-
1
-
-
84882837534
-
Signatures of mutational processes in human cancer
-
Alexandrov LB, Nik-Zainal S, Wedge DC, Aparicio SA, Behjati S, et al. 2013. Signatures of mutational processes in human cancer. Nature 500:415-21
-
(2013)
Nature
, vol.500
, pp. 415-421
-
-
Alexandrov, L.B.1
Nik-Zainal, S.2
Wedge, D.C.3
Aparicio, S.A.4
Behjati, S.5
-
2
-
-
0017807188
-
Selectivemultiplication of dihydrofolate reductase genes in methotrexate-resistant variants of cultured murine cells
-
Alt FW, Kellems RE, Bertino JR, Schimke RT. 1978. Selectivemultiplication of dihydrofolate reductase genes in methotrexate-resistant variants of cultured murine cells. J. Biol. Chem. 253:1357-70
-
(1978)
J. Biol. Chem
, vol.253
, pp. 1357-1370
-
-
Alt, F.W.1
Kellems, R.E.2
Bertino, J.R.3
Schimke, R.T.4
-
3
-
-
4444264564
-
Hotspots of mammalian chromosomal evolution
-
Bailey JA, Baertsch R, Kent WJ, Haussler D, Eichler EE. 2004. Hotspots of mammalian chromosomal evolution. Genome Biol. 5:R23
-
(2004)
Genome Biol
, vol.5
, pp. R23
-
-
Bailey, J.A.1
Baertsch, R.2
Kent, W.J.3
Haussler, D.4
Eichler, E.E.5
-
4
-
-
84888001845
-
Genome dynamics during experimental evolution
-
Barrick JE,LenskiRE. 2013. Genome dynamics during experimental evolution. Nat. Rev. Genet. 14:827-39
-
(2013)
Nat. Rev. Genet
, vol.14
, pp. 827-839
-
-
Barrick, J.E.1
Lenski, R.E.2
-
5
-
-
77249119762
-
The landscape of somatic copy-number alteration across human cancers
-
Beroukhim R, Mermel CH, Porter D, Wei G, Raychaudhuri S, et al. 2010. The landscape of somatic copy-number alteration across human cancers. Nature 463:899-905
-
(2010)
Nature
, vol.463
, pp. 899-905
-
-
Beroukhim, R.1
Mermel, C.H.2
Porter, D.3
Wei, G.4
Raychaudhuri, S.5
-
6
-
-
34548441098
-
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution
-
Bignell GR, Santarius T, Pole JC, Butler AP, Perry J, et al. 2007. Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution. Genome Res. 17:1296-303
-
(2007)
Genome Res
, vol.17
, pp. 1296-1303
-
-
Bignell, G.R.1
Santarius, T.2
Pole, J.C.3
Butler, A.P.4
Perry, J.5
-
7
-
-
78650634202
-
Micronuclei frequency in peripheral blood lymphocytes and cancer risk: Evidence from human studies
-
Bonassi S, El-Zein R, Bolognesi C, Fenech M. 2011. Micronuclei frequency in peripheral blood lymphocytes and cancer risk: evidence from human studies. Mutagenesis 26:93-100
-
(2011)
Mutagenesis
, vol.26
, pp. 93-100
-
-
Bonassi, S.1
El-Zein, R.2
Bolognesi, C.3
Fenech, M.4
-
8
-
-
26444557705
-
Engineering translocations with delayed replication: Evidence for cis control of chromosome replication timing
-
Breger KS, Smith L, Thayer MJ. 2005. Engineering translocations with delayed replication: evidence for cis control of chromosome replication timing. Hum. Mol. Genet. 14:2813-27
-
(2005)
Hum. Mol. Genet
, vol.14
, pp. 2813-2827
-
-
Breger, K.S.1
Smith, L.2
Thayer, M.J.3
-
9
-
-
84893000347
-
Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens
-
Cai H, Kumar N, Bagheri HC, von Mering C, Robinson MD, Baudis M. 2014. Chromothripsis-like patterns are recurring but heterogeneously distributed features in a survey of 22,347 cancer genome screens. BMC Genomics 15:82
-
(2014)
BMC Genomics
, vol.15
, pp. 82
-
-
Cai, H.1
Kumar, N.2
Bagheri, H.C.3
Von Mering, C.4
Robinson, M.D.5
Baudis, M.6
-
10
-
-
84884413307
-
Properties and rates of germline mutations in humans
-
Campbell CD, Eichler EE. 2013. Properties and rates of germline mutations in humans. Trends Genet. 29:575-84
-
(2013)
Trends Genet
, vol.29
, pp. 575-584
-
-
Campbell, C.D.1
Eichler, E.E.2
-
11
-
-
44349191457
-
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
-
Campbell PJ, Stephens PJ, Pleasance ED, O'Meara S, Li H, et al. 2008. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat. Genet. 40:722-29
-
(2008)
Nat. Genet
, vol.40
, pp. 722-729
-
-
Campbell, P.J.1
Stephens, P.J.2
Pleasance, E.D.3
O'Meara, S.4
Li, H.5
-
12
-
-
84907284157
-
Gibbon genome and the fast karyotype evolution of small apes
-
Carbone L, Harris RA, Gnerre S, Veeramah KR, Lorente-Galdos B, et al. 2014. Gibbon genome and the fast karyotype evolution of small apes. Nature 513:195-201
-
(2014)
Nature
, vol.513
, pp. 195-201
-
-
Carbone, L.1
Harris, R.A.2
Gnerre, S.3
Veeramah, K.R.4
Lorente-Galdos, B.5
-
13
-
-
84866405520
-
Centromere remodeling in Hoolock leuconedys (Hylobatidae) by a new transposable element unique to the gibbons
-
Carbone L, Harris RA, Mootnick AR,Milosavljevic A,Martin DI, et al. 2012. Centromere remodeling in Hoolock leuconedys (Hylobatidae) by a new transposable element unique to the gibbons. Genome Biol. Evol. 4:648-58
-
(2012)
Genome Biol. Evol
, vol.4
, pp. 648-658
-
-
Carbone, L.1
Harris, R.A.2
Mootnick, A.R.3
Milosavljevic, A.4
Martin, D.I.5
-
14
-
-
0023879118
-
Double minute chromosomes can be produced from precursors derived from a chromosomal deletion
-
Carroll SM, DeRose ML, Gaudray P, Moore CM, Needham-Vandevanter DR, et al. 1988. Double minute chromosomes can be produced from precursors derived from a chromosomal deletion. Mol. Cell. Biol. 8:1525-33
-
(1988)
Mol. Cell. Biol
, vol.8
, pp. 1525-1533
-
-
Carroll, S.M.1
DeRose, M.L.2
Gaudray, P.3
Moore, C.M.4
Needham-Vandevanter, D.R.5
-
15
-
-
85027936863
-
Replicative mechanisms for CNV formation are error prone
-
Carvalho CM, Pehlivan D, Ramocki MB, Fang P, Alleva B, et al. 2013. Replicative mechanisms for CNV formation are error prone. Nat. Genet. 45:1319-26
-
(2013)
Nat. Genet
, vol.45
, pp. 1319-1326
-
-
Carvalho, C.M.1
Pehlivan, D.2
Ramocki, M.B.3
Fang, P.4
Alleva, B.5
-
16
-
-
84948731931
-
Clusters of multiple mutations: Incidence and molecular mechanisms
-
Chan K, Gordenin DA. 2015. Clusters of multiple mutations: incidence and molecular mechanisms. Annu. Rev. Genet. 49:243-67
-
(2015)
Annu. Rev. Genet
, vol.49
, pp. 243-267
-
-
Chan, K.1
Gordenin, D.A.2
-
17
-
-
77950661675
-
Impact of replication timing on non-CpG and CpG substitution rates in mammalian genomes
-
Chen CL, Rappailles A, Duquenne L, Huvet M, Guilbaud G, et al. 2010. Impact of replication timing on non-CpG and CpG substitution rates in mammalian genomes. Genome Res. 20:447-57
-
(2010)
Genome Res
, vol.20
, pp. 447-457
-
-
Chen, C.L.1
Rappailles, A.2
Duquenne, L.3
Huvet, M.4
Guilbaud, G.5
-
18
-
-
84862777955
-
Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration
-
S1
-
Chiang C, Jacobsen JC, Ernst C, Hanscom C, Heilbut A, et al. 2012. Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration. Nat. Genet. 44:390-97, S1
-
(2012)
Nat. Genet
, vol.44
, pp. 390-397
-
-
Chiang, C.1
Jacobsen, J.C.2
Ernst, C.3
Hanscom, C.4
Heilbut, A.5
-
19
-
-
80053558376
-
Genome-wide translocation sequencing reveals mechanisms of chromosome breaks and rearrangements in B cells
-
Chiarle R, Zhang Y, Frock RL, Lewis SM,Molinie B, et al. 2011. Genome-wide translocation sequencing reveals mechanisms of chromosome breaks and rearrangements in B cells. Cell 147:107-19
-
(2011)
Cell
, vol.147
, pp. 107-119
-
-
Chiarle, R.1
Zhang, Y.2
Frock, R.L.3
Lewis, S.M.4
Molinie, B.5
-
20
-
-
0020392841
-
Double minutes and homogeneously staining regions: Gene amplification in mammalian cells
-
Cowell JK. 1982. Double minutes and homogeneously staining regions: gene amplification in mammalian cells. Annu. Rev. Genet. 16:21-59
-
(1982)
Annu. Rev. Genet
, vol.16
, pp. 21-59
-
-
Cowell, J.K.1
-
21
-
-
0026542841
-
DNA replication in cell-free extracts from Xenopus eggs is prevented by disrupting nuclear envelope function
-
Cox LS. 1992. DNA replication in cell-free extracts from Xenopus eggs is prevented by disrupting nuclear envelope function. J. Cell Sci. 101(Pt. 1):43-53
-
(1992)
J. Cell Sci
, vol.101
, pp. 43-53
-
-
Cox, L.S.1
-
22
-
-
84856424908
-
DNAbreaks and chromosome pulverization from errors in mitosis
-
Crasta K,GanemNJ, Dagher R, Lantermann AB, Ivanova EV, et al. 2012.DNAbreaks and chromosome pulverization from errors in mitosis. Nature 482:53-58
-
(2012)
Nature
, vol.482
, pp. 53-58
-
-
Crasta, K.1
Ganem, N.J.2
Dagher, R.3
Lantermann, A.B.4
Ivanova, E.V.5
-
24
-
-
0020691434
-
Unstable methotrexate resistance in human small-cell carcinoma associated with doubleminute chromosomes
-
Curt GA, Carney DN, Cowan KH, Jolivet J, Bailey BD, et al. 1983. Unstable methotrexate resistance in human small-cell carcinoma associated with doubleminute chromosomes. N. Engl. J.Med. 308:199-202
-
(1983)
N. Engl. J. Med
, vol.308
, pp. 199-202
-
-
Curt, G.A.1
Carney, D.N.2
Cowan, K.H.3
Jolivet, J.4
Bailey, B.D.5
-
25
-
-
84908695210
-
The somatic genomic landscape of chromophobe renal cell carcinoma
-
Davis CF, Ricketts CJ,Wang M, Yang L, Cherniack AD, et al. 2014. The somatic genomic landscape of chromophobe renal cell carcinoma. Cancer Cell 26:319-30
-
(2014)
Cancer Cell
, vol.26
, pp. 319-330
-
-
Davis, C.F.1
Ricketts, C.J.2
Wang, M.3
Yang, L.4
Cherniack, A.D.5
-
26
-
-
84887992179
-
Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome
-
Davoli T, Xu AW,Mengwasser KE, Sack LM, Yoon JC, et al. 2013. Cumulative haploinsufficiency and triplosensitivity drive aneuploidy patterns and shape the cancer genome. Cell 155:948-62
-
(2013)
Cell
, vol.155
, pp. 948-962
-
-
Davoli, T.1
Xu, A.W.2
Mengwasser, K.E.3
Sack, L.M.4
Yoon, J.C.5
-
27
-
-
33746425690
-
Telomere-related genome instability in cancer
-
De Lange T. 2005. Telomere-related genome instability in cancer. Cold Spring Harb. Symp. Quant. Biol. 70:197-204
-
(2005)
Cold Spring Harb. Symp. Quant. Biol
, vol.70
, pp. 197-204
-
-
De Lange, T.1
-
28
-
-
84926249075
-
Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring
-
de Pagter MS, van RoosmalenMJ, Baas AF, Renkens I, DuranKJ, et al. 2015. Chromothripsis in healthy individuals affects multiple protein-coding genes and can result in severe congenital abnormalities in offspring. Am. J. Hum. Genet. 96:651-56
-
(2015)
Am. J. Hum. Genet
, vol.96
, pp. 651-656
-
-
De Pagter, M.S.1
Van Roosmalen, M.J.2
Baas, A.F.3
Renkens, I.4
Duran, K.J.5
-
29
-
-
83255189766
-
DNA replication timing and long-range DNA interactions predict mutational landscapes of cancer genomes
-
De S, Michor F. 2011. DNA replication timing and long-range DNA interactions predict mutational landscapes of cancer genomes. Nat. Biotechnol. 29:1103-8
-
(2011)
Nat. Biotechnol
, vol.29
, pp. 1103-1108
-
-
De, S.1
Michor, F.2
-
30
-
-
84655167711
-
Common fragile sites: Mechanisms of instability revisited
-
Debatisse M, Le Tallec B, Letessier A, Dutrillaux B, BrisonO. 2012. Common fragile sites: mechanisms of instability revisited. Trends Genet. 28:22-32
-
(2012)
Trends Genet
, vol.28
, pp. 22-32
-
-
Debatisse, M.1
Le Tallec, B.2
Letessier, A.3
Dutrillaux, B.4
Brison, O.5
-
31
-
-
84896711553
-
Tolerance of wholegenome doubling propagates chromosomal instability and accelerates cancer genome evolution
-
Dewhurst SM, McGranahan N, Burrell RA, Rowan AJ, Gronroos E, et al. 2014. Tolerance of wholegenome doubling propagates chromosomal instability and accelerates cancer genome evolution. Cancer Discov. 4:175-85
-
(2014)
Cancer Discov
, vol.4
, pp. 175-185
-
-
Dewhurst, S.M.1
McGranahan, N.2
Burrell, R.A.3
Rowan, A.J.4
Gronroos, E.5
-
32
-
-
84929103936
-
Sequential cancer mutations in cultured human intestinal stem cells
-
Drost J, van Jaarsveld RH, Ponsioen B, Zimberlin C, van Boxtel R, et al. 2015. Sequential cancer mutations in cultured human intestinal stem cells. Nature 521:43-47
-
(2015)
Nature
, vol.521
, pp. 43-47
-
-
Drost, J.1
Van Jaarsveld, R.H.2
Ponsioen, B.3
Zimberlin, C.4
Van Boxtel, R.5
-
33
-
-
29144522146
-
Premature condensation induces breaks at the interface of early and late replicating chromosome bands bearing common fragile sites
-
El Achkar E, Gerbault-Seureau M, Muleris M, Dutrillaux B, Debatisse M. 2005. Premature condensation induces breaks at the interface of early and late replicating chromosome bands bearing common fragile sites. PNAS 102:18069-74
-
(2005)
PNAS
, vol.102
, pp. 18069-18074
-
-
El Achkar, E.1
Gerbault-Seureau, M.2
Muleris, M.3
Dutrillaux, B.4
Debatisse, M.5
-
35
-
-
34250187067
-
Cytokinesis-block micronucleus cytome assay
-
Fenech M. 2007. Cytokinesis-block micronucleus cytome assay. Nat. Protoc. 2:1084-104
-
(2007)
Nat. Protoc
, vol.2
, pp. 1084-1104
-
-
Fenech, M.1
-
36
-
-
78650664775
-
Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells
-
Fenech M, Kirsch-Volders M, Natarajan AT, Surralles J, Crott JW, et al. 2011. Molecular mechanisms of micronucleus, nucleoplasmic bridge and nuclear bud formation in mammalian and human cells. Mutagenesis 26:125-32
-
(2011)
Mutagenesis
, vol.26
, pp. 125-132
-
-
Fenech, M.1
Kirsch-Volders, M.2
Natarajan, A.T.3
Surralles, J.4
Crott, J.W.5
-
37
-
-
0022589981
-
Cytokinesis-block micronucleus method in human lymphocytes: Effect of in vivo ageing and low dose X-irradiation
-
Fenech M, Morley AA. 1986. Cytokinesis-block micronucleus method in human lymphocytes: effect of in vivo ageing and low dose X-irradiation. Mutat. Res. 161:193-98
-
(1986)
Mutat. Res
, vol.161
, pp. 193-198
-
-
Fenech, M.1
Morley, A.A.2
-
39
-
-
38049178545
-
Transcription-coupled nucleotide excision repair in mammalian cells: Molecular mechanisms and biological effects
-
Fousteri M, Mullenders LH. 2008. Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects. Cell Res. 18:73-84
-
(2008)
Cell Res
, vol.18
, pp. 73-84
-
-
Fousteri, M.1
Mullenders, L.H.2
-
40
-
-
84905447834
-
EGFR variant heterogeneity in glioblastoma resolved through single-nucleus sequencing
-
Francis JM, Zhang CZ, Maire CL, Jung J, Manzo VE, et al. 2014. EGFR variant heterogeneity in glioblastoma resolved through single-nucleus sequencing. Cancer Discov. 4:956-71
-
(2014)
Cancer Discov
, vol.4
, pp. 956-971
-
-
Francis, J.M.1
Zhang, C.Z.2
Maire, C.L.3
Jung, J.4
Manzo, V.E.5
-
41
-
-
27144507868
-
Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells
-
Fujiwara T, BandiM, Nitta M, Ivanova EV, Bronson RT, Pellman D. 2005. Cytokinesis failure generating tetraploids promotes tumorigenesis in p53-null cells. Nature 437:1043-47
-
(2005)
Nature
, vol.437
, pp. 1043-1047
-
-
Fujiwara, T.1
Bandi, M.2
Nitta, M.3
Ivanova, E.V.4
Bronson, R.T.5
Pellman, D.6
-
42
-
-
67649467032
-
A mechanism linking extra centrosomes to chromosomal instability
-
Ganem NJ, Godinho SA, Pellman D. 2009. A mechanism linking extra centrosomes to chromosomal instability. Nature 460:278-82
-
(2009)
Nature
, vol.460
, pp. 278-282
-
-
Ganem, N.J.1
Godinho, S.A.2
Pellman, D.3
-
43
-
-
84872026180
-
Linking abnormal mitosis to the acquisition of DNA damage
-
GanemNJ, Pellman D. 2012. Linking abnormal mitosis to the acquisition of DNA damage. J. Cell Biol. 199:871-81
-
(2012)
J. Cell Biol
, vol.199
, pp. 871-881
-
-
Ganem, N.J.1
Pellman, D.2
-
44
-
-
84912101773
-
The architecture and evolution of cancer neochromosomes
-
Garsed DW,Marshall OJ, Corbin VD,Hsu A, Di Stefano L, et al. 2014. The architecture and evolution of cancer neochromosomes. Cancer Cell 26:653-67
-
(2014)
Cancer Cell
, vol.26
, pp. 653-667
-
-
Garsed, D.W.1
Marshall, O.J.2
Corbin, V.D.3
Hsu, A.4
Di Stefano, L.5
-
46
-
-
0024542489
-
Threedimensional organization of micronuclei induced by colchicine in PtK1 cells
-
Geraud G, Laquerriere F, Masson C, Arnoult J, Labidi B, Hernandez-Verdun D. 1989. Threedimensional organization of micronuclei induced by colchicine in PtK1 cells. Exp. Cell Res. 181:27-39
-
(1989)
Exp. Cell Res
, vol.181
, pp. 27-39
-
-
Geraud, G.1
Laquerriere, F.2
Masson, C.3
Arnoult, J.4
Labidi, B.5
Hernandez-Verdun, D.6
-
47
-
-
77952519546
-
Extrachromosomal amplification mechanisms in a glioma with amplified sequences from multiple chromosome loci
-
Gibaud A, Vogt N, Hadj-Hamou NS, Meyniel JP, Hupe P, et al. 2010. Extrachromosomal amplification mechanisms in a glioma with amplified sequences from multiple chromosome loci. Hum. Mol. Genet. 19:1276-85
-
(2010)
Hum. Mol. Genet
, vol.19
, pp. 1276-1285
-
-
Gibaud, A.1
Vogt, N.2
Hadj-Hamou, N.S.3
Meyniel, J.P.4
Hupe, P.5
-
48
-
-
0035144955
-
Abnormal nuclear shape in solid tumors reflects mitotic instability
-
Gisselsson D, Bjork J, Hoglund M, Mertens F, Dal Cin P, et al. 2001. Abnormal nuclear shape in solid tumors reflects mitotic instability. Am. J. Pathol. 158:199-206
-
(2001)
Am. J. Pathol
, vol.158
, pp. 199-206
-
-
Gisselsson, D.1
Bjork, J.2
Hoglund, M.3
Mertens, F.4
Dal Cin, P.5
-
49
-
-
0345711466
-
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
-
Gisselsson D,HoglundM,Mertens F, Johansson B, Dal Cin P, et al. 1999. The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells. Hum. Genet. 104:315-25
-
(1999)
Hum. Genet
, vol.104
, pp. 315-325
-
-
Gisselsson, D.1
Hoglund, M.2
Mertens, F.3
Johansson, B.4
Dal Cin, P.5
-
50
-
-
12944329959
-
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
-
Gisselsson D, Pettersson L, Hoglund M, Heidenblad M, Gorunova L, et al. 2000. Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity. PNAS 97:5357-62
-
(2000)
PNAS
, vol.97
, pp. 5357-5362
-
-
Gisselsson, D.1
Pettersson, L.2
Hoglund, M.3
Heidenblad, M.4
Gorunova, L.5
-
51
-
-
84857192718
-
Causes and consequences of aneuploidy in cancer
-
Gordon DJ, Resio B, 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
-
52
-
-
79953032797
-
Mechanisms that promote and suppress chromosomal translocations in lymphocytes
-
Gostissa M, Alt FW, Chiarle R. 2011. Mechanisms that promote and suppress chromosomal translocations in lymphocytes. Annu. Rev. Immunol. 29:319-50
-
(2011)
Annu. Rev. Immunol
, vol.29
, pp. 319-350
-
-
Gostissa, M.1
Alt, F.W.2
Chiarle, R.3
-
53
-
-
0028965374
-
Inhibition of protein serine/threonine phosphatases directly induces premature chromosome condensation in mammalian somatic cells
-
Gotoh E, Asakawa Y, Kosaka H. 1995. Inhibition of protein serine/threonine phosphatases directly induces premature chromosome condensation in mammalian somatic cells. Biomed. Res. 16:63-68
-
(1995)
Biomed. Res
, vol.16
, pp. 63-68
-
-
Gotoh, E.1
Asakawa, Y.2
Kosaka, H.3
-
56
-
-
0021945470
-
Ultrastructural features of minute chromosomes in a methotrexate-resistant mouse 3T3 cell line
-
Hamkalo BA, Farnham PJ, Johnston R, Schimke RT. 1985. Ultrastructural features of minute chromosomes in a methotrexate-resistant mouse 3T3 cell line. PNAS 82:1126-30
-
(1985)
PNAS
, vol.82
, pp. 1126-1130
-
-
Hamkalo, B.A.1
Farnham, P.J.2
Johnston, R.3
Schimke, R.T.4
-
57
-
-
84879956366
-
Catastrophic nuclear envelope collapse in cancer cell micronuclei
-
Hatch EM, Fischer AH, Deerinck TJ, Hetzer MW. 2013. Catastrophic nuclear envelope collapse in cancer cell micronuclei. Cell 154:47-60
-
(2013)
Cell
, vol.154
, pp. 47-60
-
-
Hatch, E.M.1
Fischer, A.H.2
Deerinck, T.J.3
Hetzer, M.W.4
-
58
-
-
84861308305
-
A telomere-dependent DNA damage checkpoint induced by prolonged mitotic arrest
-
HayashiMT, Cesare AJ, Fitzpatrick JA, Lazzerini-Denchi E, Karlseder J. 2012. A telomere-dependent DNA damage checkpoint induced by prolonged mitotic arrest. Nat. Struct. Mol. Biol. 19:387-94
-
(2012)
Nat. Struct. Mol. Biol
, vol.19
, pp. 387-394
-
-
Hayashi, M.T.1
Cesare, A.J.2
Fitzpatrick, J.A.3
Lazzerini-Denchi, E.4
Karlseder, J.5
-
59
-
-
33750890143
-
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays
-
Heidenblad M, Hallor KH, Staaf J, Jonsson G, Borg A, et al. 2006. Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays. Oncogene 25:7106-16
-
(2006)
Oncogene
, vol.25
, pp. 7106-7116
-
-
Heidenblad, M.1
Hallor, K.H.2
Staaf, J.3
Jonsson, G.4
Borg, A.5
-
60
-
-
84906303775
-
Mechanisms underlying mutational signatures in human cancers
-
Helleday T, Eshtad S, Nik-Zainal S. 2014. Mechanisms underlying mutational signatures in human cancers. Nat. Rev. Genet. 15:585-98
-
(2014)
Nat. Rev. Genet
, vol.15
, pp. 585-598
-
-
Helleday, T.1
Eshtad, S.2
Nik-Zainal, S.3
-
62
-
-
77954328102
-
Increased mutagenesis and unique mutation signature associated with mitotic gene conversion
-
HicksWM, Kim M, Haber JE. 2010. Increased mutagenesis and unique mutation signature associated with mitotic gene conversion. Science 329:82-85
-
(2010)
Science
, vol.329
, pp. 82-85
-
-
Hicks, W.M.1
Kim, M.2
Haber, J.E.3
-
63
-
-
80054754012
-
The large-scale distribution of somatic mutations in cancer genomes
-
Hodgkinson A, Chen Y, Eyre-Walker A. 2012. The large-scale distribution of somatic mutations in cancer genomes. Hum. Mutat. 33:136-43
-
(2012)
Hum. Mutat
, vol.33
, pp. 136-143
-
-
Hodgkinson, A.1
Chen, Y.2
Eyre-Walker, A.3
-
64
-
-
3543013739
-
Resolution of anaphase bridges in cancer cells
-
HoffelderDR, Luo L, BurkeNA, Watkins SC, Gollin SM, SaundersWS. 2004. Resolution of anaphase bridges in cancer cells. Chromosoma 112:389-97
-
(2004)
Chromosoma
, vol.112
, pp. 389-397
-
-
Hoffelder, D.R.1
Luo, L.2
Burke, N.A.3
Watkins, S.C.4
Gollin, S.M.5
Saunders, W.S.6
-
65
-
-
84869173265
-
Chromoanagenesis and cancer: Mechanisms and consequences of localized, complex chromosomal rearrangements
-
Holland AJ, Cleveland DW. 2012. Chromoanagenesis and cancer: mechanisms and consequences of localized, complex chromosomal rearrangements. Nat. Med. 18:1630-38
-
(2012)
Nat. Med
, vol.18
, pp. 1630-1638
-
-
Holland, A.J.1
Cleveland, D.W.2
-
66
-
-
84862822270
-
Lagging chromosomes entrapped in micronuclei are not "lost" by cells
-
Huang Y, Jiang L, Yi Q, Lv L, Wang Z, et al. 2012. Lagging chromosomes entrapped in micronuclei are not "lost" by cells. Cell Res. 22:932-35
-
(2012)
Cell Res
, vol.22
, pp. 932-935
-
-
Huang, Y.1
Jiang, L.2
Yi, Q.3
Lv, L.4
Wang, Z.5
-
67
-
-
84924030504
-
Limited mitochondrial permeabilization causes DNA damage and genomic instability in the absence of cell death
-
Ichim G, Lopez J, Ahmed SU, Muthalagu N, Giampazolias E, et al. 2015. Limited mitochondrial permeabilization causes DNA damage and genomic instability in the absence of cell death. Mol. Cell 57:860-72
-
(2015)
Mol. Cell
, vol.57
, pp. 860-872
-
-
Ichim, G.1
Lopez, J.2
Ahmed, S.U.3
Muthalagu, N.4
Giampazolias, E.5
-
68
-
-
84886784734
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
-
Jager N, Schlesner M, Jones DT, Raffel S, Mallm JP, et al. 2013. Hypermutation of the inactive X chromosome is a frequent event in cancer. Cell 155:567-81
-
(2013)
Cell
, vol.155
, pp. 567-581
-
-
Jager, N.1
Schlesner, M.2
Jones, D.T.3
Raffel, S.4
Mallm, J.P.5
-
69
-
-
80053364894
-
Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations
-
Janssen A, van der Burg M, Szuhai K, Kops GJ, Medema RH. 2011. Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations. Science 333:1895-98
-
(2011)
Science
, vol.333
, pp. 1895-1898
-
-
Janssen, A.1
Van Der Burg, M.2
Szuhai, K.3
Kops, G.J.4
Medema, R.H.5
-
70
-
-
0014959463
-
Mammalian cell fusion: Induction of premature chromosome condensation in interphase nuclei
-
Johnson RT, Rao PN. 1970. Mammalian cell fusion: induction of premature chromosome condensation in interphase nuclei. Nature 226:717-22
-
(1970)
Nature
, vol.226
, pp. 717-722
-
-
Johnson, R.T.1
Rao, P.N.2
-
71
-
-
84869065150
-
Chromothripsis: Chromosomes in crisis
-
Jones MJ, Jallepalli PV. 2012. Chromothripsis: chromosomes in crisis. Dev. Cell 23:908-17
-
(2012)
Dev. Cell
, vol.23
, pp. 908-917
-
-
Jones, M.J.1
Jallepalli, P.V.2
-
72
-
-
64549093730
-
Micronuclei frequency in peripheral blood lymphocytes of thyroid cancer patients after radioiodine therapy and its relationship with metastasis
-
Joseph LJ, Bhartiya US, Raut YS, Kand P, Hawaldar RW, Nair N. 2009. Micronuclei frequency in peripheral blood lymphocytes of thyroid cancer patients after radioiodine therapy and its relationship with metastasis. Mutat. Res. 675:35-40
-
(2009)
Mutat. Res
, vol.675
, pp. 35-40
-
-
Joseph, L.J.1
Bhartiya, U.S.2
Raut, Y.S.3
Kand, P.4
Hawaldar, R.W.5
Nair, N.6
-
73
-
-
0014105051
-
Chromosome pulverization in human binucleate cells following colcemid treatment
-
Kato H, Sandberg AA. 1967. Chromosome pulverization in human binucleate cells following colcemid treatment. J. Cell Biol. 34:35-45
-
(1967)
J. Cell Biol
, vol.34
, pp. 35-45
-
-
Kato, H.1
Sandberg, A.A.2
-
74
-
-
0011815638
-
Amplified dihydrofolate reductase genes in unstably methotrexate-resistant cells are associated with double minute chromosomes
-
Kaufman RJ, Brown PC, Schimke RT. 1979. Amplified dihydrofolate reductase genes in unstably methotrexate-resistant cells are associated with double minute chromosomes. PNAS 76:5669-73
-
(1979)
PNAS
, vol.76
, pp. 5669-5673
-
-
Kaufman, R.J.1
Brown, P.C.2
Schimke, R.T.3
-
75
-
-
84873391241
-
Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes
-
Kim TM, Xi R, Luquette LJ, Park RW, Johnson MD, Park PJ. 2013. Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes. Genome Res. 23:217-27
-
(2013)
Genome Res
, vol.23
, pp. 217-227
-
-
Kim, T.M.1
Xi, R.2
Luquette, L.J.3
Park, R.W.4
Johnson, M.D.5
Park, P.J.6
-
76
-
-
84862510603
-
Combinatorics of the breakage-fusion-bridge mechanism
-
Kinsella M, Bafna V. 2012. Combinatorics of the breakage-fusion-bridge mechanism. J. Comput. Biol. 19:662-78
-
(2012)
J. Comput. Biol
, vol.19
, pp. 662-678
-
-
Kinsella, M.1
Bafna, V.2
-
79
-
-
80053502216
-
Translocation-capture sequencing reveals the extent and nature of chromosomal rearrangements in B lymphocytes
-
Klein IA, ReschW, Jankovic M, Oliveira T, Yamane A, et al. 2011. Translocation-capture sequencing reveals the extent and nature of chromosomal rearrangements in B lymphocytes. Cell 147:95-106
-
(2011)
Cell
, vol.147
, pp. 95-106
-
-
Klein, I.A.1
Resch, W.2
Jankovic, M.3
Oliveira, T.4
Yamane, A.5
-
80
-
-
84879243533
-
Chromothripsis in congenital disorders and cancer: Similarities and differences
-
Kloosterman WP, Cuppen E. 2013. Chromothripsis in congenital disorders and cancer: similarities and differences. Curr. Opin. Cell Biol. 25:341-48
-
(2013)
Curr. Opin. Cell Biol
, vol.25
, pp. 341-348
-
-
Kloosterman, W.P.1
Cuppen, E.2
-
81
-
-
79955416773
-
Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline
-
Kloosterman WP, Guryev V, van Roosmalen M, Duran KJ, de Bruijn E, et al. 2011. Chromothripsis as a mechanism driving complex de novo structural rearrangements in the germline. Hum. Mol. Genet. 20:1916-24
-
(2011)
Hum. Mol. Genet
, vol.20
, pp. 1916-1924
-
-
Kloosterman, W.P.1
Guryev, V.2
Van Roosmalen, M.3
Duran, K.J.4
De Bruijn, E.5
-
82
-
-
84890443103
-
Prevalence and clinical implications of chromothripsis in cancer genomes
-
Kloosterman WP, Koster J, Molenaar JJ. 2014. Prevalence and clinical implications of chromothripsis in cancer genomes. Curr. Opin. Oncol. 26:64-72
-
(2014)
Curr. Opin. Oncol
, vol.26
, pp. 64-72
-
-
Kloosterman, W.P.1
Koster, J.2
Molenaar, J.J.3
-
83
-
-
84863105790
-
Constitutional chromothripsis rearrangements involve clustered double-strandedDNAbreaks and nonhomologous repair mechanisms
-
Kloosterman WP, Tavakoli-Yaraki M, van Roosmalen MJ, van Binsbergen E, Renkens I, et al. 2012. Constitutional chromothripsis rearrangements involve clustered double-strandedDNAbreaks and nonhomologous repair mechanisms. Cell Rep. 1:648-55
-
(2012)
Cell Rep
, vol.1
, pp. 648-655
-
-
Kloosterman, W.P.1
Tavakoli-Yaraki, M.2
Van Roosmalen, M.J.3
Van Binsbergen, E.4
Renkens, I.5
-
84
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
Knudson AG Jr. 1971. Mutation and cancer: statistical study of retinoblastoma. PNAS 68:820-23
-
(1971)
PNAS
, vol.68
, pp. 820-823
-
-
Knudson, A.G.1
-
85
-
-
84875135862
-
Criteria for inference of chromothripsis in cancer genomes
-
Korbel JO, Campbell PJ. 2013. Criteria for inference of chromothripsis in cancer genomes. Cell 152:1226-36
-
(2013)
Cell
, vol.152
, pp. 1226-1236
-
-
Korbel, J.O.1
Campbell, P.J.2
-
86
-
-
84870955253
-
Differential relationship of DNA replication timing to different forms of human mutation and variation
-
Koren A, Polak P, Nemesh J, Michaelson JJ, Sebat J, et al. 2012. Differential relationship of DNA replication timing to different forms of human mutation and variation. Am. J. Hum. Genet. 91:1033-40
-
(2012)
Am. J. Hum. Genet
, vol.91
, pp. 1033-1040
-
-
Koren, A.1
Polak, P.2
Nemesh, J.3
Michaelson, J.J.4
Sebat, J.5
-
87
-
-
0027109075
-
Cancer p53, guardian of the genome
-
Lane DP. 1992. Cancer. p53, guardian of the genome. Nature 358:15-16
-
(1992)
Nature
, vol.358
, pp. 15-16
-
-
Lane, D.P.1
-
88
-
-
40849138236
-
Estimating the per-base-pair mutation rate in the yeast Saccharomyces cerevisiae
-
Lang GI, Murray AW. 2008. Estimating the per-base-pair mutation rate in the yeast Saccharomyces cerevisiae. Genetics 178:67-82
-
(2008)
Genetics
, vol.178
, pp. 67-82
-
-
Lang, G.I.1
Murray, A.W.2
-
89
-
-
84880507665
-
Mutational heterogeneity in cancer and the search for new cancer-associated genes
-
Lawrence MS, Stojanov P, Polak P, Kryukov GV, Cibulskis K, et al. 2013. Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature 499:214-18
-
(2013)
Nature
, vol.499
, pp. 214-218
-
-
Lawrence, M.S.1
Stojanov, P.2
Polak, P.3
Kryukov, G.V.4
Cibulskis, K.5
-
90
-
-
84881615685
-
Common fragile site profiling in epithelial and erythroid cells reveals that most recurrent cancer deletions lie in fragile sites hosting large genes
-
Le Tallec B, Millot GA, Blin ME, Brison O, Dutrillaux B, Debatisse M. 2013. Common fragile site profiling in epithelial and erythroid cells reveals that most recurrent cancer deletions lie in fragile sites hosting large genes. Cell Rep. 4:420-28
-
(2013)
Cell Rep
, vol.4
, pp. 420-428
-
-
Le Tallec, B.1
Millot, G.A.2
Blin, M.E.3
Brison, O.4
Dutrillaux, B.5
Debatisse, M.6
-
91
-
-
4344663928
-
Micronuclei with multiple copies of the X chromosome: Do chromosomes replicate in micronuclei
-
Leach NT, Jackson-Cook C. 2004. Micronuclei with multiple copies of the X chromosome: Do chromosomes replicate in micronuclei? Mutat. Res. 554:89-94
-
(2004)
Mutat. Res
, vol.554
, pp. 89-94
-
-
Leach, N.T.1
Jackson-Cook, C.2
-
92
-
-
37349109667
-
A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders
-
Lee JA, Carvalho CM, Lupski JR. 2007. A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders. Cell 131:1235-47
-
(2007)
Cell
, vol.131
, pp. 1235-1247
-
-
Lee, J.A.1
Carvalho, C.M.2
Lupski, J.R.3
-
93
-
-
0032494164
-
Dynamics of the genome during early Xenopus laevis development: Karyomeres as independent units of replication
-
Lemaitre JM, Geraud G,Mechali M. 1998. Dynamics of the genome during early Xenopus laevis development: karyomeres as independent units of replication. J. Cell Biol. 142:1159-66
-
(1998)
J. Cell Biol
, vol.142
, pp. 1159-1166
-
-
Lemaitre, J.M.1
Geraud, G.2
Mechali, M.3
-
94
-
-
0030941458
-
P53, the cellular gatekeeper for growth and division
-
Levine AJ. 1997. p53, the cellular gatekeeper for growth and division. Cell 88:323-31
-
(1997)
Cell
, vol.88
, pp. 323-331
-
-
Levine, A.J.1
-
95
-
-
84897528140
-
Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia
-
Li Y, Schwab C, Ryan SL, Papaemmanuil E, Robinson HM, et al. 2014. Constitutional and somatic rearrangement of chromosome 21 in acute lymphoblastic leukaemia. Nature 508:98-102
-
(2014)
Nature
, vol.508
, pp. 98-102
-
-
Li, Y.1
Schwab, C.2
Ryan, S.L.3
Papaemmanuil, E.4
Robinson, H.M.5
-
96
-
-
70349873824
-
Comprehensive mapping of long-range interactions reveals folding principles of the human genome
-
Lieberman-Aiden E, van Berkum NL,Williams L, Imakaev M, Ragoczy T, et al. 2009. Comprehensive mapping of long-range interactions reveals folding principles of the human genome. Science 326:289-93
-
(2009)
Science
, vol.326
, pp. 289-293
-
-
Lieberman-Aiden, E.1
Van Berkum, N.L.2
Williams, L.3
Imakaev, M.4
Ragoczy, T.5
-
97
-
-
84874585488
-
DNAreplication timing and higher-order nuclear organization determine single-nucleotide substitution patterns in cancer genomes
-
Liu L,De S,Michor F. 2013.DNAreplication timing and higher-order nuclear organization determine single-nucleotide substitution patterns in cancer genomes. Nat. Commun. 4:1502
-
(2013)
Nat. Commun
, vol.4
, pp. 1502
-
-
Liu, L.1
De, S.2
Michor, F.3
-
99
-
-
80052916562
-
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements
-
Liu P,Erez A,Nagamani SC, Dhar SU,Kolodziejska KE, et al. 2011. Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell 146:889-903
-
(2011)
Cell
, vol.146
, pp. 889-903
-
-
Liu, P.1
Erez, A.2
Nagamani, S.C.3
Dhar, S.U.4
Kolodziejska, K.E.5
-
100
-
-
80052663200
-
The CDKN2A/ CDKN2B/CDK4/CCND1 pathway is pivotal in well-differentiated and dedifferentiated liposarcoma oncogenesis: An analysis of 104 tumors
-
Louis-Brennetot C, Coindre JM, Ferreira C, Perot G, Terrier P, Aurias A. 2011. The CDKN2A/ CDKN2B/CDK4/CCND1 pathway is pivotal in well-differentiated and dedifferentiated liposarcoma oncogenesis: an analysis of 104 tumors. Genes Chromosomes Cancer 50:896-907
-
(2011)
Genes Chromosomes Cancer
, vol.50
, pp. 896-907
-
-
Louis-Brennetot, C.1
Coindre, J.M.2
Ferreira, C.3
Perot, G.4
Terrier, P.5
Aurias, A.6
-
101
-
-
79952281751
-
53BP1 nuclear bodies form around DNA lesions generated by mitotic transmission of chromosomes under replication stress
-
Lukas C, Savic V, Bekker-Jensen S,Doil C,Neumann B, et al. 2011. 53BP1 nuclear bodies form around DNA lesions generated by mitotic transmission of chromosomes under replication stress. Nat. Cell Biol. 13:243-53
-
(2011)
Nat. Cell Biol
, vol.13
, pp. 243-253
-
-
Lukas, C.1
Savic, V.2
Bekker-Jensen, S.3
Doil, C.4
Neumann, B.5
-
102
-
-
75749103383
-
Rate, molecular spectrum, and consequences of human mutation
-
Lynch M. 2010. Rate, molecular spectrum, and consequences of human mutation. PNAS 107:961-68
-
(2010)
PNAS
, vol.107
, pp. 961-968
-
-
Lynch, M.1
-
103
-
-
84877113990
-
Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms
-
Malhotra A, Lindberg M, Faust GG, Leibowitz ML, Clark RA, et al. 2013. Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms. Genome Res. 23:762-76
-
(2013)
Genome Res
, vol.23
, pp. 762-776
-
-
Malhotra, A.1
Lindberg, M.2
Faust, G.G.3
Leibowitz, M.L.4
Clark, R.A.5
-
104
-
-
84942520034
-
A cell-based model system links chromothripsis with hyperploidy
-
Mardin BR, Drainas AP, Waszak SM, Weischenfeldt J, Isokane M, et al. 2015. A cell-based model system links chromothripsis with hyperploidy. Mol. Syst. Biol. 11:828
-
(2015)
Mol. Syst. Biol
, vol.11
, pp. 828
-
-
Mardin, B.R.1
Drainas, A.P.2
Waszak, S.M.3
Weischenfeldt, J.4
Isokane, M.5
-
105
-
-
0000813303
-
The production of homozygous deficient tissues with mutant characteristics by means of the aberrant mitotic behavior of ring-shaped chromosomes
-
McClintock B. 1938. The production of homozygous deficient tissues with mutant characteristics by means of the aberrant mitotic behavior of ring-shaped chromosomes. Genetics 23:315-76
-
(1938)
Genetics
, vol.23
, pp. 315-376
-
-
McClintock, B.1
-
106
-
-
0001294157
-
The stability of broken ends of chromosomes in Zea mays
-
McClintock B. 1941. The stability of broken ends of chromosomes in Zea mays. Genetics 26:234-82
-
(1941)
Genetics
, vol.26
, pp. 234-282
-
-
McClintock, B.1
-
107
-
-
84922758305
-
Chromothriptic cure of WHIM syndrome
-
McDermott DH, Gao JL, Liu Q, Siwicki M, Martens C, et al. 2015. Chromothriptic cure of WHIM syndrome. Cell 160:686-99
-
(2015)
Cell
, vol.160
, pp. 686-699
-
-
McDermott, D.H.1
Gao, J.L.2
Liu, Q.3
Siwicki, M.4
Martens, C.5
-
108
-
-
33845986339
-
Spatial genome organization in the formation of chromosomal translocations
-
Meaburn KJ, Misteli T, Soutoglou E. 2007. Spatial genome organization in the formation of chromosomal translocations. Semin. Cancer Biol. 17:80-90
-
(2007)
Semin. Cancer Biol
, vol.17
, pp. 80-90
-
-
Meaburn, K.J.1
Misteli, T.2
Soutoglou, E.3
-
109
-
-
84975804424
-
Mapping copy number variation by population-scale genome sequencing
-
Mills RE,Walter K, Stewart C, Handsaker RE, Chen K, et al. 2011. Mapping copy number variation by population-scale genome sequencing. Nature 470:59-65
-
(2011)
Nature
, vol.470
, pp. 59-65
-
-
Mills, R.E.1
Walter, K.2
Stewart, C.3
Handsaker, R.E.4
Chen, K.5
-
110
-
-
62849083222
-
The emerging role of nuclear architecture in DNA repair and genome maintenance
-
Misteli T, Soutoglou E. 2009. The emerging role of nuclear architecture in DNA repair and genome maintenance. Nat. Rev. Mol. Cell Biol. 10:243-54
-
(2009)
Nat. Rev. Mol. Cell Biol
, vol.10
, pp. 243-254
-
-
Misteli, T.1
Soutoglou, E.2
-
111
-
-
39249083917
-
Validation of micronuclei frequency in peripheral blood lymphocytes as early cancer risk biomarker in a nested case-control study
-
Murgia E, Ballardin M, Bonassi S, Rossi AM, Barale R. 2008. Validation of micronuclei frequency in peripheral blood lymphocytes as early cancer risk biomarker in a nested case-control study. Mutat. Res. 639:27-34
-
(2008)
Mutat. Res
, vol.639
, pp. 27-34
-
-
Murgia, E.1
Ballardin, M.2
Bonassi, S.3
Rossi, A.M.4
Barale, R.5
-
112
-
-
84924267433
-
Mutations in theNHEJcomponent XRCC4 cause primordial dwarfism
-
Murray JE, van der Burg M, IJspeertH,Carroll P,WuQ, et al. 2015. Mutations in theNHEJcomponent XRCC4 cause primordial dwarfism. Am. J. Hum. Genet. 96:412-24
-
(2015)
Am. J. Hum. Genet
, vol.96
, pp. 412-424
-
-
Murray, J.E.1
Van Der Burg, M.2
I'Jspeert, H.3
Carroll, P.4
Wu, Q.5
-
113
-
-
67349187702
-
The FANC pathway and BLM collaborate during mitosis to prevent micronucleation and chromosome abnormalities
-
Naim V, Rosselli F. 2009. The FANC pathway and BLM collaborate during mitosis to prevent micronucleation and chromosome abnormalities. Nat. Cell Biol. 11:761-68
-
(2009)
Nat. Cell Biol
, vol.11
, pp. 761-768
-
-
Naim, V.1
Rosselli, F.2
-
114
-
-
84881471113
-
ERCC1 and MUS81-EME1 promote sister chromatid separation by processing late replication intermediates at common fragile sites duringmitosis
-
Naim V, Wilhelm T, Debatisse M, Rosselli F. 2013. ERCC1 and MUS81-EME1 promote sister chromatid separation by processing late replication intermediates at common fragile sites duringmitosis. Nat. Cell Biol. 15:1008-15
-
(2013)
Nat. Cell Biol
, vol.15
, pp. 1008-1015
-
-
Naim, V.1
Wilhelm, T.2
Debatisse, M.3
Rosselli, F.4
-
115
-
-
84892775264
-
Targeted therapy resistance mediated by dynamic regulation of extrachromosomal mutant EGFR DNA
-
Nathanson DA, Gini B, Mottahedeh J, Visnyei K, Koga T, et al. 2014. Targeted therapy resistance mediated by dynamic regulation of extrachromosomal mutant EGFR DNA. Science 343:72-76
-
(2014)
Science
, vol.343
, pp. 72-76
-
-
Nathanson, D.A.1
Gini, B.2
Mottahedeh, J.3
Visnyei, K.4
Koga, T.5
-
116
-
-
84861541343
-
Mutational processes molding the genomes of 21 breast cancers
-
Nik-Zainal S, Alexandrov LB,Wedge DC, Van Loo P, GreenmanCD, et al. 2012. Mutational processes molding the genomes of 21 breast cancers. Cell 149:979-93
-
(2012)
Cell
, vol.149
, pp. 979-993
-
-
Nik-Zainal, S.1
Alexandrov, L.B.2
Wedge, D.C.3
Van Loo, P.4
Greenman, C.D.5
-
117
-
-
84911734556
-
Premature chromosome condensation in micronuclei
-
Obe G, Beek B. 1982. Premature chromosome condensation in micronuclei. See Ref. 123, pp. 113-30
-
(1982)
See Ref
, vol.123
, pp. 113-130
-
-
Obe, G.1
Beek, B.2
-
118
-
-
84930638395
-
Whole-genome characterization of chemoresistant ovarian cancer
-
Patch AM, Christie EL, Etemadmoghadam D, Garsed DW, George J, et al. 2015. Whole-genome characterization of chemoresistant ovarian cancer. Nature 521:489-94
-
(2015)
Nature
, vol.521
, pp. 489-494
-
-
Patch, A.M.1
Christie, E.L.2
Etemadmoghadam, D.3
Garsed, D.W.4
George, J.5
-
119
-
-
84964696552
-
TopBP1 is required at mitosis to reduce transmission of DNA damage to G1 daughter cells
-
Pedersen RT, Kruse T, Nilsson J, Oestergaard VH, Lisby M. 2015. TopBP1 is required at mitosis to reduce transmission of DNA damage to G1 daughter cells. J. Cell Biol. 210:565-82
-
(2015)
J. Cell Biol
, vol.210
, pp. 565-582
-
-
Pedersen, R.T.1
Kruse, T.2
Nilsson, J.3
Oestergaard, V.H.4
Lisby, M.5
-
120
-
-
0032890294
-
Structure of the supernumerary ring and giant rod chromosomes in adipose tissue tumors
-
Pedeutour F, Forus A, Coindre JM, Berner JM, Nicolo G, et al. 1999. Structure of the supernumerary ring and giant rod chromosomes in adipose tissue tumors. Genes Chromosomes Cancer 24:30-41
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 30-41
-
-
Pedeutour, F.1
Forus, A.2
Coindre, J.M.3
Berner, J.M.4
Nicolo, G.5
-
121
-
-
74449093973
-
A comprehensive catalogue of somatic mutations from a human cancer genome
-
Pleasance ED, Cheetham RK, Stephens PJ, McBride DJ, Humphray SJ, et al. 2010. A comprehensive catalogue of somatic mutations from a human cancer genome. Nature 463:191-96
-
(2010)
Nature
, vol.463
, pp. 191-196
-
-
Pleasance, E.D.1
Cheetham, R.K.2
Stephens, P.J.3
McBride, D.J.4
Humphray, S.J.5
-
122
-
-
1542377277
-
Inactivation of hCDC4 can cause chromosomal instability
-
Rajagopalan H, Jallepalli PV, Rago C, Velculescu VE, Kinzler KW, et al. 2004. Inactivation of hCDC4 can cause chromosomal instability. Nature 428:77-81
-
(2004)
Nature
, vol.428
, pp. 77-81
-
-
Rajagopalan, H.1
Jallepalli, P.V.2
Rago, C.3
Velculescu, V.E.4
Kinzler, K.W.5
-
123
-
-
0035101024
-
How malleable is the eukaryotic genome? Extreme rate of chromosomal rearrangement in the genus Drosophila
-
Ranz JM, Casals F, Ruiz A. 2001. How malleable is the eukaryotic genome? Extreme rate of chromosomal rearrangement in the genus Drosophila. Genome Res. 11:230-39
-
(2001)
Genome Res
, vol.11
, pp. 230-239
-
-
Ranz, J.M.1
Casals, F.2
Ruiz, A.3
-
125
-
-
54349097938
-
Multiple origins of spontaneously arising micronuclei in HeLa cells: Direct evidence from long-term live cell imaging
-
Rao X, Zhang Y, Yi Q, HouH, Xu B, et al. 2008. Multiple origins of spontaneously arising micronuclei in HeLa cells: direct evidence from long-term live cell imaging. Mutat. Res. 646:41-49
-
(2008)
Mutat. Res
, vol.646
, pp. 41-49
-
-
Rao, X.1
Zhang, Y.2
Yi, Q.3
Hou, H.4
Xu, B.5
-
126
-
-
84862907577
-
Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations
-
Rausch T, Jones DT, Zapatka M, Stutz AM, Zichner T, et al. 2012. Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations. Cell 148:59-71
-
(2012)
Cell
, vol.148
, pp. 59-71
-
-
Rausch, T.1
Jones, D.T.2
Zapatka, M.3
Stutz, A.M.4
Zichner, T.5
-
127
-
-
84923322262
-
A haploid genetics toolbox for Arabidopsis thaliana
-
Ravi M, Marimuthu MP, Tan EH, Maheshwari S, Henry IM, et al. 2014. A haploid genetics toolbox for Arabidopsis thaliana. Nat. Commun. 5:5334
-
(2014)
Nat. Commun
, vol.5
, pp. 5334
-
-
Ravi, M.1
Marimuthu, M.P.2
Tan, E.H.3
Maheshwari, S.4
Henry, I.M.5
-
128
-
-
84874608346
-
Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations
-
Robberecht C, Voet T, Zamani Esteki M, Nowakowska BA, Vermeesch JR. 2013. Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations. Genome Res. 23:411-18
-
(2013)
Genome Res
, vol.23
, pp. 411-418
-
-
Robberecht, C.1
Voet, T.2
Zamani, E.M.3
Nowakowska, B.A.4
Vermeesch, J.R.5
-
129
-
-
84861460657
-
Clustered mutations in yeast and in human cancers can arise from damaged long single-strand DNA regions
-
Roberts SA, Sterling J, Thompson C, Harris S,Mav D, et al. 2012. Clustered mutations in yeast and in human cancers can arise from damaged long single-strand DNA regions. Mol. Cell 46:424-35
-
(2012)
Mol. Cell
, vol.46
, pp. 424-435
-
-
Roberts, S.A.1
Sterling, J.2
Thompson, C.3
Harris, S.4
Mav, D.5
-
130
-
-
76049094187
-
Mutation patterns in cancer genomes
-
Rubin AF, Green P. 2009. Mutation patterns in cancer genomes. PNAS 106:21766-70
-
(2009)
PNAS
, vol.106
, pp. 21766-21770
-
-
Rubin, A.F.1
Green, P.2
-
131
-
-
84885074156
-
Double minute chromosomes in glioblastoma multiforme are revealed by precise reconstruction of oncogenic amplicons
-
Sanborn JZ, Salama SR, Grifford M, Brennan CW, Mikkelsen T, et al. 2013. Double minute chromosomes in glioblastoma multiforme are revealed by precise reconstruction of oncogenic amplicons. Cancer Res. 73:6036-45
-
(2013)
Cancer Res
, vol.73
, pp. 6036-6045
-
-
Sanborn, J.Z.1
Salama, S.R.2
Grifford, M.3
Brennan, C.W.4
Mikkelsen, T.5
-
132
-
-
84923230005
-
Deciphering the evolutionary history of open and closed mitosis
-
Sazer S, Lynch M, Needleman D. 2014. Deciphering the evolutionary history of open and closed mitosis. Curr. Biol. 24:R1099-103
-
(2014)
Curr. Biol
, vol.24
, pp. R1099-R1103
-
-
Sazer, S.1
Lynch, M.2
Needleman, D.3
-
133
-
-
84865248380
-
Chromatin organization is a major influence on regionalmutation rates in human cancer cells
-
Schuster-Bockler B, Lehner B. 2012. Chromatin organization is a major influence on regionalmutation rates in human cancer cells. Nature 488:504-7
-
(2012)
Nature
, vol.488
, pp. 504-507
-
-
Schuster-Bockler, B.1
Lehner, B.2
-
134
-
-
0024377243
-
Model for the formation of double minutes from prematurely condensed chromosomes of replicatingmicronuclei in drug-treatedChinese hamster ovary cells undergoing DNA amplification
-
Sen S, Hittelman WN, Teeter LD, Kuo MT. 1989. Model for the formation of double minutes from prematurely condensed chromosomes of replicatingmicronuclei in drug-treatedChinese hamster ovary cells undergoing DNA amplification. Cancer Res. 49:6731-37
-
(1989)
Cancer Res
, vol.49
, pp. 6731-6737
-
-
Sen, S.1
Hittelman, W.N.2
Teeter, L.D.3
Kuo, M.T.4
-
135
-
-
20544462642
-
Segmental duplications and copynumber variation in the human genome
-
Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, et al. 2005. Segmental duplications and copynumber variation in the human genome. Am. J. Hum. Genet. 77:78-88
-
(2005)
Am. J. Hum. Genet
, vol.77
, pp. 78-88
-
-
Sharp, A.J.1
Locke, D.P.2
McGrath, S.D.3
Cheng, Z.4
Bailey, J.A.5
-
136
-
-
80051871652
-
Aneuploidy drives genomic instability in yeast
-
Sheltzer JM, Blank HM, Pfau SJ, Tange Y, George BM, et al. 2011. Aneuploidy drives genomic instability in yeast. Science 333:1026-30
-
(2011)
Science
, vol.333
, pp. 1026-1030
-
-
Sheltzer, J.M.1
Blank, H.M.2
Pfau, S.J.3
Tange, Y.4
George, B.M.5
-
137
-
-
0037356808
-
Phenotype-based identification of mouse chromosome instability mutants
-
Shima N, Hartford SA, Duffy T, Wilson LA, Schimenti KJ, Schimenti JC. 2003. Phenotype-based identification of mouse chromosome instability mutants. Genetics 163:1031-40
-
(2003)
Genetics
, vol.163
, pp. 1031-1040
-
-
Shima, N.1
Hartford, S.A.2
Duffy, T.3
Wilson, L.A.4
Schimenti, K.J.5
Schimenti, J.C.6
-
138
-
-
83455176258
-
Mosaic amplification ofmultiple receptor tyrosine kinase genes in glioblastoma
-
Snuderl M, Fazlollahi L, Le LP, Nitta M, Zhelyazkova BH, et al. 2011. Mosaic amplification ofmultiple receptor tyrosine kinase genes in glioblastoma. Cancer Cell 20:810-17
-
(2011)
Cancer Cell
, vol.20
, pp. 810-817
-
-
Snuderl, M.1
Fazlollahi, L.2
Le, L.P.3
Nitta, M.4
Zhelyazkova, B.H.5
-
139
-
-
63449141981
-
Human mutation rate associated with DNA replication timing
-
Stamatoyannopoulos JA, Adzhubei I, Thurman RE, Kryukov GV, Mirkin SM, Sunyaev SR. 2009. Human mutation rate associated with DNA replication timing. Nat. Genet. 41:393-95
-
(2009)
Nat. Genet
, vol.41
, pp. 393-395
-
-
Stamatoyannopoulos, J.A.1
Adzhubei, I.2
Thurman, R.E.3
Kryukov, G.V.4
Mirkin, S.M.5
Sunyaev, S.R.6
-
140
-
-
0036591666
-
Molecular-evolutionarymechanisms for genomic disorders
-
Stankiewicz P, Lupski JR. 2002. Molecular-evolutionarymechanisms for genomic disorders. Curr. Opin. Genet. Dev. 12:312-19
-
(2002)
Curr. Opin. Genet. Dev
, vol.12
, pp. 312-319
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
142
-
-
78650959663
-
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
-
Stephens PJ, Greenman CD, Fu B, Yang F, Bignell GR, et al. 2011. Massive genomic rearrangement acquired in a single catastrophic event during cancer development. Cell 144:27-40
-
(2011)
Cell
, vol.144
, pp. 27-40
-
-
Stephens, P.J.1
Greenman, C.D.2
Fu, B.3
Yang, F.4
Bignell, G.R.5
-
143
-
-
72949119310
-
Complex landscapes of somatic rearrangement in human breast cancer genomes
-
Stephens PJ,McBride DJ, LinML, Varela I, Pleasance ED, et al. 2009. Complex landscapes of somatic rearrangement in human breast cancer genomes. Nature 462:1005-10
-
(2009)
Nature
, vol.462
, pp. 1005-1010
-
-
Stephens, P.J.1
McBride, D.J.2
Lin, M.L.3
Varela, I.4
Pleasance, E.D.5
-
144
-
-
33749506269
-
Genome-wide genetic analysis of polyploidy in yeast
-
Storchova Z, Breneman A, Cande J, Dunn J, Burbank K, et al. 2006. Genome-wide genetic analysis of polyploidy in yeast. Nature 443:541-47
-
(2006)
Nature
, vol.443
, pp. 541-547
-
-
Storchova, Z.1
Breneman, A.2
Cande, J.3
Dunn, J.4
Burbank, K.5
-
145
-
-
77956277959
-
Gene amplification as doubleminutes or homogeneously staining regions in solid tumors: Origin and structure
-
Storlazzi CT, Lonoce A, Guastadisegni MC, Trombetta D, D'Addabbo P, et al. 2010. Gene amplification as doubleminutes or homogeneously staining regions in solid tumors: origin and structure. Genome Res. 20:1198-206
-
(2010)
Genome Res
, vol.20
, pp. 1198-1206
-
-
Storlazzi, C.T.1
Lonoce, A.2
Guastadisegni, M.C.3
Trombetta, D.4
D'Addabbo, P.5
-
146
-
-
84925615834
-
Differential DNA mismatch repair underlies mutation rate variation across the human genome
-
Supek F, Lehner B. 2015. Differential DNA mismatch repair underlies mutation rate variation across the human genome. Nature 521:81-84
-
(2015)
Nature
, vol.521
, pp. 81-84
-
-
Supek, F.1
Lehner, B.2
-
147
-
-
80755187806
-
Double-strand break end resection and repair pathway choice
-
Symington LS, Gautier J. 2011. Double-strand break end resection and repair pathway choice. Annu. Rev. Genet. 45:247-71
-
(2011)
Annu. Rev. Genet
, vol.45
, pp. 247-271
-
-
Symington, L.S.1
Gautier, J.2
-
148
-
-
84857397985
-
Intratumoral heterogeneity of receptor tyrosine kinases EGFR and PDGFRA amplification in glioblastoma defines subpopulations with distinct growth factor response
-
Szerlip NJ, Pedraza A, Chakravarty D, Azim M, McGuire J, et al. 2012. Intratumoral heterogeneity of receptor tyrosine kinases EGFR and PDGFRA amplification in glioblastoma defines subpopulations with distinct growth factor response. PNAS 109:3041-46
-
(2012)
PNAS
, vol.109
, pp. 3041-3046
-
-
Szerlip, N.J.1
Pedraza, A.2
Chakravarty, D.3
Azim, M.4
McGuire, J.5
-
149
-
-
84930683882
-
Catastrophic chromosomal restructuring during genome elimination in plants
-
Tan EH, Henry IM, Ravi M, Bradnam KR, Mandakova T, et al. 2015. Catastrophic chromosomal restructuring during genome elimination in plants. eLife 4:e06516
-
(2015)
ELife
, vol.4
, pp. e06516
-
-
Tan, E.H.1
Henry, I.M.2
Ravi, M.3
Bradnam, K.R.4
Mandakova, T.5
-
150
-
-
84879061509
-
DNA deaminases induce breakassociated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis
-
Taylor BJ, Nik-Zainal S, Wu YL, Stebbings LA, Raine K, et al. 2013. DNA deaminases induce breakassociated mutation showers with implication of APOBEC3B and 3A in breast cancer kataegis. eLife 2:e00534
-
(2013)
ELife
, vol.2
, pp. e00534
-
-
Taylor, B.J.1
Nik-Zainal, S.2
Wu, Y.L.3
Stebbings, L.A.4
Raine, K.5
-
151
-
-
84856807056
-
Frequent alterations and epigenetic silencing of differentiation pathway genes in structurally rearranged liposarcomas
-
Taylor BS, DeCarolis PL, Angeles CV, Brenet F, Schultz N, et al. 2011. Frequent alterations and epigenetic silencing of differentiation pathway genes in structurally rearranged liposarcomas. Cancer Discov. 1:587-97
-
(2011)
Cancer Discov
, vol.1
, pp. 587-597
-
-
Taylor, B.S.1
DeCarolis, P.L.2
Angeles, C.V.3
Brenet, F.4
Schultz, N.5
-
152
-
-
84878264650
-
Gene fusions by chromothripsis of chromosome 5q in the VCaP prostate cancer cell line
-
Teles Alves I, Hiltemann S, Hartjes T, van der Spek P, Stubbs A, et al. 2013. Gene fusions by chromothripsis of chromosome 5q in the VCaP prostate cancer cell line. Hum. Genet. 132:709-13
-
(2013)
Hum. Genet
, vol.132
, pp. 709-713
-
-
Teles, A.I.1
Hiltemann, S.2
Hartjes, T.3
Van Der Spek, P.4
Stubbs, A.5
-
153
-
-
83555176004
-
Nuclear envelope defects impede a proper response to micronuclear DNA lesions
-
Terradas M, Martín M, Hernandez L, Tusell L, Genesca A. 2012. Nuclear envelope defects impede a proper response to micronuclear DNA lesions. Mutat. Res. 729:35-40
-
(2012)
Mutat. Res
, vol.729
, pp. 35-40
-
-
Terradas, M.1
Martín, M.2
Hernandez, L.3
Tusell, L.4
Genesca, A.5
-
154
-
-
70149107457
-
DNA lesions sequestered in micronuclei induce a local defective-damage response
-
Terradas M, Martin M, Tusell L, Genesca A. 2009. DNA lesions sequestered in micronuclei induce a local defective-damage response. DNA Repair 8:1225-34
-
(2009)
DNA Repair
, vol.8
, pp. 1225-1234
-
-
Terradas, M.1
Martin, M.2
Tusell, L.3
Genesca, A.4
-
155
-
-
77952585411
-
Genetic activities in micronuclei: Is the DNA entrapped in micronuclei lost for the cell
-
Terradas M, Martín M, Tusell L, Genesca A. 2010. Genetic activities in micronuclei: Is the DNA entrapped in micronuclei lost for the cell? Mutat. Res. 705:60-67
-
(2010)
Mutat. Res
, vol.705
, pp. 60-67
-
-
Terradas, M.1
Martín, M.2
Tusell, L.3
Genesca, A.4
-
156
-
-
81055141515
-
Chromosome missegregation in human cells arises through specific types of kinetochore-microtubule attachment errors
-
Thompson SL,Compton DA. 2011. Chromosome missegregation in human cells arises through specific types of kinetochore-microtubule attachment errors. PNAS 108:17974-78
-
(2011)
PNAS
, vol.108
, pp. 17974-17978
-
-
Thompson, S.L.1
Compton, D.A.2
-
157
-
-
84889563685
-
ATR prohibits replication catastrophe by preventing global exhaustion of RPA
-
Toledo LI, Altmeyer M, Rask MB, Lukas C, Larsen DH, et al. 2013. ATR prohibits replication catastrophe by preventing global exhaustion of RPA. Cell 155:1088-103
-
(2013)
Cell
, vol.155
, pp. 1088-1103
-
-
Toledo, L.I.1
Altmeyer, M.2
Rask, M.B.3
Lukas, C.4
Larsen, D.H.5
-
158
-
-
34548131710
-
Effects of aneuploidy on cellular physiology and cell division in haploid yeast
-
Torres EM, Sokolsky T, Tucker CM, Chan LY, Boselli M, et al. 2007. Effects of aneuploidy on cellular physiology and cell division in haploid yeast. Science 317:916-24
-
(2007)
Science
, vol.317
, pp. 916-924
-
-
Torres, E.M.1
Sokolsky, T.2
Tucker, C.M.3
Chan, L.Y.4
Boselli, M.5
-
159
-
-
79952120598
-
Cancer: When catastrophe strikes a cell
-
Tubio JM, Estivill X. 2011. Cancer: when catastrophe strikes a cell. Nature 470:476-77
-
(2011)
Nature
, vol.470
, pp. 476-477
-
-
Tubio, J.M.1
Estivill, X.2
-
161
-
-
3843101398
-
Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas
-
Vogt N, Lefevre SH, Apiou F,Dutrillaux AM, Cor A, et al. 2004. Molecular structure of double-minute chromosomes bearing amplified copies of the epidermal growth factor receptor gene in gliomas. PNAS 101:11368-73
-
(2004)
PNAS
, vol.101
, pp. 11368-11373
-
-
Vogt, N.1
Lefevre, S.H.2
Apiou, F.3
Dutrillaux, A.M.4
Cor, A.5
-
162
-
-
0026705145
-
Elimination of extrachromosomally amplified MYC genes from human tumor cells reduces their tumorigenicity
-
Von Hoff DD, McGill JR, Forseth BJ, Davidson KK, Bradley TP, et al. 1992. Elimination of extrachromosomally amplified MYC genes from human tumor cells reduces their tumorigenicity. PNAS 89:8165-69
-
(1992)
PNAS
, vol.89
, pp. 8165-8169
-
-
Von Hoff, D.D.1
McGill, J.R.2
Forseth, B.J.3
Davidson, K.K.4
Bradley, T.P.5
-
163
-
-
0012176213
-
Amplified human MYC oncogenes localized to replicating submicroscopic circular DNA molecules
-
Von Hoff DD, Needham-VanDevanter DR, Yucel J, Windle BE,Wahl GM. 1988. Amplified human MYC oncogenes localized to replicating submicroscopic circular DNA molecules. PNAS 85:4804-8
-
(1988)
PNAS
, vol.85
, pp. 4804-4808
-
-
Von Hoff, D.D.1
Needham-VanDevanter, D.R.2
Yucel, J.3
Windle, B.E.4
Wahl, G.M.5
-
164
-
-
84924056345
-
Whole genomes redefine the mutational landscape of pancreatic cancer
-
Waddell N, Pajic M, Patch AM, Chang DK, Kassahn KS, et al. 2015. Whole genomes redefine the mutational landscape of pancreatic cancer. Nature 518:495-501
-
(2015)
Nature
, vol.518
, pp. 495-501
-
-
Waddell, N.1
Pajic, M.2
Patch, A.M.3
Chang, D.K.4
Kassahn, K.S.5
-
165
-
-
0024574074
-
The importance of circular DNA in mammalian gene amplification
-
Wahl GM. 1989. The importance of circular DNA in mammalian gene amplification. Cancer Res. 49:1333-40
-
(1989)
Cancer Res
, vol.49
, pp. 1333-1340
-
-
Wahl, G.M.1
-
166
-
-
80052663689
-
High-resolution genomic mapping reveals consistent amplification of the fibroblast growth factor receptor substrate 2 gene in well-differentiated and dedifferentiated liposarcoma
-
Wang X, Asmann YW, Erickson-Johnson MR, Oliveira JL, Zhang H, et al. 2011. High-resolution genomic mapping reveals consistent amplification of the fibroblast growth factor receptor substrate 2 gene in well-differentiated and dedifferentiated liposarcoma. Genes Chromosomes Cancer 50:849-58
-
(2011)
Genes Chromosomes Cancer
, vol.50
, pp. 849-858
-
-
Wang, X.1
Asmann, Y.W.2
Erickson-Johnson, M.R.3
Oliveira, J.L.4
Zhang, H.5
-
167
-
-
0026018901
-
Acentral role for chromosome breakage in gene amplification, deletion formation, and amplicon integration
-
Windle B, Draper BW,Yin YX,O'Gorman S,WahlGM. 1991.Acentral role for chromosome breakage in gene amplification, deletion formation, and amplicon integration. Genes Dev. 5:160-74
-
(1991)
Genes Dev
, vol.5
, pp. 160-174
-
-
Windle, B.1
Draper, B.W.2
Yin, Y.X.3
O'Gorman, S.4
Wahl, G.M.5
-
168
-
-
84866067741
-
DNA replication timing and selection shape the landscape of nucleotide variation in cancer genomes
-
Woo YH, Li WH. 2012. DNA replication timing and selection shape the landscape of nucleotide variation in cancer genomes. Nat. Commun. 3:1004
-
(2012)
Nat. Commun
, vol.3
, pp. 1004
-
-
Woo, Y.H.1
Li, W.H.2
-
169
-
-
67649982842
-
Mobile elements create structural variation: Analysis of a complete human genome
-
Xing J, Zhang Y, Han K, Salem AH, Sen SK, et al. 2009. Mobile elements create structural variation: analysis of a complete human genome. Genome Res. 19:1516-26
-
(2009)
Genome Res
, vol.19
, pp. 1516-1526
-
-
Xing, J.1
Zhang, Y.2
Han, K.3
Salem, A.H.4
Sen, S.K.5
-
170
-
-
84877722178
-
Diverse mechanisms of somatic structural variations in human cancer genomes
-
Yang L, Luquette LJ, Gehlenborg N, Xi R, Haseley PS, et al. 2013. Diverse mechanisms of somatic structural variations in human cancer genomes. Cell 153:919-29
-
(2013)
Cell
, vol.153
, pp. 919-929
-
-
Yang, L.1
Luquette, L.J.2
Gehlenborg, N.3
Xi, R.4
Haseley, P.S.5
-
172
-
-
84885008220
-
Pan-cancer patterns of somatic copy number alteration
-
Zack TI, Schumacher SE, Carter SL, Cherniack AD, Saksena G, et al. 2013. Pan-cancer patterns of somatic copy number alteration. Nat. Genet. 45:1134-40
-
(2013)
Nat. Genet
, vol.45
, pp. 1134-1140
-
-
Zack, T.I.1
Schumacher, S.E.2
Carter, S.L.3
Cherniack, A.D.4
Saksena, G.5
-
173
-
-
67650001851
-
Complex human chromosomal and genomic rearrangements
-
Zhang F, Carvalho CM, Lupski JR. 2009. Complex human chromosomal and genomic rearrangements. Trends Genet. 25:298-307
-
(2009)
Trends Genet
, vol.25
, pp. 298-307
-
-
Zhang, F.1
Carvalho, C.M.2
Lupski, J.R.3
-
174
-
-
84888869068
-
Chromothripsis and beyond: Rapid genome evolution from complex chromosomal rearrangements
-
Zhang CZ, Leibowitz ML, Pellman D. 2013. Chromothripsis and beyond: rapid genome evolution from complex chromosomal rearrangements. Genes Dev. 27:2513-30
-
(2013)
Genes Dev
, vol.27
, pp. 2513-2530
-
-
Zhang, C.Z.1
Leibowitz, M.L.2
Pellman, D.3
-
175
-
-
84930941966
-
Chromothripsis from DNA damage in micronuclei
-
Zhang CZ, Spektor A, Cornils H, Francis JM, Jackson EK, et al. 2015. Chromothripsis from DNA damage in micronuclei. Nature 522:179-84
-
(2015)
Nature
, vol.522
, pp. 179-184
-
-
Zhang, C.Z.1
Spektor, A.2
Cornils, H.3
Francis, J.M.4
Jackson, E.K.5
-
176
-
-
84914695543
-
A nontranscriptional role for Oct4 in the regulation of mitotic entry
-
Zhao R, Deibler RW, Lerou PH, Ballabeni A, Heffner GC, et al. 2014. A nontranscriptional role for Oct4 in the regulation of mitotic entry. PNAS 111:15768-73
-
(2014)
PNAS
, vol.111
, pp. 15768-15773
-
-
Zhao, R.1
Deibler, R.W.2
Lerou, P.H.3
Ballabeni, A.4
Heffner, G.C.5
-
177
-
-
0014086536
-
Chromosomal changes of similar nature in seven established cell lines derived from the peripheral blood of patients with leukemia
-
zur Hausen H. 1967. Chromosomal changes of similar nature in seven established cell lines derived from the peripheral blood of patients with leukemia. J. Natl. Cancer Inst. 38:683-96
-
(1967)
J. Natl. Cancer Inst
, vol.38
, pp. 683-696
-
-
Hausen, H.1
|