Partial porcine kidney resection in vivo using a 1.92 μm fiber laser system

2009 ◽  
Author(s):  
Dirk Theisen-Kunde ◽  
Sönke Tedsen ◽  
Veit Danicke ◽  
Ralf Brinkmann
2009 ◽  
Author(s):  
Sönke Tedsen ◽  
Dirk Theisen-Kunde ◽  
Christian Doehn ◽  
Ingo Kausch ◽  
Dieter Jocham

2018 ◽  
Author(s):  
Ksenia V. Shatilova ◽  
Georgii A. Aloian ◽  
Ilya V. Yaroslavsky ◽  
Gregory B. Altshuler ◽  
Maria Karabut ◽  
...  
Keyword(s):  
Ex Vivo ◽  

2007 ◽  
Author(s):  
D. Theisen-Kunde ◽  
S. Tedsen ◽  
K. Herrmann ◽  
V. Danicke ◽  
R. Brinkmann

2011 ◽  
Vol 26 (4) ◽  
pp. 509-514 ◽  
Author(s):  
Dirk Theisen-Kunde ◽  
Sönke Tedsen ◽  
Christian Doehn ◽  
Dieter Jocham ◽  
Ingo Kausch von Schmeling

2007 ◽  
Vol 18 (8) ◽  
pp. 1005-1010 ◽  
Author(s):  
Paul F. Laeseke ◽  
Lisa A. Sampson ◽  
Tina M. Frey ◽  
Rajat Mukherjee ◽  
Thomas C. Winter ◽  
...  

2007 ◽  
Vol 177 (2) ◽  
pp. 219-229 ◽  
Author(s):  
Naoya Uematsu ◽  
Eric Weterings ◽  
Ken-ichi Yano ◽  
Keiko Morotomi-Yano ◽  
Burkhard Jakob ◽  
...  

The DNA-dependent protein kinase catalytic subunit (DNA-PKCS) plays an important role during the repair of DNA double-strand breaks (DSBs). It is recruited to DNA ends in the early stages of the nonhomologous end-joining (NHEJ) process, which mediates DSB repair. To study DNA-PKCS recruitment in vivo, we used a laser system to introduce DSBs in a specified region of the cell nucleus. We show that DNA-PKCS accumulates at DSB sites in a Ku80-dependent manner, and that neither the kinase activity nor the phosphorylation status of DNA-PKCS influences its initial accumulation. However, impairment of both of these functions results in deficient DSB repair and the maintained presence of DNA-PKCS at unrepaired DSBs. The use of photobleaching techniques allowed us to determine that the kinase activity and phosphorylation status of DNA-PKCS influence the stability of its binding to DNA ends. We suggest a model in which DNA-PKCS phosphorylation/autophosphorylation facilitates NHEJ by destabilizing the interaction of DNA-PKCS with the DNA ends.


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