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

Nichole Owen

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
DNA Repair|March 16, 2015
BLM protein mitigates formaldehyde-induced genomic instabilityAnuradha Kumari, Nichole Owen, Eleonora Juarez, et al.
Journal of Clinical Immunology|March 8, 2023
Phenotypic Variability of SOCS1 HaploinsufficiencyRebecca C Hale, Nichole Owen, Bo Yuan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 30, 2010
Multiple loci contribute to genome-wide recombination levels in male miceBrenda Murdoch, Nichole Owen, Sofia Shirley, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Expansion of the clinical phenotype of GALE deficiencyRebecca Markovitz, Nichole Owen, Lisa Forbes Satter, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2021
Enhanced cytarabine-induced killing in OGG1-deficient acute myeloid leukemia cellsNichole Owen, Irina G Minko, Samantha A Moellmer, et al.
DNA Repair|November 4, 2018
An RNAi screen in human cell lines reveals conserved DNA damage repair pathways that mitigate formaldehyde sensitivityEleonora Juarez, Nyasha Chambwe, Weiliang Tang, et al.
Cytogenetic and Genome Research|March 14, 2015
Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLMNichole Owen, James Hejna, Scott Rennie, et al.
DNA Repair|November 8, 2016
Enhanced sensitivity of Neil1<sup>-/-</sup> mice to chronic UVB exposureMarcus J Calkins, Vladimir Vartanian, Nichole Owen, et al.
Molecular Genetics & Genomic Medicine|February 26, 2024
Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing lossRyan J German, Blake Vuocolo, Liesbeth Vossaert, et al.
Molecular Genetics & Genomic Medicine|August 24, 2023
Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved populationCara P Ford, Rebecca O Littlejohn, Ryan German, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
DNA Repair|March 16, 2015
BLM protein mitigates formaldehyde-induced genomic instabilityAnuradha Kumari, Nichole Owen, Eleonora Juarez, et al.
Journal of Clinical Immunology|March 8, 2023
Phenotypic Variability of SOCS1 HaploinsufficiencyRebecca C Hale, Nichole Owen, Bo Yuan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 30, 2010
Multiple loci contribute to genome-wide recombination levels in male miceBrenda Murdoch, Nichole Owen, Sofia Shirley, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Expansion of the clinical phenotype of GALE deficiencyRebecca Markovitz, Nichole Owen, Lisa Forbes Satter, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 10, 2021
Enhanced cytarabine-induced killing in OGG1-deficient acute myeloid leukemia cellsNichole Owen, Irina G Minko, Samantha A Moellmer, et al.
DNA Repair|November 4, 2018
An RNAi screen in human cell lines reveals conserved DNA damage repair pathways that mitigate formaldehyde sensitivityEleonora Juarez, Nyasha Chambwe, Weiliang Tang, et al.
Cytogenetic and Genome Research|March 14, 2015
Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLMNichole Owen, James Hejna, Scott Rennie, et al.
DNA Repair|November 8, 2016
Enhanced sensitivity of Neil1<sup>-/-</sup> mice to chronic UVB exposureMarcus J Calkins, Vladimir Vartanian, Nichole Owen, et al.
Molecular Genetics & Genomic Medicine|February 26, 2024
Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing lossRyan J German, Blake Vuocolo, Liesbeth Vossaert, et al.
Molecular Genetics & Genomic Medicine|August 24, 2023
Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved populationCara P Ford, Rebecca O Littlejohn, Ryan German, et al.
Pageof 2