-
1
-
-
4043133287
-
ATR couples FANCD2 monoubiquitination to the DNA-damage response
-
Andreassen, P. R., A. D. D'Andrea, and T. Taniguchi. 2004. ATR couples FANCD2 monoubiquitination to the DNA-damage response. Genes Dev. 18:1958-1963.
-
(2004)
Genes Dev.
, vol.18
, pp. 1958-1963
-
-
Andreassen, P.R.1
D'Andrea, A.D.2
Taniguchi, T.3
-
2
-
-
0032508504
-
Enhanced phosphorylation of p53 by ATM in response to DNA damage
-
Banin, S., L. Moyal, S. Shieh, Y. Taya, C. Anderson, L. Chessa, N. Smorodinsky, C. Prives, Y. Reiss, Y. Shiloh, and Y. Ziv. 1998. Enhanced phosphorylation of p53 by ATM in response to DNA damage. Science 281:1674-1677.
-
(1998)
Science
, vol.281
, pp. 1674-1677
-
-
Banin, S.1
Moyal, L.2
Shieh, S.3
Taya, Y.4
Anderson, C.5
Chessa, L.6
Smorodinsky, N.7
Prives, C.8
Reiss, Y.9
Shiloh, Y.10
Ziv, Y.11
-
3
-
-
25144503943
-
The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair
-
Bridge, W. L., C. J. Vandenberg, R. J. Franklin, and K. Hiom. 2005. The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair. Nat. Genet. 37:953-957.
-
(2005)
Nat. Genet.
, vol.37
, pp. 953-957
-
-
Bridge, W.L.1
Vandenberg, C.J.2
Franklin, R.J.3
Hiom, K.4
-
4
-
-
0032508608
-
Activation of the ATM kinase by ionizing radiation and phosphorylation of p53
-
Canman, C. E., D. S. Lim, K. A. Cimprich, Y. Taya, K. Tamai, K. Sakaguchi, E. Appella, M. B. Kastan, and J. D. Siliciano. 1998. Activation of the ATM kinase by ionizing radiation and phosphorylation of p53. Science 281:1677-1679.
-
(1998)
Science
, vol.281
, pp. 1677-1679
-
-
Canman, C.E.1
Lim, D.S.2
Cimprich, K.A.3
Taya, Y.4
Tamai, K.5
Sakaguchi, K.6
Appella, E.7
Kastan, M.B.8
Siliciano, J.D.9
-
5
-
-
0033527717
-
Requirement of ATM-dependent phosphorylation of brca1 in the DNA damage response to double-strand breaks
-
Cortez, D., Y. Wang, J. Qin, and S. J. Elledge. 1999. Requirement of ATM-dependent phosphorylation of brca1 in the DNA damage response to double-strand breaks. Science 286:1162-1166.
-
(1999)
Science
, vol.286
, pp. 1162-1166
-
-
Cortez, D.1
Wang, Y.2
Qin, J.3
Elledge, S.J.4
-
6
-
-
0037268338
-
The Fanconi anaemia/BRCA pathway
-
D'Andrea, A. D., and M. Grompe. 2003. The Fanconi anaemia/BRCA pathway. Nat. Rev. Cancer 3:23-34.
-
(2003)
Nat. Rev. Cancer
, vol.3
, pp. 23-34
-
-
D'Andrea, A.D.1
Grompe, M.2
-
7
-
-
0034813499
-
Fanconi anemia protein, FANCG, is a phosphoprotein and is upregulated with FANCA after TNF-alpha treatment
-
Fulaki, M., S. Watanabe, S. Kajigaya, and J. M. Liu. 2001. Fanconi anemia protein, FANCG, is a phosphoprotein and is upregulated with FANCA after TNF-alpha treatment. Biochem. Biophys. Res. Commun. 281:347-351.
-
(2001)
Biochem. Biophys. Res. Commun.
, vol.281
, pp. 347-351
-
-
Fulaki, M.1
Watanabe, S.2
Kajigaya, S.3
Liu, J.M.4
-
8
-
-
0035105291
-
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway
-
Garcia-Higuera, I., T. Taniguchi, S. Ganesan, M. S. Meyn, C. Timmers, J. Hejna, M. Grompe, and A. D. D'Andrea. 2001. Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway. Mol. Cell 7:249-262.
-
(2001)
Mol. Cell
, vol.7
, pp. 249-262
-
-
Garcia-Higuera, I.1
Taniguchi, T.2
Ganesan, S.3
Meyn, M.S.4
Timmers, C.5
Hejna, J.6
Grompe, M.7
D'Andrea, A.D.8
-
9
-
-
0034125103
-
Role for ATM in DNA damage-induced phosphorylation of BRCA1
-
Gatei, M., S. P. Scott, I., Filippovitch, N. Soronika, M. F. Lavin, B. Weber, and K. K. Khanna. 2000. Role for ATM in DNA damage-induced phosphorylation of BRCA1. Cancer Res. 60:3299-3304.
-
(2000)
Cancer Res.
, vol.60
, pp. 3299-3304
-
-
Gatei, M.1
Scott, S.P.2
Filippovitch, I.3
Soronika, N.4
Lavin, M.F.5
Weber, B.6
Khanna, K.K.7
-
10
-
-
0038644654
-
Fanconi anemia protein complex: Mapping protein interactions in the yeast 2- and 3-hybrid systems
-
Gordon, S. M., and M. Buchwald. 2003. Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems. Blood 102:136-141.
-
(2003)
Blood
, vol.102
, pp. 136-141
-
-
Gordon, S.M.1
Buchwald, M.2
-
11
-
-
0035379611
-
The emerging genetic and molecular basis of Fanconi anaemia
-
Joenje, H., and K. J. Patel. 2001. The emerging genetic and molecular basis of Fanconi anaemia. Nat. Rev. Genet. 2:446-457.
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 446-457
-
-
Joenje, H.1
Patel, K.J.2
-
12
-
-
29144506137
-
The Fanconi anemia/BRCA pathway: New faces in the crowd
-
Kennedy, R. D., and A. D. D'Andrea. 2005. The Fanconi anemia/BRCA pathway: new faces in the crowd. Genes Dev. 19:2925-2940.
-
(2005)
Genes Dev.
, vol.19
, pp. 2925-2940
-
-
Kennedy, R.D.1
D'Andrea, A.D.2
-
13
-
-
0033621392
-
Substrate specificities and identification of putative substrates of ATM kinase family members
-
Kim, S. T., D. S. Lim, C. E. Canman, and M. B. Kastan. 1999. Substrate specificities and identification of putative substrates of ATM kinase family members. J. Biol. Chem. 274:37538-37543.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 37538-37543
-
-
Kim, S.T.1
Lim, D.S.2
Canman, C.E.3
Kastan, M.B.4
-
14
-
-
0036500555
-
Involvement of the cohesin protein, Smc1, in Atm-dependent and independent responses to DNA damage
-
Kim, S. T., B. Xu, and M. B. Kastan. 2002. Involvement of the cohesin protein, Smc1, in Atm-dependent and independent responses to DNA damage. Genes Dev. 16:560-570.
-
(2002)
Genes Dev.
, vol.16
, pp. 560-570
-
-
Kim, S.T.1
Xu, B.2
Kastan, M.B.3
-
15
-
-
25144457604
-
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group
-
Levitus, M., Q. Waisfisz, B. C. Godthelp, Y. de Vries, S. Hussain, W. W. Wiegant, E. Elghalbzouri-Maghrani, J. Steltenpool, M. A. Roolmans, G. Pals, F. Arwert, C. G. Mathew, M. Z. Zdzienicka, K. Hiom, J. P. De Winter, and H. Joenje. 2005. The DNA helicase BRIP1 is defective in Fanconi anemia complementation group Nat. Genet. 37:934-935.
-
(2005)
Nat. Genet.
, vol.37
, pp. 934-935
-
-
Levitus, M.1
Waisfisz, Q.2
Godthelp, B.C.3
De Vries, Y.4
Hussain, S.5
Wiegant, W.W.6
Elghalbzouri-Maghrani, E.7
Steltenpool, J.8
Roolmans, M.A.9
Pals, G.10
Arwert, F.11
Mathew, C.G.12
Zdzienicka, M.Z.13
Hiom, K.14
De Winter, J.P.15
Joenje, H.16
-
16
-
-
25144497571
-
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
-
Levran, O., C. Attwooll, R. T. Henry, K. L. Milton, K. Neveling, P. Rio, S. D. Batish, R. Kalb, E. Velleuer, S. Barral, J. Ott, J. Petrini, D. Schindler, H. Hanenberg, and A. D. Auerbach. 2005. The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia. Nat. Genet. 37:931-933
-
(2005)
Nat. Genet.
, vol.37
, pp. 931-933
-
-
Levran, O.1
Attwooll, C.2
Henry, R.T.3
Milton, K.L.4
Neveling, K.5
Rio, P.6
Batish, S.D.7
Kalb, R.8
Velleuer, E.9
Barral, S.10
Ott, J.11
Petrini, J.12
Schindler, D.13
Hanenberg, H.14
Auerbach, A.D.15
-
17
-
-
0034611728
-
ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway
-
Lim, D. S., S. T. Kim, B. Xu, R. S. Maser, J. Lin, J. H. Petrini, and M. B. Kastan. 2000. ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway. Nature 404:613-617.
-
(2000)
Nature
, vol.404
, pp. 613-617
-
-
Lim, D.S.1
Kim, S.T.2
Xu, B.3
Maser, R.S.4
Lin, J.5
Petrini, J.H.6
Kastan, M.B.7
-
18
-
-
24944575242
-
BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ
-
Litman, R., M. Peng, Z. Jin, F. Zhang, J. Zhang, S. Powell, P. R. Andreassen, and S. B. Cantor. 2005. BACH1 is critical for homologous recombination and appears to be the Fanconi anemia gene product FANCJ. Cancer Cell 8:255-265.
-
(2005)
Cancer Cell
, vol.8
, pp. 255-265
-
-
Litman, R.1
Peng, M.2
Jin, Z.3
Zhang, F.4
Zhang, J.5
Powell, S.6
Andreassen, P.R.7
Cantor, S.B.8
-
19
-
-
0141484612
-
A novel ubiquitin ligase is deficient in Fanconi anemia
-
Meetei, A. R., J. P. de Winter, A. L. Medhurst, M. Wallisch, Q. Waisfisz, H. J. van de Vrugt, A. B. Oostra, Z. Yan, C. Ling, C. E. Bishop, M. E. Hoatlin, H. Joenje, and W. Wang. 2003. A novel ubiquitin ligase is deficient in Fanconi anemia. Nat. Genet. 35:165-170.
-
(2003)
Nat. Genet.
, vol.35
, pp. 165-170
-
-
Meetei, A.R.1
De Winter, J.P.2
Medhurst, A.L.3
Wallisch, M.4
Waisfisz, Q.5
Van De Vrugt, H.J.6
Oostra, A.B.7
Yan, Z.8
Ling, C.9
Bishop, C.E.10
Hoatlin, M.E.11
Joenje, H.12
Wang, W.13
-
20
-
-
25144449181
-
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M
-
Meetei, A. R., A. L. Medhurst, C. Ling, Y. Xue, T. R. Singh, P. Bier, J. Steltenpool, S. Stone, I. Dokal, C. G. Mathew, M. Hoatlin, H. Joenje, J. P. de Winter, and W. Wang. 2005. A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M. Nat. Genet. 37:958-963.
-
(2005)
Nat. Genet.
, vol.37
, pp. 958-963
-
-
Meetei, A.R.1
Medhurst, A.L.2
Ling, C.3
Xue, Y.4
Singh, T.R.5
Bier, P.6
Steltenpool, J.7
Stone, S.8
Dokal, I.9
Mathew, C.G.10
Hoatlin, M.11
Joenje, H.12
De Winter, J.P.13
Wang, W.14
-
21
-
-
0038642027
-
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome
-
Meetei, A. R., S. Sechi, M. Wallisch, D. Yang, M. K. Young, H. Joenje, M. E. Hoatlin, and W. Wang. 2003. A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome. Mol. Cell. Biol. 23:3417-3426.
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 3417-3426
-
-
Meetei, A.R.1
Sechi, S.2
Wallisch, M.3
Yang, D.4
Young, M.K.5
Joenje, H.6
Hoatlin, M.E.7
Wang, W.8
-
22
-
-
11244337035
-
The Fanconi anemia core complex associates with chromatin during S phase
-
Mi, J., and G. M. Kupfer. 2004. The Fanconi anemia core complex associates with chromatin during S phase. Blood 105:759-766.
-
(2004)
Blood
, vol.105
, pp. 759-766
-
-
Mi, J.1
Kupfer, G.M.2
-
23
-
-
4544253225
-
FANCG is phosphorylated at serines 383 and 387 during mitosis
-
Mi, J., F. Qiao, J. B. Wilson, A. A. High, M. J. Schroeder, P. T. Stukenberg, A. Moss, J. Shabanowitz, D. F. Hunt, N. J. Jones, and G. M. Kupfer. 2004. FANCG is phosphorylated at serines 383 and 387 during mitosis. Mol. Cell. Biol. 24:8576-8585.
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 8576-8585
-
-
Mi, J.1
Qiao, F.2
Wilson, J.B.3
High, A.A.4
Schroeder, M.J.5
Stukenberg, P.T.6
Moss, A.7
Shabanowitz, J.8
Hunt, D.F.9
Jones, N.J.10
Kupfer, G.M.11
-
24
-
-
12844263398
-
Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatin
-
Montes de Oca, R., P. R. Andreassen, S. P. Margossian, R. C. Gregory, T. Taniguchi, X. Wang, S. Houghtaling, M. Grompe, and A. D. D'Andrea. 2005. Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatin. Blood 105:1003-1009.
-
(2005)
Blood
, vol.105
, pp. 1003-1009
-
-
De Montes Oca, R.1
Andreassen, P.R.2
Margossian, S.P.3
Gregory, R.C.4
Taniguchi, T.5
Wang, X.6
Houghtaling, S.7
Grompe, M.8
D'Andrea, A.D.9
-
25
-
-
0030969423
-
Fragments of ATM which have dominant-negative or complementing activity
-
Morgan, S. E., C. Lovly, T. K. Pandita, Y. Shiloh, and M. B. Kastan. 1997. Fragments of ATM which have dominant-negative or complementing activity. Mol. Cell. Biol. 17:2020-2029.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 2020-2029
-
-
Morgan, S.E.1
Lovly, C.2
Pandita, T.K.3
Shiloh, Y.4
Kastan, M.B.5
-
26
-
-
26944499485
-
The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway
-
Mosedale, G., W. Niedzwiedz, A. Alpi, F. Perrina, J. B. Pereira-Leal, M. Johnson, F. Langevin, P. Pace, and K. J. Patel. 2005. The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway. Nat. Struct. Mol. Biol. 12:763-771.
-
(2005)
Nat. Struct. Mol. Biol.
, vol.12
, pp. 763-771
-
-
Mosedale, G.1
Niedzwiedz, W.2
Alpi, A.3
Perrina, F.4
Pereira-Leal, J.B.5
Johnson, M.6
Langevin, F.7
Pace, P.8
Patel, K.J.9
-
27
-
-
0031657241
-
Functional activity of the Fanconi anemia protein FAA requires FAC binding and nuclear localization
-
Naf, D., G. M. Kupfer, A. Suliman, K. Lambert, and A. D. D'Andrea. 1998. Functional activity of the Fanconi anemia protein FAA requires FAC binding and nuclear localization. Mol. Cell. Biol. 18:5952-5960.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 5952-5960
-
-
Naf, D.1
Kupfer, G.M.2
Suliman, A.3
Lambert, K.4
D'Andrea, A.D.5
-
28
-
-
12844286052
-
Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair
-
Nakanishi, K., Y. G. Yang, A. J. Pierce, T. Taniguchi, M. Digweed, A. D. D'Andrea, Z. Q. Wang, and M. Jasin. 2005. Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair. Proc. Natl. Acad. Sci. USA 102:1110-1115.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 1110-1115
-
-
Nakanishi, K.1
Yang, Y.G.2
Pierce, A.J.3
Taniguchi, T.4
Digweed, M.5
D'Andrea, A.D.6
Wang, Z.Q.7
Jasin, M.8
-
29
-
-
13244291457
-
The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway
-
Nijman, S. M., T. T. Huang, A. M. Dirac, T. R. Brummelkamp, R. M. Kerkhoven, A. D. D'Andrea, and R. Bernards. 2005. The deubiquitinating enzyme USP1 regulates the Fanconi anemia pathway. Mol. Cell 17:331-339.
-
(2005)
Mol. Cell
, vol.17
, pp. 331-339
-
-
Nijman, S.M.1
Huang, T.T.2
Dirac, A.M.3
Brummelkamp, T.R.4
Kerkhoven, R.M.5
D'Andrea, A.D.6
Bernards, R.7
-
30
-
-
18444384217
-
FANCE: The link between Fanconi anaemia complex assembly and activity
-
Pace, P., M. Johnson, W. M. Tan, G. Mosedale, C. Sng, M. Hoatlin, J. de Winter, H. Joenje, F. Gergely, and K. J. Patel. 2002. FANCE: the link between Fanconi anaemia complex assembly and activity. EMBO J. 21:3414-3423.
-
(2002)
EMBO J.
, vol.21
, pp. 3414-3423
-
-
Pace, P.1
Johnson, M.2
Tan, W.M.3
Mosedale, G.4
Sng, C.5
Hoatlin, M.6
De Winter, J.7
Joenje, H.8
Gergely, F.9
Patel, K.J.10
-
31
-
-
3242670803
-
ATR and ATM regulate the timing of DNA replication origin firing
-
Shechter, D., V. Costanzo, and J. Gautier. 2004. ATR and ATM regulate the timing of DNA replication origin firing. Nat. Cell Biol. 6:648-655.
-
(2004)
Nat. Cell Biol.
, vol.6
, pp. 648-655
-
-
Shechter, D.1
Costanzo, V.2
Gautier, J.3
-
32
-
-
21444434023
-
ATM and ATR check in on origins: A dynamic model for origin selection and activation
-
Shechter, D., and J. Gautier. 2005. ATM and ATR check in on origins: a dynamic model for origin selection and activation. Cell Cycle 4:235-238.
-
(2005)
Cell Cycle
, vol.4
, pp. 235-238
-
-
Shechter, D.1
Gautier, J.2
-
33
-
-
20244388673
-
Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets, and DNA breakage
-
Syljuasen, R. G., C. S. Sorensen, L. T. Hansen, K. Fugger, C. Lundin, F. Johansson, T. Helleday, M. Sehested, J. Lukas, and J. Bartek. 2005. Inhibition of human Chk1 causes increased initiation of DNA replication, phosphorylation of ATR targets, and DNA breakage. Mol. Cell. Biol. 25:3553-3562.
-
(2005)
Mol. Cell. Biol.
, vol.25
, pp. 3553-3562
-
-
Syljuasen, R.G.1
Sorensen, C.S.2
Hansen, L.T.3
Fugger, K.4
Lundin, C.5
Johansson, F.6
Helleday, T.7
Sehested, M.8
Lukas, J.9
Bartek, J.10
-
34
-
-
0036785375
-
S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51
-
Taniguchi, T., I. Garcia-Higuera, P. R. Andreassen, R. C. Gregory, M. Grompe, and A. D. D'Andrea. 2002. S-phase-specific interaction of the Fanconi anemia protein, FANCD2, with BRCA1 and RAD51. Blood 100:2414-2420.
-
(2002)
Blood
, vol.100
, pp. 2414-2420
-
-
Taniguchi, T.1
Garcia-Higuera, I.2
Andreassen, P.R.3
Gregory, R.C.4
Grompe, M.5
D'Andrea, A.D.6
-
35
-
-
0037123768
-
Convergence of the Fanconi anemia and ataxia telangiectasia signaling pathways
-
Taniguchi, T., I. Garcia-Higuera, B. Xu, P. R. Andreassen, R. C. Gregory, S. T. Kim, W. S. Lane, M. B. Kastan, and A. D. D'Andrea. 2002. Convergence of the Fanconi anemia and ataxia telangiectasia signaling pathways. Cell 109:459-472.
-
(2002)
Cell
, vol.109
, pp. 459-472
-
-
Taniguchi, T.1
Garcia-Higuera, I.2
Xu, B.3
Andreassen, P.R.4
Gregory, R.C.5
Kim, S.T.6
Lane, W.S.7
Kastan, M.B.8
D'Andrea, A.D.9
-
36
-
-
2942705849
-
Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin
-
Wang, X., P. R. Andreassen, and A. D. D'Andrea. 2004. Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin. Mol. Cell. Biol. 24:5850-5862.
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 5850-5862
-
-
Wang, X.1
Andreassen, P.R.2
D'Andrea, A.D.3
-
37
-
-
0034713466
-
ATM phosphorylation of Nijmegen breakage syndrome protein is required in a DNA damage response
-
Wu, X., V. Ranganathan, D. S. Weisman, W. F. Heine, D. N. Ciccone, T. B. O'Neill, K. E. Crick, K. A. Pierce, W. S. Lane, G. Rathbun, D. M. Livingston, and D. T. Weaver. 2000. ATM phosphorylation of Nijmegen breakage syndrome protein is required in a DNA damage response. Nature 405:477-482.
-
(2000)
Nature
, vol.405
, pp. 477-482
-
-
Wu, X.1
Ranganathan, V.2
Weisman, D.S.3
Heine, W.F.4
Ciccone, D.N.5
O'Neill, T.B.6
Crick, K.E.7
Pierce, K.A.8
Lane, W.S.9
Rathbun, G.10
Livingston, D.M.11
Weaver, D.T.12
-
39
-
-
0032573229
-
The Fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation
-
Yamashita, T., G. M. Kupfer, D. Naf, A. Suliman, H. Joenje, S. Asano, and A. D. D'Andrea. 1998. The Fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation. Proc. Natl. Acad. Sci. USA 95:13085-13090.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13085-13090
-
-
Yamashita, T.1
Kupfer, G.M.2
Naf, D.3
Suliman, A.4
Joenje, H.5
Asano, S.6
D'Andrea, A.D.7
-
40
-
-
0036500690
-
SMC1 is a downstream effector in the ATM/NBS1 branch of the human S-phase checkpoint
-
Yazdi, P. T., Y. Wang, S. Zhao, N. Patel, E. Y. Lee, and J. Qin. 2002. SMC1 is a downstream effector in the ATM/NBS1 branch of the human S-phase checkpoint. Genes Dev. 16:571-582.
-
(2002)
Genes Dev.
, vol.16
, pp. 571-582
-
-
Yazdi, P.T.1
Wang, Y.2
Zhao, S.3
Patel, N.4
Lee, E.Y.5
Qin, J.6
-
41
-
-
20744436198
-
ATM activation and its recruitment to damaged DNA require binding to the C terminus of Nbsl
-
You, Z., C. Chahwan, J. Bailis, T. Hunter, and P. Russell. 2005. ATM activation and its recruitment to damaged DNA require binding to the C terminus of Nbsl. Mol. Cell. Biol. 25:5363-5379.
-
(2005)
Mol. Cell. Biol.
, vol.25
, pp. 5363-5379
-
-
You, Z.1
Chahwan, C.2
Bailis, J.3
Hunter, T.4
Russell, P.5
-
42
-
-
0019506288
-
Cell death, chromosome damage and mitotic delay in normal human, ataxia telangiectasia and retinoblastoma fibroblasts after X-irradiation
-
Zampetti-Bosseler, F., and D. Scott. 1981. Cell death, chromosome damage and mitotic delay in normal human, ataxia telangiectasia and retinoblastoma fibroblasts after X-irradiation. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 39:547-558.
-
(1981)
Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med.
, vol.39
, pp. 547-558
-
-
Zampetti-Bosseler, F.1
Scott, D.2
-
43
-
-
0034713393
-
Functional link between ataxia-telangiectasia and Nijmegen breakage syndrome gene products
-
Zhao, S., Y.-C. Weng, S.-S. F. Yuan, Y.-T. Lin, H.-C. Hsu, S.-C. J. Lin, E. Gerbino, M.-H. Song, M. Z. Zdzienicka, R. A. Gatti, J. W. Shay, Y. Ziv, Y. Shiloh, and E. Y.-H. P. Lee. 2000. Functional link between ataxia-telangiectasia and Nijmegen breakage syndrome gene products. Nature 405:473-477.
-
(2000)
Nature
, vol.405
, pp. 473-477
-
-
Zhao, S.1
Weng, Y.-C.2
Yuan, S.-S.F.3
Lin, Y.-T.4
Hsu, H.-C.5
Lin, S.-C.J.6
Gerbino, E.7
Song, M.-H.8
Zdzienicka, M.Z.9
Gatti, R.A.10
Shay, J.W.11
Ziv, Y.12
Shiloh, Y.13
Lee, E.Y.-H.P.14
-
44
-
-
0030797708
-
Recombinant ATM protein complements the cellular A-T phenotype
-
Ziv, Y., A. Bar-Shira, I. Pecker, P. Russell, T. J. Jorgensen, I. Tsarfati, and Y. Shiloh. 1997. Recombinant ATM protein complements the cellular A-T phenotype. Oncogene 15:159-167.
-
(1997)
Oncogene
, vol.15
, pp. 159-167
-
-
Ziv, Y.1
Bar-Shira, A.2
Pecker, I.3
Russell, P.4
Jorgensen, T.J.5
Tsarfati, I.6
Shiloh, Y.7
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