-
1
-
-
0037178719
-
Segregating sister genomes: The molecular biology of chromosome separation
-
Nasmyth, K. (2002) Segregating sister genomes: The molecular biology of chromosome separation. Science 297, 559-565.
-
(2002)
Science
, vol.297
, pp. 559-565
-
-
Nasmyth, K.1
-
2
-
-
84883212203
-
Cohesin in development and disease
-
Remeseiro, S., Cuadrado, A. and Losada, A. (2013) Cohesin in development and disease. Development 140, 3715-3718.
-
(2013)
Development
, vol.140
, pp. 3715-3718
-
-
Remeseiro, S.1
Cuadrado, A.2
Losada, A.3
-
3
-
-
0034645067
-
Characterization of vertebrate cohesin complexes and their regulation in prophase
-
Sumara, I., Vorlaufer, E., Gieffers, C., Peters, B. H. and Peters, J. M. (2000) Characterization of vertebrate cohesin complexes and their regulation in prophase. J. Cell Biol. 151, 749-762.
-
(2000)
J. Cell Biol.
, vol.151
, pp. 749-762
-
-
Sumara, I.1
Vorlaufer, E.2
Gieffers, C.3
Peters, B.H.4
Peters, J.M.5
-
4
-
-
47549115780
-
The cohesin ring concatenates sister DNA molecules
-
Haering, C. H., Farcas, A. M., Arumugam, P., Metson, J. and Nasmyth, K. (2008) The cohesin ring concatenates sister DNA molecules. Nature 454, 297-301.
-
(2008)
Nature
, vol.454
, pp. 297-301
-
-
Haering, C.H.1
Farcas, A.M.2
Arumugam, P.3
Metson, J.4
Nasmyth, K.5
-
5
-
-
70449731229
-
Differential regulation of telomere and centromere cohesion by the Scc3 homologues SA1 and SA2, respectively, in human cells
-
Canudas, S. and Smith, S. (2009) Differential regulation of telomere and centromere cohesion by the Scc3 homologues SA1 and SA2, respectively, in human cells. J. Cell Biol. 187, 165-173.
-
(2009)
J. Cell Biol.
, vol.187
, pp. 165-173
-
-
Canudas, S.1
Smith, S.2
-
6
-
-
84860507563
-
Cohesin-SA1 deficiency drives aneuploidy and tumourigenesis in mice due to impaired replication of telomeres
-
Remeseiro, S., Cuadrado, A., Carretero, M., Martínez, P., Drosopoulos, W. C., Canamero, M., Schildkraut, C. L., Blasco, M. A. and Losada, A. (2012) Cohesin-SA1 deficiency drives aneuploidy and tumourigenesis in mice due to impaired replication of telomeres. EMBO J. 31, 2076-2089.
-
(2012)
EMBO J.
, vol.31
, pp. 2076-2089
-
-
Remeseiro, S.1
Cuadrado, A.2
Carretero, M.3
Martínez, P.4
Drosopoulos, W.C.5
Canamero, M.6
Schildkraut, C.L.7
Blasco, M.A.8
Losada, A.9
-
7
-
-
84871820710
-
Cohesin in gametogenesis
-
McNicoll, F., Stevense, M. and Jessberger, R. (2013) Cohesin in gametogenesis. Curr. Top. Dev. Biol. 102, 1-34.
-
(2013)
Curr. Top. Dev. Biol.
, vol.102
, pp. 1-34
-
-
McNicoll, F.1
Stevense, M.2
Jessberger, R.3
-
8
-
-
1842557791
-
Drosophila nipped-B protein supports sister chromatid cohesion and opposes the stromalin/Scc3 cohesion factor to facilitate long-range activation of the cut gene
-
Rollins, R. A., Korom, M., Aulner, N., Martens, A. and Dorsett, D. (2004) Drosophila nipped-B protein supports sister chromatid cohesion and opposes the stromalin/Scc3 cohesion factor to facilitate long-range activation of the cut gene. Mol. Cell. Biol. 24, 3100-3111.
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 3100-3111
-
-
Rollins, R.A.1
Korom, M.2
Aulner, N.3
Martens, A.4
Dorsett, D.5
-
9
-
-
33747368147
-
Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance
-
Seitan, V. C., Banks, P., Laval, S., Majid, N. A., Dorsett, D., Rana, A., Smith, J., Bateman, A., Krpic, S., Hostert, A., Rollins, R. A., Erdjument-Bromage, H., Tempst, P., Benard, C. Y., Hekimi, S., Newbury, S. F. and Strachan, T. (2006) Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance. PLoS Biol. 4, e242.
-
(2006)
PLoS Biol.
, vol.4
-
-
Seitan, V.C.1
Banks, P.2
Laval, S.3
Majid, N.A.4
Dorsett, D.5
Rana, A.6
Smith, J.7
Bateman, A.8
Krpic, S.9
Hostert, A.10
Rollins, R.A.11
Erdjument-Bromage, H.12
Tempst, P.13
Benard, C.Y.14
Hekimi, S.15
Newbury, S.F.16
Strachan, T.17
-
10
-
-
84885592677
-
Wapl is an essential regulator of chromatin structure and chromosome segregation
-
Tedeschi, A., Wutz, G., Huet, S., Jaritz, M., Wuensche, A., Schirghuber, E., Davidson, I. F., Tang, W., Cisneros, D. A., Bhaskara, V., Nishiyama, T., Vaziri, A., Wutz, A., Ellenberg, J. and Peters, J. M. (2013) Wapl is an essential regulator of chromatin structure and chromosome segregation. Nature 501, 564-568.
-
(2013)
Nature
, vol.501
, pp. 564-568
-
-
Tedeschi, A.1
Wutz, G.2
Huet, S.3
Jaritz, M.4
Wuensche, A.5
Schirghuber, E.6
Davidson, I.F.7
Tang, W.8
Cisneros, D.A.9
Bhaskara, V.10
Nishiyama, T.11
Vaziri, A.12
Wutz, A.13
Ellenberg, J.14
Peters, J.M.15
-
11
-
-
84887819535
-
Pds5B is required for cohesion establishment and Aurora B accumulation at centromeres
-
Carretero, M., Ruiz-Torres, M., Rodríguez-Corsino, M., Barthelemy, I. and Losada, A. (2013) Pds5B is required for cohesion establishment and Aurora B accumulation at centromeres. EMBO J. 32, 2938-2949.
-
(2013)
EMBO J.
, vol.32
, pp. 2938-2949
-
-
Carretero, M.1
Ruiz-Torres, M.2
Rodríguez-Corsino, M.3
Barthelemy, I.4
Losada, A.5
-
12
-
-
46149100946
-
Acetylation of Smc3 by Eco1 is required for S phase sister chromatid cohesion in both human and yeast
-
Zhang, J., Shi, X., Li, Y., Kim, B. J., Jia, J., Huang, Z., Yang, T., Fu, X., Jung, S. Y., Wang, Y., Zhang, P., Kim, S. T., Pan, X. and Qin, J. (2008) Acetylation of Smc3 by Eco1 is required for S phase sister chromatid cohesion in both human and yeast. Mol. Cell 31, 143-151.
-
(2008)
Mol. Cell
, vol.31
, pp. 143-151
-
-
Zhang, J.1
Shi, X.2
Li, Y.3
Kim, B.J.4
Jia, J.5
Huang, Z.6
Yang, T.7
Fu, X.8
Jung, S.Y.9
Wang, Y.10
Zhang, P.11
Kim, S.T.12
Pan, X.13
Qin, J.14
-
13
-
-
48249142388
-
A molecular determinant for the establishment of sister chromatid cohesion
-
Unal, E., Heidinger-Pauli, J. M., Kim, W., Guacci, V., Onn, I., Gygi, S. P. and Koshland, D. E. (2008) A molecular determinant for the establishment of sister chromatid cohesion. Science 321, 566-569.
-
(2008)
Science
, vol.321
, pp. 566-569
-
-
Unal, E.1
Heidinger-Pauli, J.M.2
Kim, W.3
Guacci, V.4
Onn, I.5
Gygi, S.P.6
Koshland, D.E.7
-
14
-
-
17044424182
-
Sororin, a substrate of the anaphase-promoting complex, is required for sister chromatid cohesion in vertebrates
-
Rankin, S., Ayad, N. G. and Kirschner, M. W. (2005) Sororin, a substrate of the anaphase-promoting complex, is required for sister chromatid cohesion in vertebrates. Mol. Cell 18, 185-200.
-
(2005)
Mol. Cell
, vol.18
, pp. 185-200
-
-
Rankin, S.1
Ayad, N.G.2
Kirschner, M.W.3
-
15
-
-
18044393595
-
Dissociation of cohesin from chromosome arms and loss of arm cohesion during early mitosis depends on phosphorylation of SA2
-
Hauf, S., Roitinger, E., Koch, B., Dittrich, C. M., Mechtler, K. and Peters, J. M. (2005) Dissociation of cohesin from chromosome arms and loss of arm cohesion during early mitosis depends on phosphorylation of SA2. PLoS Biol. 3, e69.
-
(2005)
PLoS Biol.
, vol.3
-
-
Hauf, S.1
Roitinger, E.2
Koch, B.3
Dittrich, C.M.4
Mechtler, K.5
Peters, J.M.6
-
16
-
-
4444224967
-
Vertebrate shugoshin links sister centromere cohesion and kinetochore microtubule stability in mitosis
-
Salic, A., Waters, J. C. and Mitchison, T. J. (2004) Vertebrate shugoshin links sister centromere cohesion and kinetochore microtubule stability in mitosis. Cell 118, 567-578.
-
(2004)
Cell
, vol.118
, pp. 567-578
-
-
Salic, A.1
Waters, J.C.2
Mitchison, T.J.3
-
17
-
-
0030448251
-
Anaphase initiation in Saccharomyces cerevisiae is controlled by the APC-dependent degradation of the anaphase inhibitor Pds1p
-
Cohen-Fix, O., Peters, J. M., Kirschner, M. W. and Koshland, D. (1996) Anaphase initiation in Saccharomyces cerevisiae is controlled by the APC-dependent degradation of the anaphase inhibitor Pds1p. Genes Dev. 10, 3081-3093.
-
(1996)
Genes Dev.
, vol.10
, pp. 3081-3093
-
-
Cohen-Fix, O.1
Peters, J.M.2
Kirschner, M.W.3
Koshland, D.4
-
18
-
-
0033168496
-
Sister-chromatid separation at anaphase onset is promoted by cleavage of the cohesin subunit Scc1
-
Uhlmann, F., Lottspeich, F. and Nasmyth, K. (1999) Sister-chromatid separation at anaphase onset is promoted by cleavage of the cohesin subunit Scc1. Nature 400, 37-42.
-
(1999)
Nature
, vol.400
, pp. 37-42
-
-
Uhlmann, F.1
Lottspeich, F.2
Nasmyth, K.3
-
19
-
-
84880696794
-
Cohesin: functions beyond sister chromatid cohesion
-
Mehta, G. D., Kumar, R., Srivastava, S. and Ghosh, S. K. (2013) Cohesin: functions beyond sister chromatid cohesion. FEBS Lett. 587, 2299-2312.
-
(2013)
FEBS Lett.
, vol.587
, pp. 2299-2312
-
-
Mehta, G.D.1
Kumar, R.2
Srivastava, S.3
Ghosh, S.K.4
-
20
-
-
39149121436
-
Cohesin mediates transcriptional insulation by CCCTC-binding factor
-
Wendt, K. S., Yoshida, K., Itoh, T., Bando, M., Koch, B., Schirghuber, E., Tsutsumi, S., Nagae, G., Ishihara, K., Mishiro, T., Yahata, K., Imamoto, F., Aburatani, H., Nakao, M., Imamoto, N., Maeshima, K., Shirahige, K. and Peters, J. M. (2008) Cohesin mediates transcriptional insulation by CCCTC-binding factor. Nature 451, 796-801.
-
(2008)
Nature
, vol.451
, pp. 796-801
-
-
Wendt, K.S.1
Yoshida, K.2
Itoh, T.3
Bando, M.4
Koch, B.5
Schirghuber, E.6
Tsutsumi, S.7
Nagae, G.8
Ishihara, K.9
Mishiro, T.10
Yahata, K.11
Imamoto, F.12
Aburatani, H.13
Nakao, M.14
Imamoto, N.15
Maeshima, K.16
Shirahige, K.17
Peters, J.M.18
-
21
-
-
38849121606
-
Cohesins functionally associate with CTCF on mammalian chromosome arms
-
Parelho, V., Hadjur, S., Spivakov, M., Leleu, M., Sauer, S., Gregson, H. C., Jarmuz, A., Canzonetta, C., Webster, Z., Nesterova, T., Cobb, B. S., Yokomori, K., Dillon, N., Aragon, L., Fisher, A. G. and Merkenschlager, M. (2008) Cohesins functionally associate with CTCF on mammalian chromosome arms. Cell 132, 422-433.
-
(2008)
Cell
, vol.132
, pp. 422-433
-
-
Parelho, V.1
Hadjur, S.2
Spivakov, M.3
Leleu, M.4
Sauer, S.5
Gregson, H.C.6
Jarmuz, A.7
Canzonetta, C.8
Webster, Z.9
Nesterova, T.10
Cobb, B.S.11
Yokomori, K.12
Dillon, N.13
Aragon, L.14
Fisher, A.G.15
Merkenschlager, M.16
-
22
-
-
79958065572
-
Specific sites in the C terminus of CTCF interact with the SA2 subunit of the cohesin complex and are required for cohesin-dependent insulation activity
-
Xiao, T., Wallace, J. and Felsenfeld, G. (2011) Specific sites in the C terminus of CTCF interact with the SA2 subunit of the cohesin complex and are required for cohesin-dependent insulation activity. Mol. Cell. Biol. 31, 2174-2183.
-
(2011)
Mol. Cell. Biol.
, vol.31
, pp. 2174-2183
-
-
Xiao, T.1
Wallace, J.2
Felsenfeld, G.3
-
23
-
-
77957139539
-
Mediator and cohesin connect gene expression and chromatin architecture
-
Kagey, M. H., Newman, J. J., Bilodeau, S., Zhan, Y., Orlando, D. A., van Berkum, N. L., Ebmeier, C. C., Goossens, J., Rahl, P. B., Levine, S. S., Taatjes, D. J., Dekker, J. and Young, R. A. (2010) Mediator and cohesin connect gene expression and chromatin architecture. Nature 467, 430-435.
-
(2010)
Nature
, vol.467
, pp. 430-435
-
-
Kagey, M.H.1
Newman, J.J.2
Bilodeau, S.3
Zhan, Y.4
Orlando, D.A.5
van Berkum, N.L.6
Ebmeier, C.C.7
Goossens, J.8
Rahl, P.B.9
Levine, S.S.10
Taatjes, D.J.11
Dekker, J.12
Young, R.A.13
-
24
-
-
84876895132
-
Suv4-20h2 mediates chromatin compaction and is important for cohesin recruitment to heterochromatin
-
Hahn, M., Dambacher, S., Dulev, S., Kuznetsova, A. Y., Eck, S., Worz, S., Sadic, D., Schulte, M., Mallm, J. P., Maiser, A., Debs, P., von Melchner, H., Leonhardt, H., Schermelleh, L., Rohr, K., Rippe, K., Storchova, Z. and Schotta, G. (2013) Suv4-20h2 mediates chromatin compaction and is important for cohesin recruitment to heterochromatin. Genes Dev. 27, 859-872.
-
(2013)
Genes Dev.
, vol.27
, pp. 859-872
-
-
Hahn, M.1
Dambacher, S.2
Dulev, S.3
Kuznetsova, A.Y.4
Eck, S.5
Worz, S.6
Sadic, D.7
Schulte, M.8
Mallm, J.P.9
Maiser, A.10
Debs, P.11
von Melchner, H.12
Leonhardt, H.13
Schermelleh, L.14
Rohr, K.15
Rippe, K.16
Storchova, Z.17
Schotta, G.18
-
25
-
-
2642542322
-
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
-
Krantz, I. D., McCallum, J., DeScipio, C., Kaur, M., Gillis, L. A., Yaeger, D., Jukofsky, L., Wasserman, N., Bottani, A., Morris, C. A., Nowaczyk, M. J., Toriello, H., Bamshad, M. J., Carey, J. C., Rappaport, E., Kawauchi, S., Lander, A. D., Calof, A. L., Li, H. H., Devoto, M. and Jackson, L. G. (2004) Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B. Nat. Genet. 36, 631-635.
-
(2004)
Nat. Genet.
, vol.36
, pp. 631-635
-
-
Krantz, I.D.1
McCallum, J.2
DeScipio, C.3
Kaur, M.4
Gillis, L.A.5
Yaeger, D.6
Jukofsky, L.7
Wasserman, N.8
Bottani, A.9
Morris, C.A.10
Nowaczyk, M.J.11
Toriello, H.12
Bamshad, M.J.13
Carey, J.C.14
Rappaport, E.15
Kawauchi, S.16
Lander, A.D.17
Calof, A.L.18
Li, H.H.19
Devoto, M.20
Jackson, L.G.21
more..
-
26
-
-
2642565901
-
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome
-
Tonkin, E. T., Wang, T. J., Lisgo, S., Bamshad, M. J. and Strachan, T. (2004) NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome. Nat. Genet. 36, 636-641.
-
(2004)
Nat. Genet.
, vol.36
, pp. 636-641
-
-
Tonkin, E.T.1
Wang, T.J.2
Lisgo, S.3
Bamshad, M.J.4
Strachan, T.5
-
27
-
-
33646379870
-
X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations
-
Musio, A., Selicorni, A., Focarelli, M. L., Gervasini, C., Milani, D., Russo, S., Vezzoni, P. and Larizza, L. (2006) X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations. Nat. Genet. 38, 528-530.
-
(2006)
Nat. Genet.
, vol.38
, pp. 528-530
-
-
Musio, A.1
Selicorni, A.2
Focarelli, M.L.3
Gervasini, C.4
Milani, D.5
Russo, S.6
Vezzoni, P.7
Larizza, L.8
-
28
-
-
33847196427
-
Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation
-
Deardorff, M. A., Kaur, M., Yaeger, D., Rampuria, A., Korolev, S., Pie, J., Gil-Rodriguez, C., Arnedo, M., Loeys, B., Kline, A. D., Wilson, M., Lillquist, K., Siu, V., Ramos, F. J., Musio, A., Jackson, L. S., Dorsett, D. and Krantz, I. D. (2007) Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation. Am. J. Hum. Genet. 80, 485-494.
-
(2007)
Am. J. Hum. Genet.
, vol.80
, pp. 485-494
-
-
Deardorff, M.A.1
Kaur, M.2
Yaeger, D.3
Rampuria, A.4
Korolev, S.5
Pie, J.6
Gil-Rodriguez, C.7
Arnedo, M.8
Loeys, B.9
Kline, A.D.10
Wilson, M.11
Lillquist, K.12
Siu, V.13
Ramos, F.J.14
Musio, A.15
Jackson, L.S.16
Dorsett, D.17
Krantz, I.D.18
-
29
-
-
84862142852
-
RAD21 mutations cause a human cohesinopathy
-
Deardorff, M. A., Wilde, J. J., Albrecht, M., Dickinson, E., Tennstedt, S., Braunholz, D., Monnich, M., Yan, Y., Xu, W., Gil-Rodriguez, M. C., Clark, D., Hakonarson, H., Halbach, S., Michelis, L. D., Rampuria, A., Rossier, E., Spranger, S., Van Maldergem, L., Lynch, S. A., Gillessen-Kaesbach, G., Ludecke, H. J., Ramsay, R. G., McKay, M. J., Krantz, I. D., Xu, H., Horsfield, J. A. and Kaiser, F. J. (2012) RAD21 mutations cause a human cohesinopathy. Am. J. Hum. Genet. 90, 1014-1027.
-
(2012)
Am. J. Hum. Genet.
, vol.90
, pp. 1014-1027
-
-
Deardorff, M.A.1
Wilde, J.J.2
Albrecht, M.3
Dickinson, E.4
Tennstedt, S.5
Braunholz, D.6
Monnich, M.7
Yan, Y.8
Xu, W.9
Gil-Rodriguez, M.C.10
Clark, D.11
Hakonarson, H.12
Halbach, S.13
Michelis, L.D.14
Rampuria, A.15
Rossier, E.16
Spranger, S.17
Van Maldergem, L.18
Lynch, S.A.19
Gillessen-Kaesbach, G.20
Ludecke, H.J.21
Ramsay, R.G.22
McKay, M.J.23
Krantz, I.D.24
Xu, H.25
Horsfield, J.A.26
Kaiser, F.J.27
more..
-
30
-
-
24344440548
-
Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome
-
Kaur, M., DeScipio, C., McCallum, J., Yaeger, D., Devoto, M., Jackson, L. G., Spinner, N. B. and Krantz, I. D. (2005) Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome. Am. J. Med. Genet. 138A, 27-31.
-
(2005)
Am. J. Med. Genet.
, vol.138 A
, pp. 27-31
-
-
Kaur, M.1
DeScipio, C.2
McCallum, J.3
Yaeger, D.4
Devoto, M.5
Jackson, L.G.6
Spinner, N.B.7
Krantz, I.D.8
-
31
-
-
70349878942
-
Premature chromatid separation is not a useful diagnostic marker for Cornelia de Lange syndrome
-
Castronovo, P., Gervasini, C., Cereda, A., Masciadri, M., Milani, D., Russo, S., Selicorni, A. and Larizza, L. (2009) Premature chromatid separation is not a useful diagnostic marker for Cornelia de Lange syndrome. Chromosome Res. 17, 763-771.
-
(2009)
Chromosome Res.
, vol.17
, pp. 763-771
-
-
Castronovo, P.1
Gervasini, C.2
Cereda, A.3
Masciadri, M.4
Milani, D.5
Russo, S.6
Selicorni, A.7
Larizza, L.8
-
32
-
-
66249144416
-
Transcriptional dysregulation in NIPBL and cohesin mutant human cells
-
Liu, J., Zhang, Z., Bando, M., Itoh, T., Deardorff, M. A., Clark, D., Kaur, M., Tandy, S., Kondoh, T., Rappaport, E., Spinner, N. B., Vega, H., Jackson, L. G., Shirahige, K. and Krantz, I. D. (2009) Transcriptional dysregulation in NIPBL and cohesin mutant human cells. PLoS Biol. 7, e1000119.
-
(2009)
PLoS Biol.
, vol.7
-
-
Liu, J.1
Zhang, Z.2
Bando, M.3
Itoh, T.4
Deardorff, M.A.5
Clark, D.6
Kaur, M.7
Tandy, S.8
Kondoh, T.9
Rappaport, E.10
Spinner, N.B.11
Vega, H.12
Jackson, L.G.13
Shirahige, K.14
Krantz, I.D.15
-
33
-
-
70349690201
-
Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome
-
Kawauchi, S., Calof, A. L., Santos, R., Lopez-Burks, M. E., Young, C. M., Hoang, M. P., Chua, A., Lao, T., Lechner, M. S., Daniel, J. A., Nussenzweig, A., Kitzes, L., Yokomori, K., Hallgrimsson, B. and Lander, A. D. (2009) Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome. PLoS Genet. 5, e1000650.
-
(2009)
PLoS Genet.
, vol.5
-
-
Kawauchi, S.1
Calof, A.L.2
Santos, R.3
Lopez-Burks, M.E.4
Young, C.M.5
Hoang, M.P.6
Chua, A.7
Lao, T.8
Lechner, M.S.9
Daniel, J.A.10
Nussenzweig, A.11
Kitzes, L.12
Yokomori, K.13
Hallgrimsson, B.14
Lander, A.D.15
-
34
-
-
84860539709
-
A unique role of cohesin-SA1 in gene regulation and development
-
Remeseiro, S., Cuadrado, A., Gómez-López, G., Pisano, D. G. and Losada, A. (2012) A unique role of cohesin-SA1 in gene regulation and development. EMBO J. 31, 2090-2102.
-
(2012)
EMBO J.
, vol.31
, pp. 2090-2102
-
-
Remeseiro, S.1
Cuadrado, A.2
Gómez-López, G.3
Pisano, D.G.4
Losada, A.5
-
35
-
-
81955161806
-
Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature
-
Schrier, S. A., Sherer, I., Deardorff, M. A., Clark, D., Audette, L., Gillis, L., Kline, A. D., Ernst, L., Loomes, K., Krantz, I. D. and Jackson, L. G. (2011) Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature. Am. J. Med. Genet. 155A, 3007-3024.
-
(2011)
Am. J. Med. Genet.
, vol.155 A
, pp. 3007-3024
-
-
Schrier, S.A.1
Sherer, I.2
Deardorff, M.A.3
Clark, D.4
Audette, L.5
Gillis, L.6
Kline, A.D.7
Ernst, L.8
Loomes, K.9
Krantz, I.D.10
Jackson, L.G.11
-
36
-
-
84895433616
-
Mutant cohesin in premature ovarian failure
-
Caburet, S., Arboleda, V. A., Llano, E., Overbeek, P. A., Barbero, J. L., Oka, K., Harrison, W., Vaiman, D., Ben-Neriah, Z., Garcia-Tunon, I., Fellous, M., Pendas, A. M., Veitia, R. A. and Vilain, E. (2014) Mutant cohesin in premature ovarian failure. N. Engl. J. Med. 370, 943-949.
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 943-949
-
-
Caburet, S.1
Arboleda, V.A.2
Llano, E.3
Overbeek, P.A.4
Barbero, J.L.5
Oka, K.6
Harrison, W.7
Vaiman, D.8
Ben-Neriah, Z.9
Garcia-Tunon, I.10
Fellous, M.11
Pendas, A.M.12
Veitia, R.A.13
Vilain, E.14
-
37
-
-
79952284127
-
Hallmarks of cancer:The next generation
-
Hanahan, D. and Weinberg, R. A. (2011) Hallmarks of cancer:The next generation. Cell 144, 646-674.
-
(2011)
Cell
, vol.144
, pp. 646-674
-
-
Hanahan, D.1
Weinberg, R.A.2
-
38
-
-
84857192718
-
Causes and consequences of aneuploidy in cancer
-
Gordon, D. J., Resio, B. and Pellman, D. (2012) Causes and consequences of aneuploidy in cancer. Nat. Rev. Genet. 13, 189-203.
-
(2012)
Nat. Rev. Genet.
, vol.13
, pp. 189-203
-
-
Gordon, D.J.1
Resio, B.2
Pellman, D.3
-
39
-
-
40849149557
-
Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers
-
Barber, T. D., McManus, K., Yuen, K. W., Reis, M., Parmigiani, G., Shen, D., Barrett, I., Nouhi, Y., Spencer, F., Markowitz, S., Velculescu, V. E., Kinzler, K. W., Vogelstein, B., Lengauer, C. and Hieter, P. (2008) Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers. Proc. Natl. Acad. Sci. U. S. A. 105, 3443-3448.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 3443-3448
-
-
Barber, T.D.1
McManus, K.2
Yuen, K.W.3
Reis, M.4
Parmigiani, G.5
Shen, D.6
Barrett, I.7
Nouhi, Y.8
Spencer, F.9
Markowitz, S.10
Velculescu, V.E.11
Kinzler, K.W.12
Vogelstein, B.13
Lengauer, C.14
Hieter, P.15
-
40
-
-
77956476356
-
Alteration of cohesin genes in myeloid diseases
-
Rocquain, J., Gelsi-Boyer, V., Adelaide, J., Murati, A., Carbuccia, N., Vey, N., Birnbaum, D., Mozziconacci, M. J. and Chaffanet, M. (2010) Alteration of cohesin genes in myeloid diseases. Am. J. Hematol. 85, 717-719.
-
(2010)
Am. J. Hematol.
, vol.85
, pp. 717-719
-
-
Rocquain, J.1
Gelsi-Boyer, V.2
Adelaide, J.3
Murati, A.4
Carbuccia, N.5
Vey, N.6
Birnbaum, D.7
Mozziconacci, M.J.8
Chaffanet, M.9
-
41
-
-
80051874823
-
Mutational inactivation of STAG2 causes aneuploidy in human cancer
-
Solomon, D. A., Kim, T., Diaz-Martinez, L. A., Fair, J., Elkahloun, A. G., Harris, B. T., Toretsky, J. A., Rosenberg, S. A., Shukla, N., Ladanyi, M., Samuels, Y., James, C. D., Yu, H., Kim, J. S. and Waldman, T. (2011) Mutational inactivation of STAG2 causes aneuploidy in human cancer. Science 333, 1039-1043.
-
(2011)
Science
, vol.333
, pp. 1039-1043
-
-
Solomon, D.A.1
Kim, T.2
Diaz-Martinez, L.A.3
Fair, J.4
Elkahloun, A.G.5
Harris, B.T.6
Toretsky, J.A.7
Rosenberg, S.A.8
Shukla, N.9
Ladanyi, M.10
Samuels, Y.11
James, C.D.12
Yu, H.13
Kim, J.S.14
Waldman, T.15
-
42
-
-
84862776906
-
Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing
-
Ding, L., Ley, T. J., Larson, D. E., Miller, C. A., Koboldt, D. C., Welch, J. S., Ritchey, J. K., Young, M. A., Lamprecht, T., McLellan, M. D., McMichael, J. F., Wallis, J. W., Lu, C., Shen, D., Harris, C. C., Dooling, D. J., Fulton, R. S., Fulton, L. L., Chen, K., Schmidt, H., Kalicki-Veizer, J., Magrini, V. J., Cook, L., McGrath, S. D., Vickery, T. L., Wendl, M. C., Heath, S., Watson, M. A., Link, D. C., Tomasson, M. H., Shannon, W. D., Payton, J. E., Kulkarni, S., Westervelt, P., Walter, M. J., Graubert, T. A., Mardis, E. R., Wilson, R. K. and DiPersio, J. F. (2012) Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing. Nature 481, 506-510.
-
(2012)
Nature
, vol.481
, pp. 506-510
-
-
Ding, L.1
Ley, T.J.2
Larson, D.E.3
Miller, C.A.4
Koboldt, D.C.5
Welch, J.S.6
Ritchey, J.K.7
Young, M.A.8
Lamprecht, T.9
McLellan, M.D.10
McMichael, J.F.11
Wallis, J.W.12
Lu, C.13
Shen, D.14
Harris, C.C.15
Dooling, D.J.16
Fulton, R.S.17
Fulton, L.L.18
Chen, K.19
Schmidt, H.20
Kalicki-Veizer, J.21
Magrini, V.J.22
Cook, L.23
McGrath, S.D.24
Vickery, T.L.25
Wendl, M.C.26
Heath, S.27
Watson, M.A.28
Link, D.C.29
Tomasson, M.H.30
Shannon, W.D.31
Payton, J.E.32
Kulkarni, S.33
Westervelt, P.34
Walter, M.J.35
Graubert, T.A.36
Mardis, E.R.37
Wilson, R.K.38
DiPersio, J.F.39
more..
-
43
-
-
84863337617
-
Clonal architecture of secondary acute myeloid leukemia
-
Walter, M. J., Shen, D., Ding, L., Shao, J., Koboldt, D. C., Chen, K., Larson, D. E., McLellan, M. D., Dooling, D., Abbott, R., Fulton, R., Magrini, V., Schmidt, H., Kalicki-Veizer, J., O'Laughlin, M., Fan, X., Grillot, M., Witowski, S., Heath, S., Frater, J. L., Eades, W., Tomasson, M., Westervelt, P., DiPersio, J. F., Link, D. C., Mardis, E. R., Ley, T. J., Wilson, R. K. and Graubert, T. A. (2012) Clonal architecture of secondary acute myeloid leukemia. N. Engl. J. Med. 366, 1090-1098.
-
(2012)
N. Engl. J. Med.
, vol.366
, pp. 1090-1098
-
-
Walter, M.J.1
Shen, D.2
Ding, L.3
Shao, J.4
Koboldt, D.C.5
Chen, K.6
Larson, D.E.7
McLellan, M.D.8
Dooling, D.9
Abbott, R.10
Fulton, R.11
Magrini, V.12
Schmidt, H.13
Kalicki-Veizer, J.14
O'Laughlin, M.15
Fan, X.16
Grillot, M.17
Witowski, S.18
Heath, S.19
Frater, J.L.20
Eades, W.21
Tomasson, M.22
Westervelt, P.23
DiPersio, J.F.24
Link, D.C.25
Mardis, E.R.26
Ley, T.J.27
Wilson, R.K.28
Graubert, T.A.29
more..
-
44
-
-
84864255882
-
The origin and evolution of mutations in acute myeloid leukemia
-
Welch, J. S., Ley, T. J., Link, D. C., Miller, C. A., Larson, D. E., Koboldt, D. C., Wartman, L. D., Lamprecht, T. L., Liu, F., Xia, J., Kandoth, C., Fulton, R. S., McLellan, M. D., Dooling, D. J., Wallis, J. W., Chen, K., Harris, C. C., Schmidt, H. K., Kalicki-Veizer, J. M., Lu, C., Zhang, Q., Lin, L., O'Laughlin, M. D., McMichael, J. F., Delehaunty, K. D., Fulton, L. A., Magrini, V. J., McGrath, S. D., Demeter, R. T., Vickery, T. L., Hundal, J., Cook, L. L., Swift, G. W., Reed, J. P., Alldredge, P. A., Wylie, T. N., Walker, J. R., Watson, M. A., Heath, S. E., Shannon, W. D., Varghese, N., Nagarajan, R., Payton, J. E., Baty, J. D., Kulkarni, S., Klco, J. M., Tomasson, M. H., Westervelt, P., Walter, M. J., Graubert, T. A., DiPersio, J. F., Ding, L., Mardis, E. R. and Wilson, R. K. (2012) The origin and evolution of mutations in acute myeloid leukemia. Cell 150, 264-278.
-
(2012)
Cell
, vol.150
, pp. 264-278
-
-
Welch, J.S.1
Ley, T.J.2
Link, D.C.3
Miller, C.A.4
Larson, D.E.5
Koboldt, D.C.6
Wartman, L.D.7
Lamprecht, T.L.8
Liu, F.9
Xia, J.10
Kandoth, C.11
Fulton, R.S.12
McLellan, M.D.13
Dooling, D.J.14
Wallis, J.W.15
Chen, K.16
Harris, C.C.17
Schmidt, H.K.18
Kalicki-Veizer, J.M.19
Lu, C.20
Zhang, Q.21
Lin, L.22
O'Laughlin, M.D.23
McMichael, J.F.24
Delehaunty, K.D.25
Fulton, L.A.26
Magrini, V.J.27
McGrath, S.D.28
Demeter, R.T.29
Vickery, T.L.30
Hundal, J.31
Cook, L.L.32
Swift, G.W.33
Reed, J.P.34
Alldredge, P.A.35
Wylie, T.N.36
Walker, J.R.37
Watson, M.A.38
Heath, S.E.39
Shannon, W.D.40
Varghese, N.41
Nagarajan, R.42
Payton, J.E.43
Baty, J.D.44
Kulkarni, S.45
Klco, J.M.46
Tomasson, M.H.47
Westervelt, P.48
Walter, M.J.49
Graubert, T.A.50
DiPersio, J.F.51
Ding, L.52
Mardis, E.R.53
Wilson, R.K.54
more..
-
45
-
-
84878372012
-
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia
-
The Cancer Genome Atlas Research Network
-
The Cancer Genome Atlas Research Network. (2013) Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia. N. Engl. J. Med. 368, 2059-2074.
-
(2013)
N. Engl. J. Med.
, vol.368
, pp. 2059-2074
-
-
-
46
-
-
84885021313
-
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms
-
Kon, A., Shih, L. Y., Minamino, M., Sanada, M., Shiraishi, Y., Nagata, Y., Yoshida, K., Okuno, Y., Bando, M., Nakato, R., Ishikawa, S., Sato-Otsubo, A., Nagae, G., Nishimoto, A., Haferlach, C., Nowak, D., Sato, Y., Alpermann, T., Nagasaki, M., Shimamura, T., Tanaka, H., Chiba, K., Yamamoto, R., Yamaguchi, T., Otsu, M., Obara, N., Sakata-Yanagimoto, M., Nakamaki, T., Ishiyama, K., Nolte, F., Hofmann, W. K., Miyawaki, S., Chiba, S., Mori, H., Nakauchi, H., Koeffler, H. P., Aburatani, H., Haferlach, T., Shirahige, K., Miyano, S. and Ogawa, S. (2013) Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms. Nat. Genet. 45, 1232-1237.
-
(2013)
Nat. Genet.
, vol.45
, pp. 1232-1237
-
-
Kon, A.1
Shih, L.Y.2
Minamino, M.3
Sanada, M.4
Shiraishi, Y.5
Nagata, Y.6
Yoshida, K.7
Okuno, Y.8
Bando, M.9
Nakato, R.10
Ishikawa, S.11
Sato-Otsubo, A.12
Nagae, G.13
Nishimoto, A.14
Haferlach, C.15
Nowak, D.16
Sato, Y.17
Alpermann, T.18
Nagasaki, M.19
Shimamura, T.20
Tanaka, H.21
Chiba, K.22
Yamamoto, R.23
Yamaguchi, T.24
Otsu, M.25
Obara, N.26
Sakata-Yanagimoto, M.27
Nakamaki, T.28
Ishiyama, K.29
Nolte, F.30
Hofmann, W.K.31
Miyawaki, S.32
Chiba, S.33
Mori, H.34
Nakauchi, H.35
Koeffler, H.P.36
Aburatani, H.37
Haferlach, T.38
Shirahige, K.39
Miyano, S.40
Ogawa, S.41
more..
-
47
-
-
84897573903
-
Mutations in the cohesin complex in acute myeloid leukemia:clinical and prognostic implications
-
Thol, F., Bollin, R., Gehlhaar, M., Walter, C., Dugas, M., Suchanek, K. J., Kirchner, A., Huang, L., Chaturvedi, A., Wichmann, M., Wiehlmann, L., Shahswar, R., Damm, F., Gohring, G., Schlegelberger, B., Schlenk, R., Dohner, K., Dohner, H., Krauter, J., Ganser, A. and Heuser, M. (2014) Mutations in the cohesin complex in acute myeloid leukemia:clinical and prognostic implications. Blood 123, 914-920.
-
(2014)
Blood
, vol.123
, pp. 914-920
-
-
Thol, F.1
Bollin, R.2
Gehlhaar, M.3
Walter, C.4
Dugas, M.5
Suchanek, K.J.6
Kirchner, A.7
Huang, L.8
Chaturvedi, A.9
Wichmann, M.10
Wiehlmann, L.11
Shahswar, R.12
Damm, F.13
Gohring, G.14
Schlegelberger, B.15
Schlenk, R.16
Dohner, K.17
Dohner, H.18
Krauter, J.19
Ganser, A.20
Heuser, M.21
more..
-
48
-
-
0036727413
-
Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome
-
Wechsler, J., Greene, M., McDevitt, M. A., Anastasi, J., Karp, J. E., Le Beau, M. M. and Crispino, J. D. (2002) Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome. Nat. Genet. 32, 148-152.
-
(2002)
Nat. Genet.
, vol.32
, pp. 148-152
-
-
Wechsler, J.1
Greene, M.2
McDevitt, M.A.3
Anastasi, J.4
Karp, J.E.5
Le Beau, M.M.6
Crispino, J.D.7
-
49
-
-
84887117736
-
The landscape of somatic mutations in Down syndrome-related myeloid disorders
-
Yoshida, K., Toki, T., Okuno, Y., Kanezaki, R., Shiraishi, Y., Sato-Otsubo, A., Sanada, M., Park, M., Terui, K., Suzuki, H., Kon, A., Nagata, Y., Sato, Y., Wang, R., Shiba, N., Chiba, K., Tanaka, H., Hama, A., Muramatsu, H., Hasegawa, D., Nakamura, K., Kanegane, H., Tsukamoto, K., Adachi, S., Kawakami, K., Kato, K., Nishimura, R., Izraeli, S., Hayashi, Y., Miyano, S., Kojima, S., Ito, E. and Ogawa, S. (2013) The landscape of somatic mutations in Down syndrome-related myeloid disorders. Nat. Genet. 45, 1293-1299.
-
(2013)
Nat. Genet.
, vol.45
, pp. 1293-1299
-
-
Yoshida, K.1
Toki, T.2
Okuno, Y.3
Kanezaki, R.4
Shiraishi, Y.5
Sato-Otsubo, A.6
Sanada, M.7
Park, M.8
Terui, K.9
Suzuki, H.10
Kon, A.11
Nagata, Y.12
Sato, Y.13
Wang, R.14
Shiba, N.15
Chiba, K.16
Tanaka, H.17
Hama, A.18
Muramatsu, H.19
Hasegawa, D.20
Nakamura, K.21
Kanegane, H.22
Tsukamoto, K.23
Adachi, S.24
Kawakami, K.25
Kato, K.26
Nishimura, R.27
Izraeli, S.28
Hayashi, Y.29
Miyano, S.30
Kojima, S.31
Ito, E.32
Ogawa, S.33
more..
-
50
-
-
84888340419
-
Frequent truncating mutations of STAG2 in bladder cancer
-
Solomon, D. A., Kim, J. S., Bondaruk, J., Shariat, S. F., Wang, Z. F., Elkahloun, A. G., Ozawa, T., Gerard, J., Zhuang, D., Zhang, S., Navai, N., Siefker-Radtke, A., Phillips, J. J., Robinson, B. D., Rubin, M. A., Volkmer, B., Hautmann, R., Kufer, R., Hogendoorn, P. C. W., Netto, G., Theodorescu, D., James, C. D., Czerniak, B., Miettinen, M. and Waldman, T. (2013) Frequent truncating mutations of STAG2 in bladder cancer. Nat. Genet. 45, 1428-1430.
-
(2013)
Nat. Genet.
, vol.45
, pp. 1428-1430
-
-
Solomon, D.A.1
Kim, J.S.2
Bondaruk, J.3
Shariat, S.F.4
Wang, Z.F.5
Elkahloun, A.G.6
Ozawa, T.7
Gerard, J.8
Zhuang, D.9
Zhang, S.10
Navai, N.11
Siefker-Radtke, A.12
Phillips, J.J.13
Robinson, B.D.14
Rubin, M.A.15
Volkmer, B.16
Hautmann, R.17
Kufer, R.18
Hogendoorn, P.C.W.19
Netto, G.20
Theodorescu, D.21
James, C.D.22
Czerniak, B.23
Miettinen, M.24
Waldman, T.25
more..
-
51
-
-
84888354078
-
Recurrent inactivation of STAG2 in bladder is not associated with aneuploidy
-
Balbas-Martinez, C., Sagrera, A., Carrillo-de-Santa-Pau, E., Earl, J., Marquez, M., Vazquez, M., Lapi, E., Castro-Giner, F., Beltran, S., Bayes, M., Carrato, A., Cigudosa, J. C., Dominguez, O., Gut, M., Herranz, J., Juanpere, N., Kogevinas, M., Langa, X., Lopez-Knowles, E., Lorente, J. A., Lloreta, J., Pisano, D. G., Richart, L., Rico, D., Salgado, R. N., Tardon, A., Chanock, S., Heath, S., Valencia, A., Losada, A., Gut, I., Malats, N. and Real, F. X. (2013) Recurrent inactivation of STAG2 in bladder is not associated with aneuploidy. Nat. Genet. 45, 1464-1469.
-
(2013)
Nat. Genet.
, vol.45
, pp. 1464-1469
-
-
Balbas-Martinez, C.1
Sagrera, A.2
Carrillo-de-Santa-Pau, E.3
Earl, J.4
Marquez, M.5
Vazquez, M.6
Lapi, E.7
Castro-Giner, F.8
Beltran, S.9
Bayes, M.10
Carrato, A.11
Cigudosa, J.C.12
Dominguez, O.13
Gut, M.14
Herranz, J.15
Juanpere, N.16
Kogevinas, M.17
Langa, X.18
Lopez-Knowles, E.19
Lorente, J.A.20
Lloreta, J.21
Pisano, D.G.22
Richart, L.23
Rico, D.24
Salgado, R.N.25
Tardon, A.26
Chanock, S.27
Heath, S.28
Valencia, A.29
Losada, A.30
Gut, I.31
Malats, N.32
Real, F.X.33
more..
-
52
-
-
84888380730
-
Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation
-
Guo, G., Sun, X., Chen, C., Wu, S., Huang, P., Li, Z., Dean, M., Huang, Y., Jia, W., Zhou, Q., Tang, A., Yang, Z., Li, X., Song, P., Zhao, X., Ye, R., Zhang, S., Lin, Z., Qi, M., Wan, S., Xie, L., Fan, F., Nickerson, M. L., Zou, X., Hu, X., Xing, L., Lv, Z., Mei, H., Gao, S., Liang, C., Gao, Z., Lu, J., Yu, Y., Liu, C., Li, L., Fang, X., Jiang, Z., Yang, J., Li, C., Zhao, X., Chen, J., Zhang, F., Lai, Y., Lin, Z., Zhou, F., Chen, H., Chan, H. C., Tsang, S., Theodorescu, D., Li, Y., Zhang, X., Wang, J., Yang, H., Gui, Y., Wang, J. and Cai, Z. (2013) Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation. Nat. Genet. 45, 1459-1463.
-
(2013)
Nat. Genet.
, vol.45
, pp. 1459-1463
-
-
Guo, G.1
Sun, X.2
Chen, C.3
Wu, S.4
Huang, P.5
Li, Z.6
Dean, M.7
Huang, Y.8
Jia, W.9
Zhou, Q.10
Tang, A.11
Yang, Z.12
Li, X.13
Song, P.14
Zhao, X.15
Ye, R.16
Zhang, S.17
Lin, Z.18
Qi, M.19
Wan, S.20
Xie, L.21
Fan, F.22
Nickerson, M.L.23
Zou, X.24
Hu, X.25
Xing, L.26
Lv, Z.27
Mei, H.28
Gao, S.29
Liang, C.30
Gao, Z.31
Lu, J.32
Yu, Y.33
Liu, C.34
Li, L.35
Fang, X.36
Jiang, Z.37
Yang, J.38
Li, C.39
Zhao, X.40
Chen, J.41
Zhang, F.42
Lai, Y.43
Lin, Z.44
Zhou, F.45
Chen, H.46
Chan, H.C.47
Tsang, S.48
Theodorescu, D.49
Li, Y.50
Zhang, X.51
Wang, J.52
Yang, H.53
Gui, Y.54
Wang, J.55
Cai, Z.56
more..
-
53
-
-
84897865695
-
Frequent inactivating mutations of STAG2 in bladder cancer are associated with low tumour grade and stage and inversely related to chromosomal copy number changes
-
Taylor, C. F., Platt, F. M., Hurst, C. D., Thygesen, H. H. and Knowles, M. A. (2014) Frequent inactivating mutations of STAG2 in bladder cancer are associated with low tumour grade and stage and inversely related to chromosomal copy number changes. Hum. Mol. Genet. 23, 1964-1974.
-
(2014)
Hum. Mol. Genet.
, vol.23
, pp. 1964-1974
-
-
Taylor, C.F.1
Platt, F.M.2
Hurst, C.D.3
Thygesen, H.H.4
Knowles, M.A.5
-
54
-
-
84903614391
-
Comprehensive molecular characterization of urothelial bladder carcinoma
-
The Cancer Genome Atlas Research Network
-
The Cancer Genome Atlas Research Network. (2014) Comprehensive molecular characterization of urothelial bladder carcinoma. Nature 507, 515-522.
-
(2014)
Nature
, vol.507
, pp. 515-522
-
-
-
55
-
-
84883894030
-
Mutational signature of aristolochic acid exposure as revealed by whole-exome sequencing
-
197ra102
-
Hoang, M. L., Chen, C. H., Sidorenko, V. S., He, J., Dickman, K. G., Yun, B. H., Moriya, M., Niknafs, N., Douville, C., Karchin, R., Turesky, R. J., Pu, Y. S., Vogelstein, B., Papadopoulos, N., Grollman, A. P., Kinzler, K. W. and Rosenquist, T. A. (2013) Mutational signature of aristolochic acid exposure as revealed by whole-exome sequencing. Sci. Transl. Med. 5, 197ra102.
-
(2013)
Sci. Transl. Med.
, vol.5
-
-
Hoang, M.L.1
Chen, C.H.2
Sidorenko, V.S.3
He, J.4
Dickman, K.G.5
Yun, B.H.6
Moriya, M.7
Niknafs, N.8
Douville, C.9
Karchin, R.10
Turesky, R.J.11
Pu, Y.S.12
Vogelstein, B.13
Papadopoulos, N.14
Grollman, A.P.15
Kinzler, K.W.16
Rosenquist, T.A.17
-
56
-
-
84879890360
-
Comprehensive molecular characterization of clear cell re nal cell carcinoma
-
Cancer Genome Atlas Research Network
-
Cancer Genome Atlas Research Network. (2013) Comprehensive molecular characterization of clear cell re nal cell carcinoma. Nature 499, 43-49.
-
(2013)
Nature
, vol.499
, pp. 43-49
-
-
-
57
-
-
84885074034
-
The somatic genomic landscape of glioblastoma
-
The Cancer Genome Atlas Research Network
-
Brennan, C. W., Verhaak, R. G., McKenna, A., Campos, B., Noushmehr, H., Salama, S. R., Zheng, S., Chakravarty, D., Sanborn, J. Z., Berman, S. H., Beroukhim, R., Bernard, B., Wu, C. J., Genovese, G., Shmulevich, I., Barnholtz-Sloan, J., Zou, L., Vegesna, R., Shukla, S. A., Ciriello, G., Yung, W. K., Zhang, W., Sougnez, C., Mikkelsen, T., Aldape, K., Bigner, D. D., Van Meir, E. G., Prados, M., Sloan, A., Black, K. L., Eschbacher, J., Finocchiaro, G., Friedman, W., Andrews, D. W., Guha, A., Iacocca, M., O'Neill, B. P., Foltz, G., Myers, J., Weisenberger, D. J., Penny, R., Kucherlapati, R., Perou, C. M., Hayes, D. N., Gibbs, R., Marra, M., Mills, G. B., Lander, E., Spellman, P., Wilson, R., Sander, C., Weinstein, J., Meyerson, M., Gabriel, S., Laird, P. W., Haussler, D., Getz, G., Chin, L. and The Cancer Genome Atlas Research Network. (2013) The somatic genomic landscape of glioblastoma. Cell 155, 462-477.
-
(2013)
Cell
, vol.155
, pp. 462-477
-
-
Brennan, C.W.1
Verhaak, R.G.2
McKenna, A.3
Campos, B.4
Noushmehr, H.5
Salama, S.R.6
Zheng, S.7
Chakravarty, D.8
Sanborn, J.Z.9
Berman, S.H.10
Beroukhim, R.11
Bernard, B.12
Wu, C.J.13
Genovese, G.14
Shmulevich, I.15
Barnholtz-Sloan, J.16
Zou, L.17
Vegesna, R.18
Shukla, S.A.19
Ciriello, G.20
Yung, W.K.21
Zhang, W.22
Sougnez, C.23
Mikkelsen, T.24
Aldape, K.25
Bigner, D.D.26
Van Meir, E.G.27
Prados, M.28
Sloan, A.29
Black, K.L.30
Eschbacher, J.31
Finocchiaro, G.32
Friedman, W.33
Andrews, D.W.34
Guha, A.35
Iacocca, M.36
O'Neill, B.P.37
Foltz, G.38
Myers, J.39
Weisenberger, D.J.40
Penny, R.41
Kucherlapati, R.42
Perou, C.M.43
Hayes, D.N.44
Gibbs, R.45
Marra, M.46
Mills, G.B.47
Lander, E.48
Spellman, P.49
Wilson, R.50
Sander, C.51
Weinstein, J.52
Meyerson, M.53
Gabriel, S.54
Laird, P.W.55
Haussler, D.56
Getz, G.57
Chin, L.58
more..
-
58
-
-
84864419974
-
Dissecting the genomic complexity underlying medulloblastoma
-
Jones, D. T., Jager, N., Kool, M., Zichner, T., Hutter, B., Sultan, M., Cho, Y. J., Pugh, T. J., Hovestadt, V., Stutz, A. M., Rausch, T., Warnatz, H. J., Ryzhova, M., Bender, S., Sturm, D., Pleier, S., Cin, H., Pfaff, E., Sieber, L., Wittmann, A., Remke, M., Witt, H., Hutter, S., Tzaridis, T., Weischenfeldt, J., Raeder, B., Avci, M., Amstislavskiy, V., Zapatka, M., Weber, U. D., Wang, Q., Lasitschka, B., Bartholomae, C. C., Schmidt, M., von Kalle, C., Ast, V., Lawerenz, C., Eils, J., Kabbe, R., Benes, V., van Sluis, P., Koster, J., Volckmann, R., Shih, D., Betts, M. J., Russell, R. B., Coco, S., Tonini, G. P., Schuller, U., Hans, V., Graf, N., Kim, Y. J., Monoranu, C., Roggendorf, W., Unterberg, A., Herold-Mende, C., Milde, T., Kulozik, A. E., von Deimling, A., Witt, O., Maass, E., Rossler, J., Ebinger, M., Schuhmann, M. U., Fruhwald, M. C., Hasselblatt, M., Jabado, N., Rutkowski, S., von Bueren, A. O., Williamson, D., Clifford, S. C., McCabe, M. G., Collins, V. P., Wolf, S., Wiemann, S., Lehrach, H., Brors, B., Scheurlen, W., Felsberg, J., Reifenberger, G., Northcott, P. A., Taylor, M. D., Meyerson, M., Pomeroy, S. L., Yaspo, M. L., Korbel, J. O., Korshunov, A., Eils, R., Pfister, S. M. and Lichter, P. (2012) Dissecting the genomic complexity underlying medulloblastoma. Nature 488, 100-105.
-
(2012)
Nature
, vol.488
, pp. 100-105
-
-
Jones, D.T.1
Jager, N.2
Kool, M.3
Zichner, T.4
Hutter, B.5
Sultan, M.6
Cho, Y.J.7
Pugh, T.J.8
Hovestadt, V.9
Stutz, A.M.10
Rausch, T.11
Warnatz, H.J.12
Ryzhova, M.13
Bender, S.14
Sturm, D.15
Pleier, S.16
Cin, H.17
Pfaff, E.18
Sieber, L.19
Wittmann, A.20
Remke, M.21
Witt, H.22
Hutter, S.23
Tzaridis, T.24
Weischenfeldt, J.25
Raeder, B.26
Avci, M.27
Amstislavskiy, V.28
Zapatka, M.29
Weber, U.D.30
Wang, Q.31
Lasitschka, B.32
Bartholomae, C.C.33
Schmidt, M.34
von Kalle, C.35
Ast, V.36
Lawerenz, C.37
Eils, J.38
Kabbe, R.39
Benes, V.40
van Sluis, P.41
Koster, J.42
Volckmann, R.43
Shih, D.44
Betts, M.J.45
Russell, R.B.46
Coco, S.47
Tonini, G.P.48
Schuller, U.49
Hans, V.50
Graf, N.51
Kim, Y.J.52
Monoranu, C.53
Roggendorf, W.54
Unterberg, A.55
Herold-Mende, C.56
Milde, T.57
Kulozik, A.E.58
von Deimling, A.59
Witt, O.60
Maass, E.61
Rossler, J.62
Ebinger, M.63
Schuhmann, M.U.64
Fruhwald, M.C.65
Hasselblatt, M.66
Jabado, N.67
Rutkowski, S.68
von Bueren, A.O.69
Williamson, D.70
Clifford, S.C.71
McCabe, M.G.72
Collins, V.P.73
Wolf, S.74
Wiemann, S.75
Lehrach, H.76
Brors, B.77
Scheurlen, W.78
Felsberg, J.79
Reifenberger, G.80
Northcott, P.A.81
Taylor, M.D.82
Meyerson, M.83
Pomeroy, S.L.84
Yaspo, M.L.85
Korbel, J.O.86
Korshunov, A.87
Eils, R.88
Pfister, S.M.89
Lichter, P.90
more..
-
59
-
-
84861576201
-
The landscape of cancer genes and mutational processes in breast cancer
-
Oslo Breast Cancer Consortium (OSBREAC)
-
Stephens, P. J., Tarpey, P. S., Davies, H., Van Loo, P., Greenman, C., Wedge, D. C., Nik-Zainal, S., Martin, S., Varela, I., Bignell, G. R., Yates, L. R., Papaemmanuil, E., Beare, D., Butler, A., Cheverton, A., Gamble, J., Hinton, J., Jia, M., Jayakumar, A., Jones, D., Latimer, C., Lau, K. W., McLaren, S., McBride, D. J., Menzies, A., Mudie, L., Raine, K., Rad, R., Chapman, M. S., Teague, J., Easton, D., Langerod, A., Oslo Breast Cancer Consortium (OSBREAC), Lee, M. T., Shen, C. Y., Tee, B. T., Huimin, B. W., Broeks, A., Vargas, A. C., Turashvili, G., Martens, J., Fatima, A., Miron, P., Chin, S. F., Thomas, G., Boyault, S., Mariani, O., Lakhani, S. R., van de Vijver, M., van 't Veer, L., Foekens, J., Desmedt, C., Sotiriou, C., Tutt, A., Caldas, C., Reis-Filho, J. S, Aparicio, S. A., Salomon, A. V., Borresen-Dale, A. L., Richardson, A. L., Campbell, P. J., Futreal, P. A. and Stratton, M. R. (2012) The landscape of cancer genes and mutational processes in breast cancer. Nature 486, 400-404.
-
(2012)
Nature
, vol.486
, pp. 400-404
-
-
Stephens, P.J.1
Tarpey, P.S.2
Davies, H.3
Van Loo, P.4
Greenman, C.5
Wedge, D.C.6
Nik-Zainal, S.7
Martin, S.8
Varela, I.9
Bignell, G.R.10
Yates, L.R.11
Papaemmanuil, E.12
Beare, D.13
Butler, A.14
Cheverton, A.15
Gamble, J.16
Hinton, J.17
Jia, M.18
Jayakumar, A.19
Jones, D.20
Latimer, C.21
Lau, K.W.22
McLaren, S.23
McBride, D.J.24
Menzies, A.25
Mudie, L.26
Raine, K.27
Rad, R.28
Chapman, M.S.29
Teague, J.30
Easton, D.31
Langerod, A.32
Lee, M.T.33
Shen, C.Y.34
Tee, B.T.35
Huimin, B.W.36
Broeks, A.37
Vargas, A.C.38
Turashvili, G.39
Martens, J.40
Fatima, A.41
Miron, P.42
Chin, S.F.43
Thomas, G.44
Boyault, S.45
Mariani, O.46
Lakhani, S.R.47
van de Vijver, M.48
van't Veer, L.49
Foekens, J.50
Desmedt, C.51
Sotiriou, C.52
Tutt, A.53
Caldas, C.54
Reis-Filho, J.S.55
Aparicio, S.A.56
Salomon, A.V.57
Borresen-Dale, A.L.58
Richardson, A.L.59
Campbell, P.J.60
Futreal, P.A.61
Stratton, M.R.62
more..
-
60
-
-
84896702480
-
STAG2 is a clinically relevant tumor suppressor in pancreatic ductal adenocarcinoma
-
Evers, L., Perez-Mancera, P. A., Lenkiewicz, E., Tang, N., Aust, D., Knosel, T., Rummele, P., Holley, T., Kassner, M., Aziz, M., Ramanathan, R. K., Von Hoff, D. D., Yin, H., Pilarsky, C. and Barrett, M. T. (2014) STAG2 is a clinically relevant tumor suppressor in pancreatic ductal adenocarcinoma. Genome Med. 6, 9.
-
(2014)
Genome Med.
, vol.6
, pp. 9
-
-
Evers, L.1
Perez-Mancera, P.A.2
Lenkiewicz, E.3
Tang, N.4
Aust, D.5
Knosel, T.6
Rummele, P.7
Holley, T.8
Kassner, M.9
Aziz, M.10
Ramanathan, R.K.11
Von Hoff, D.D.12
Yin, H.13
Pilarsky, C.14
Barrett, M.T.15
-
61
-
-
84884418423
-
Frameshift mutations of chromosome cohesion-related genes SGOL1 and PDS5B in gastric and colorectal cancers with high microsatellite instability
-
Kim, M. S., An, C. H., Yoo, N. J. and Lee, S. H. (2013) Frameshift mutations of chromosome cohesion-related genes SGOL1 and PDS5B in gastric and colorectal cancers with high microsatellite instability. Hum. Pathol. 44, 2234-2240.
-
(2013)
Hum. Pathol.
, vol.44
, pp. 2234-2240
-
-
Kim, M.S.1
An, C.H.2
Yoo, N.J.3
Lee, S.H.4
-
62
-
-
0027059030
-
Cloning and characterization of rad21 an essential gene of Schizosaccharomyces pombe involved in DNA double-strand-break repair
-
Birkenbihl, R. P. and Subramani, S. (1992) Cloning and characterization of rad21 an essential gene of Schizosaccharomyces pombe involved in DNA double-strand-break repair. Nucleic Acids Res. 20, 6605-6611.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 6605-6611
-
-
Birkenbihl, R.P.1
Subramani, S.2
-
63
-
-
0035954251
-
Sister chromatid cohesion is required for postreplicative double-strand break repair in Saccharomyces cerevisiae
-
Sjogren, C. and Nasmyth, K. (2001) Sister chromatid cohesion is required for postreplicative double-strand break repair in Saccharomyces cerevisiae. Curr. Biol. 11, 991-995.
-
(2001)
Curr. Biol.
, vol.11
, pp. 991-995
-
-
Sjogren, C.1
Nasmyth, K.2
-
64
-
-
10944232673
-
Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair
-
Strom, L., Lindroos, H. B., Shirahige, K. and Sjogren, C. (2004) Postreplicative recruitment of cohesin to double-strand breaks is required for DNA repair. Mol. Cell 16, 1003-1015.
-
(2004)
Mol. Cell
, vol.16
, pp. 1003-1015
-
-
Strom, L.1
Lindroos, H.B.2
Shirahige, K.3
Sjogren, C.4
-
65
-
-
34447549077
-
Postreplicative formation of cohesion is required for repair and induced by a single DNA break
-
Strom, L., Karlsson, C., Lindroos, H. B., Wedahl, S., Katou, Y., Shirahige, K. and Sjogren, C. (2007) Postreplicative formation of cohesion is required for repair and induced by a single DNA break. Science 317, 242-245.
-
(2007)
Science
, vol.317
, pp. 242-245
-
-
Strom, L.1
Karlsson, C.2
Lindroos, H.B.3
Wedahl, S.4
Katou, Y.5
Shirahige, K.6
Sjogren, C.7
-
66
-
-
77449141863
-
Cohesin promotes the repair of ionizing radiation-induced DNA double-strand breaks in replicated chromatin
-
Bauerschmidt, C., Arrichiello, C., Burdak-Rothkamm, S., Woodcock, M., Hill, M. A., Stevens, D. L. and Rothkamm, K. (2010) Cohesin promotes the repair of ionizing radiation-induced DNA double-strand breaks in replicated chromatin. Nucleic Acids Res. 38, 477-487.
-
(2010)
Nucleic Acids Res.
, vol.38
, pp. 477-487
-
-
Bauerschmidt, C.1
Arrichiello, C.2
Burdak-Rothkamm, S.3
Woodcock, M.4
Hill, M.A.5
Stevens, D.L.6
Rothkamm, K.7
-
67
-
-
84867399846
-
Cohesin association to replication sites depends on rad50 and promotes fork restart
-
Tittel-Elmer, M., Lengronne, A., Davidson, M. B., Bacal, J., Francois, P., Hohl, M., Petrini, J. H., Pasero, P. and Cobb, J. A. (2012) Cohesin association to replication sites depends on rad50 and promotes fork restart. Mol. Cell 48, 98-108.
-
(2012)
Mol. Cell
, vol.48
, pp. 98-108
-
-
Tittel-Elmer, M.1
Lengronne, A.2
Davidson, M.B.3
Bacal, J.4
Francois, P.5
Hohl, M.6
Petrini, J.H.7
Pasero, P.8
Cobb, J.A.9
-
68
-
-
84355166398
-
SMC1A codon 496 mutations affect the cellular response to genotoxic treatments
-
Mannini, L., Menga, S., Tonelli, A., Zanotti, S., Bassi, M. T., Magnani, C. and Musio, A. (2012) SMC1A codon 496 mutations affect the cellular response to genotoxic treatments. Am. J. Med. Genet. 158A, 224-228.
-
(2012)
Am. J. Med. Genet.
, vol.158 A
, pp. 224-228
-
-
Mannini, L.1
Menga, S.2
Tonelli, A.3
Zanotti, S.4
Bassi, M.T.5
Magnani, C.6
Musio, A.7
-
69
-
-
84896309068
-
Glioblastoma cells containing mutations in the cohesin component STAG2 are sensitive to PARP inhibition
-
Bailey, M. L., O'Neil, N. J., van Pel, D. M., Solomon, D. A., Waldman, T. and Hieter, P. (2014) Glioblastoma cells containing mutations in the cohesin component STAG2 are sensitive to PARP inhibition. Mol. Cancer Ther. 13, 724-732.
-
(2014)
Mol. Cancer Ther.
, vol.13
, pp. 724-732
-
-
Bailey, M.L.1
O'Neil, N.J.2
van Pel, D.M.3
Solomon, D.A.4
Waldman, T.5
Hieter, P.6
|