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Charles C Valentine

Showing results (1-10 of 18) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 15, 2020
Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencingCharles C Valentine, Robert R Young, Mark R Fielden, et al.
Biology of Reproduction|February 12, 2025
Duplex sequencing identifies unique characteristics of ENU-induced mutations in male mouse germ cells†Danielle P M LeBlanc, Gu Zhou, Andrew Williams, et al.
Nature Ecology & Evolution|February 16, 2024
Mitochondrial haplotype and mito-nuclear matching drive somatic mutation and selection throughout ageingIsabel M Serrano, Misa Hirose, Charles C Valentine, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Mitochondrial haplotype and mito-nuclear matching drive somatic mutation and selection throughout agingIsabel M Serrano, Misa Hirose, Charles C Valentine, et al.
Nature Ecology & Evolution|January 30, 2025
Author Correction: Mitochondrial somatic mutation and selection throughout ageingIsabel M Serrano, Misa Hirose, Charles C Valentine, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 30, 2017
Mutational spectra of aflatoxin B<sub>1</sub> in vivo establish biomarkers of exposure for human hepatocellular carcinomaSupawadee Chawanthayatham, Charles C Valentine, Bogdan I Fedeles, et al.
Archives of Toxicology|June 21, 2023
Duplex sequencing provides detailed characterization of mutation frequencies and spectra in the bone marrow of MutaMouse males exposed to procarbazine hydrochlorideAnnette E Dodge, Danielle P M LeBlanc, Gu Zhou, et al.
Bioinformatics Advances|November 27, 2025
MutSeqR: an open source R package for standardized analysis of error-corrected next-generation sequencing data in genetic toxicologyAnnette E Dodge, Andrew Williams, Danielle P M LeBlanc, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Quantification of measurable residual disease using duplex sequencing in adults with acute myeloid leukemiaLaura W Dillon, Jake Higgins, Hassan Nasif, et al.
Mutagenesis|June 10, 2023
Next Generation Sequencing Workshop at the Royal Society of Medicine (London, May 2022): how genomics is on the path to modernizing genetic toxicologyAnthony M Lynch, Thalita B Zanoni, Jesse J Salk, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Proceedings of the National Academy of Sciences of the United States of America|December 15, 2020
Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencingCharles C Valentine, Robert R Young, Mark R Fielden, et al.
Biology of Reproduction|February 12, 2025
Duplex sequencing identifies unique characteristics of ENU-induced mutations in male mouse germ cells†Danielle P M LeBlanc, Gu Zhou, Andrew Williams, et al.
Nature Ecology & Evolution|February 16, 2024
Mitochondrial haplotype and mito-nuclear matching drive somatic mutation and selection throughout ageingIsabel M Serrano, Misa Hirose, Charles C Valentine, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Mitochondrial haplotype and mito-nuclear matching drive somatic mutation and selection throughout agingIsabel M Serrano, Misa Hirose, Charles C Valentine, et al.
Nature Ecology & Evolution|January 30, 2025
Author Correction: Mitochondrial somatic mutation and selection throughout ageingIsabel M Serrano, Misa Hirose, Charles C Valentine, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 30, 2017
Mutational spectra of aflatoxin B<sub>1</sub> in vivo establish biomarkers of exposure for human hepatocellular carcinomaSupawadee Chawanthayatham, Charles C Valentine, Bogdan I Fedeles, et al.
Archives of Toxicology|June 21, 2023
Duplex sequencing provides detailed characterization of mutation frequencies and spectra in the bone marrow of MutaMouse males exposed to procarbazine hydrochlorideAnnette E Dodge, Danielle P M LeBlanc, Gu Zhou, et al.
Bioinformatics Advances|November 27, 2025
MutSeqR: an open source R package for standardized analysis of error-corrected next-generation sequencing data in genetic toxicologyAnnette E Dodge, Andrew Williams, Danielle P M LeBlanc, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Quantification of measurable residual disease using duplex sequencing in adults with acute myeloid leukemiaLaura W Dillon, Jake Higgins, Hassan Nasif, et al.
Mutagenesis|June 10, 2023
Next Generation Sequencing Workshop at the Royal Society of Medicine (London, May 2022): how genomics is on the path to modernizing genetic toxicologyAnthony M Lynch, Thalita B Zanoni, Jesse J Salk, et al.
Pageof 2