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

C Lovell

Showing results (151-160 of 160) with videos related to

Pageof 16
Sort By:
You have reached the last page of results.This site can display upto 160 results.
Plos Genetics|October 31, 2017
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian developmentLiam A Ridge, Karen Mitchell, Ali Al-Anbaki, et al.
Protein Science : a Publication of the Protein Society|October 26, 2017
MolProbity: More and better reference data for improved all-atom structure validationChristopher J Williams, Jeffrey J Headd, Nigel W Moriarty, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 7, 2026
Domain-specific mechanisms of YAP1 variants in ocular coloboma revealed by in-vitro and organoid studiesSrishti Silvano, Van Annika Rick-Lenze, James Bagnall, et al.
Cell Death & Disease|October 21, 2020
EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewalRoberto Paredes, James R Kelly, Bethany Geary, et al.
Open Research Europe|October 15, 2024
Atacama Large Aperture Submillimeter Telescope (AtLAST) science: Surveying the distant UniverseEelco van Kampen, Tom Bakx, Carlos De Breuck, et al.
Protein Science : a Publication of the Protein Society|April 25, 2012
The interface of protein structure, protein biophysics, and molecular evolutionDavid A Liberles, Sarah A Teichmann, Ivet Bahar, et al.
Science Immunology|December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.
Nature Genetics|January 11, 2011
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signatureTracy A Briggs, Gillian I Rice, Sarah Daly, et al.
Nature Genetics|September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signatureGillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
Nature Genetics|January 24, 2012
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plusBeverley H Anderson, Paul R Kasher, Josephine Mayer, et al.
Pageof 16

Showing results (151-160 of 160) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 160 results.
Plos Genetics|October 31, 2017
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian developmentLiam A Ridge, Karen Mitchell, Ali Al-Anbaki, et al.
Protein Science : a Publication of the Protein Society|October 26, 2017
MolProbity: More and better reference data for improved all-atom structure validationChristopher J Williams, Jeffrey J Headd, Nigel W Moriarty, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 7, 2026
Domain-specific mechanisms of YAP1 variants in ocular coloboma revealed by in-vitro and organoid studiesSrishti Silvano, Van Annika Rick-Lenze, James Bagnall, et al.
Cell Death & Disease|October 21, 2020
EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewalRoberto Paredes, James R Kelly, Bethany Geary, et al.
Open Research Europe|October 15, 2024
Atacama Large Aperture Submillimeter Telescope (AtLAST) science: Surveying the distant UniverseEelco van Kampen, Tom Bakx, Carlos De Breuck, et al.
Protein Science : a Publication of the Protein Society|April 25, 2012
The interface of protein structure, protein biophysics, and molecular evolutionDavid A Liberles, Sarah A Teichmann, Ivet Bahar, et al.
Science Immunology|December 15, 2019
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in <i>STAT2</i>Christopher J A Duncan, Benjamin J Thompson, Rui Chen, et al.
Nature Genetics|January 11, 2011
Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signatureTracy A Briggs, Gillian I Rice, Sarah Daly, et al.
Nature Genetics|September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signatureGillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
Nature Genetics|January 24, 2012
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plusBeverley H Anderson, Paul R Kasher, Josephine Mayer, et al.
Pageof 16