-
1
-
-
80051580618
-
Cancer statistics, 2011: The impact of eliminating socioeconomic and racial disparities on premature cancer deaths
-
Siegel R, Ward E, Brawley O, Jemal A. Cancer statistics, 2011: the impact of eliminating socioeconomic and racial disparities on premature cancer deaths. CA Cancer J Clin 2011;61:212-36.
-
(2011)
CA Cancer J Clin
, vol.61
, pp. 212-236
-
-
Siegel, R.1
Ward, E.2
Brawley, O.3
Jemal, A.4
-
3
-
-
78349235127
-
Prostate cancer risk-associated variants reported from genome-wide association studies: Meta-analysis and their contribution to genetic variation
-
Kim ST, Cheng Y, Hsu FC, et al. Prostate cancer risk-associated variants reported from genome-wide association studies: meta-analysis and their contribution to genetic variation. Prostate 2010;70: 1729-38.
-
(2010)
Prostate
, vol.70
, pp. 1729-1738
-
-
Kim, S.T.1
Cheng, Y.2
Hsu, F.C.3
-
4
-
-
79960924160
-
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study
-
Kote-Jarai Z, Olama AA, Giles GG, et al. Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. Nat Genet 2011;43:785- 91.
-
(2011)
Nat Genet
, vol.43
, pp. 785-791
-
-
Kote-Jarai, Z.1
Olama, A.A.2
Giles, G.G.3
-
5
-
-
0345374575
-
Genome-Wide Scan for Prostate Cancer Susceptibility Genes Using Families from the University of Michigan Prostate Cancer Genetics Project Finds Evidence for Linkage on Chromosome 17 Near BRCA1
-
DOI 10.1002/pros.10307
-
Lange EM, Gillanders EM, Davis CC, et al. Genome-wide scan for prostate cancer susceptibility genes using families from the University of Michigan Prostate Cancer Genetics Project finds evidence for linkage on chromosome 17 near BRCA1. Prostate 2003;57:326-34. (Pubitemid 37487078)
-
(2003)
Prostate
, vol.57
, Issue.4
, pp. 326-334
-
-
Lange, E.M.1
Gillanders, E.M.2
Davis, C.C.3
Brown, W.M.4
Campbell, J.K.5
Jones, M.6
Gildea, D.7
Riedesel, E.8
Albertus, J.9
Freas-Lutz, D.10
Markey, C.11
Giri, V.12
Dimmer, J.B.13
Montie, J.E.14
Trent, J.M.15
Cooney, K.A.16
-
6
-
-
4344565052
-
Combined genome-wide scan for prostate cancer susceptibility genes
-
DOI 10.1093/jnci/djh228
-
Gillanders EM, Xu J, Chang BL, et al. Combined genome-wide scan for prostate cancer susceptibility genes. J Natl Cancer Inst 2004;96:1240-7. (Pubitemid 39232715)
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.16
, pp. 1240-1247
-
-
Gillanders, E.M.1
Xu, J.2
Chang, B.-L.3
Lange, E.M.4
Wiklund, F.5
Bailey-Wilson, J.E.6
Baffoe-Bonnie, A.7
Jones, M.P.8
Gildea, D.9
Riedesel, E.10
Albertus, J.11
Isaacs, S.D.12
Wiley, K.E.13
Mohai, C.E.14
Matikainen, M.P.15
Tammela, T.L.J.16
Zheng, S.L.17
Brown, W.M.18
Rokman, A.19
Carpten, J.D.20
Meyers, D.A.21
Walsh, P.C.P.C.22
Schleutker, J.23
Gronberg, H.24
Cooney, K.A.25
Isaacs, W.B.26
Trent, J.M.27
more..
-
7
-
-
22544431928
-
A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the International Consortium for Prostate Cancer Genetics
-
Xu J, Dimitrov L, Chang BL, et al. A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the International Consortium for Prostate Cancer Genetics. Am J Hum Genet 2005;77:219- 29.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 219-229
-
-
Xu, J.1
Dimitrov, L.2
Chang, B.L.3
-
8
-
-
33947283656
-
Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis
-
Lange EM, Robbins CM, Gillanders EM, et al. Fine-mapping the putative chromosome 17q21-22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis. Hum Genet 2007;121:49- 55.
-
(2007)
Hum Genet
, vol.121
, pp. 49-55
-
-
Lange, E.M.1
Robbins, C.M.2
Gillanders, E.M.3
-
9
-
-
84857121123
-
-
Seattle: NHLBI Exome Sequencing Project
-
Exome variant server. Seattle: NHLBI Exome Sequencing Project (http://snp.gs .washington.edu/EVS).
-
Exome Variant Server
-
-
-
10
-
-
79959524146
-
A haplotype map of the human genome
-
The International HapMap Consortium
-
The International HapMap Consortium. A haplotype map of the human genome. Nature 2005;437:1299-320.
-
(2005)
Nature
, vol.437
, pp. 1299-1320
-
-
-
12
-
-
84862964059
-
Early onset prostate cancer has a significant genetic component
-
May 2 (Epub ahead of print)
-
Lange EM, Salinas CA, Zuhlke KA, et al. Early onset prostate cancer has a significant genetic component. Prostate 2011 May 2 (Epub ahead of print).
-
(2011)
Prostate
-
-
Lange, E.M.1
Salinas, C.A.2
Zuhlke, K.A.3
-
13
-
-
59849113507
-
Genome-wide linkage scan for prostate cancer susceptibility from the University of Michigan Prostate Cancer Genetics Project: Suggestive evidence for linkage at 16q23
-
Lange EM, Beebe-Dimmer JL, Ray AM, et al. Genome-wide linkage scan for prostate cancer susceptibility from the University of Michigan Prostate Cancer Genetics Project: suggestive evidence for linkage at 16q23. Prostate 2009;69:385-91.
-
(2009)
Prostate
, vol.69
, pp. 385-391
-
-
Lange, E.M.1
Beebe-Dimmer, J.L.2
Ray, A.M.3
-
14
-
-
18644386765
-
Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk
-
Xu J, Zheng SL, Komiya A, et al. Germline mutations and sequence variants of the macrophage scavenger receptor 1 gene are associated with prostate cancer risk. Nat Genet 2002;32:321-5.
-
(2002)
Nat Genet
, vol.32
, pp. 321-325
-
-
Xu, J.1
Zheng, S.L.2
Komiya, A.3
-
15
-
-
35548944499
-
Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans
-
DOI 10.1093/jnci/djm169
-
Zheng SL, Sun J, Cheng Y, et al. Association between two unlinked loci at 8q24 and prostate cancer risk among European Americans. J Natl Cancer Inst 2007;99: 1525-33. (Pubitemid 351767236)
-
(2007)
Journal of the National Cancer Institute
, vol.99
, Issue.20
, pp. 1525-1533
-
-
Zheng, S.L.1
Sun, J.2
Cheng, Y.3
Li, G.4
Hsu, F.-C.5
Zhu, Y.6
Chang, B.-L.7
Liu, W.8
Kim, J.W.9
Turner, A.R.10
Gielzak, M.11
Yan, G.12
Isaacs, S.D.13
Wiley, K.E.14
Sauvageot, J.15
Chen, H.-S.16
Gurganus, R.17
Mangold, L.A.18
Trock, B.J.19
Gronberg, H.20
Duggan, D.21
Carpten, J.D.22
Partin, A.W.23
Walsh, P.C.24
Xu, J.25
Isaacs, W.B.26
more..
-
16
-
-
48249153087
-
Homozygous deletions and recurrent amplifications implicate new genes involved in prostate cancer
-
Liu W, Xie CC, Zhu Y, et al. Homozygous deletions and recurrent amplifications implicate new genes involved in prostate cancer. Neoplasia 2008;10:897- 907.
-
(2008)
Neoplasia
, vol.10
, pp. 897-907
-
-
Liu, W.1
Xie, C.C.2
Zhu, Y.3
-
17
-
-
33750353461
-
Predicting the effects of amino acid substitutions on protein function
-
DOI 10.1146/annurev.genom.7.080505.115630
-
Ng PC, Henikoff S. Predicting the effects of amino acid substitutions on protein function. Annu Rev Genomics Hum Genet 2006;7:61-80. (Pubitemid 44627922)
-
(2006)
Annual Review of Genomics and Human Genetics
, vol.7
, pp. 61-80
-
-
Ng, P.C.1
Henikoff, S.2
-
18
-
-
0036713510
-
Human non-synonymous SNPs: Server and survey
-
Ramensky V, Bork P, Sunyaev S. Human non-synonymous SNPs: server and survey. Nucleic Acids Res 2002;30:3894- 900.
-
(2002)
Nucleic Acids Res
, vol.30
, pp. 3894-3900
-
-
Ramensky, V.1
Bork, P.2
Sunyaev, S.3
-
19
-
-
11144327574
-
Range of HOX/TALE superclass associations and protein domain requirements for HOXA13:MEIS interaction
-
DOI 10.1016/j.ydbio.2004.10.004, PII S0012160604007195
-
Williams TM, Williams ME, Innis JW. Range of HOX/TALE superclass associations and protein domain requirements for HOXA13:MEIS interaction. Dev Biol 2005;277:457-71. (Pubitemid 40022964)
-
(2005)
Developmental Biology
, vol.277
, Issue.2
, pp. 457-471
-
-
Williams, T.M.1
Williams, M.E.2
Innis, J.W.3
-
20
-
-
79957581659
-
Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21
-
Haiman CA, Chen GK, Blot WJ, et al. Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. Nat Genet 2011;43:570-3.
-
(2011)
Nat Genet
, vol.43
, pp. 570-573
-
-
Haiman, C.A.1
Chen, G.K.2
Blot, W.J.3
-
21
-
-
34547510624
-
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
-
DOI 10.1038/ng2062, PII NG2062
-
Gudmundsson J, Sulem P, Steinthorsdottir V, et al. Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. Nat Genet 2007;39:977-83. (Pubitemid 47185170)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 977-983
-
-
Gudmundsson, J.1
Sulem, P.2
Steinthorsdottir, V.3
Bergthorsson, J.T.4
Thorleifsson, G.5
Manolescu, A.6
Rafnar, T.7
Gudbjartsson, D.8
Agnarsson, B.A.9
Baker, A.10
Sigurdsson, A.11
Benediktsdottir, K.R.12
Jakobsdottir, M.13
Blondal, T.14
Stacey, S.N.15
Helgason, A.16
Gunnarsdottir, S.17
Olafsdottir, A.18
Kristinsson, K.T.19
Birgisdottir, B.20
Ghosh, S.21
Thorlacius, S.22
Magnusdottir, D.23
Stefansdottir, G.24
Kristjansson, K.25
Bagger, Y.26
Wilensky, R.L.27
Reilly, M.P.28
Morris, A.D.29
Kimber, C.H.30
Adeyemo, A.31
Chen, Y.32
Zhou, J.33
So, W.-Y.34
Tong, P.C.Y.35
Ng, M.C.Y.36
Hansen, T.37
Andersen, G.38
Borch-Johnsen, K.39
Jorgensen, T.40
Tres, A.41
Fuertes, F.42
Ruiz-Echarri, M.43
Asin, L.44
Saez, B.45
Van Boven, E.46
Klaver, S.47
Swinkels, D.W.48
Aben, K.K.49
Graif, T.50
Cashy, J.51
Suarez, B.K.52
Van Vierssen, T.O.53
Frigge, M.L.54
Ober, C.55
Hofker, M.H.56
Wijmenga, C.57
Christiansen, C.58
Rader, D.J.59
Palmer, C.N.A.60
Rotimi, C.61
Chan, J.C.N.62
Pedersen, O.63
Sigurdsson, G.64
Benediktsson, R.65
Jonsson, E.66
Einarsson, G.V.67
Mayordomo, J.I.68
Catalona, W.J.69
Kiemeney, L.A.70
Barkardottir, R.B.71
Gulcher, J.R.72
Thorsteinsdottir, U.73
Kong, A.74
Stefansson, K.75
more..
-
22
-
-
0028675512
-
The Hox code out on a limb
-
Graham A. Developmental patterning: the Hox code out on a limb. Curr Biol 1994;4:1135-7. (Pubitemid 124001604)
-
(1994)
Current Biology
, vol.4
, Issue.12
, pp. 1135-1137
-
-
Graham, A.1
-
23
-
-
0035159735
-
Human HOX gene mutations
-
DOI 10.1034/j.1399-0004.2001.590101.x
-
Goodman FR, Scambler PJ. Human HOX gene mutations. Clin Genet 2001;59: 1-11. (Pubitemid 32049120)
-
(2001)
Clinical Genetics
, vol.59
, Issue.1
, pp. 1-11
-
-
Goodman, F.R.1
Scambler, P.J.2
-
24
-
-
0345505285
-
Hoxb13 mutations cause overgrowth of caudal spinal cordand tail vertebrae
-
DOI 10.1016/S0012-1606(02)00137-9
-
Economides KD, Zeltser L, Capecchi MR. Hoxb13 mutations cause overgrowth of caudal spinal cord and tail vertebrae. Dev Biol 2003;256:317-30. (Pubitemid 36390101)
-
(2003)
Developmental Biology
, vol.256
, Issue.2
, pp. 317-330
-
-
Economides, K.D.1
Zeltser, L.2
Capecchi, M.R.3
-
25
-
-
0038074197
-
Hoxb13 is required for normal differentiation and secretory function of the ventral prostate
-
DOI 10.1242/dev.00432
-
Economides KD, Capecchi MR. Hoxb13 is required for normal differentiation and secretory function of the ventral prostate. Development 2003;130:2061-9. (Pubitemid 36656703)
-
(2003)
Development
, vol.130
, Issue.10
, pp. 2061-2069
-
-
Economides, K.D.1
Capecchi, M.R.2
-
26
-
-
0034747741
-
Defining roles for HOX and MEIS1 genes in induction of acute myeloid leukemia
-
Thorsteinsdottir U, Kroon E, Jerome L, Blasi F, Sauvageau G. Defining roles for HOX and MEIS1 genes in induction of acute myeloid leukemia. Mol Cell Biol 2001;21:224-34.
-
(2001)
Mol Cell Biol
, vol.21
, pp. 224-234
-
-
Thorsteinsdottir, U.1
Kroon, E.2
Jerome, L.3
Blasi, F.4
Sauvageau, G.5
-
27
-
-
10844266655
-
HOXB13 induces growth suppression of prostate cancer cells as a repressor of hormone-activated androgen receptor signaling
-
DOI 10.1158/0008-5472.CAN-04-1330
-
Jung C, Kim RS, Zhang HJ, Lee SJ, Jeng MH. HOXB13 induces growth suppression of prostate cancer cells as a repressor of hormone-activated androgen receptor signaling. Cancer Res 2004;64: 9185-92. (Pubitemid 39665535)
-
(2004)
Cancer Research
, vol.64
, Issue.24
, pp. 9185-9192
-
-
Jung, C.1
Kim, R.-S.2
Zhang, H.-J.3
Lee, S.-J.4
Jeng, M.-H.5
-
28
-
-
70449123571
-
The homeodomain protein HOXB13 regulates the cellular response to androgens
-
Norris JD, Chang CY, Wittmann BM, et al. The homeodomain protein HOXB13 regulates the cellular response to androgens. Mol Cell 2009;36:405-16.
-
(2009)
Mol Cell
, vol.36
, pp. 405-416
-
-
Norris, J.D.1
Chang, C.Y.2
Wittmann, B.M.3
-
29
-
-
34548567066
-
Integrative analysis of genomic aberrations associated with prostate cancer progression
-
DOI 10.1158/0008-5472.CAN-07-1297
-
Kim JH, Dhanasekaran SM, Mehra R, et al. Integrative analysis of genomic aberrations associated with prostate cancer progression. Cancer Res 2007;67:8229-39. (Pubitemid 47395160)
-
(2007)
Cancer Research
, vol.67
, Issue.17
, pp. 8229-8239
-
-
Kim, J.H.1
Dhanasekaran, S.M.2
Mehra, R.3
Tomlins, S.A.4
Gu, W.5
Yu, J.6
Kumar-Sinha, C.7
Cao, X.8
Dash, A.9
Wang, L.10
Ghosh, D.11
Shedden, K.12
Montie, J.E.13
Rubin, M.A.14
Pienta, K.J.15
Shah, R.B.16
Chinnaiyan, A.M.17
-
30
-
-
50649102100
-
Genetic changes in pT2 and pT3 prostate cancer detected by comparative genomic hybridization
-
Fukasawa S, Kino M, Kobayashi M, et al. Genetic changes in pT2 and pT3 prostate cancer detected by comparative genomic hybridization. Prostate Cancer Prostatic Dis 2008;11:303-10.
-
(2008)
Prostate Cancer Prostatic Dis
, vol.11
, pp. 303-310
-
-
Fukasawa, S.1
Kino, M.2
Kobayashi, M.3
-
31
-
-
20044385928
-
Expression analysis onto microarrays of randomly selected cDNA clones highlights HOXB13 as a marker of human prostate cancer
-
Edwards S, Campbell C, Flohr P, et al. Expression analysis onto microarrays of randomly selected cDNA clones highlights HOXB13 as a marker of human prostate cancer. Br J Cancer 2005;92:376- 81.
-
(2005)
Br J Cancer
, vol.92
, pp. 376-381
-
-
Edwards, S.1
Campbell, C.2
Flohr, P.3
-
33
-
-
54049130531
-
The role of the BRCA2 gene in susceptibility to prostate cancer revisited
-
Ostrander EA, Udler MS. The role of the BRCA2 gene in susceptibility to prostate cancer revisited. Cancer Epidemiol Biomarkers Prev 2008;17:1843-8.
-
(2008)
Cancer Epidemiol Biomarkers Prev
, vol.17
, pp. 1843-1848
-
-
Ostrander, E.A.1
Udler, M.S.2
-
34
-
-
0034162984
-
BRCA1 and BRCA2 have a limited role in familial prostate cancer
-
Schehl-Sinclair C, Berry R, Schaid D, Thibodeau SN, Couch FJ. BRCA1 and BRCA2 have a limited role in familial prostate cancer. Cancer Res 2000;60:1371-5. (Pubitemid 30152009)
-
(2000)
Cancer Research
, vol.60
, Issue.5
, pp. 1371-1375
-
-
Sinclair, C.S.1
Berry, R.2
Schaid, D.3
Thibodeau, S.N.4
Couch, F.J.5
-
35
-
-
4644363085
-
Truncating BRCA1 mutations are uncommon in a cohort of hereditary prostate cancer families with evidence of linkage to 17q markers
-
DOI 10.1158/1078-0432.CCR-04-0554
-
Zuhlke KA, Madeoy JJ, Beebe-Dimmer J, et al. Truncating BRCA1 mutations are uncommon in a cohort of hereditary prostate cancer families with evidence of linkage to 17q markers. Clin Cancer Res 2004;10:5975-80. (Pubitemid 39287501)
-
(2004)
Clinical Cancer Research
, vol.10
, Issue.18 I
, pp. 5975-5980
-
-
Zuhlke, K.A.1
Madeoy, J.J.2
Beebe-Dimmer, J.3
White, K.A.4
Griffin, A.5
Lange, E.M.6
Gruber, S.B.7
Ostrander, E.A.8
Cooney, K.A.9
|