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Genes, Brain, and Behavior|June 17, 2023
Spontaneous allelic variant in deafness-blindness gene Ush1g resulting in an expanded phenotypeVladimir Vartanian, Jocelyn F Krey, Paroma Chatterjee, et al.
DNA Repair|November 17, 2019
Recognition of DNA adducts by edited and unedited forms of DNA glycosylase NEIL1Irina G Minko, Vladimir L Vartanian, Naoto N Tozaki, et al.
Oncology Reports|December 16, 2014
Case-control study of the PERIOD3 clock gene length polymorphism and colorectal adenoma formationMelannie Alexander, James B Burch, Susan E Steck, et al.
DNA Repair|May 18, 2019
Characterization of rare NEIL1 variants found in East Asian populationsIrina G Minko, Vladimir L Vartanian, Naoto N Tozaki, et al.
Scientific Reports|January 17, 2018
Modulation of UVB-induced Carcinogenesis by Activation of Alternative DNA Repair PathwaysYan Sha, Vladimir Vartanian, Nichole Owen, et al.
DNA Repair|June 29, 2021
DNA glycosylase deficiency leads to decreased severity of lupus in the Polb-Y265C mouse modelSesha L Paluri, Matthew Burak, Alireza G Senejani, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 5, 2017
NEIL1 protects against aflatoxin-induced hepatocellular carcinoma in miceVladimir Vartanian, Irina G Minko, Supawadee Chawanthayatham, et al.
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