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Jun Ho Ko

Showing results (1-10 of 8) with videos related to

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Genesis (New York, N.Y. : 2000)|October 22, 2008
High-throughput knock-in coupling gene targeting with the HPRT minigene and Cre-mediated recombinationTae Moon Kim, Yong Jun Choi, Jun Ho Ko, et al.
The Review of Scientific Instruments|February 3, 2026
Commissioning of the linear accelerator for the extreme ultraviolet synchrotron of the Pohang Accelerator LaboratoryJun Ho Ko, Min Woo Kim, Jang-Hui Han, et al.
The Review of Scientific Instruments|July 2, 2018
Coherent synchrotron radiation monitor for microbunching instability in XFELJun Ho Ko, Gyujin Kim, Changbum Kim, et al.
Mutation Research|April 5, 2011
The phenotype of FancB-mutant mouse embryonic stem cellsTae Moon Kim, Jun Ho Ko, Yong Jun Choi, et al.
Cell Reports|January 4, 2024
TREX2 deficiency suppresses spontaneous and genotoxin-associated mutagenesisTeresa Marple, Mi Young Son, Xiaodong Cheng, et al.
Molecular and Cellular Biology|July 11, 2012
RAD51 mutants cause replication defects and chromosomal instabilityTae Moon Kim, Jun Ho Ko, Lingchuan Hu, et al.
Cell Reports|December 28, 2020
TREX2 Exonuclease Causes Spontaneous Mutations and Stress-Induced Replication Fork Defects in Cells Expressing RAD51<sup>K133A</sup>Jun Ho Ko, Mi Young Son, Qing Zhou, et al.
Journal of Synchrotron Radiation|July 6, 2019
Hard X-ray self-seeding commissioning at PAL-XFELChang Ki Min, Inhyuk Nam, Haeryong Yang, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genesis (New York, N.Y. : 2000)|October 22, 2008
High-throughput knock-in coupling gene targeting with the HPRT minigene and Cre-mediated recombinationTae Moon Kim, Yong Jun Choi, Jun Ho Ko, et al.
The Review of Scientific Instruments|February 3, 2026
Commissioning of the linear accelerator for the extreme ultraviolet synchrotron of the Pohang Accelerator LaboratoryJun Ho Ko, Min Woo Kim, Jang-Hui Han, et al.
The Review of Scientific Instruments|July 2, 2018
Coherent synchrotron radiation monitor for microbunching instability in XFELJun Ho Ko, Gyujin Kim, Changbum Kim, et al.
Mutation Research|April 5, 2011
The phenotype of FancB-mutant mouse embryonic stem cellsTae Moon Kim, Jun Ho Ko, Yong Jun Choi, et al.
Cell Reports|January 4, 2024
TREX2 deficiency suppresses spontaneous and genotoxin-associated mutagenesisTeresa Marple, Mi Young Son, Xiaodong Cheng, et al.
Molecular and Cellular Biology|July 11, 2012
RAD51 mutants cause replication defects and chromosomal instabilityTae Moon Kim, Jun Ho Ko, Lingchuan Hu, et al.
Cell Reports|December 28, 2020
TREX2 Exonuclease Causes Spontaneous Mutations and Stress-Induced Replication Fork Defects in Cells Expressing RAD51<sup>K133A</sup>Jun Ho Ko, Mi Young Son, Qing Zhou, et al.
Journal of Synchrotron Radiation|July 6, 2019
Hard X-ray self-seeding commissioning at PAL-XFELChang Ki Min, Inhyuk Nam, Haeryong Yang, et al.
Pageof 1