-
1
-
-
0034790947
-
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
-
Date, H., Onodera, O., Tanaka, H., Iwabuchi, K., Uekawa, K., Igarashi, S., Koike, R., Hiroi, T., Yuasa, T., Awaya, Y. et al. (2001) Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene. Nat. Genet., 29, 184-188.
-
(2001)
Nat. Genet
, vol.29
, pp. 184-188
-
-
Date, H.1
Onodera, O.2
Tanaka, H.3
Iwabuchi, K.4
Uekawa, K.5
Igarashi, S.6
Koike, R.7
Hiroi, T.8
Yuasa, T.9
Awaya, Y.10
-
2
-
-
0034785531
-
The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/ Zn-finger protein aprataxin
-
Moreira, M.C., Barbot, C., Tachi, N., Kozuka, N., Uchida, E., Gibson, T., Mendonca, P., Costa, M., Barros, J., Yanagisawa, T. et al. (2001) The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/ Zn-finger protein aprataxin. Nat. Genet., 29, 189-193.
-
(2001)
Nat. Genet
, vol.29
, pp. 189-193
-
-
Moreira, M.C.1
Barbot, C.2
Tachi, N.3
Kozuka, N.4
Uchida, E.5
Gibson, T.6
Mendonca, P.7
Costa, M.8
Barros, J.9
Yanagisawa, T.10
-
3
-
-
0037183505
-
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: The aprataxin gene mutations
-
Shimazaki, H., Takiyama, Y., Sakoe, K., Ikeguchi, K., Niijima, K., Kaneko, J., Namekawa, M., Ogawa, T., Date, H., Tsuji, S. et al. (2002) Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations. Neurology, 59, 590-595.
-
(2002)
Neurology
, vol.59
, pp. 590-595
-
-
Shimazaki, H.1
Takiyama, Y.2
Sakoe, K.3
Ikeguchi, K.4
Niijima, K.5
Kaneko, J.6
Namekawa, M.7
Ogawa, T.8
Date, H.9
Tsuji, S.10
-
4
-
-
0037432279
-
Phenotypic variability of aprataxin gene mutations
-
Tranchant, C., Fleury, M., Moreira, M.C., Koenig, M. and Warter, J.M. (2003) Phenotypic variability of aprataxin gene mutations. Neurology 60, 868-870.
-
(2003)
Neurology
, vol.60
, pp. 868-870
-
-
Tranchant, C.1
Fleury, M.2
Moreira, M.C.3
Koenig, M.4
Warter, J.M.5
-
5
-
-
4644369308
-
Aprataxin gene mutations in Tunisian families
-
Amouri, R., Moreira, M.C., Zouari, M., El Euch, G., Barhoumi, C., Kefi, M., Belal, S., Koenig, M. and Hentati, F. (2004) Aprataxin gene mutations in Tunisian families. Neurology, 63, 928-929.
-
(2004)
Neurology
, vol.63
, pp. 928-929
-
-
Amouri, R.1
Moreira, M.C.2
Zouari, M.3
El Euch, G.4
Barhoumi, C.5
Kefi, M.6
Belal, S.7
Koenig, M.8
Hentati, F.9
-
6
-
-
2542495194
-
Aprataxin mutations are a rare cause of early onset ataxia in Germany
-
Habeck, M., Zuhlke, C., Bentele, K.H., Unkelbach, S., Kress, W., Burk, K., Schwinger, E. and Hellenbroich, Y. (2004) Aprataxin mutations are a rare cause of early onset ataxia in Germany. J. Neurol., 251 591-594.
-
(2004)
J. Neurol
, vol.251
, pp. 591-594
-
-
Habeck, M.1
Zuhlke, C.2
Bentele, K.H.3
Unkelbach, S.4
Kress, W.5
Burk, K.6
Schwinger, E.7
Hellenbroich, Y.8
-
7
-
-
34248180071
-
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. and Ueno, S. (2007) Short half-lives of ataxia-associated aprataxin proteins in neuronal cells. Neurosci. Lett., 419, 184-187.
-
(2007)
Neurosci. Lett
, vol.419
, pp. 184-187
-
-
Hirano, M.1
Asai, H.2
Kiriyama, T.3
Furiya, Y.4
Iwamoto, T.5
Nishiwaki, T.6
Yamamoto, A.7
Mori, T.8
Ueno, S.9
-
8
-
-
4544341920
-
The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4
-
Clements, P.M., Breslin, C., Deeks, E.D., Byrd, P.J., Ju, L., Bieganowski, P., Brenner, C., Moreira, M.C., Taylor, A.M. and Caldecott, K.W. (2004) The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4. DNA Repair (Amst), 3, 1493-1502.
-
(2004)
DNA Repair (Amst)
, vol.3
, pp. 1493-1502
-
-
Clements, P.M.1
Breslin, C.2
Deeks, E.D.3
Byrd, P.J.4
Ju, L.5
Bieganowski, P.6
Brenner, C.7
Moreira, M.C.8
Taylor, A.M.9
Caldecott, K.W.10
-
9
-
-
2542612903
-
Aprataxin, a novel protein that protects against genotoxic stress
-
Gueven, N., Becherel, O.J., Kijas, A.W., Chen, P., Howe, O., Rudolph, J.H., Gatti, R., Date, H., Onodera, O., Taucher-Scholz, G. et al. (2004) Aprataxin, a novel protein that protects against genotoxic stress. Hum. Mol. Genet., 13, 1081-1093.
-
(2004)
Hum. Mol. Genet
, vol.13
, pp. 1081-1093
-
-
Gueven, N.1
Becherel, O.J.2
Kijas, A.W.3
Chen, P.4
Howe, O.5
Rudolph, J.H.6
Gatti, R.7
Date, H.8
Onodera, O.9
Taucher-Scholz, G.10
-
10
-
-
4544314723
-
A new XRCC1-containing complex and its role in cellular survival of methyl methanesulfonate treatment
-
Luo, H., Chan, D.W., Yang, T., Rodriguez, M., Chen, B.P., Leng, M., Mu, J.J., Chen, D., Songyang, Z., Wang, Y. et al. (2004) A new XRCC1-containing complex and its role in cellular survival of methyl methanesulfonate treatment. Mol. Cell. Biol., 24, 8356-8365.
-
(2004)
Mol. Cell. Biol
, vol.24
, pp. 8356-8365
-
-
Luo, H.1
Chan, D.W.2
Yang, T.3
Rodriguez, M.4
Chen, B.P.5
Leng, M.6
Mu, J.J.7
Chen, D.8
Songyang, Z.9
Wang, Y.10
-
11
-
-
33847645440
-
DNA single-strand break repair is impaired in aprataxin-related ataxia
-
Hirano, M., Yamamoto, A., Mori, T., Lan, L., Iwamoto, T.A., Aoki, M., Shimada, K., Furiya, Y., Kariya, S., Asai, H. et al. (2007) DNA single-strand break repair is impaired in aprataxin-related ataxia. Ann. Neurol., 61, 162-174.
-
(2007)
Ann. Neurol
, vol.61
, pp. 162-174
-
-
Hirano, M.1
Yamamoto, A.2
Mori, T.3
Lan, L.4
Iwamoto, T.A.5
Aoki, M.6
Shimada, K.7
Furiya, Y.8
Kariya, S.9
Asai, H.10
-
12
-
-
10744228698
-
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. and Tsuji, S. (2004) Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein. Ann. Neurol., 55, 241-249.
-
(2004)
Ann. Neurol
, vol.55
, pp. 241-249
-
-
Sano, Y.1
Date, H.2
Igarashi, S.3
Onodera, O.4
Oyake, M.5
Takahashi, T.6
Hayashi, S.7
Morimatsu, M.8
Takahashi, H.9
Makifuchi, T.10
Fukuhara, N.11
Tsuji, S.12
-
13
-
-
8844265438
-
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. and Onodera, O. (2004) The FHA domain of aprataxin interacts with the C-terminal region of XRCC1. Biochem. Biophys. Res. Commun., 325, 1279-1285.
-
(2004)
Biochem. Biophys. Res. Commun
, vol.325
, pp. 1279-1285
-
-
Date, H.1
Igarashi, S.2
Sano, Y.3
Takahashi, T.4
Takahashi, T.5
Takano, H.6
Tsuji, S.7
Nishizawa, M.8
Onodera, O.9
-
14
-
-
0029842307
-
Reconstitution of DNA base excision-repair with purified human proteins: Interaction between DNA polymerase beta and the XRCC1 protein
-
Kubota, Y., Nash, R.A., Klungland, A., Schar, P., Barnes, D.E. and Lindahl, T. (1996) Reconstitution of DNA base excision-repair with purified human proteins: Interaction between DNA polymerase beta and the XRCC1 protein. EMBO J., 15, 6662-6670.
-
(1996)
EMBO J
, vol.15
, pp. 6662-6670
-
-
Kubota, Y.1
Nash, R.A.2
Klungland, A.3
Schar, P.4
Barnes, D.E.5
Lindahl, T.6
-
15
-
-
0031844311
-
XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage
-
Masson, M., Niedergang, C., Schreiber, V., Muller, S., Menissier-de Murcia, J. and de Murcia, G. (1998) XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage. Mol. Cell. Biol., 18, 3563-3571.
-
(1998)
Mol. Cell. Biol
, vol.18
, pp. 3563-3571
-
-
Masson, M.1
Niedergang, C.2
Schreiber, V.3
Muller, S.4
Menissier-de Murcia, J.5
de Murcia, G.6
-
16
-
-
0035890069
-
XRCC1 coordinates the initial and late stages of DNA abasic site repair through protein-protein interactions
-
Vidal, A.E., Boiteux, S., Hickson, I.D. and Radicella, J.P. (2001) XRCC1 coordinates the initial and late stages of DNA abasic site repair through protein-protein interactions. EMBO J., 20, 6530-6539.
-
(2001)
EMBO J
, vol.20
, pp. 6530-6539
-
-
Vidal, A.E.1
Boiteux, S.2
Hickson, I.D.3
Radicella, J.P.4
-
17
-
-
2342627913
-
-
Fan, J., Otterlei, M., Wong, H.K., Tomkinson, A.E. and Wilson, D.M. 3rd (2004) XRCC1 co-localizes and physically interacts with PCNA. Nucleic Acids Res., 32, 2193-2201.
-
Fan, J., Otterlei, M., Wong, H.K., Tomkinson, A.E. and Wilson, D.M. 3rd (2004) XRCC1 co-localizes and physically interacts with PCNA. Nucleic Acids Res., 32, 2193-2201.
-
-
-
-
18
-
-
61749094512
-
Defective DNA ligation during short-patch single-strand break repair in ataxia oculomotor apraxia-1
-
Reynolds, J.J., El-Khamisy, S.F., Katyal, S., Clements, P., McKinnon, P.J. and Caldecott, K.W. (2008) Defective DNA ligation during short-patch single-strand break repair in ataxia oculomotor apraxia-1. Mol. Cell. Biol, 29, 1354-1362.
-
(2008)
Mol. Cell. Biol
, vol.29
, pp. 1354-1362
-
-
Reynolds, J.J.1
El-Khamisy, S.F.2
Katyal, S.3
Clements, P.4
McKinnon, P.J.5
Caldecott, K.W.6
-
19
-
-
33749821755
-
The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates
-
Ahel, I., Rass, U., El-Khamisy, S.F., Katyal, S., Clements, P.M., McKinnon, P.J., Caldecott, K.W. and West, S.C. (2006) The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates. Nature, 443, 713-716.
-
(2006)
Nature
, vol.443
, pp. 713-716
-
-
Ahel, I.1
Rass, U.2
El-Khamisy, S.F.3
Katyal, S.4
Clements, P.M.5
McKinnon, P.J.6
Caldecott, K.W.7
West, S.C.8
-
20
-
-
34248215322
-
Actions of aprataxin in multiple DNA repair pathways
-
Rass, U., Ahel, I. and West, S.C. (2007) Actions of aprataxin in multiple DNA repair pathways. J. Biol. Chem., 282, 9469-9474.
-
(2007)
J. Biol. Chem
, vol.282
, pp. 9469-9474
-
-
Rass, U.1
Ahel, I.2
West, S.C.3
-
21
-
-
0028927261
-
Reactions of oxyl radicals with DNA
-
Breen, A.P. and Murphy, J.A. (1995) Reactions of oxyl radicals with DNA. Free Radic. Biol. Med., 18, 1033-1077.
-
(1995)
Free Radic. Biol. Med
, vol.18
, pp. 1033-1077
-
-
Breen, A.P.1
Murphy, J.A.2
-
22
-
-
62349120246
-
Base excision repair: The long and short of it
-
Robertson, A.B., Klungland, A., Rognes, T. and Leiros, I. (2009) Base excision repair: The long and short of it. Cell. Mol. Life Sci., 66, 981-993.
-
(2009)
Cell. Mol. Life Sci
, vol.66
, pp. 981-993
-
-
Robertson, A.B.1
Klungland, A.2
Rognes, T.3
Leiros, I.4
-
23
-
-
48249095920
-
Single-strand break repair and genetic disease
-
Caldecott, K.W. (2008) Single-strand break repair and genetic disease. Nat. Rev. Genet., 9, 619-631.
-
(2008)
Nat. Rev. Genet
, vol.9
, pp. 619-631
-
-
Caldecott, K.W.1
-
24
-
-
0142009654
-
A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage
-
El-Khamisy, S.F., Masutani, M., Suzuki, H. and Caldecott, K.W. (2003) A requirement for PARP-1 for the assembly or stability of XRCC1 nuclear foci at sites of oxidative DNA damage. Nucleic Acids Res., 31 5526-5533.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 5526-5533
-
-
El-Khamisy, S.F.1
Masutani, M.2
Suzuki, H.3
Caldecott, K.W.4
-
25
-
-
4344685333
-
The PARP superfamily
-
Ame, J.C., Spenlehauer, C. and de Murcia, G. (2004) The PARP superfamily. Bioessays, 26, 882-893.
-
(2004)
Bioessays
, vol.26
, pp. 882-893
-
-
Ame, J.C.1
Spenlehauer, C.2
de Murcia, G.3
-
26
-
-
0034720734
-
Base excision repair is impaired in mammalian cells lacking Poly(ADP-ribose) polymerase-1
-
Dantzer, F., de La Rubia, G., Menissier-De Murcia, J., Hostomsky, Z., de Murcia, G. and Schreiber, V. (2000) Base excision repair is impaired in mammalian cells lacking Poly(ADP-ribose) polymerase-1. Biochemistry 39, 7559-7569.
-
(2000)
Biochemistry
, vol.39
, pp. 7559-7569
-
-
Dantzer, F.1
de La Rubia, G.2
Menissier-De Murcia, J.3
Hostomsky, Z.4
de Murcia, G.5
Schreiber, V.6
-
27
-
-
34547225606
-
Poly(ADP-ribose) polymerase 1 accelerates single-strand break repair in concert with poly(ADP-ribose) glycohydrolase
-
Fisher, A.E., Hochegger, H., Takeda, S. and Caldecott, K.W. (2007) Poly(ADP-ribose) polymerase 1 accelerates single-strand break repair in concert with poly(ADP-ribose) glycohydrolase. Mol. Cell. Biol., 27, 5597-5605.
-
(2007)
Mol. Cell. Biol
, vol.27
, pp. 5597-5605
-
-
Fisher, A.E.1
Hochegger, H.2
Takeda, S.3
Caldecott, K.W.4
-
28
-
-
0038381446
-
Poly(ADP-ribose) polymerase-1 (PARP-1) is required in murine cell lines for base excision repair of oxidative DNA damage in the absence of DNA polymerase beta
-
Le Page, F., Schreiber, V., Dherin, C., De Murcia, G. and Boiteux, S. (2003) Poly(ADP-ribose) polymerase-1 (PARP-1) is required in murine cell lines for base excision repair of oxidative DNA damage in the absence of DNA polymerase beta. J. Biol. Chem., 278, 18471-18477.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 18471-18477
-
-
Le Page, F.1
Schreiber, V.2
Dherin, C.3
De Murcia, G.4
Boiteux, S.5
-
29
-
-
11244280890
-
Involvement of Poly(ADP-ribose) Polymerase-1 and XRCC1/DNA Ligase III in an Alternative Route for DNA Double-strand Breaks Rejoining
-
Audebert, S. and Calsou (2004) Involvement of Poly(ADP-ribose) Polymerase-1 and XRCC1/DNA Ligase III in an Alternative Route for DNA Double-strand Breaks Rejoining. J. Biol. Chem., 279, 55117-55126.
-
(2004)
J. Biol. Chem
, vol.279
, pp. 55117-55126
-
-
Audebert, S.1
Calsou2
-
30
-
-
0032102896
-
DNA repair defect in poly(ADP-ribose) polymerase-deficient cell lines
-
Trucco, C., Oliver, F.J., de Murcia, G. and Menissier-de Murcia, J. (1998) DNA repair defect in poly(ADP-ribose) polymerase-deficient cell lines. Nucleic Acids Res., 26, 2644-2649.
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 2644-2649
-
-
Trucco, C.1
Oliver, F.J.2
de Murcia, G.3
Menissier-de Murcia, J.4
-
31
-
-
0034656991
-
Domain specific interaction in the XRCC1-DNA polymerase beta complex
-
Marintchev, A., Robertson, A., Dimitriadis, E.K., Prasad, R., Wilson, S.H. and Mullen, G.P. (2000) Domain specific interaction in the XRCC1-DNA polymerase beta complex. Nucleic Acids Res., 28, 2049-2059.
-
(2000)
Nucleic Acids Res
, vol.28
, pp. 2049-2059
-
-
Marintchev, A.1
Robertson, A.2
Dimitriadis, E.K.3
Prasad, R.4
Wilson, S.H.5
Mullen, G.P.6
-
32
-
-
0035837587
-
The major human abasic endonuclease: Formation, consequences and repair of abasic lesions in DNA
-
Wilson, D.M. III and Barsky, D. (2001) The major human abasic endonuclease: Formation, consequences and repair of abasic lesions in DNA. Mutat. Res., 485, 283-307.
-
(2001)
Mutat. Res
, vol.485
, pp. 283-307
-
-
Wilson III, D.M.1
Barsky, D.2
-
33
-
-
3142770341
-
APE1 is the major 30-phosphoglycolate activity in human cell extracts
-
Parsons, J.L., Dianova, I.I. and Dianov, G.L. (2004) APE1 is the major 30-phosphoglycolate activity in human cell extracts. Nucleic Acids Res., 32, 3531-3536.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 3531-3536
-
-
Parsons, J.L.1
Dianova, I.I.2
Dianov, G.L.3
-
34
-
-
17844365289
-
APE1-dependent repair of DNA single-strand breaks containing 3′-end 8-oxoguanine
-
Parsons, J.L., Dianova, I.I. and Dianov, G.L. (2005) APE1-dependent repair of DNA single-strand breaks containing 3′-end 8-oxoguanine. Nucleic Acids Res., 33, 2204-2209.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 2204-2209
-
-
Parsons, J.L.1
Dianova, I.I.2
Dianov, G.L.3
-
35
-
-
0036828697
-
AP endonuclease 1 coordinates flap endonuclease 1 and DNA ligase I activity in long patch base excision repair
-
Ranalli, T.A., Tom, S. and Bambara, R.A. (2002) AP endonuclease 1 coordinates flap endonuclease 1 and DNA ligase I activity in long patch base excision repair. J. Biol. Chem., 277, 41715-41724.
-
(2002)
J. Biol. Chem
, vol.277
, pp. 41715-41724
-
-
Ranalli, T.A.1
Tom, S.2
Bambara, R.A.3
-
36
-
-
0030740948
-
Interaction of human apurinic endonuclease and DNA polymerase beta in the base excision repair pathway
-
Bennett, R.A., Wilson, D.M. III, Wong, D. and Demple, B. (1997) Interaction of human apurinic endonuclease and DNA polymerase beta in the base excision repair pathway. Proc. Natl Acad. Sci. USA., 94, 7166-7169.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 7166-7169
-
-
Bennett, R.A.1
Wilson III, D.M.2
Wong, D.3
Demple, B.4
-
37
-
-
0032167424
-
Base excision repair initiation revealed by crystal structures and binding kinetics of human uracil-DNA glycosylase with DNA
-
Parikh, S.S., Mol, C.D., Slupphaug, G., Bharati, S., Krokan, H.E. and Tainer, J.A. (1998) Base excision repair initiation revealed by crystal structures and binding kinetics of human uracil-DNA glycosylase with DNA. EMBO J., 17, 5214-5226.
-
(1998)
EMBO J
, vol.17
, pp. 5214-5226
-
-
Parikh, S.S.1
Mol, C.D.2
Slupphaug, G.3
Bharati, S.4
Krokan, H.E.5
Tainer, J.A.6
-
38
-
-
0035869114
-
Mechanism of stimulation of the DNA glycosylase activity of hOGG1 by the major human AP endonuclease: Bypass of the AP lyase activity step
-
Vidal, A.E., Hickson, I.D., Boiteux, S. and Radicella, J.P. (2001) Mechanism of stimulation of the DNA glycosylase activity of hOGG1 by the major human AP endonuclease: Bypass of the AP lyase activity step. Nucleic Acids Res., 29, 1285-1292.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 1285-1292
-
-
Vidal, A.E.1
Hickson, I.D.2
Boiteux, S.3
Radicella, J.P.4
-
39
-
-
0034719372
-
DNA-bound structures and mutants reveal abasic DNA binding by APE1 and DNA repair coordination
-
Mol, C.D., Izumi, T., Mitra, S. and Tainer, J.A. (2000) DNA-bound structures and mutants reveal abasic DNA binding by APE1 and DNA repair coordination. Nature, 403, 451-456.
-
(2000)
Nature
, vol.403
, pp. 451-456
-
-
Mol, C.D.1
Izumi, T.2
Mitra, S.3
Tainer, J.A.4
-
40
-
-
0034093291
-
Passing the baton in base excision repair
-
Wilson, S.H. and Kunkel, T.A. (2000) Passing the baton in base excision repair. Nat. Struct. Biol., 7, 176-178.
-
(2000)
Nat. Struct. Biol
, vol.7
, pp. 176-178
-
-
Wilson, S.H.1
Kunkel, T.A.2
-
41
-
-
0035863739
-
Stimulation of human 8-oxoguanine-DNA glycosylase by AP-endonuclease: Potential coordination of the initial steps in base excision repair
-
Hill, J.W., Hazra, T.K., Izumi, T. and Mitra, S. (2001) Stimulation of human 8-oxoguanine-DNA glycosylase by AP-endonuclease: Potential coordination of the initial steps in base excision repair. Nucleic Acids Res., 29, 430-438.
-
(2001)
Nucleic Acids Res
, vol.29
, pp. 430-438
-
-
Hill, J.W.1
Hazra, T.K.2
Izumi, T.3
Mitra, S.4
-
42
-
-
0030816108
-
Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae
-
Radicella, J.P., Dherin, C., Desmaze, C., Fox, M.S. and Boiteux, S. (1997) Cloning and characterization of hOGG1, a human homolog of the OGG1 gene of Saccharomyces cerevisiae. Proc. Natl Acad. Sci. USA., 94, 8010-8015.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 8010-8015
-
-
Radicella, J.P.1
Dherin, C.2
Desmaze, C.3
Fox, M.S.4
Boiteux, S.5
-
43
-
-
34547138954
-
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. et al. (2007) Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends. Nucleic Acids Res., 35, 3797-3809.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 3797-3809
-
-
Takahashi, T.1
Tada, M.2
Igarashi, S.3
Koyama, A.4
Date, H.5
Yokoseki, A.6
Shiga, A.7
Yoshida, Y.8
Tsuji, S.9
Nishizawa, M.10
-
44
-
-
5744246254
-
MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder
-
Delia, D., Piane, M., Buscemi, G., Savio, C., Palmeri, S., Lulli, P., Carlessi, L., Fontanella, E. and Chessa, L. (2004) MRE11 mutations and impaired ATM-dependent responses in an Italian family with ataxia-telangiectasia-like disorder. Hum. Mol. Genet., 13, 2155-2163.
-
(2004)
Hum. Mol. Genet
, vol.13
, pp. 2155-2163
-
-
Delia, D.1
Piane, M.2
Buscemi, G.3
Savio, C.4
Palmeri, S.5
Lulli, P.6
Carlessi, L.7
Fontanella, E.8
Chessa, L.9
-
45
-
-
65149095154
-
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder
-
Waltes, R., Kalb, R., Gatei, M., Kijas, A.W., Stumm, M., Sobeck, A., Wieland, B., Varon, R., Lerenthal, Y., Lavin, M.F., Schindler, D. and Dörk, T. Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder. Am. J. Hum. Genet., 84, 605-616.
-
Am. J. Hum. Genet
, vol.84
, pp. 605-616
-
-
Waltes, R.1
Kalb, R.2
Gatei, M.3
Kijas, A.W.4
Stumm, M.5
Sobeck, A.6
Wieland, B.7
Varon, R.8
Lerenthal, Y.9
Lavin, M.F.10
Schindler, D.11
Dörk, T.12
-
46
-
-
0028157948
-
An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III
-
Caldecott, K., McKeown, C., Tucker, J., Ljungquist, S. and Thompson, L. (1994) An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III. Mol. Cell. Biol., 14, 68-76.
-
(1994)
Mol. Cell. Biol
, vol.14
, pp. 68-76
-
-
Caldecott, K.1
McKeown, C.2
Tucker, J.3
Ljungquist, S.4
Thompson, L.5
-
47
-
-
0018906390
-
(ADP-ribose)n participates in DNA excision repair
-
Durkacz, B.W., Omidiji, O., Gray, D.A. and Shall, S. (1980) (ADP-ribose)n participates in DNA excision repair. Nature, 283 593-596.
-
(1980)
Nature
, vol.283
, pp. 593-596
-
-
Durkacz, B.W.1
Omidiji, O.2
Gray, D.A.3
Shall, S.4
-
48
-
-
0035289536
-
Protective effects of PJ34, a novel, potent inhibitor of poly(ADP-ribose) polymerase (PARP) in in vitro and in vivo models of stroke
-
Abdelkarim, G.E., Gertz, K., Harms, C., Katchanov, J., Dirnagl, U., Szabó, C. and Endres, M. (2001) Protective effects of PJ34, a novel, potent inhibitor of poly(ADP-ribose) polymerase (PARP) in in vitro and in vivo models of stroke. Int. J. Mol. Med., 7, 255-260.
-
(2001)
Int. J. Mol. Med
, vol.7
, pp. 255-260
-
-
Abdelkarim, G.E.1
Gertz, K.2
Harms, C.3
Katchanov, J.4
Dirnagl, U.5
Szabó, C.6
Endres, M.7
-
49
-
-
19544376983
-
Live cell imaging of heavy-ion-induced radiation responses by beamline microscopy
-
Jakob, B., Rudolph, J.H., Gueven, N., Lavin, M.F. and Taucher-Scholz, G. (2005) Live cell imaging of heavy-ion-induced radiation responses by beamline microscopy. Radiat. Res., 163, 681-690.
-
(2005)
Radiat. Res
, vol.163
, pp. 681-690
-
-
Jakob, B.1
Rudolph, J.H.2
Gueven, N.3
Lavin, M.F.4
Taucher-Scholz, G.5
-
50
-
-
0038301384
-
Biological imaging of heavy charged-particle tracks
-
Jakob, B., Scholz, M. and Taucher-Scholz, G. (2003) Biological imaging of heavy charged-particle tracks. Radiat. Res., 159, 676-684.
-
(2003)
Radiat. Res
, vol.159
, pp. 676-684
-
-
Jakob, B.1
Scholz, M.2
Taucher-Scholz, G.3
-
51
-
-
0035109757
-
Recessive ataxia with ocular apraxia: Review of 22 Portuguese patients
-
Barbot, C., Coutinho, P., Chorao, R., Ferreira, C., Barros, J., Fineza, I., Dias, K., Monteiro, J., Guimaraes, A., Mendonca, P. et al. (2001) Recessive ataxia with ocular apraxia: Review of 22 Portuguese patients. Arch. Neurol., 58, 201-205.
-
(2001)
Arch. Neurol
, vol.58
, pp. 201-205
-
-
Barbot, C.1
Coutinho, P.2
Chorao, R.3
Ferreira, C.4
Barros, J.5
Fineza, I.6
Dias, K.7
Monteiro, J.8
Guimaraes, A.9
Mendonca, P.10
-
52
-
-
42649132797
-
Oxidative stress in neurodegeneration and available means of protection
-
Fatokun, A.A., Stone, T.W. and Smith, R.A. (2008) Oxidative stress in neurodegeneration and available means of protection. Front. Biosci. 13, 3288-3311.
-
(2008)
Front. Biosci
, vol.13
, pp. 3288-3311
-
-
Fatokun, A.A.1
Stone, T.W.2
Smith, R.A.3
-
53
-
-
34247177448
-
A subgroup of spinocerebellar ataxias defective in DNA damage responses
-
Gueven, N., Chen, P., Nakamura, J., Becherel, O.J., Kijas, A.W., Grattan-Smith, P. and Lavin, M.F. (2007) A subgroup of spinocerebellar ataxias defective in DNA damage responses. Neuroscience, 145 1418-1425.
-
(2007)
Neuroscience
, vol.145
, pp. 1418-1425
-
-
Gueven, N.1
Chen, P.2
Nakamura, J.3
Becherel, O.J.4
Kijas, A.W.5
Grattan-Smith, P.6
Lavin, M.F.7
-
54
-
-
15044357229
-
The novel human gene aprataxin is directly involved in DNA single-strand-break repair
-
Mosesso, P., Piane, M., Palitti, F., Pepe, G., Penna, S. and Chessa, L. (2005) The novel human gene aprataxin is directly involved in DNA single-strand-break repair. Cell. Mol. Life Sci., 62, 485-491.
-
(2005)
Cell. Mol. Life Sci
, vol.62
, pp. 485-491
-
-
Mosesso, P.1
Piane, M.2
Palitti, F.3
Pepe, G.4
Penna, S.5
Chessa, L.6
-
55
-
-
33744937625
-
Aprataxin forms a discrete branch in the HIT (histidine triad) superfamily of proteins with both DNA/RNA binding and nucleotide hydrolase activities
-
Kijas, A.W., Harris, J.L., Harris, J.M. and Lavin, M.F. (2006) Aprataxin forms a discrete branch in the HIT (histidine triad) superfamily of proteins with both DNA/RNA binding and nucleotide hydrolase activities. J. Biol. Chem., 281, 13939-13948.
-
(2006)
J. Biol. Chem
, vol.281
, pp. 13939-13948
-
-
Kijas, A.W.1
Harris, J.L.2
Harris, J.M.3
Lavin, M.F.4
-
56
-
-
33745614891
-
Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription
-
Becherel, O.J., Gueven, N., Birrell, G.W., Schreiber, V., Suraweera, A., Jakob, B., Taucher-Scholz, G. and Lavin, M.F. (2006) Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription. Hum. Mol. Genet., 15, 2239-2249.
-
(2006)
Hum. Mol. Genet
, vol.15
, pp. 2239-2249
-
-
Becherel, O.J.1
Gueven, N.2
Birrell, G.W.3
Schreiber, V.4
Suraweera, A.5
Jakob, B.6
Taucher-Scholz, G.7
Lavin, M.F.8
-
57
-
-
0030271885
-
A Method for Isolation and Purification of Specific Antibodies to a Protein Fused to the GST
-
Bar-Peled, M. and Raikhel, V. (1996) A Method for Isolation and Purification of Specific Antibodies to a Protein Fused to the GST. Analytical Biochem., 241, 140-142.
-
(1996)
Analytical Biochem
, vol.241
, pp. 140-142
-
-
Bar-Peled, M.1
Raikhel, V.2
-
58
-
-
34250775522
-
Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage
-
Suraweera, A., Becherel, O.J., Chen, P., Rundle, N., Woods, R., Nakamura, J., Gatei, M., Criscuolo, C., Filla, A., Chessa, L. et al. (2007) Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage. J. Cell. Biol. 177, 969-979.
-
(2007)
J. Cell. Biol
, vol.177
, pp. 969-979
-
-
Suraweera, A.1
Becherel, O.J.2
Chen, P.3
Rundle, N.4
Woods, R.5
Nakamura, J.6
Gatei, M.7
Criscuolo, C.8
Filla, A.9
Chessa, L.10
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