-
1
-
-
0035137882
-
Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB
-
Baldwin AS. 2001. Control of oncogenesis and cancer therapy resistance by the transcription factor NF-kappaB. J Clin Invest 107:241-246.
-
(2001)
J Clin Invest
, vol.107
, pp. 241-246
-
-
Baldwin, A.S.1
-
2
-
-
3843084078
-
The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website
-
Bamford S, Dawson E, Forbes S, Clements J, Pettett R, Dogan A, Flanagan A, Teague J, Futreal PA, Stratton MR, Wooster R. 2004. The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website. Br J Cancer 91(2):355-358.
-
(2004)
Br J Cancer
, vol.91
, Issue.2
, pp. 355-358
-
-
Bamford, S.1
Dawson, E.2
Forbes, S.3
Clements, J.4
Pettett, R.5
Dogan, A.6
Flanagan, A.7
Teague, J.8
Futreal, P.A.9
Stratton, M.R.10
Wooster, R.11
-
3
-
-
0037040444
-
Microsomal epoxide hydrolase polymorphism and susceptibility to ovarian cancer
-
Baxter SW, Choong DY, Campbell IG. 2002. Microsomal epoxide hydrolase polymorphism and susceptibility to ovarian cancer. Cancer Lett 177:75-81.
-
(2002)
Cancer Lett
, vol.177
, pp. 75-81
-
-
Baxter, S.W.1
Choong, D.Y.2
Campbell, I.G.3
-
4
-
-
0001677717
-
Controlling the false discovery rate: A practical and powerful approach to multiple testing
-
Benjamini Y, Hochberg Y. 1995. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc B 57:289-300.
-
(1995)
J R Stat Soc B
, vol.57
, pp. 289-300
-
-
Benjamini, Y.1
Hochberg, Y.2
-
5
-
-
0035902180
-
Oncogenic kinase signalling
-
Blume-Jensen P, Hunter T. 2001. Oncogenic kinase signalling. Nature 411:355-365.
-
(2001)
Nature
, vol.411
, pp. 355-365
-
-
Blume-Jensen, P.1
Hunter, T.2
-
6
-
-
0037255072
-
The SWISSPROT protein knowledgebase and its supplement TrEMBL in 2003
-
Boeckmann B, Bairoch A, Apweiler R, Blatter MC, Estreicher A, Gasteiger E, Martin MJ, Michoud K, O'Donovan C, Phan I, Pilbout S, Schneider M. 2003. The SWISSPROT protein knowledgebase and its supplement TrEMBL in 2003. Nucleic Acids Res 31:365-370.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 365-370
-
-
Boeckmann, B.1
Bairoch, A.2
Apweiler, R.3
Blatter, M.C.4
Estreicher, A.5
Gasteiger, E.6
Martin, M.J.7
Michoud, K.8
O'Donovan, C.9
Phan, I.10
Pilbout, S.11
Schneider, M.12
-
7
-
-
28044431588
-
Protein variety and functional diversity: Swiss-Prot annotation in its biological context
-
Boeckmann B, Blatter MC, Famiglietti L, Hinz U, Lane L, Roechert B, Bairoch A. 2005. Protein variety and functional diversity: Swiss-Prot annotation in its biological context. CR Biol 328:882-899.
-
(2005)
CR Biol
, vol.328
, pp. 882-899
-
-
Boeckmann, B.1
Blatter, M.C.2
Famiglietti, L.3
Hinz, U.4
Lane, L.5
Roechert, B.6
Bairoch, A.7
-
8
-
-
0037373275
-
Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
-
Botstein D, Risch N. 2003. Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet 33(Suppl):228-237.
-
(2003)
Nat Genet
, vol.33
, Issue.SUPPL.
, pp. 228-237
-
-
Botstein, D.1
Risch, N.2
-
9
-
-
0032991552
-
Characterization of single-nucleotide polymorphisms in coding regions of human genes
-
Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N, Shaw N, Lane CR, Lim EP, Kalyanaraman N, Nemesh J, Ziaugra L, Friedland L, Rolfe A, Warrington J, Lipshutz R, Daley GQ, Lander ES. 1999. Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat Genet 22:231-238.
-
(1999)
Nat Genet
, vol.22
, pp. 231-238
-
-
Cargill, M.1
Altshuler, D.2
Ireland, J.3
Sklar, P.4
Ardlie, K.5
Patil, N.6
Shaw, N.7
Lane, C.R.8
Lim, E.P.9
Kalyanaraman, N.10
Nemesh, J.11
Ziaugra, L.12
Friedland, L.13
Rolfe, A.14
Warrington, J.15
Lipshutz, R.16
Daley, G.Q.17
Lander, E.S.18
-
10
-
-
1342309591
-
Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: A population-based study in northern Sweden
-
Cederquist K, Emanuelsson M, Goransson I, Holinski-Feder E, Muller-Koch Y, Golovleva I, Gronberg H. 2004. Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. Int J Cancer 109:370-376.
-
(2004)
Int J Cancer
, vol.109
, pp. 370-376
-
-
Cederquist, K.1
Emanuelsson, M.2
Goransson, I.3
Holinski-Feder, E.4
Muller-Koch, Y.5
Golovleva, I.6
Gronberg, H.7
-
11
-
-
0034799051
-
Candidate genes and single nucleotide polymorphisms (SNPs) in the study of human disease
-
Chanock S. 2001. Candidate genes and single nucleotide polymorphisms (SNPs) in the study of human disease. Dis Markers 17:89-98.
-
(2001)
Dis Markers
, vol.17
, pp. 89-98
-
-
Chanock, S.1
-
12
-
-
0034541557
-
Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium?
-
Charames GS, Millar AL, Pal T, Narod S, Bapat B. 2000. Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium? Hum Genet 107:623-629.
-
(2000)
Hum Genet
, vol.107
, pp. 623-629
-
-
Charames, G.S.1
Millar, A.L.2
Pal, T.3
Narod, S.4
Bapat, B.5
-
13
-
-
0035937259
-
Predicting the functional consequences of nonsynonymous single nucleotide polymorphisms: Structure-based assessment of amino acid variation
-
Chasman D, Adams RM. 2001. Predicting the functional consequences of nonsynonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation. J Mol Biol 307:683-706.
-
(2001)
J Mol Biol
, vol.307
, pp. 683-706
-
-
Chasman, D.1
Adams, R.M.2
-
14
-
-
33846073818
-
MINT: The Molecular INTeraction database
-
Chatr-aryamontri A, Ceol A, Palazzi LM, Nardelli G, Schneider MV, Castagnoli L, Cesareni G. 2007. MINT: the Molecular INTeraction database. Nucleic Acids Res 35(Database issue):D572-D574.
-
(2007)
Nucleic Acids Res 35(Database issue)
-
-
Chatr-aryamontri, A.1
Ceol, A.2
Palazzi, L.M.3
Nardelli, G.4
Schneider, M.V.5
Castagnoli, L.6
Cesareni, G.7
-
15
-
-
21044445279
-
Mutation in the tyrosine kinase domain of epidermal growth factor receptor is a predictive and prognostic factor for gefitinib treatment in patients with non-small cell lung cancer
-
Chou TY, Chiu CH, Li LH, Hsiao CY, Tzen CY, Chang KT, Chen YM, Perng RP, Tsai SF, Tsai CM. 2005. Mutation in the tyrosine kinase domain of epidermal growth factor receptor is a predictive and prognostic factor for gefitinib treatment in patients with non-small cell lung cancer. Clin Cancer Res 11:3750-3757.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 3750-3757
-
-
Chou, T.Y.1
Chiu, C.H.2
Li, L.H.3
Hsiao, C.Y.4
Tzen, C.Y.5
Chang, K.T.6
Chen, Y.M.7
Perng, R.P.8
Tsai, S.F.9
Tsai, C.M.10
-
16
-
-
65649090889
-
The caBIG terminology review process
-
Cimino JJ, Hayamizu TF, Bodenreider O, Davis B, Stafford GA, Ringwald M. 2009. The caBIG terminology review process. J Biomed Inform 42:571-580.
-
(2009)
J Biomed Inform
, vol.42
, pp. 571-580
-
-
Cimino, J.J.1
Hayamizu, T.F.2
Bodenreider, O.3
Davis, B.4
Stafford, G.A.5
Ringwald, M.6
-
17
-
-
7244245445
-
Roles and regulation of stat family transcription factors in human breast cancer
-
Clevenger CV. 2004. Roles and regulation of stat family transcription factors in human breast cancer. Am J Pathol 165:1449-1460.
-
(2004)
Am J Pathol
, vol.165
, pp. 1449-1460
-
-
Clevenger, C.V.1
-
19
-
-
58549095879
-
Replacement of normal with mutant alleles in the genome of normal human cells unveils mutation-specific drug responses
-
Di Nicolantonio F, Arena S, Gallicchio M, Zecchin D, Martini M, Flonta SE, Stella GM, Lamba S, Cancelliere C, Russo M, Geuna M, Appendino G, Fantozzi R, Medico E, Bardelli A. 2008. Replacement of normal with mutant alleles in the genome of normal human cells unveils mutation-specific drug responses. Proc Natl Acad Sci USA 105:20864-20869.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 20864-20869
-
-
Di Nicolantonio, F.1
Arena, S.2
Gallicchio, M.3
Zecchin, D.4
Martini, M.5
Flonta, S.E.6
Stella, G.M.7
Lamba, S.8
Cancelliere, C.9
Russo, M.10
Geuna, M.11
Appendino, G.12
Fantozzi, R.13
Medico, E.14
Bardelli, A.15
-
20
-
-
13844321724
-
Chasing mutations in the epidermal growth factor in lung cancer
-
Dowell JE, Minna JD. 2005. Chasing mutations in the epidermal growth factor in lung cancer. N Engl J Med 352:830-832.
-
(2005)
N Engl J Med
, vol.352
, pp. 830-832
-
-
Dowell, J.E.1
Minna, J.D.2
-
21
-
-
33645124451
-
Using high-throughput SNP technologies to study cancer
-
Engle LJ, Simpson CL, Landers JE. 2006. Using high-throughput SNP technologies to study cancer. Oncogene 25:1594-1601.
-
(2006)
Oncogene
, vol.25
, pp. 1594-1601
-
-
Engle, L.J.1
Simpson, C.L.2
Landers, J.E.3
-
22
-
-
65649152988
-
Involvement of a novel chemokine decoy receptor CCX-CKR in breast cancer growth, metastasis and patient survival
-
Feng LY, Ou ZL, Wu FY, Shen ZZ, Shao ZM. 2009. Involvement of a novel chemokine decoy receptor CCX-CKR in breast cancer growth, metastasis and patient survival. Clin Cancer Res 15:2962-2970.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 2962-2970
-
-
Feng, L.Y.1
Ou, Z.L.2
Wu, F.Y.3
Shen, Z.Z.4
Shao, Z.M.5
-
23
-
-
33846266906
-
Modeling the evolution of protein domain architectures using maximum parsimony
-
Fong JH, Geer LY, Panchenko AR, Bryant SH. 2007.Modeling the evolution of protein domain architectures using maximum parsimony. J Mol Biol 366:307-315.
-
(2007)
J Mol Biol
, vol.366
, pp. 307-315
-
-
Fong, J.H.1
Geer, L.Y.2
Panchenko, A.R.3
Bryant, S.H.4
-
24
-
-
0036081484
-
HGVbase: A human sequence variation database emphasizing data quality and a broad spectrum of data sources
-
Fredman D, Siegfried M, Yuan YP, Bork P, Lehvaslaiho H, Brookes AJ. 2002. HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources. Nucleic Acids Res 30:387-391.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 387-391
-
-
Fredman, D.1
Siegfried, M.2
Yuan, Y.P.3
Bork, P.4
Lehvaslaiho, H.5
Brookes, A.J.6
-
25
-
-
32544435114
-
Nonsynonymous SNPs: Validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection
-
Fredman D, Sawyer SL, Stromqvist L, Mottagui-Tabar S, Kidd KK, Wahlestedt C, Chanock SJ, Brookes AJ. 2006. Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection. Hum Mutat 27:173-186.
-
(2006)
Hum Mutat
, vol.27
, pp. 173-186
-
-
Fredman, D.1
Sawyer, S.L.2
Stromqvist, L.3
Mottagui-Tabar, S.4
Kidd, K.K.5
Wahlestedt, C.6
Chanock, S.J.7
Brookes, A.J.8
-
26
-
-
1542515338
-
A census of human cancer genes
-
Futreal PA, Coin L, Marshall M, Down T, Hubbard T, Wooster R, Rahman N, Stratton MR. 2004. A census of human cancer genes. Nat Rev Cancer 4:177-183.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 177-183
-
-
Futreal, P.A.1
Coin, L.2
Marshall, M.3
Down, T.4
Hubbard, T.5
Wooster, R.6
Rahman, N.7
Stratton, M.R.8
-
27
-
-
33947101019
-
Patterns of somatic mutation in human cancer genomes
-
Greenman C, Stephens P, Smith R, Dalgliesh GL, Hunter C, Bignell G, Davies H, Teague J, Butler A, Stevens C, and others. 2007. Patterns of somatic mutation in human cancer genomes. Nature 446:153-158.
-
(2007)
Nature
, vol.446
, pp. 153-158
-
-
Greenman, C.1
Stephens, P.2
Smith, R.3
Dalgliesh, G.L.4
Hunter, C.5
Bignell, G.6
Davies, H.7
Teague, J.8
Butler, A.9
Stevens, C.10
and others11
-
28
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
Halushka MK, Fan JB, Bentley K, Hsie L, Shen N, Weder A, Cooper R, Lipshutz R, Chakravarti A. 1999. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis. Nat Genet 22:239-247.
-
(1999)
Nat Genet
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
Hsie, L.4
Shen, N.5
Weder, A.6
Cooper, R.7
Lipshutz, R.8
Chakravarti, A.9
-
29
-
-
13444266370
-
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
-
Hamosh A, Scott AF, Amberger JS, Bocchini CA, McKusick VA. 2005. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res 33(Database issue):D514-D517.
-
(2005)
Nucleic Acids Res 33(Database issue)
-
-
Hamosh, A.1
Scott, A.F.2
Amberger, J.S.3
Bocchini, C.A.4
McKusick, V.A.5
-
30
-
-
33747864499
-
SNP@Domain: A web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences
-
Han A, Kang HJ, Cho Y, Lee S, Kim YJ, Gong S. 2006. SNP@Domain: a web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences. Nucleic Acids Res 34(Web Server issue):W642-W644.
-
(2006)
Nucleic Acids Res 34(Web Server issue)
-
-
Han, A.1
Kang, H.J.2
Cho, Y.3
Lee, S.4
Kim, Y.J.5
Gong, S.6
-
32
-
-
0032235209
-
Polymorphisms of N-acetyltransferases, glutathione S-transferases, microsomal epoxide hydrolase and sulfotransferases: Influence on cancer susceptibility
-
Hengstler JG, Arand M, Herrero ME, Oesch F. 1998. Polymorphisms of N-acetyltransferases, glutathione S-transferases, microsomal epoxide hydrolase and sulfotransferases: influence on cancer susceptibility. Recent Results Cancer Res 154:47-85.
-
(1998)
Recent Results Cancer Res
, vol.154
, pp. 47-85
-
-
Hengstler, J.G.1
Arand, M.2
Herrero, M.E.3
Oesch, F.4
-
33
-
-
0035902108
-
Genome maintenance mechanisms for preventing cancer
-
Hoeijmakers JH. 2001. Genome maintenance mechanisms for preventing cancer. Nature 411:366-374.
-
(2001)
Nature
, vol.411
, pp. 366-374
-
-
Hoeijmakers, J.H.1
-
34
-
-
2542557724
-
Breast cancer: When proteomics challenges biological complexity
-
Hondermarck H. 2003. Breast cancer: when proteomics challenges biological complexity. Mol Cell Proteomics 2:281-291.
-
(2003)
Mol Cell Proteomics
, vol.2
, pp. 281-291
-
-
Hondermarck, H.1
-
35
-
-
33846071416
-
PolyDoms: A whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease
-
Jegga AG, Gowrisankar S, Chen J, Aronow BJ. 2007. PolyDoms: a whole genome database for the identification of non-synonymous coding SNPs with the potential to impact disease. Nucleic Acids Res 35(Database issue): D700-D706.
-
(2007)
Nucleic Acids Res 35(Database issue)
-
-
Jegga, A.G.1
Gowrisankar, S.2
Chen, J.3
Aronow, B.J.4
-
36
-
-
20844461337
-
LS-SNP: Large-scale annotation of coding non-synonymous SNPs based on multiple information sources
-
Karchin R, Diekhans M, Kelly L, Thomas DJ, Pieper U, Eswar N, Haussler D, Sali A. 2005. LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources. Bioinformatics 21:2814-2820.
-
(2005)
Bioinformatics
, vol.21
, pp. 2814-2820
-
-
Karchin, R.1
Diekhans, M.2
Kelly, L.3
Thomas, D.J.4
Pieper, U.5
Eswar, N.6
Haussler, D.7
Sali, A.8
-
37
-
-
33846047770
-
IntAct-open source resource for molecular interaction data
-
Kerrien S, Alam-Faruque Y, Aranda B, Bancarz I, Bridge A, Derow C, Dimmer E, Feuermann M, Friedrichsen A, Huntley R, Kohler C, Khadake J, Leroy C, Liban A, Lieftink C, Montecchi-Palazzi L, Orchard S, Risse J, Robbe K, Roechert B, Thorneycroft D, Zhang Y, Apweiler R, Hermjakob H. 2007. IntAct-open source resource for molecular interaction data. Nucleic Acids Res 35(Database issue):D561-D565.
-
(2007)
Nucleic Acids Res 35(Database issue)
-
-
Kerrien, S.1
Alam-Faruque, Y.2
Aranda, B.3
Bancarz, I.4
Bridge, A.5
Derow, C.6
Dimmer, E.7
Feuermann, M.8
Friedrichsen, A.9
Huntley, R.10
Kohler, C.11
Khadake, J.12
Leroy, C.13
Liban, A.14
Lieftink, C.15
Montecchi-Palazzi, L.16
Orchard, S.17
Risse, J.18
Robbe, K.19
Roechert, B.20
Thorneycroft, D.21
Zhang, Y.22
Apweiler, R.23
Hermjakob, H.24
more..
-
38
-
-
58149193222
-
Human Protein Reference Database-2009 update
-
Keshava Prasad TS, Goel R, Kandasamy K, Keerthikumar S, Kumar S, Mathivanan S, Telikicherla D, Raju R, Shafreen B, Venugopal A, Balakrishnan L, Marimuthu A, Banerjee S, Somanathan DS, Sebastian A, Rani S, Ray S, Harrys Kishore CJ, Kanth S, Ahmed M, Kashyap MK, Mohmood R, Ramachandra YL, Krishna V, Rahiman BA, Mohan S, Ranganathan P, Ramabadran S, Chaerkady R, Pandey A. 2009. Human Protein Reference Database-2009 update. Nucleic Acids Res 37(Database issue):D767-D772.
-
(2009)
Nucleic Acids Res 37(Database issue)
-
-
Keshava Prasad, T.S.1
Goel, R.2
Kandasamy, K.3
Keerthikumar, S.4
Kumar, S.5
Mathivanan, S.6
Telikicherla, D.7
Raju, R.8
Shafreen, B.9
Venugopal, A.10
Balakrishnan, L.11
Marimuthu, A.12
Banerjee, S.13
Somanathan, D.S.14
Sebastian, A.15
Rani, S.16
Ray, S.17
Harrys Kishore, C.J.18
Kanth, S.19
Ahmed, M.20
Kashyap, M.K.21
Mohmood, R.22
Ramachandra, Y.L.23
Krishna, V.24
Rahiman, B.A.25
Mohan, S.26
Ranganathan, P.27
Ramabadran, S.28
Chaerkady, R.29
Pandey, A.30
more..
-
39
-
-
33645213803
-
Distribution of human SNPs and its effect on high-throughput genotyping
-
Koboldt DC, Miller RD, Kwok PY. 2006. Distribution of human SNPs and its effect on high-throughput genotyping. Hum Mutat 27:249-254.
-
(2006)
Hum Mutat
, vol.27
, pp. 249-254
-
-
Koboldt, D.C.1
Miller, R.D.2
Kwok, P.Y.3
-
40
-
-
0034667593
-
Meaningful relationships: The regulation of the Ras/Raf/MEK/ERK pathway by protein interactions
-
Kolch W. 2000. Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions. Biochem J 351(Pt 2):289-305.
-
(2000)
Biochem J
, vol.351
, Issue.PART 2
, pp. 289-305
-
-
Kolch, W.1
-
41
-
-
33846617807
-
Cancer-associated mutations in the MDM2 zinc finger domain disrupt ribosomal protein interaction and attenuate MDM2-induced p53 degradation
-
Lindstrom MS, Jin A, Deisenroth C, White Wolf G, Zhang Y. 2007. Cancer-associated mutations in the MDM2 zinc finger domain disrupt ribosomal protein interaction and attenuate MDM2-induced p53 degradation. Mol Cell Biol 27:1056-1068.
-
(2007)
Mol Cell Biol
, vol.27
, pp. 1056-1068
-
-
Lindstrom, M.S.1
Jin, A.2
Deisenroth, C.3
White Wolf, G.4
Zhang, Y.5
-
42
-
-
58149177166
-
Reactome knowledgebase of human biological pathways and processes
-
Matthews L, Gopinath G, Gillespie M, Caudy M, Croft D, de Bono B, Garapati P, Hemish J, Hermjakob H, Jassal B, Kanapin A, Lewis S, Mahajan S, May B, Schmidt E, Vastrik I, Wu G, Birhey E, Stein L, D'Eustachio P. 2009. Reactome knowledgebase of human biological pathways and processes. Nucleic Acids Res 37(Database issue):D619-D622.
-
(2009)
Nucleic Acids Res 37(Database issue)
-
-
Matthews, L.1
Gopinath, G.2
Gillespie, M.3
Caudy, M.4
Croft, D.5
de Bono, B.6
Garapati, P.7
Hemish, J.8
Hermjakob, H.9
Jassal, B.10
Kanapin, A.11
Lewis, S.12
Mahajan, S.13
May, B.14
Schmidt, E.15
Vastrik, I.16
Wu, G.17
Birhey, E.18
Stein, L.19
D'Eustachio, P.20
more..
-
43
-
-
33645111448
-
Glutathione S-transferase polymorphisms: Cancer incidence and therapy
-
McIlwain CC, Townsend DM, Tew KD. 2006. Glutathione S-transferase polymorphisms: cancer incidence and therapy. Oncogene 25:1639-1648.
-
(2006)
Oncogene
, vol.25
, pp. 1639-1648
-
-
McIlwain, C.C.1
Townsend, D.M.2
Tew, K.D.3
-
44
-
-
38549170927
-
-
Mewes HW, Dietmann S, Frishman D, Gregory R, Mannhaupt G, Mayer KF, Munsterkotter M, Ruepp A, Spannagl M, Stumpflen V, Rattei T. 2008. MIPS: analysis and annotation of genome information in 2007. Nucleic Acids Res 36(Database issue):D196-D201.
-
Mewes HW, Dietmann S, Frishman D, Gregory R, Mannhaupt G, Mayer KF, Munsterkotter M, Ruepp A, Spannagl M, Stumpflen V, Rattei T. 2008. MIPS: analysis and annotation of genome information in 2007. Nucleic Acids Res 36(Database issue):D196-D201.
-
-
-
-
45
-
-
0030949463
-
Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC
-
Morin PJ, Sparks AB, Korinek V, Barker N, Clevers H, Vogelstein B, Kinzler KW. 1997. Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC. Science 275:1787-1790.
-
(1997)
Science
, vol.275
, pp. 1787-1790
-
-
Morin, P.J.1
Sparks, A.B.2
Korinek, V.3
Barker, N.4
Clevers, H.5
Vogelstein, B.6
Kinzler, K.W.7
-
46
-
-
0035282432
-
Involvement of chemokine receptors in breast cancer metastasis
-
Muller A, Homey B, Soto H, Ge N, Catron D, Buchanan ME, McClanahan T, Murphy E, Yuan W, Wagner SN, Barrera JL, Mohan A, Verastegui E, Zlotnik A. 2001. Involvement of chemokine receptors in breast cancer metastasis. Nature 410:50-56.
-
(2001)
Nature
, vol.410
, pp. 50-56
-
-
Muller, A.1
Homey, B.2
Soto, H.3
Ge, N.4
Catron, D.5
Buchanan, M.E.6
McClanahan, T.7
Murphy, E.8
Yuan, W.9
Wagner, S.N.10
Barrera, J.L.11
Mohan, A.12
Verastegui, E.13
Zlotnik, A.14
-
48
-
-
61649116600
-
Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: Proposed guidelines for improving data collection, distribution, and integration
-
Olivier M, Petitjean A, Teague J, Forbes S, Dunnick JK, den Dunnen JT, Langerod A, Wilkinson JM, Vihinen M, Cotton RG, Hainaut P. 2009. Somatic mutation databases as tools for molecular epidemiology and molecular pathology of cancer: proposed guidelines for improving data collection, distribution, and integration. Hum Mutat 30:275-282.
-
(2009)
Hum Mutat
, vol.30
, pp. 275-282
-
-
Olivier, M.1
Petitjean, A.2
Teague, J.3
Forbes, S.4
Dunnick, J.K.5
den Dunnen, J.T.6
Langerod, A.7
Wilkinson, J.M.8
Vihinen, M.9
Cotton, R.G.10
Hainaut, P.11
-
49
-
-
2342624080
-
EGFR mutations in lung cancer: Correlation with clinical response to gefitinib therapy
-
Paez JG, Janne PA, Lee JC, Tracy S, Greulich H, Gabriel S, Herman P, Kaye FJ, Lindeman N, Boggon TJ, Naoki K, Sasaki H, Fujii Y, Eck MJ, Sellers WR, Johnson BE, Meyerson M. 2004. EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy. Science 304: 1497-1500.
-
(2004)
Science
, vol.304
, pp. 1497-1500
-
-
Paez, J.G.1
Janne, P.A.2
Lee, J.C.3
Tracy, S.4
Greulich, H.5
Gabriel, S.6
Herman, P.7
Kaye, F.J.8
Lindeman, N.9
Boggon, T.J.10
Naoki, K.11
Sasaki, H.12
Fujii, Y.13
Eck, M.J.14
Sellers, W.R.15
Johnson, B.E.16
Meyerson, M.17
-
50
-
-
4444344330
-
EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib
-
Pao W, Miller V, Zakowski M, Doherty J, Politi K, Sarkaria I, Singh B, Heelan R, Rusch V, Fulton L, Mardis E, Kupfer D, Wilson R, Kris M, Varmus H. 2004. EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib. Proc Natl Acad Sci USA 101:13306-13311.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 13306-13311
-
-
Pao, W.1
Miller, V.2
Zakowski, M.3
Doherty, J.4
Politi, K.5
Sarkaria, I.6
Singh, B.7
Heelan, R.8
Rusch, V.9
Fulton, L.10
Mardis, E.11
Kupfer, D.12
Wilson, R.13
Kris, M.14
Varmus, H.15
-
51
-
-
47749097979
-
Evolution of the phospho-tyrosine signaling machinery in premetazoan lineages
-
Pincus D, Letunic I, Bork P, Lim WA. 2008. Evolution of the phospho-tyrosine signaling machinery in premetazoan lineages. Proc Natl Acad Sci USA 105:9680-9684.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 9680-9684
-
-
Pincus, D.1
Letunic, I.2
Bork, P.3
Lim, W.A.4
-
52
-
-
0036713510
-
Human non-synonymous SNPs: Server and survey
-
Ramensky V, Bork P, Sunyaev S. 2002. Human non-synonymous SNPs: server and survey. Nucleic Acids Res 30:3894-3900.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunyaev, S.3
-
53
-
-
13444270842
-
SNPeffect: A database mapping molecular phenotypic effects of human nonsynonymous coding SNPs
-
Reumers J, Schymkowitz J, Ferkinghoff-Borg J, Stricher F, Serrano L, Rousseau F. 2005. SNPeffect: a database mapping molecular phenotypic effects of human nonsynonymous coding SNPs. Nucleic Acids Res 33(Database issue):D527-D532.
-
(2005)
Nucleic Acids Res 33(Database issue)
-
-
Reumers, J.1
Schymkowitz, J.2
Ferkinghoff-Borg, J.3
Stricher, F.4
Serrano, L.5
Rousseau, F.6
-
54
-
-
61649111743
-
MedRefSNP: A database of medically investigated SNPs
-
Rhee H, Lee JS. 2009. MedRefSNP: a database of medically investigated SNPs. Hum Mutat 30:E460-E466.
-
(2009)
Hum Mutat
, vol.30
-
-
Rhee, H.1
Lee, J.S.2
-
55
-
-
36849065315
-
Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer
-
CombMJ
-
Rikova K, Guo A, Zeng Q, Possemato A, Yu J, Haack H, Nardone J, Lee K, Reeves C, Li Y, Hu Y, Tan Z, Stokes M, Sullivan L, Mitchell J, Wetzel R, Macneill J, Ren JM, Yuan J, Bakalarski CE, Villen J, Kornhauser JM, Smith B, Li D, Zhou X, Gygi SP, Gu TL, Polakiewicz RD, Rush J, CombMJ. 2007. Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. Cell 131:1190-1203.
-
(2007)
Cell
, vol.131
, pp. 1190-1203
-
-
Rikova, K.1
Guo, A.2
Zeng, Q.3
Possemato, A.4
Yu, J.5
Haack, H.6
Nardone, J.7
Lee, K.8
Reeves, C.9
Li, Y.10
Hu, Y.11
Tan, Z.12
Stokes, M.13
Sullivan, L.14
Mitchell, J.15
Wetzel, R.16
Macneill, J.17
Ren, J.M.18
Yuan, J.19
Bakalarski, C.E.20
Villen, J.21
Kornhauser, J.M.22
Smith, B.23
Li, D.24
Zhou, X.25
Gygi, S.P.26
Gu, T.L.27
Polakiewicz, R.D.28
Rush, J.29
more..
-
56
-
-
34249807325
-
A mass spectrometry-friendly database for cSNP identification
-
Schandorff S, Olsen JV, Bunkenborg J, Blagoev B, Zhang Y, Andersen JS, Mann M. 2007. A mass spectrometry-friendly database for cSNP identification. Nat Methods 4:465-466.
-
(2007)
Nat Methods
, vol.4
, pp. 465-466
-
-
Schandorff, S.1
Olsen, J.V.2
Bunkenborg, J.3
Blagoev, B.4
Zhang, Y.5
Andersen, J.S.6
Mann, M.7
-
57
-
-
33749993417
-
The consensus coding sequences of human breast and colorectal cancers
-
Sjoblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, Mandelker D, Leary RJ, Ptak J, Silliman N, Szabo S, Buckhautts P, Farrell C, Meeh P, Markowitz SD, Willis J, Dawson D, Willson JK, Gazdar AF, Hartigan J, Wu L, Liu C, Parmigiani G, Park BH, Bachman KE, Papadopoulos N, Vogelstein B, Kinzler KW, Velculescu VE. 2006. The consensus coding sequences of human breast and colorectal cancers. Science 314:268-274.
-
(2006)
Science
, vol.314
, pp. 268-274
-
-
Sjoblom, T.1
Jones, S.2
Wood, L.D.3
Parsons, D.W.4
Lin, J.5
Barber, T.D.6
Mandelker, D.7
Leary, R.J.8
Ptak, J.9
Silliman, N.10
Szabo, S.11
Buckhautts, P.12
Farrell, C.13
Meeh, P.14
Markowitz, S.D.15
Willis, J.16
Dawson, D.17
Willson, J.K.18
Gazdar, A.F.19
Hartigan, J.20
Wu, L.21
Liu, C.22
Parmigiani, G.23
Park, B.H.24
Bachman, K.E.25
Papadopoulos, N.26
Vogelstein, B.27
Kinzler, K.W.28
Velculescu, V.E.29
more..
-
58
-
-
61649083057
-
BioMart-biological queries made easy
-
Smedley D, Haider S, Ballester B, Holland R, London D, Thorisson G, Kasprzyk A. 2009. BioMart-biological queries made easy. BMC Genomics 10:22.
-
(2009)
BMC Genomics
, vol.10
, pp. 22
-
-
Smedley, D.1
Haider, S.2
Ballester, B.3
Holland, R.4
London, D.5
Thorisson, G.6
Kasprzyk, A.7
-
59
-
-
0037903275
-
Human Gene Mutation Database (HGMD): 2003 update
-
Stenson PD, Ball EV, Mort M, Phillips AD, Shiel JA, Thomas NS, Abeysinghe S, Krawczak M, Cooper DN. 2003. Human Gene Mutation Database (HGMD): 2003 update. Hum Mutat 21:577-581.
-
(2003)
Hum Mutat
, vol.21
, pp. 577-581
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
Phillips, A.D.4
Shiel, J.A.5
Thomas, N.S.6
Abeysinghe, S.7
Krawczak, M.8
Cooper, D.N.9
-
60
-
-
0035869223
-
Prediction of deleterious human alleles
-
Sunyaev S, Ramensky V, Koch I, Lathe 3rd W, Kondrashov AS, Bork P. 2001. Prediction of deleterious human alleles. Hum Mol Genet 10:591-597.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 591-597
-
-
Sunyaev, S.1
Ramensky, V.2
Koch, I.3
Lathe 3rd, W.4
Kondrashov, A.S.5
Bork, P.6
-
61
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
TCGA CGARN. 2008. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 455:1061-1068.
-
(2008)
Nature
, vol.455
, pp. 1061-1068
-
-
CGARN, T.C.G.A.1
-
62
-
-
45849097153
-
Pilot study of mutant ras peptide-based vaccine as an adjuvant treatment in pancreatic and colorectal cancers
-
Toubaji A, Achtar M, Provenzano M, Herrin VE, Behrens R, Hamilton M, Bernstein S, Venzon D, Gause B, Marincola F, and others. 2008. Pilot study of mutant ras peptide-based vaccine as an adjuvant treatment in pancreatic and colorectal cancers. Cancer Immunol Immunother 57:1413-1420.
-
(2008)
Cancer Immunol Immunother
, vol.57
, pp. 1413-1420
-
-
Toubaji, A.1
Achtar, M.2
Provenzano, M.3
Herrin, V.E.4
Behrens, R.5
Hamilton, M.6
Bernstein, S.7
Venzon, D.8
Gause, B.9
Marincola, F.10
and others11
-
64
-
-
21044443147
-
Peptide-based vaccination for colorectal cancer
-
Tsuruma T, Hata F, Furuhata T, Ohmura T, Katsuramaki T, Yamaguchi K, Kimura Y, Torigoe T, Sato N, Hirata K. 2005. Peptide-based vaccination for colorectal cancer. Expert Opin Biol Ther 5:799-807.
-
(2005)
Expert Opin Biol Ther
, vol.5
, pp. 799-807
-
-
Tsuruma, T.1
Hata, F.2
Furuhata, T.3
Ohmura, T.4
Katsuramaki, T.5
Yamaguchi, K.6
Kimura, Y.7
Torigoe, T.8
Sato, N.9
Hirata, K.10
-
65
-
-
34547611433
-
Structure SNP (StSNP): A web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways
-
Uzun A, Leslin CM, Abyzov A, Ilyin V. 2007. Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways. Nucleic Acids Res 35(Web Server issue):W384-W392.
-
(2007)
Nucleic Acids Res 35(Web Server issue)
-
-
Uzun, A.1
Leslin, C.M.2
Abyzov, A.3
Ilyin, V.4
-
66
-
-
33744953182
-
-
von Eschenbach AC, Buetow K. 2007. Cancer Informatics Vision: caBIG. Cancer Inform 2:22-24.
-
von Eschenbach AC, Buetow K. 2007. Cancer Informatics Vision: caBIG. Cancer Inform 2:22-24.
-
-
-
-
67
-
-
0035065485
-
SNPs, protein structure, and disease
-
Wang Z, Moult J. 2001. SNPs, protein structure, and disease. Hum Mutat 17: 263-270.
-
(2001)
Hum Mutat
, vol.17
, pp. 263-270
-
-
Wang, Z.1
Moult, J.2
-
68
-
-
0037025173
-
Cancer. Addiction to oncogenes-the Achilles heal of cancer
-
Weinstein IB. 2002. Cancer. Addiction to oncogenes-the Achilles heal of cancer. Science 297:63-64.
-
(2002)
Science
, vol.297
, pp. 63-64
-
-
Weinstein, I.B.1
-
69
-
-
37649009370
-
Plexin-B1 mutations in prostate cancer
-
Wong OG, Nitkunan T, Oinuma I, Zhou C, Blanc V, Brown RS, Bott SR, Nariculam J, Box G, Munson P, Constantinou J, Feneley MR, Klocker H, Eccles SA, Negishi M, Freeman A, Masters JR,Williamson M. 2007. Plexin-B1 mutations in prostate cancer. Proc Natl Acad Sci USA 104:19040-19045.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 19040-19045
-
-
Wong, O.G.1
Nitkunan, T.2
Oinuma, I.3
Zhou, C.4
Blanc, V.5
Brown, R.S.6
Bott, S.R.7
Nariculam, J.8
Box, G.9
Munson, P.10
Constantinou, J.11
Feneley, M.R.12
Klocker, H.13
Eccles, S.A.14
Negishi, M.15
Freeman, A.16
Masters, J.R.17
Williamson, M.18
-
70
-
-
0036088133
-
DIP, the Database of Interacting Proteins: A research tool for studying cellular networks of protein interactions
-
Xenarios I, Salwinski L, Duan XJ, Higney P, Kim SM, Eisenberg D. 2002. DIP, the Database of Interacting Proteins: a research tool for studying cellular networks of protein interactions. Nucleic Acids Res 30:303-305.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 303-305
-
-
Xenarios, I.1
Salwinski, L.2
Duan, X.J.3
Higney, P.4
Kim, S.M.5
Eisenberg, D.6
-
71
-
-
58149185118
-
SysPIMP: The web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometry
-
Xi H, Park J, Ding G, Lee YH, Li Y. 2009. SysPIMP: the web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometry. Nucleic Acids Res 37(Database issue):D913-D920.
-
(2009)
Nucleic Acids Res 37(Database issue)
-
-
Xi, H.1
Park, J.2
Ding, G.3
Lee, Y.H.4
Li, Y.5
-
72
-
-
2342596530
-
The Swiss-Prot variant page and the ModSNP database: A resource for sequence and structure information on human protein variants
-
Yip YL, Scheib H, Diemand AV, Gattiker A, Famiglietti LM, Gasteiger E, Bairoch A. 2004. The Swiss-Prot variant page and the ModSNP database: a resource for sequence and structure information on human protein variants. Hum Mutat 23:464-470.
-
(2004)
Hum Mutat
, vol.23
, pp. 464-470
-
-
Yip, Y.L.1
Scheib, H.2
Diemand, A.V.3
Gattiker, A.4
Famiglietti, L.M.5
Gasteiger, E.6
Bairoch, A.7
-
73
-
-
45849115106
-
Menin critically links MLL proteins with LEDGF on cancer-associated target genes
-
Yokoyama A, Cleary ML. 2008. Menin critically links MLL proteins with LEDGF on cancer-associated target genes. Cancer Cell 14:36-46.
-
(2008)
Cancer Cell
, vol.14
, pp. 36-46
-
-
Yokoyama, A.1
Cleary, M.L.2
|