Limei Ju - JoVE Visualize

Showing results (11-20 of 14) with videos related to

Pageof 2

Sort By:

You have reached the last page of results.This site can display upto 14 results.

DNA Repair|September 24, 2004

The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4Paula M Clements, Claire Breslin, Emma D Deeks, et al.

Cerebral Cortex (New York, N.Y. : 1991)|April 3, 2017

Deficiency of Cks1 Leads to Learning and Long-Term Memory Defects and p27 Dependent Formation of Neuronal Cofilin AggregatesAlexander Kukalev, Yiu-Ming Ng, Limei Ju, et al.

Nature|December 22, 2016

XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxiaNicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, et al.

DNA Repair|March 23, 2013

SMC6 is an essential gene in mice, but a hypomorphic mutant in the ATPase domain has a mild phenotype with a range of subtle abnormalitiesLimei Ju, Jonathan Wing, Elaine Taylor, et al.

Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

DNA Repair|September 24, 2004

The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4Paula M Clements, Claire Breslin, Emma D Deeks, et al.

Cerebral Cortex (New York, N.Y. : 1991)|April 3, 2017

Deficiency of Cks1 Leads to Learning and Long-Term Memory Defects and p27 Dependent Formation of Neuronal Cofilin AggregatesAlexander Kukalev, Yiu-Ming Ng, Limei Ju, et al.

Nature|December 22, 2016

XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxiaNicolas C Hoch, Hana Hanzlikova, Stuart L Rulten, et al.

DNA Repair|March 23, 2013

SMC6 is an essential gene in mice, but a hypomorphic mutant in the ATPase domain has a mild phenotype with a range of subtle abnormalitiesLimei Ju, Jonathan Wing, Elaine Taylor, et al.

Pageof 2