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

R Sampson

Showing results (451-460 of 518) with videos related to

Pageof 52
Sort By:
Oncogene|January 10, 2019
Correction: Loss of tuberous sclerosis complex 2 sensitizes tumors to nelfinavir-bortezomib therapy to intensify endoplasmic reticulum stress-induced cell deathCharlotte E Johnson, Elaine A Dunlop, Sara Seifan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 16, 2014
A CRISPR-Cas system enhances envelope integrity mediating antibiotic resistance and inflammasome evasionTimothy R Sampson, Brooke A Napier, Max R Schroeder, et al.
Nature Communications|June 28, 2023
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repairKitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.
Arthritis and Rheumatism|March 17, 2012
Conditional activation of β-catenin signaling in mice leads to severe defects in intervertebral disc tissueMeina Wang, Dezhi Tang, Bing Shu, et al.
Nature Communications|June 19, 2023
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repairKitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
Elife|February 12, 2020
A gut bacterial amyloid promotes α-synuclein aggregation and motor impairment in miceTimothy R Sampson, Collin Challis, Neha Jain, et al.
Nucleic Acids Research|December 8, 2017
Improving CRISPR-Cas specificity with chemical modifications in single-guide RNAsDaniel E Ryan, David Taussig, Israel Steinfeld, et al.
European Journal of Human Genetics : EJHG|March 17, 2011
Determining the pathogenicity of patient-derived TSC2 mutations by functional characterization and clinical evidenceElaine A Dunlop, Kayleigh M Dodd, Stephen C Land, et al.
Frontiers in Pediatrics|May 10, 2024
Tonsils at Telethon: developing a standardised collection of tonsil photographs for group A streptococcal (GAS) researchMarianne J Mullane, Hannah M Thomas, Jonathan R Carapetis, et al.
Pageof 52

Showing results (451-460 of 518) with videos related to

Sort By:
Pageof 52
Oncogene|January 10, 2019
Correction: Loss of tuberous sclerosis complex 2 sensitizes tumors to nelfinavir-bortezomib therapy to intensify endoplasmic reticulum stress-induced cell deathCharlotte E Johnson, Elaine A Dunlop, Sara Seifan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 16, 2014
A CRISPR-Cas system enhances envelope integrity mediating antibiotic resistance and inflammasome evasionTimothy R Sampson, Brooke A Napier, Max R Schroeder, et al.
Nature Communications|June 28, 2023
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repairKitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
American Journal of Medical Genetics. Part A|February 28, 2006
NTNG1 mutations are a rare cause of Rett syndromeHayley L Archer, Julie C Evans, David S Millar, et al.
Arthritis and Rheumatism|March 17, 2012
Conditional activation of β-catenin signaling in mice leads to severe defects in intervertebral disc tissueMeina Wang, Dezhi Tang, Bing Shu, et al.
Nature Communications|June 19, 2023
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repairKitty Sherwood, Joseph C Ward, Ignacio Soriano, et al.
Elife|February 12, 2020
A gut bacterial amyloid promotes α-synuclein aggregation and motor impairment in miceTimothy R Sampson, Collin Challis, Neha Jain, et al.
Nucleic Acids Research|December 8, 2017
Improving CRISPR-Cas specificity with chemical modifications in single-guide RNAsDaniel E Ryan, David Taussig, Israel Steinfeld, et al.
European Journal of Human Genetics : EJHG|March 17, 2011
Determining the pathogenicity of patient-derived TSC2 mutations by functional characterization and clinical evidenceElaine A Dunlop, Kayleigh M Dodd, Stephen C Land, et al.
Frontiers in Pediatrics|May 10, 2024
Tonsils at Telethon: developing a standardised collection of tonsil photographs for group A streptococcal (GAS) researchMarianne J Mullane, Hannah M Thomas, Jonathan R Carapetis, et al.
Pageof 52