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

Laurel Thomas

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
Nature Communications|October 17, 2023
Neural deficits in a mouse model of PACS1 syndrome are corrected with PACS1- or HDAC6-targeting therapySabrina Villar-Pazos, Laurel Thomas, Yunhan Yang, et al.
Research Square|February 7, 2023
RNA-targeted therapy corrects neuronal deficits in PACS1 syndrome miceSabrina Villar-Pazos, Laurel Thomas, Yunhan Yang, et al.
Molecular Cell|November 13, 2018
An Insulin-Responsive Sensor in the SIRT1 Disordered Region Binds DBC1 and PACS-2 to Control Enzyme ActivityTroy C Krzysiak, Laurel Thomas, You-Jin Choi, et al.
Protein Science : a Publication of the Protein Society|March 27, 2024
Inhibitory protein-protein interactions of the SIRT1 deacetylase are choreographed by post-translational modificationTroy C Krzysiak, You-Jin Choi, Yong Joon Kim, et al.
Nature Communications|June 26, 2015
The sorting protein PACS-2 promotes ErbB signalling by regulating recycling of the metalloproteinase ADAM17Sarah Louise Dombernowsky, Jacob Samsøe-Petersen, Camilla Hansson Petersen, et al.
Molecular Cell|June 2, 2009
Akt and 14-3-3 control a PACS-2 homeostatic switch that integrates membrane traffic with TRAIL-induced apoptosisJoseph E Aslan, Huihong You, Danielle M Williamson, et al.
Molecular Biology of the Cell|August 13, 2010
Small molecule inhibition of HIV-1-induced MHC-I down-regulation identifies a temporally regulated switch in Nef actionJimmy D Dikeakos, Katelyn M Atkins, Laurel Thomas, et al.
American Journal of Human Genetics|April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Nature Communications|October 17, 2023
Neural deficits in a mouse model of PACS1 syndrome are corrected with PACS1- or HDAC6-targeting therapySabrina Villar-Pazos, Laurel Thomas, Yunhan Yang, et al.
Research Square|February 7, 2023
RNA-targeted therapy corrects neuronal deficits in PACS1 syndrome miceSabrina Villar-Pazos, Laurel Thomas, Yunhan Yang, et al.
Molecular Cell|November 13, 2018
An Insulin-Responsive Sensor in the SIRT1 Disordered Region Binds DBC1 and PACS-2 to Control Enzyme ActivityTroy C Krzysiak, Laurel Thomas, You-Jin Choi, et al.
Protein Science : a Publication of the Protein Society|March 27, 2024
Inhibitory protein-protein interactions of the SIRT1 deacetylase are choreographed by post-translational modificationTroy C Krzysiak, You-Jin Choi, Yong Joon Kim, et al.
Nature Communications|June 26, 2015
The sorting protein PACS-2 promotes ErbB signalling by regulating recycling of the metalloproteinase ADAM17Sarah Louise Dombernowsky, Jacob Samsøe-Petersen, Camilla Hansson Petersen, et al.
Molecular Cell|June 2, 2009
Akt and 14-3-3 control a PACS-2 homeostatic switch that integrates membrane traffic with TRAIL-induced apoptosisJoseph E Aslan, Huihong You, Danielle M Williamson, et al.
Molecular Biology of the Cell|August 13, 2010
Small molecule inhibition of HIV-1-induced MHC-I down-regulation identifies a temporally regulated switch in Nef actionJimmy D Dikeakos, Katelyn M Atkins, Laurel Thomas, et al.
American Journal of Human Genetics|April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Pageof 3