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Hepatitis C virus inhibits DNA damage repair through reactive oxygen and nitrogen species and by interfering with the ATM-NBS1/Mre11/Rad50 DNA repair pathway in monocytes and hepatocytes.

Machida K, McNamara G, Cheng KT, Huang J, Wang CH, Comai L, Ou JH, Lai MM.

J Immunol. 2010 Dec 1;185(11):6985-98. doi: 10.4049/jimmunol.1000618. Epub 2010 Oct 25.


Hepatitis B virus pre-S2 mutant large surface protein inhibits DNA double-strand break repair and leads to genome instability in hepatocarcinogenesis.

Hsieh YH, Chang YY, Su IJ, Yen CJ, Liu YR, Liu RJ, Hsieh WC, Tsai HW, Wang LH, Huang W.

J Pathol. 2015 Jul;236(3):337-47. doi: 10.1002/path.4531. Epub 2015 Apr 22.


Microtubule-targeting agents augment the toxicity of DNA-damaging agents by disrupting intracellular trafficking of DNA repair proteins.

Poruchynsky MS, Komlodi-Pasztor E, Trostel S, Wilkerson J, Regairaz M, Pommier Y, Zhang X, Kumar Maity T, Robey R, Burotto M, Sackett D, Guha U, Fojo AT.

Proc Natl Acad Sci U S A. 2015 Feb 3;112(5):1571-6. doi: 10.1073/pnas.1416418112. Epub 2015 Jan 20.


Hepatitis C virus core protein overcomes H2O2-induced apoptosis by downregulating p14 expression via DNA methylation.

Seo YL, Heo S, Jang KL.

J Gen Virol. 2015 Apr;96(Pt 4):822-32. doi: 10.1099/vir.0.000032. Epub 2014 Dec 22.


Loss of nuclear PTEN in HCV-infected human hepatocytes.

Bao W, Florea L, Wu N, Wang Z, Banaudha K, Qian J, Houzet L, Kumar R, Kumar A.

Infect Agent Cancer. 2014 Jul 18;9:23. doi: 10.1186/1750-9378-9-23. eCollection 2014.


Concerted action of Nrf2-ARE pathway, MRN complex, HMGB1 and inflammatory cytokines - implication in modification of radiation damage.

Anuranjani, Bala M.

Redox Biol. 2014 Feb 28;2:832-46. doi: 10.1016/j.redox.2014.02.008. eCollection 2014. Review.


Rad50 and CARD9, missing links in cytosolic DNA-stimulated inflammation.

Bowie AG.

Nat Immunol. 2014 Jun;15(6):534-6. doi: 10.1038/ni.2894. No abstract available.


The Rad50 hook domain regulates DNA damage signaling and tumorigenesis.

Roset R, Inagaki A, Hohl M, Brenet F, Lafrance-Vanasse J, Lange J, Scandura JM, Tainer JA, Keeney S, Petrini JH.

Genes Dev. 2014 Mar 1;28(5):451-62. doi: 10.1101/gad.236745.113. Epub 2014 Feb 14.


Hepatitis C virus core protein regulates NANOG expression via the stat3 pathway.

Zhou JJ, Chen RF, Deng XG, Zhou Y, Ye X, Yu M, Tang J, He XY, Cheng D, Zeng B, Zhou QB, Li ZH.

FEBS Lett. 2014 Feb 14;588(4):566-73. doi: 10.1016/j.febslet.2013.11.041. Epub 2014 Jan 21.


Non-homologous end joining pathway is the major route of protection against 4β-hydroxywithanolide E-induced DNA damage in MCF-7 cells.

You BJ, Wu YC, Lee CL, Lee HZ.

Food Chem Toxicol. 2014 Mar;65:205-12. doi: 10.1016/j.fct.2013.12.026. Epub 2013 Dec 25.


Radiation-induced telomere length variations in normal and in Nijmegen Breakage Syndrome cells.

Berardinelli F, Sgura A, Di Masi A, Leone S, Cirrone GA, Romano F, Tanzarella C, Antoccia A.

Int J Radiat Biol. 2014 Jan;90(1):45-52. doi: 10.3109/09553002.2014.859400.


A potential cellular host factor homologous to ZNF-136 can interact with truncated nonstructural protein 2 of hepatitis C virus.

Liu C, Chen X.

Arch Virol. 2014 Apr;159(4):785-9. doi: 10.1007/s00705-013-1888-z. Epub 2013 Oct 18.


Chlamydia infection promotes host DNA damage and proliferation but impairs the DNA damage response.

Chumduri C, Gurumurthy RK, Zadora PK, Mi Y, Meyer TF.

Cell Host Microbe. 2013 Jun 12;13(6):746-58. doi: 10.1016/j.chom.2013.05.010.


SHIP2 regulates epithelial cell polarity through its lipid product, which binds to Dlg1, a pathway subverted by hepatitis C virus core protein.

Awad A, Sar S, Barré R, Cariven C, Marin M, Salles JP, Erneux C, Samuel D, Gassama-Diagne A.

Mol Biol Cell. 2013 Jul;24(14):2171-85. doi: 10.1091/mbc.E12-08-0626. Epub 2013 May 22.


Hepatitis C virus NS2 protein inhibits DNA damage pathway by sequestering p53 to the cytoplasm.

Bittar C, Shrivastava S, Bhanja Chowdhury J, Rahal P, Ray RB.

PLoS One. 2013 Apr 30;8(4):e62581. doi: 10.1371/journal.pone.0062581. Print 2013.


Culture under low physiological oxygen conditions improves the stemness and quality of induced pluripotent stem cells.

Guo CW, Kawakatsu M, Idemitsu M, Urata Y, Goto S, Ono Y, Hamano K, Li TS.

J Cell Physiol. 2013 Nov;228(11):2159-66. doi: 10.1002/jcp.24389.


Sodium tungstate modulates ATM function upon DNA damage.

Rodriguez-Hernandez CJ, Llorens-Agost M, Calbó J, Murguia JR, Guinovart JJ.

FEBS Lett. 2013 May 21;587(10):1579-86. doi: 10.1016/j.febslet.2013.04.003. Epub 2013 Apr 12.


SIRT4 has tumor-suppressive activity and regulates the cellular metabolic response to DNA damage by inhibiting mitochondrial glutamine metabolism.

Jeong SM, Xiao C, Finley LW, Lahusen T, Souza AL, Pierce K, Li YH, Wang X, Laurent G, German NJ, Xu X, Li C, Wang RH, Lee J, Csibi A, Cerione R, Blenis J, Clish CB, Kimmelman A, Deng CX, Haigis MC.

Cancer Cell. 2013 Apr 15;23(4):450-63. doi: 10.1016/j.ccr.2013.02.024. Epub 2013 Apr 4.


Nitric oxide coordinates development of genomic instability in realization of combined effect with ionizing radiation.

Mikhailenko VM, Diomina EA, Muzalov II, Gerashchenko BI.

Exp Oncol. 2013 Mar;35(1):58-64.


Ataxia telangiectasia-mutated (ATM) kinase activity is regulated by ATP-driven conformational changes in the Mre11/Rad50/Nbs1 (MRN) complex.

Lee JH, Mand MR, Deshpande RA, Kinoshita E, Yang SH, Wyman C, Paull TT.

J Biol Chem. 2013 May 3;288(18):12840-51. doi: 10.1074/jbc.M113.460378. Epub 2013 Mar 22.

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