, 2016
Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humansJavier Quilez, Audrey Guilmatre, Paras Garg, et al.
Plos Genetics|June 14, 2012
The App-Runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a Down syndrome mouse modelMatthieu Raveau, Jacques M Lignon, Valérie Nalesso, et al.
Genome Medicine|January 26, 2016
Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's diseaseCorey T Watson, Panos Roussos, Paras Garg, et al.
Pageof 9