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 Copeland

Showing results (341-350 of 352) with videos related to

Pageof 36
Sort By:
DNA Repair|November 4, 2017
DNA polymerase β: A missing link of the base excision repair machinery in mammalian mitochondriaRajendra Prasad, Melike Çağlayan, Da-Peng Dai, et al.
JAMA Oncology|September 10, 2020
Assessment of Doxorubicin and Pembrolizumab in Patients With Advanced Anthracycline-Naive Sarcoma: A Phase 1/2 Nonrandomized Clinical TrialSeth M Pollack, Mary W Redman, Kelsey K Baker, et al.
Environmental and Molecular Mutagenesis|January 6, 2006
Mitochondrial toxicity in hearts of CD-1 mice following perinatal exposure to AZT, 3TC, or AZT/3TC in combinationSherine S L Chan, Janine H Santos, Joel N Meyer, et al.
Nature Biotechnology|August 20, 2008
High-resolution metagenomics targets specific functional types in complex microbial communitiesMarina G Kalyuzhnaya, Alla Lapidus, Natalia Ivanova, et al.
Plos One|September 4, 2019
Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromesMargaret A Gustafson, Elizabeth M McCormick, Lalith Perera, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonismLionel Van Maldergem, Arnaud Besse, Boel De Paepe, et al.
Environmental Health Perspectives|August 16, 2014
Mitochondria, energetics, epigenetics, and cellular responses to stressDaniel T Shaughnessy, Kimberly McAllister, Leroy Worth, et al.
The Journal of Biological Chemistry|October 2, 2001
Eukaryotic DNA polymerases: proposal for a revised nomenclatureP M Burgers, E V Koonin, E Bruford, et al.
Human Mutation|June 12, 2008
Molecular and clinical genetics of mitochondrial diseases due to POLG mutationsLee-Jun C Wong, Robert K Naviaux, Nicola Brunetti-Pierri, et al.
Molecular Genetics and Metabolism|December 28, 2014
Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communitiesMarni J Falk, Lishuang Shen, Michael Gonzalez, et al.
Pageof 36

Showing results (341-350 of 352) with videos related to

Sort By:
Pageof 36
DNA Repair|November 4, 2017
DNA polymerase β: A missing link of the base excision repair machinery in mammalian mitochondriaRajendra Prasad, Melike Çağlayan, Da-Peng Dai, et al.
JAMA Oncology|September 10, 2020
Assessment of Doxorubicin and Pembrolizumab in Patients With Advanced Anthracycline-Naive Sarcoma: A Phase 1/2 Nonrandomized Clinical TrialSeth M Pollack, Mary W Redman, Kelsey K Baker, et al.
Environmental and Molecular Mutagenesis|January 6, 2006
Mitochondrial toxicity in hearts of CD-1 mice following perinatal exposure to AZT, 3TC, or AZT/3TC in combinationSherine S L Chan, Janine H Santos, Joel N Meyer, et al.
Nature Biotechnology|August 20, 2008
High-resolution metagenomics targets specific functional types in complex microbial communitiesMarina G Kalyuzhnaya, Alla Lapidus, Natalia Ivanova, et al.
Plos One|September 4, 2019
Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromesMargaret A Gustafson, Elizabeth M McCormick, Lalith Perera, et al.
Annals of Clinical and Translational Neurology|January 13, 2017
POLG2 deficiency causes adult-onset syndromic sensory neuropathy, ataxia and parkinsonismLionel Van Maldergem, Arnaud Besse, Boel De Paepe, et al.
Environmental Health Perspectives|August 16, 2014
Mitochondria, energetics, epigenetics, and cellular responses to stressDaniel T Shaughnessy, Kimberly McAllister, Leroy Worth, et al.
The Journal of Biological Chemistry|October 2, 2001
Eukaryotic DNA polymerases: proposal for a revised nomenclatureP M Burgers, E V Koonin, E Bruford, et al.
Human Mutation|June 12, 2008
Molecular and clinical genetics of mitochondrial diseases due to POLG mutationsLee-Jun C Wong, Robert K Naviaux, Nicola Brunetti-Pierri, et al.
Molecular Genetics and Metabolism|December 28, 2014
Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communitiesMarni J Falk, Lishuang Shen, Michael Gonzalez, et al.
Pageof 36