-
1
-
-
84922527340
-
Systematic analysis of noncoding somatic mutations and gene expression alterations across 14 tumor types
-
Fredriksson, N. J., Ny, L., Nilsson, J. A. & Larsson, E. Systematic analysis of noncoding somatic mutations and gene expression alterations across 14 tumor types. Nat. Genet. 46, 1258-1263 (2014).
-
(2014)
Nat. Genet
, vol.46
, pp. 1258-1263
-
-
Fredriksson, N.J.1
Ny, L.2
Nilsson, J.A.3
Larsson, E.4
-
2
-
-
84908894973
-
Genome-wide analysis of noncoding regulatory mutations in cancer
-
Weinhold, N., Jacobsen, A., Schultz, N., Sander, C. & Lee, W. Genome-wide analysis of noncoding regulatory mutations in cancer. Nat. Genet. 46, 1160-1165 (2014).
-
(2014)
Nat. Genet
, vol.46
, pp. 1160-1165
-
-
Weinhold, N.1
Jacobsen, A.2
Schultz, N.3
Sander, C.4
Lee, W.5
-
3
-
-
84956615603
-
Identification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterations
-
Araya, C. L. et al. Identification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterations. Nat. Genet. 48, 117-125 (2016).
-
(2016)
Nat. Genet
, vol.48
, pp. 117-125
-
-
Araya, C.L.1
-
4
-
-
84933278181
-
Recurrent somatic mutations in regulatory regions of human cancer genomes
-
Melton, C., Reuter, J. A., Spacek, D. V. & Snyder, M. Recurrent somatic mutations in regulatory regions of human cancer genomes. Nat. Genet. 47, 710-716 (2015).
-
(2015)
Nat. Genet
, vol.47
, pp. 710-716
-
-
Melton, C.1
Reuter, J.A.2
Spacek, D.V.3
Snyder, M.4
-
5
-
-
84973594792
-
Landscape of somatic mutations in 560 breast cancer whole-genome sequences
-
Nik-Zainal, S. et al. Landscape of somatic mutations in 560 breast cancer whole-genome sequences. Nature 534, 47-54 (2016).
-
(2016)
Nature
, vol.534
, pp. 47-54
-
-
Nik-Zainal, S.1
-
6
-
-
84892833777
-
Discovery and saturation analysis of cancer genes across 21 tumour types
-
Lawrence, M. S. et al. Discovery and saturation analysis of cancer genes across 21 tumour types. Nature 505, 495-501 (2014).
-
(2014)
Nature
, vol.505
, pp. 495-501
-
-
Lawrence, M.S.1
-
7
-
-
84874025843
-
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
-
Cibulskis, K. et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat. Biotechnol. 31, 213-219 (2013).
-
(2013)
Nat. Biotechnol
, vol.31
, pp. 213-219
-
-
Cibulskis, K.1
-
8
-
-
84880507665
-
Mutational heterogeneity in cancer and the search for new cancer-associated genes
-
Lawrence, M. S. et al. Mutational heterogeneity in cancer and the search for new cancer-associated genes. Nature 499, 214-218 (2013).
-
(2013)
Nature
, vol.499
, pp. 214-218
-
-
Lawrence, M.S.1
-
9
-
-
84861541343
-
Mutational processes molding the genomes of 21 breast cancers
-
Nik-Zainal, S. et al. Mutational processes molding the genomes of 21 breast cancers. Cell 149, 979-993 (2012).
-
(2012)
Cell
, vol.149
, pp. 979-993
-
-
Nik-Zainal, S.1
-
10
-
-
84943613527
-
Comprehensive molecular portraits of invasive lobular breast cancer
-
Ciriello, G. et al. Comprehensive molecular portraits of invasive lobular breast cancer. Cell 163, 506-519 (2015).
-
(2015)
Cell
, vol.163
, pp. 506-519
-
-
Ciriello, G.1
-
11
-
-
84877028141
-
Comprehensive molecular portraits of human breast tumours
-
The Cancer Genome Atlas Network
-
The Cancer Genome Atlas Network. Comprehensive molecular portraits of human breast tumours. Nature 490, 61-70 (2012).
-
(2012)
Nature
, vol.490
, pp. 61-70
-
-
-
12
-
-
84862584058
-
Whole-genome analysis informs breast cancer response to aromatase inhibition
-
Ellis, M. J. et al. Whole-genome analysis informs breast cancer response to aromatase inhibition. Nature 486, 353-360 (2012).
-
(2012)
Nature
, vol.486
, pp. 353-360
-
-
Ellis, M.J.1
-
13
-
-
84861576201
-
The landscape of cancer genes and mutational processes in breast cancer
-
Stephens, P. J. et al. The landscape of cancer genes and mutational processes in breast cancer. Nature 486, 400-404 (2012).
-
(2012)
Nature
, vol.486
, pp. 400-404
-
-
Stephens, P.J.1
-
14
-
-
84862523863
-
Sequence analysis of mutations and translocations across breast cancer subtypes
-
Banerji, S. et al. Sequence analysis of mutations and translocations across breast cancer subtypes. Nature 486, 405-409 (2012).
-
(2012)
Nature
, vol.486
, pp. 405-409
-
-
Banerji, S.1
-
15
-
-
34548680046
-
Comment on "The consensus coding sequences of human breast and colorectal cancers"
-
Getz, G. et al. Comment on "The consensus coding sequences of human breast and colorectal cancers". Science 317, 1500 (2007).
-
(2007)
Science
, vol.317
, pp. 1500
-
-
Getz, G.1
-
16
-
-
84882837534
-
Signatures of mutational processes in human cancer
-
Alexandrov, L. B. et al. Signatures of mutational processes in human cancer. Nature 500, 415-421 (2013).
-
(2013)
Nature
, vol.500
, pp. 415-421
-
-
Alexandrov, L.B.1
-
17
-
-
84883432724
-
An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers
-
Roberts, S. A. et al. An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers. Nat. Genet. 45, 970-976 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 970-976
-
-
Roberts, S.A.1
-
18
-
-
84964308124
-
Somatic ERCC2 mutations are associated with a distinct genomic signature in urothelial tumors
-
Kim, J. et al. Somatic ERCC2 mutations are associated with a distinct genomic signature in urothelial tumors. Nat. Genet. 48, 600-606 (2016).
-
(2016)
Nat. Genet
, vol.48
, pp. 600-606
-
-
Kim, J.1
-
19
-
-
84860782006
-
Absolute quantification of somatic DNA alterations in human cancer
-
Carter, S. L. et al. Absolute quantification of somatic DNA alterations in human cancer. Nat. Biotechnol. 30, 413-421 (2012).
-
(2012)
Nat. Biotechnol
, vol.30
, pp. 413-421
-
-
Carter, S.L.1
-
20
-
-
84874191269
-
TERT promoter mutations in familial and sporadic melanoma
-
Horn, S. et al. TERT promoter mutations in familial and sporadic melanoma. Science 339, 959-961 (2013).
-
(2013)
Science
, vol.339
, pp. 959-961
-
-
Horn, S.1
-
21
-
-
84874189784
-
Highly recurrent TERT promoter mutations in human melanoma
-
Huang, F. W. et al. Highly recurrent TERT promoter mutations in human melanoma. Science 339, 957-959 (2013).
-
(2013)
Science
, vol.339
, pp. 957-959
-
-
Huang, F.W.1
-
22
-
-
84951288125
-
DDX5 and its associated lncRNA Rmrp modulate TH17 cell effector functions
-
Huang, W. et al. DDX5 and its associated lncRNA Rmrp modulate TH17 cell effector functions. Nature 528, 517-522 (2015).
-
(2015)
Nature
, vol.528
, pp. 517-522
-
-
Huang, W.1
-
23
-
-
84911486777
-
The long noncoding RNA Neat1 is required for mammary gland development and lactation
-
Standaert, L. et al. The long noncoding RNA Neat1 is required for mammary gland development and lactation. RNA 20, 1844-1849 (2014).
-
(2014)
RNA
, vol.20
, pp. 1844-1849
-
-
Standaert, L.1
-
24
-
-
22144486551
-
Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the Forkhead protein FoxA1
-
Carroll, J. S. et al. Chromosome-wide mapping of estrogen receptor binding reveals long-range regulation requiring the Forkhead protein FoxA1. Cell 122, 33-43 (2005).
-
(2005)
Cell
, vol.122
, pp. 33-43
-
-
Carroll, J.S.1
-
25
-
-
78651250284
-
FOXA1 is a key determinant of estrogen receptor function and endocrine response
-
Hurtado, A., Holmes, K. A., Ross-Innes, C. S., Schmidt, D. & Carroll, J. S. FOXA1 is a key determinant of estrogen receptor function and endocrine response. Nat. Genet. 43, 27-33 (2011).
-
(2011)
Nat. Genet
, vol.43
, pp. 27-33
-
-
Hurtado, A.1
Holmes, K.A.2
Ross-Innes, C.S.3
Schmidt, D.4
Carroll, J.S.5
-
26
-
-
84856008906
-
Differential oestrogen receptor binding is associated with clinical outcome in breast cancer
-
Ross-Innes, C. S. et al. Differential oestrogen receptor binding is associated with clinical outcome in breast cancer. Nature 481, 389-393 (2012).
-
(2012)
Nature
, vol.481
, pp. 389-393
-
-
Ross-Innes, C.S.1
-
27
-
-
34547691136
-
FOXA1 expression in breast cancer-correlation with luminal subtype A and survival
-
Badve, S. et al. FOXA1 expression in breast cancer-correlation with luminal subtype A and survival. Clin. Cancer Res. 13, 4415-4421 (2007).
-
(2007)
Clin. Cancer Res
, vol.13
, pp. 4415-4421
-
-
Badve, S.1
-
28
-
-
40449117593
-
Forkhead box A1 expression in breast cancer is associated with luminal subtype and good prognosis
-
Thorat, M. A. et al. Forkhead box A1 expression in breast cancer is associated with luminal subtype and good prognosis. J. Clin. Pathol. 61, 327-332 (2008).
-
(2008)
J. Clin. Pathol
, vol.61
, pp. 327-332
-
-
Thorat, M.A.1
-
29
-
-
85028112875
-
FOXA1 is an independent prognostic marker for ER-positive breast cancer
-
Mehta, R. J. et al. FOXA1 is an independent prognostic marker for ER-positive breast cancer. Breast Cancer Res. Treat. 131, 881-890 (2012).
-
(2012)
Breast Cancer Res. Treat
, vol.131
, pp. 881-890
-
-
Mehta, R.J.1
-
30
-
-
84992371656
-
FOXA1 overexpression mediates endocrine resistance by altering the ER transcriptome and IL-8 expression in ER-positive breast cancer
-
Fu, X. et al. FOXA1 overexpression mediates endocrine resistance by altering the ER transcriptome and IL-8 expression in ER-positive breast cancer. Proc. Natl Acad. Sci. USA 113, E6600-E6609 (2016).
-
(2016)
Proc. Natl Acad. Sci. USA
, vol.113
, pp. E6600-E6609
-
-
Fu, X.1
-
31
-
-
85006247048
-
TransCONFIRM: Identification of a genetic signature of response to fulvestrant in advanced hormone receptor-positive breast cancer
-
Jeselsohn, R. et al. TransCONFIRM: identification of a genetic signature of response to fulvestrant in advanced hormone receptor-positive breast cancer. Clin. Cancer Res. 22, 5755 (2016)
-
(2016)
Clin. Cancer Res
, vol.22
, pp. 5755
-
-
Jeselsohn, R.1
-
32
-
-
78650762588
-
A scalable, fully automated process for construction of sequenceready human exome targeted capture libraries
-
Fisher, S. et al. A scalable, fully automated process for construction of sequenceready human exome targeted capture libraries. Genome Biol. 12, R1 (2011).
-
(2011)
Genome Biol
, vol.12
, pp. R1
-
-
Fisher, S.1
-
33
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
Gnirke, A. et al. Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat. Biotechnol. 27, 182-189 (2009).
-
(2009)
Nat. Biotechnol
, vol.27
, pp. 182-189
-
-
Gnirke, A.1
-
34
-
-
84928412505
-
Reply
-
Pugh, T. J., Banerji, S. & Meyerson, M. Pugh et al. reply. Nature 520, E12-E14 (2015).
-
(2015)
Nature
, vol.520
, pp. E12-E14
-
-
Pugh, T.J.1
Banerji, S.2
Pugh, M.M.3
-
35
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li, H. & Durbin, R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25, 1754-1760 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
36
-
-
80052707308
-
ContEst: Estimating cross-contamination of human samples in next-generation sequencing data
-
Cibulskis, K. et al. ContEst: estimating cross-contamination of human samples in next-generation sequencing data. Bioinformatics 27, 2601-2602 (2011).
-
(2011)
Bioinformatics
, vol.27
, pp. 2601-2602
-
-
Cibulskis, K.1
-
37
-
-
84876020288
-
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation
-
Costello, M. et al. Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation. Nucleic Acids Res. 41, e67 (2013).
-
(2013)
Nucleic Acids Res
, vol.41
, pp. e67
-
-
Costello, M.1
-
38
-
-
84925965197
-
Oncotator: Cancer variant annotation tool
-
Ramos, A. H. et al. Oncotator: cancer variant annotation tool. Hum. Mutat. 36, E2423-E2429 (2015).
-
(2015)
Hum. Mutat
, vol.36
, pp. E2423-E2429
-
-
Ramos, A.H.1
-
39
-
-
79955166265
-
GISTIC2. 0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers
-
Mermel, C. H. et al. GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers. Genome Biol. 12, R41 (2011).
-
(2011)
Genome Biol
, vol.12
, pp. R41
-
-
Mermel, C.H.1
-
40
-
-
84945302209
-
Mutations driving CLL and their evolution in progression and relapse
-
Landau, D. A. et al. Mutations driving CLL and their evolution in progression and relapse. Nature 526, 525-530 (2015).
-
(2015)
Nature
, vol.526
, pp. 525-530
-
-
Landau, D.A.1
-
41
-
-
84893904007
-
A polygenic burden of rare disruptive mutations in schizophrenia
-
Purcell, S. M. et al. A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506, 185-190 (2014).
-
(2014)
Nature
, vol.506
, pp. 185-190
-
-
Purcell, S.M.1
-
42
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price, A. L. et al. Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet. 38, 904-909 (2006).
-
(2006)
Nat. Genet
, vol.38
, pp. 904-909
-
-
Price, A.L.1
-
44
-
-
84949034526
-
LARVA: An integrative framework for large-scale analysis of recurrent variants in noncoding annotations
-
Lochovsky, L., Zhang, J., Fu, Y., Khurana, E. & Gerstein, M. LARVA: an integrative framework for large-scale analysis of recurrent variants in noncoding annotations. Nucleic Acids Res. 43, 8123-8134 (2015).
-
(2015)
Nucleic Acids Res
, vol.43
, pp. 8123-8134
-
-
Lochovsky, L.1
Zhang, J.2
Fu, Y.3
Khurana, E.4
Gerstein, M.5
-
45
-
-
84929991442
-
Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin
-
Martincorena, I. et al. Tumor evolution. High burden and pervasive positive selection of somatic mutations in normal human skin. Science 348, 880-886 (2015).
-
(2015)
Science
, vol.348
, pp. 880-886
-
-
Martincorena, I.1
-
46
-
-
84864598664
-
MuSiC: Identifying mutational significance in cancer genomes
-
Dees, N. D. et al. MuSiC: identifying mutational significance in cancer genomes. Genome Res. 22, 1589-1598 (2012).
-
(2012)
Genome Res
, vol.22
, pp. 1589-1598
-
-
Dees, N.D.1
-
47
-
-
31144472543
-
Fuzzy and randomized confidence intervals and P values
-
Geyer, C. J. & Meeden, G. D. Fuzzy and randomized confidence intervals and P values. Stat. Sci. 20, 358-366 (2005).
-
(2005)
Stat. Sci
, vol.20
, pp. 358-366
-
-
Geyer, C.J.1
Meeden, G.D.2
-
48
-
-
84988075071
-
Practicing safe statistics with the mid-p
-
Routledge, R. Practicing safe statistics with the mid-p. Can. J. Stat. 22, 103-110 (1994).
-
(1994)
Can. J. Stat
, vol.22
, pp. 103-110
-
-
Routledge, R.1
-
49
-
-
84943411478
-
Comprehensive assessment of cancer missense mutation clustering in protein structures
-
Kamburov, A. et al. Comprehensive assessment of cancer missense mutation clustering in protein structures. Proc. Natl Acad. Sci. USA 112, E5486-E5495 (2015).
-
(2015)
Proc. Natl Acad. Sci. USA
, vol.112
, pp. E5486-E5495
-
-
Kamburov, A.1
-
51
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini, Y. & Hochberg, Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J. Roy. Stat. Soc. B 57, 289-300 (1995).
-
(1995)
J. Roy. Stat. Soc. B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
52
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
The ENCODE Project Consortium. An integrated encyclopedia of DNA elements in the human genome. Nature 489, 57-74 (2012).
-
(2012)
Nature
, vol.489
, pp. 57-74
-
-
-
53
-
-
0037208166
-
TRANSFAC: Transcriptional regulation, from patterns to profiles
-
Matys, V. et al. TRANSFAC: transcriptional regulation, from patterns to profiles. Nucleic Acids Res. 31, 374-378 (2003).
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 374-378
-
-
Matys, V.1
-
54
-
-
0347125328
-
JASPAR: An open-access database for eukaryotic transcription factor binding profiles
-
Sandelin, A., Alkema, W., Engström, P., Wasserman, W. W. & Lenhard, B. JASPAR: an open-access database for eukaryotic transcription factor binding profiles. Nucleic Acids Res. 32, D91-D94 (2004).
-
(2004)
Nucleic Acids Res
, vol.32
, pp. D91-D94
-
-
Sandelin, A.1
Alkema, W.2
Engström, P.3
Wasserman, W.W.4
Lenhard, B.5
-
55
-
-
30344439849
-
Genome-wide prediction of mammalian enhancers based on analysis of transcription-factor binding affinity
-
Hallikas, O. et al. Genome-wide prediction of mammalian enhancers based on analysis of transcription-factor binding affinity. Cell 124, 47-59 (2006).
-
(2006)
Cell
, vol.124
, pp. 47-59
-
-
Hallikas, O.1
-
56
-
-
77953006022
-
Multiplexed massively parallel SELEX for characterization of human transcription factor binding specificities
-
Jolma, A. et al. Multiplexed massively parallel SELEX for characterization of human transcription factor binding specificities. Genome Res. 20, 861-873 (2010).
-
(2010)
Genome Res
, vol.20
, pp. 861-873
-
-
Jolma, A.1
-
57
-
-
84872540994
-
DNA-binding specificities of human transcription factors
-
Jolma, A. et al. DNA-binding specificities of human transcription factors. Cell 152, 327-339 (2013).
-
(2013)
Cell
, vol.152
, pp. 327-339
-
-
Jolma, A.1
-
58
-
-
77954954652
-
Genome-wide analysis of ETS-family DNA-binding in vitro and in vivo
-
Wei, G. H. et al. Genome-wide analysis of ETS-family DNA-binding in vitro and in vivo. EMBO J. 29, 2147-2160 (2010).
-
(2010)
EMBO J
, vol.29
, pp. 2147-2160
-
-
Wei, G.H.1
-
59
-
-
39049165160
-
Efficient and accurate P value computation for position weight matrices
-
Touzet, H. & Varré, J. S. Efficient and accurate P value computation for position weight matrices. Algorithms Mol. Biol. 2, 15 (2007).
-
(2007)
Algorithms Mol. Biol
, vol.2
, pp. 15
-
-
Touzet, H.1
Varré, J.S.2
-
60
-
-
84932628860
-
Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas
-
The Cancer Genome Atlas Research
-
The Cancer Genome Atlas Research. Comprehensive, integrative genomic analysis of diffuse lower-grade gliomas. N. Engl. J. Med. 372, 2481-2498 (2015).
-
(2015)
N. Engl. J. Med
, vol.372
, pp. 2481-2498
-
-
-
61
-
-
68549104404
-
The sequence alignment/map format and samtools
-
Li, H. et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics 25, 2078-2079 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
-
62
-
-
84868198825
-
Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression
-
Cowper-Sal lari, R. et al. Breast cancer risk-associated SNPs modulate the affinity of chromatin for FOXA1 and alter gene expression. Nat. Genet. 44, 1191-1198 (2012).
-
(2012)
Nat. Genet
, vol.44
, pp. 1191-1198
-
-
Cowper-Sal Lari, R.1
-
63
-
-
77952567987
-
Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities
-
Heinz, S. et al. Simple combinations of lineage-determining transcription factors prime cis-regulatory elements required for macrophage and B cell identities. Mol. Cell 38, 576-589 (2010).
-
(2010)
Mol. Cell
, vol.38
, pp. 576-589
-
-
Heinz, S.1
-
64
-
-
77949587674
-
Lentiviral vectors to probe and manipulate the Wnt signaling pathway
-
Fuerer, C. & Nusse, R. Lentiviral vectors to probe and manipulate the Wnt signaling pathway. PLoS ONE 5, e9370 (2010).
-
(2010)
PLoS ONE
, vol.5
, pp. e9370
-
-
Fuerer, C.1
Nusse, R.2
-
65
-
-
0026609875
-
Independent binding of the retinoblastoma protein and p107 to the transcription factor E2F
-
Cao, L. et al. Independent binding of the retinoblastoma protein and p107 to the transcription factor E2F. Nature 355, 176-179 (1992).
-
(1992)
Nature
, vol.355
, pp. 176-179
-
-
Cao, L.1
-
66
-
-
0141814666
-
Specificity in the activation and control of transcription factor E2F-dependent apoptosis
-
Hallstrom, T. C. & Nevins, J. R. Specificity in the activation and control of transcription factor E2F-dependent apoptosis. Proc. Natl Acad. Sci. USA 100, 10848-10853 (2003).
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 10848-10853
-
-
Hallstrom, T.C.1
Nevins, J.R.2
-
67
-
-
23744507860
-
E2F1 is crucial for E2F-dependent apoptosis
-
Lazzerini Denchi, E. & Helin, K. E2F1 is crucial for E2F-dependent apoptosis. EMBO Rep. 6, 661-668 (2005).
-
(2005)
EMBO Rep
, vol.6
, pp. 661-668
-
-
Lazzerini Denchi, E.1
Helin, K.2
-
68
-
-
0141927097
-
PRB contains an E2F1-specific binding domain that allows E2F1-induced apoptosis to be regulated separately from other E2F activities
-
Dick, F. A. & Dyson, N. pRB contains an E2F1-specific binding domain that allows E2F1-induced apoptosis to be regulated separately from other E2F activities. Mol. Cell 12, 639-649 (2003).
-
(2003)
Mol. Cell
, vol.12
, pp. 639-649
-
-
Dick, F.A.1
Dyson, N.2
-
69
-
-
70149114591
-
Antiestrogen-resistant subclones of MCF-7 human breast cancer cells are derived from a common monoclonal drug-resistant progenitor
-
Coser, K. R. et al. Antiestrogen-resistant subclones of MCF-7 human breast cancer cells are derived from a common monoclonal drug-resistant progenitor. Proc. Natl Acad. Sci. USA 106, 14536-14541 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 14536-14541
-
-
Coser, K.R.1
-
70
-
-
78651271733
-
Integrative genomics viewer
-
Robinson, J. T. et al. Integrative genomics viewer. Nat. Biotechnol. 29, 24-26 (2011).
-
(2011)
Nat. Biotechnol
, vol.29
, pp. 24-26
-
-
Robinson, J.T.1
|