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Moonsook Lee

Showing results (31-40 of 39) with videos related to

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Human Molecular Genetics|February 26, 2009
Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in miceGo Suzuki, Kathryn M Harper, Takeshi Hiramoto, et al.
Biorxiv : the Preprint Server for Biology|May 20, 2024
Negative Selection Allows DNA Mismatch Repair-Deficient Mouse Fibroblasts <i>In Vitro</i> to Tolerate High Levels of Somatic MutationsLei Zhang, Moonsook Lee, Xiaoxiao Hao, et al.
Science Advances|October 27, 2021
Maintenance of genome sequence integrity in long- and short-lived rodent speciesLei Zhang, Xiao Dong, Xiao Tian, et al.
Human Molecular Genetics|July 21, 2009
Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceGo Suzuki, Kathryn M Harper, Takeshi Hiramoto, et al.
Plos One|April 18, 2014
The progeroid phenotype of Ku80 deficiency is dominant over DNA-PKCS deficiencyErwin Reiling, Martijn E T Dollé, Sameh A Youssef, et al.
Nature Genetics|April 12, 2022
Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smokingZhenqiu Huang, Shixiang Sun, Moonsook Lee, et al.
Plos One|January 28, 2014
Deletion of individual Ku subunits in mice causes an NHEJ-independent phenotype potentially by altering apurinic/apyrimidinic site repairYong Jun Choi, Han Li, Mi Young Son, et al.
Innovation (Cambridge (Mass.))|October 20, 2025
Divergent accumulation patterns of SNVs and INDELs reveal negative selection in noncancerous cellsLei Zhang, Moonsook Lee, Xiaoxiao Hao, et al.
Nature Aging|November 17, 2025
Single-cell analysis of the somatic mutational landscape in human chondrocytes during aging and in osteoarthritisPeijun Ren, Chen Zheng, Yidan Pang, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Human Molecular Genetics|February 26, 2009
Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in miceGo Suzuki, Kathryn M Harper, Takeshi Hiramoto, et al.
Biorxiv : the Preprint Server for Biology|May 20, 2024
Negative Selection Allows DNA Mismatch Repair-Deficient Mouse Fibroblasts <i>In Vitro</i> to Tolerate High Levels of Somatic MutationsLei Zhang, Moonsook Lee, Xiaoxiao Hao, et al.
Science Advances|October 27, 2021
Maintenance of genome sequence integrity in long- and short-lived rodent speciesLei Zhang, Xiao Dong, Xiao Tian, et al.
Human Molecular Genetics|July 21, 2009
Over-expression of a human chromosome 22q11.2 segment including TXNRD2, COMT and ARVCF developmentally affects incentive learning and working memory in miceGo Suzuki, Kathryn M Harper, Takeshi Hiramoto, et al.
Plos One|April 18, 2014
The progeroid phenotype of Ku80 deficiency is dominant over DNA-PKCS deficiencyErwin Reiling, Martijn E T Dollé, Sameh A Youssef, et al.
Nature Genetics|April 12, 2022
Single-cell analysis of somatic mutations in human bronchial epithelial cells in relation to aging and smokingZhenqiu Huang, Shixiang Sun, Moonsook Lee, et al.
Plos One|January 28, 2014
Deletion of individual Ku subunits in mice causes an NHEJ-independent phenotype potentially by altering apurinic/apyrimidinic site repairYong Jun Choi, Han Li, Mi Young Son, et al.
Innovation (Cambridge (Mass.))|October 20, 2025
Divergent accumulation patterns of SNVs and INDELs reveal negative selection in noncancerous cellsLei Zhang, Moonsook Lee, Xiaoxiao Hao, et al.
Nature Aging|November 17, 2025
Single-cell analysis of the somatic mutational landscape in human chondrocytes during aging and in osteoarthritisPeijun Ren, Chen Zheng, Yidan Pang, et al.
Pageof 4