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

Timothy B Palculict

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2013
Rare variant detection using family-based sequencing analysisGang Peng, Yu Fan, Timothy B Palculict, et al.
Cancer Research|May 2, 2013
Hypoxia triggers hedgehog-mediated tumor-stromal interactions in pancreatic cancerTaly R Spivak-Kroizman, Galen Hostetter, Richard Posner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2021
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafishSheng-Jia Lin, Barbara Vona, Patricia G Barbalho, et al.
American Journal of Human Genetics|January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctionJoery den Hoed, Elke de Boer, Norine Voisin, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2013
Rare variant detection using family-based sequencing analysisGang Peng, Yu Fan, Timothy B Palculict, et al.
Cancer Research|May 2, 2013
Hypoxia triggers hedgehog-mediated tumor-stromal interactions in pancreatic cancerTaly R Spivak-Kroizman, Galen Hostetter, Richard Posner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2021
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafishSheng-Jia Lin, Barbara Vona, Patricia G Barbalho, et al.
American Journal of Human Genetics|January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctionJoery den Hoed, Elke de Boer, Norine Voisin, et al.
Pageof 1