scholarly journals Precision medicine based on surgical oncology in the era of genome-scale analysis and genome editing technology

2018 ◽  
Vol 2 (2) ◽  
pp. 106-115 ◽  
Author(s):  
Shinji Tanaka
Author(s):  
Marcel Böhrer ◽  
Bart Rymen ◽  
Christophe Himber ◽  
Aude Gerbaud ◽  
David Pflieger ◽  
...  

2018 ◽  
Vol 66 ◽  
pp. 43-47 ◽  
Author(s):  
Juan Á. Patiño-Galindo ◽  
Francisco Domínguez ◽  
María T. Cuevas ◽  
Elena Delgado ◽  
Mónica Sánchez ◽  
...  

2020 ◽  
Vol 69 (7) ◽  
pp. 1293-1305
Author(s):  
Guoshu Bi ◽  
Zhencong Chen ◽  
Xiaodong Yang ◽  
Jiaqi Liang ◽  
Zhengyang Hu ◽  
...  

2019 ◽  
Vol 14 (4) ◽  
pp. 608-641 ◽  
Author(s):  
Sudhanshu P. Raikwar ◽  
Nidhi S. Kikkeri ◽  
Ragha Sakuru ◽  
Daniyal Saeed ◽  
Haris Zahoor ◽  
...  

2020 ◽  
Vol 10 (3) ◽  
pp. 652-654.e17
Author(s):  
B.P.D. Purkayastha ◽  
E.R. Chan ◽  
D. Ravillah ◽  
L. Ravi ◽  
R. Gupta ◽  
...  

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Joana Ferreira da Silva ◽  
Sejla Salic ◽  
Marc Wiedner ◽  
Paul Datlinger ◽  
Patrick Essletzbichler ◽  
...  

Abstract The mutagenic repair of Cas9 generated breaks is thought to predominantly rely on non-homologous end-joining (NHEJ), leading to insertions and deletions within DNA that culminate in gene knock-out (KO). In this study, by taking focused as well as genome-wide approaches, we show that this pathway is dispensable for the repair of such lesions. Genetic ablation of NHEJ is fully compensated for by alternative end joining (alt-EJ), in a POLQ-dependent manner, resulting in a distinct repair signature with larger deletions that may be exploited for large-scale genome editing. Moreover, we show that cells deficient for both NHEJ and alt-EJ were still able to repair CRISPR-mediated DNA double-strand breaks, highlighting how little is yet known about the mechanisms of CRISPR-based genome editing.


2011 ◽  
Vol 6 (6) ◽  
pp. 870-895 ◽  
Author(s):  
Tyrone Ryba ◽  
Dana Battaglia ◽  
Benjamin D Pope ◽  
Ichiro Hiratani ◽  
David M Gilbert

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