Citations for
1DCLRE1C, ERCC1, ERCC4, MUS81
DNA replication stress triggers rapid DNA replication fork breakage by Artemis and XPF.
Bétous R, Goullet de Rugy T, Pelegrini AL, Queille S, de Villartay JP, Hoffmann JS.
PLoS Genet 14(7):e1007541. doi: 10.1371/journal.pgen.1007541. eCollection 2018 Jul. 2018
2DCLRE1C, PAXIP1
PTIP associates with Artemis to dictate DNA repair pathway choice.
Wang J, Aroumougame A, Lobrich M, Li Y, Chen D, Chen J, Gong Z.
Genes Dev 28(24):2693-8. doi: 10.1101/gad.252478.114. 2014
3DCLRE1C, SETMAR
Trimming of damaged 3' overhangs of DNA double-strand breaks by the Metnase and Artemis endonucleases.
Mohapatra S, Yannone SM, Lee SH, Hromas RA, Akopiants K, Menon V, Ramsden DA, Povirk LF.
DNA Repair (Amst) 12(6):422-32. doi: 10.1016/j.dnarep.2013.03.005. 2013
4DCLRE1C, LIG4
Structural basis of DNA ligase IV-Artemis interaction in nonhomologous end-joining.
De Ioannes P, Malu S, Cortes P, Aggarwal AK.
Cell Rep 2(6):1505-12. doi: 10.1016/j.celrep.2012.11.004. Epub 2012 Dec 7. 2012
5DCLRE1C, SCIDA
A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis.
Jacobs C, Huang Y, Masud T, Lu W, Westfield G, Giblin W, Sekiguchi JM.
Hum Mol Genet 20(4):806-19. Epub 2010 Dec 8. 2011
6DCLRE1C
Artemis is a negative regulator of p53 in response to oxidative stress.
Zhang X, Zhu Y, Geng L, Wang H, Legerski RJ.
Oncogene 28(22):2196-204. Epub 2009 Apr 27. 2009
7DCLRE1A, DCLRE1B, DCLRE1C
SNM1A acts downstream of ATM to promote the G1 cell cycle checkpoint.
Akhter S, Legerski RJ.
Biochem Biophys Res Commun 377(1):236-41. Epub 2008 Oct 9. 2008
8DCLRE1C
Processing of 3'-phosphoglycolate-terminated DNA double strand breaks by Artemis nuclease.
Povirk LF, Zhou T, Zhou R, Cowan MJ, Yannone SM.
J Biol Chem 282(6):3547-58. Epub 2006 Nov 22. 2007
9DCLRE1C
Role of Artemis in DSB repair and guarding chromosomal stability following exposure to ionizing radiation at different stages of cell cycle.
Darroudi F, Wiegant W, Meijers M, Friedl AA, van der Burg M, Fomina J, van Dongen JJ, van Gent DC, Zdzienicka MZ.
Mutat Res 615(1-2):111-24. Epub 2006 Dec 12. 2007
10DCLRE1C, XRCC6
Interplay between Ku, Artemis, and the DNA-dependent protein kinase catalytic subunit at DNA ends.
Drouet J, Frit P, Delteil C, de Villartay JP, Salles B, Calsou P.
J Biol Chem 281(38):27784-93. Epub 2006 Jul 19. 2006
11DCLRE1C
The DNA-dependent protein kinase catalytic subunit phosphorylation sites in human Artemis.
Ma Y, Pannicke U, Lu H, Niewolik D, Schwarz K, Lieber MR.
J Biol Chem 280(40):33839-46. Epub 2005 Aug 10. 2005
12DCLRE1C
The Artemis:DNA-PKcs endonuclease cleaves DNA loops, flaps, and gaps.
Ma Y, Schwarz K, Lieber MR.
DNA Repair (Amst) 4(7):845-51. 2005
13ATM, ATR, DCLRE1C
Artemis is a phosphorylation target of ATM and ATR and is involved in the G2/M DNA damage checkpoint response.
Zhang X, Succi J, Feng Z, Prithivirajsingh S, Story MD, Legerski RJ.
Mol Cell Biol 24(20):9207-20. 2004
14DCLRE1C, SCIDA
Novel Artemis gene mutations of radiosensitive severe combined immunodeficiency in Japanese families.
Kobayashi N, Agematsu K, Sugita K, Sako M, Nonoyama S, Yachie A, Kumaki S, Tsuchiya S, Ochs HD, Sugita K, Fukushima Y, Komiyama A.
Hum Genet 112(4):348-52. Epub 2003 Feb 19. 2003
15CPSF3, DCLRE1A, DCLRE1B, DCLRE1C, ELAC2
hSnm1 colocalizes and physically associates with 53BP1 before and after DNA damage.
Richie CT, Peterson C, Lu T, Hittelman WN, Carpenter PB, Legerski RJ.
Mol Cell Biol 22(24):8635-47. 2002
16DCLRE1C
Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.
Moshous D, Callebaut I, de Chasseval R, Corneo B, Cavazzana-Calvo M, Le Deist F, Tezcan I, Sanal O, Bertrand Y, Philippe N, Fischer A, de Villartay JP.
Cell 105(2):177-86. 2001
17DCLRE1C
A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p.
Moshous D, Li L, Chasseval R, Philippe N, Jabado N, Cowan MJ, Fischer A, Villartay JP.
Hum Mol Genet 9(4):583-588. 2000
18DCLRE1C
The gene for severe combined immunodeficiency disease in athabascan-speaking native Americans is located on chromoosme 10p.
Li L, Drayna D, Hu D, Hayward A, Gahagan S, Pabst H, Cowan MJ.
Am J Hum Genet 62(1):136-44. 1998
19DCLRE1C
A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency.
Nicolas N, Moshous D, Cavazzana-Calvo M, Papadopoulo D, de Chasseval R, Le Deist F, Fischer A, de Villartay JP.
J Exp Med 188(4):627-34. 1998
20DCLRE1C
Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.
Cavazzana-Calvo M, Le Deist F, De Saint Basile G, Papadopoulo D, De Villartay JP, Fischer A.
J Clin Invest 91(3):1214-8. 1993