Similar articles for PMID: 17315206

Year	Number of Results
1999	1
2001	2
2002	1
2003	5
2004	15
2005	18
2006	18
2007	20
2008	9
2009	15
2010	2
2011	7
2012	5
2013	8
2014	7
2015	9
2016	2
2017	9
2018	7
2019	3
2020	7
2021	3
2022	7
2023	2
2024	0

1

DNA single-strand break repair is impaired in aprataxin-related ataxia.

Hirano M, Yamamoto A, Mori T, Lan L, Iwamoto TA, Aoki M, Shimada K, Furiya Y, Kariya S, Asai H, Yasui A, Nishiwaki T, Imoto K, Kobayashi N, Kiriyama T, Nagata T, Konishi N, Itoyama Y, Ueno S. Hirano M, et al. Ann Neurol. 2007 Feb;61(2):162-74. doi: 10.1002/ana.21078. Ann Neurol. 2007. PMID: 17315206

2

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein.

Sano Y, Date H, Igarashi S, Onodera O, Oyake M, Takahashi T, Hayashi S, Morimatsu M, Takahashi H, Makifuchi T, Fukuhara N, Tsuji S. Sano Y, et al. Ann Neurol. 2004 Feb;55(2):241-9. doi: 10.1002/ana.10808. Ann Neurol. 2004. PMID: 14755728

3

The FHA domain of aprataxin interacts with the C-terminal region of XRCC1.

Date H, Igarashi S, Sano Y, Takahashi T, Takahashi T, Takano H, Tsuji S, Nishizawa M, Onodera O. Date H, et al. Biochem Biophys Res Commun. 2004 Dec 24;325(4):1279-85. doi: 10.1016/j.bbrc.2004.10.162. Biochem Biophys Res Commun. 2004. PMID: 15555565

4

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.

Tada M, Yokoseki A, Sato T, Makifuchi T, Onodera O. Tada M, et al. Adv Exp Med Biol. 2010;685:21-33. doi: 10.1007/978-1-4419-6448-9_3. Adv Exp Med Biol. 2010. PMID: 20687492 Review.

5

A novel nonsense mutation in the APTX gene associated with delayed DNA single-strand break removal fails to enhance sensitivity to different genotoxic agents.

Crimella C, Cantoni O, Guidarelli A, Vantaggiato C, Martinuzzi A, Fiorani M, Azzolini C, Orso G, Bresolin N, Bassi MT. Crimella C, et al. Hum Mutat. 2011 Apr;32(4):E2118-33. doi: 10.1002/humu.21464. Epub 2011 Feb 8. Hum Mutat. 2011. PMID: 21412945

6

Aprataxin, a novel protein that protects against genotoxic stress.

Gueven N, Becherel OJ, Kijas AW, Chen P, Howe O, Rudolph JH, Gatti R, Date H, Onodera O, Taucher-Scholz G, Lavin MF. Gueven N, et al. Hum Mol Genet. 2004 May 15;13(10):1081-93. doi: 10.1093/hmg/ddh122. Epub 2004 Mar 25. Hum Mol Genet. 2004. PMID: 15044383

7

Short half-lives of ataxia-associated aprataxin proteins in neuronal cells.

Hirano M, Asai H, Kiriyama T, Furiya Y, Iwamoto T, Nishiwaki T, Yamamoto A, Mori T, Ueno S. Hirano M, et al. Neurosci Lett. 2007 May 29;419(2):184-7. doi: 10.1016/j.neulet.2007.04.044. Epub 2007 Apr 25. Neurosci Lett. 2007. PMID: 17485165

8

[DNA repair and neurodegeneration].

Onodera O. Onodera O. Rinsho Shinkeigaku. 2005 Nov;45(11):979-81. Rinsho Shinkeigaku. 2005. PMID: 16447779 Japanese.

9

Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends.

Takahashi T, Tada M, Igarashi S, Koyama A, Date H, Yokoseki A, Shiga A, Yoshida Y, Tsuji S, Nishizawa M, Onodera O. Takahashi T, et al. Nucleic Acids Res. 2007;35(11):3797-809. doi: 10.1093/nar/gkm158. Epub 2007 May 22. Nucleic Acids Res. 2007. PMID: 17519253 Free PMC article.

10

Short-patch single-strand break repair in ataxia oculomotor apraxia-1.

Reynolds JJ, El-Khamisy SF, Caldecott KW. Reynolds JJ, et al. Biochem Soc Trans. 2009 Jun;37(Pt 3):577-81. doi: 10.1042/BST0370577. Biochem Soc Trans. 2009. PMID: 19442253 Review.

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