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

Jonathan J Wilde

Showing results (1-10 of 11) with videos related to

Pageof 2
Sort By:
Annual Review of Genetics|October 9, 2014
Genetic, epigenetic, and environmental contributions to neural tube closureJonathan J Wilde, Juliette R Petersen, Lee Niswander
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 4, 2017
Diencephalic Size Is Restricted by a Novel Interplay Between GCN5 Acetyltransferase Activity and Retinoic Acid SignalingJonathan J Wilde, Julie A Siegenthaler, Sharon Y R Dent, et al.
Elife|January 8, 2015
Potassium dependent rescue of a myopathy with core-like structures in mouseM Gartz Hanson, Jonathan J Wilde, Rosa L Moreno, et al.
Cell|May 27, 2021
Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repairJonathan J Wilde, Tomomi Aida, Ricardo C H Del Rosario, et al.
Nature Communications|May 13, 2020
Multiplex precise base editing in cynomolgus monkeysWenhui Zhang, Tomomi Aida, Ricardo C H Del Rosario, et al.
Cell|November 3, 2023
Circuit-specific gene therapy reverses core symptoms in a primate Parkinson's disease modelYefei Chen, Zexuan Hong, Jingyi Wang, et al.
Cell Reports|August 18, 2024
Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytesPlaton Megagiannis, Yuan Mei, Rachel E Yan, et al.
American Journal of Human Genetics|May 29, 2012
RAD21 mutations cause a human cohesinopathyMatthew A Deardorff, Jonathan J Wilde, Melanie Albrecht, et al.
Nature|August 14, 2012
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycleMatthew A Deardorff, Masashige Bando, Ryuichiro Nakato, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Annual Review of Genetics|October 9, 2014
Genetic, epigenetic, and environmental contributions to neural tube closureJonathan J Wilde, Juliette R Petersen, Lee Niswander
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 4, 2017
Diencephalic Size Is Restricted by a Novel Interplay Between GCN5 Acetyltransferase Activity and Retinoic Acid SignalingJonathan J Wilde, Julie A Siegenthaler, Sharon Y R Dent, et al.
Elife|January 8, 2015
Potassium dependent rescue of a myopathy with core-like structures in mouseM Gartz Hanson, Jonathan J Wilde, Rosa L Moreno, et al.
Cell|May 27, 2021
Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repairJonathan J Wilde, Tomomi Aida, Ricardo C H Del Rosario, et al.
Nature Communications|May 13, 2020
Multiplex precise base editing in cynomolgus monkeysWenhui Zhang, Tomomi Aida, Ricardo C H Del Rosario, et al.
Cell|November 3, 2023
Circuit-specific gene therapy reverses core symptoms in a primate Parkinson's disease modelYefei Chen, Zexuan Hong, Jingyi Wang, et al.
Cell Reports|August 18, 2024
Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytesPlaton Megagiannis, Yuan Mei, Rachel E Yan, et al.
American Journal of Human Genetics|May 29, 2012
RAD21 mutations cause a human cohesinopathyMatthew A Deardorff, Jonathan J Wilde, Melanie Albrecht, et al.
Nature|August 14, 2012
HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycleMatthew A Deardorff, Masashige Bando, Ryuichiro Nakato, et al.
Human Molecular Genetics|January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritanceFrank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Pageof 2