-
1
-
-
0034329424
-
Cloning of TC-1 (C8orf4), a novel gene found to be overexpressed in thyroid cancer
-
EL Chua L Young WM Wu JR Turtle Q Dong 2000 Cloning of TC-1 (C8orf4), a novel gene found to be overexpressed in thyroid cancer Genomics 69 342 347
-
(2000)
Genomics
, vol.69
, pp. 342-347
-
-
Chua, E.L.1
Young, L.2
Wu, W.M.3
Turtle, J.R.4
Dong, Q.5
-
2
-
-
31544462050
-
TC1 (C8orf4) enhances the Wnt/β-catenin pathway by relieving antagonistic activity of Chibby
-
DOI 10.1158/0008-5472.CAN-05-3124
-
Y Jung 2006 TC1 (C8orf4) enhances the Wnt/beta-catenin pathway by relieving antagonistic activity of Chibby Cancer Res 66 723 728 (Pubitemid 43165934)
-
(2006)
Cancer Research
, vol.66
, Issue.2
, pp. 723-728
-
-
Jung, Y.1
Bang, S.2
Choi, K.3
Kim, E.4
Kim, Y.5
Kim, J.6
Park, J.7
Koo, H.8
Moon, R.T.9
Song, K.10
Lee, I.11
-
3
-
-
13844261745
-
TC-1 Is a Novel Tumorigenic and Natively Disordered Protein Associated with Thyroid Cancer
-
DOI 10.1158/0008-5472.CAN-03-2093
-
M Sunde 2004 TC-1 is a novel tumorigenic and natively disordered protein associated with thyroid cancer Cancer Res 64 2766 2773 (Pubitemid 38500614)
-
(2004)
Cancer Research
, vol.64
, Issue.8
, pp. 2766-2773
-
-
Sunde, M.1
McGrath, K.C.Y.2
Young, L.3
Matthews, J.M.4
Chua, E.L.5
Mackay, J.P.6
Death, A.K.7
-
4
-
-
34548078977
-
Transforming properties of TC-1 in human breast cancer: Interaction with FGFR2 and β-catenin signaling pathways
-
DOI 10.1002/ijc.22831
-
ZQ Yang AB Moffa R Haddad KL Streicher SP Ethier 2007 Transforming properties of TC-1 in human breast cancer: interaction with FGFR2 and beta-catenin signaling pathways Int J Cancer 121 1265 1273 (Pubitemid 47293794)
-
(2007)
International Journal of Cancer
, vol.121
, Issue.6
, pp. 1265-1273
-
-
Yang, Z.-Q.1
Moffa, A.B.2
Haddad, R.3
Streicher, K.L.4
Ethier, S.P.5
-
5
-
-
33646903027
-
TC1(C8orf4) is upregulated by IL-1β/TNF-α and enhances proliferation of human follicular dendritic cells
-
DOI 10.1016/j.febslet.2006.05.036, PII S0014579306006302
-
Y Kim 2006 TC1(C8orf4) is upregulated by IL-1beta/TNF-alpha and enhances proliferation of human follicular dendritic cells FEBS Lett 580 3519 3524 (Pubitemid 43795901)
-
(2006)
FEBS Letters
, vol.580
, Issue.14
, pp. 3519-3524
-
-
Kim, Y.1
Kim, J.2
Park, J.3
Bang, S.4
Jung, Y.5
Choe, J.6
Song, K.7
Lee, I.8
-
7
-
-
33745192244
-
TC1(C8orf4) correlates with Wnt/beta-catenin target genes and aggressive biological behavior in gastric cancer
-
B Kim 2006 TC1(C8orf4) correlates with Wnt/beta-catenin target genes and aggressive biological behavior in gastric cancer Clin Cancer Res 12 3541 3548
-
(2006)
Clin Cancer Res
, vol.12
, pp. 3541-3548
-
-
Kim, B.1
-
8
-
-
35648982507
-
The intrinsically disordered TC-1 interacts with Chibby via regions with high helical propensity
-
DOI 10.1110/ps.073062707
-
C Gall H Xu A Brickenden X Ai WY Choy 2007 The intrinsically disordered TC-1 interacts with chibby via regions with high helical propensity Protein Sci 16 2510 2518 (Pubitemid 350036756)
-
(2007)
Protein Science
, vol.16
, Issue.11
, pp. 2510-2518
-
-
Gall, C.1
Xu, H.2
Brickenden, A.3
Ai, X.4
Wing, Y.C.5
-
9
-
-
70349313133
-
TC1(C8orf4) is a novel endothelial inflammatory regulator enhancing NF-kappaB activity
-
J Kim 2009 TC1(C8orf4) is a novel endothelial inflammatory regulator enhancing NF-kappaB activity J Immunol 183 3996 4002
-
(2009)
J Immunol
, vol.183
, pp. 3996-4002
-
-
Kim, J.1
-
10
-
-
55249112997
-
TC1 (C8orf4) is involved in ERK1/2 pathway-regulated G(1)- to S-phase transition
-
YD Wang 2008 TC1 (C8orf4) is involved in ERK1/2 pathway-regulated G(1)- to S-phase transition BMB Rep 41 733 738
-
(2008)
BMB Rep
, vol.41
, pp. 733-738
-
-
Wang, Y.D.1
-
11
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
MJ Walter 2009 Acquired copy number alterations in adult acute myeloid leukemia genomes Proc Natl Acad Sci U S A 106 12950 12955
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 12950-12955
-
-
Walter, M.J.1
-
13
-
-
29444450702
-
Common deletions and SNPs are in linkage disequilibrium in the human genome
-
DOI 10.1038/ng1695
-
DA Hinds AP Kloek M Jen X Chen KA Frazer 2006 Common deletions and SNPs are in linkage disequilibrium in the human genome Nat Genet 38 82 85 (Pubitemid 43011886)
-
(2006)
Nature Genetics
, vol.38
, Issue.1
, pp. 82-85
-
-
Hinds, D.A.1
Kloek, A.P.2
Jen, M.3
Chen, X.4
Frazer, K.A.5
-
14
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
DOI 10.1038/ng1416
-
AJ Iafrate 2004 Detection of large-scale variation in the human genome Nat Genet 36 949 951 (Pubitemid 39167488)
-
(2004)
Nature Genetics
, vol.36
, Issue.9
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
Scherer, S.W.7
Lee, C.8
-
15
-
-
43049143055
-
Mapping and sequencing of structural variation from eight human genomes
-
DOI 10.1038/nature06862, PII NATURE06862
-
JM Kidd 2008 Mapping and sequencing of structural variation from eight human genomes Nature 453 56 64 (Pubitemid 351630326)
-
(2008)
Nature
, vol.453
, Issue.7191
, pp. 56-64
-
-
Kidd, J.M.1
Cooper, G.M.2
Donahue, W.F.3
Hayden, H.S.4
Sampas, N.5
Graves, T.6
Hansen, N.7
Teague, B.8
Alkan, C.9
Antonacci, F.10
Haugen, E.11
Zerr, T.12
Yamada, N.A.13
Tsang, P.14
Newman, T.L.15
Tuzun, E.16
Cheng, Z.17
Ebling, H.M.18
Tusneem, N.19
David, R.20
Gillett, W.21
Phelps, K.A.22
Weaver, M.23
Saranga, D.24
Brand, A.25
Tao, W.26
Gustafson, E.27
McKernan, K.28
Chen, L.29
Malig, M.30
Smith, J.D.31
Korn, J.M.32
McCarroll, S.A.33
Altshuler, D.A.34
Peiffer, D.A.35
Dorschner, M.36
Stamatoyannopoulos, J.37
Schwartz, D.38
Nickerson, D.A.39
Mullikin, J.C.40
Wilson, R.K.41
Bruhn, L.42
Olson, M.V.43
Kaul, R.44
Smith, D.R.45
Eichler, E.E.46
more..
-
16
-
-
35348988679
-
Paired-end mapping reveals extensive structural variation in the human genome
-
DOI 10.1126/science.1149504
-
JO Korbel 2007 Paired-end mapping reveals extensive structural variation in the human genome Science 318 420 426 (Pubitemid 47614521)
-
(2007)
Science
, vol.318
, Issue.5849
, pp. 420-426
-
-
Korbel, J.O.1
Urban, A.E.2
Affourtit, J.P.3
Godwin, B.4
Grubert, F.5
Simons, J.F.6
Kim, P.M.7
Palejev, D.8
Carriero, N.J.9
Du, L.10
Taillon, B.E.11
Chen, Z.12
Tanzer, A.13
Saunders, A.C.E.14
Chi, J.15
Yang, F.16
Carter, N.P.17
Hurles, M.E.18
Weissman, S.M.19
Harkins, T.T.20
Gerstein, M.B.21
Egholm, M.22
Snyder, M.23
more..
-
17
-
-
29444457877
-
Common deletion polymorphisms in the human genome
-
SA [tmp] McCarroll 2006 Common deletion polymorphisms in the human genome Nat Genet 38 86 92
-
(2006)
Nat Genet
, vol.38
, pp. 86-92
-
-
McCarroll, S.A.1
-
18
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
R Redon 2006 Global variation in copy number in the human genome Nature 444 444 454 (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
19
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
DOI 10.1126/science.1098918
-
J Sebat 2004 Large-scale copy number polymorphism in the human genome Science 305 525 528 (Pubitemid 38971344)
-
(2004)
Science
, vol.305
, Issue.5683
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
Maner, S.7
Massa, H.8
Walker, M.9
Chi, M.10
Navin, N.11
Lucito, R.12
Healy, J.13
Hicks, J.14
Ye, K.15
Reiner, A.16
Gilliam, T.C.17
Trask, B.18
Patterson, N.19
Zetterberg, A.20
Wigler, M.21
more..
-
20
-
-
22844451617
-
Fine-scale structural variation of the human genome
-
DOI 10.1038/ng1562
-
E Tuzun 2005 Fine-scale structural variation of the human genome Nat Genet 37 727 732 (Pubitemid 41754889)
-
(2005)
Nature Genetics
, vol.37
, Issue.7
, pp. 727-732
-
-
Tuzun, E.1
Sharp, A.J.2
Bailey, J.A.3
Kaul, R.4
Morrison, V.A.5
Pertz, L.M.6
Haugen, E.7
Hayden, H.8
Albertson, D.9
Pinkel, D.10
Olson, M.V.11
Eichler, E.E.12
-
21
-
-
34547204201
-
Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome
-
DOI 10.1073/pnas.0703834104
-
JO Korbel 2007 Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome Proc Natl Acad Sci U S A 104 10110 10115 (Pubitemid 47175271)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.24
, pp. 10110-10115
-
-
Korbel, J.O.1
Urban, A.E.2
Grubert, F.3
Du, J.4
Royce, T.E.5
Starr, P.6
Zhong, G.7
Emanuel, B.S.8
Weissman, S.M.9
Snyder, M.10
Gerstein, M.B.11
-
22
-
-
20044377204
-
The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility
-
DOI 10.1126/science.1101160
-
E Gonzalez 2005 The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility Science 307 1434 1440 (Pubitemid 40321934)
-
(2005)
Science
, vol.307
, Issue.5714
, pp. 1434-1440
-
-
Gonzalez, E.1
Kulkarni, H.2
Bolivar, H.3
Mangano, A.4
Sanchez, R.5
Catano, G.6
Nibbs, R.J.7
Freedman, B.I.8
Quinones, M.P.9
Bamshad, M.J.10
Murthy, K.K.11
Rovin, B.H.12
Bradley, W.13
Clark, R.A.14
Anderson, S.A.15
O'Connell, R.J.16
Agan, B.K.17
Ahuja, S.S.18
Bologna, R.19
Sen, L.20
Dolan, M.J.21
Ahuja, S.K.22
more..
-
23
-
-
39549091294
-
Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis
-
C [tmp] McKinney 2008 Evidence for an influence of chemokine ligand 3-like 1 (CCL3L1) gene copy number on susceptibility to rheumatoid arthritis Ann Rheum Dis 67 409 413
-
(2008)
Ann Rheum Dis
, vol.67
, pp. 409-413
-
-
McKinney, C.1
-
24
-
-
29444442794
-
APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy
-
DOI 10.1038/ng1718
-
A Rovelet-Lecrux 2006 APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy Nat Genet 38 24 26 (Pubitemid 43011878)
-
(2006)
Nature Genetics
, vol.38
, Issue.1
, pp. 24-26
-
-
Rovelet-Lecrux, A.1
Hannequin, D.2
Raux, G.3
Le Meur, N.4
Laquerriere, A.5
Vital, A.6
Dumanchin, C.7
Feuillette, S.8
Brice, A.9
Vercelletto, M.10
Dubas, F.11
Frebourg, T.12
Campion, D.13
-
25
-
-
0242300619
-
α-Synuclein Locus Triplication Causes Parkinson's Disease
-
DOI 10.1126/science.1090278
-
AB Singleton 2003 Alpha-Synuclein locus triplication causes Parkinson's disease Science 302 841 (Pubitemid 37339619)
-
(2003)
Science
, vol.302
, Issue.5646
, pp. 841
-
-
Singleton, A.B.1
Farrer, M.2
Johnson, J.3
Singleton, A.4
Hague, S.5
Kachergus, J.6
Hulihan, M.7
Peuralinna, T.8
Dutra, A.9
Nussbaum, R.10
Lincoln, S.11
Crawley, A.12
Hanson, M.13
Maraganore, D.14
Adler, C.15
Cookson, M.R.16
Muenter, M.17
Baptista, M.18
Miller, D.19
Blancato, J.20
Hardy, J.21
Gwinn-Hardy, K.22
more..
-
26
-
-
77952499379
-
Multi-platform whole-genome microarray analyses refine the epigenetic signature of breast cancer metastasis with gene expression and copy number
-
Andrews J, et al. Multi-platform whole-genome microarray analyses refine the epigenetic signature of breast cancer metastasis with gene expression and copy number. PLoS One. 5:e8665.
-
PLoS One
, vol.5
-
-
Andrews, J.1
-
27
-
-
67649289900
-
Copy number variation at 1q21.1 associated with neuroblastoma
-
SJ Diskin 2009 Copy number variation at 1q21.1 associated with neuroblastoma Nature 459 987 991
-
(2009)
Nature
, vol.459
, pp. 987-991
-
-
Diskin, S.J.1
-
28
-
-
65549150968
-
Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer
-
W Liu 2009 Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer Cancer Res 69 2176 2179
-
(2009)
Cancer Res
, vol.69
, pp. 2176-2179
-
-
Liu, W.1
-
29
-
-
60849118132
-
Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA)
-
V Grubor 2009 Novel genomic alterations and clonal evolution in chronic lymphocytic leukemia revealed by representational oligonucleotide microarray analysis (ROMA) Blood 113 1294 1303
-
(2009)
Blood
, vol.113
, pp. 1294-1303
-
-
Grubor, V.1
-
30
-
-
45349086985
-
Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia - A comparative study of four differently designed, high resolution microarray platforms
-
DOI 10.1002/gcc.20575
-
R Gunnarsson 2008 Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia-a comparative study of four differently designed, high resolution microarray platforms Genes Chromosomes Cancer 47 697 711 (Pubitemid 351847582)
-
(2008)
Genes Chromosomes and Cancer
, vol.47
, Issue.8
, pp. 697-711
-
-
Gunnarsson, R.1
Staaf, J.2
Jansson, M.3
Ottesen, A.M.4
Goransson, H.5
Liljedahl, U.6
Ralfkiaer, U.7
Mansouri, M.8
Buhl, A.M.9
Smedby, K.E.10
Hjalgrim, H.11
Syvanen, A.-C.12
Borg, A.13
Isaksson, A.14
Jurlander, J.15
Juliusson, G.16
Rosenquist, R.17
-
31
-
-
75849157716
-
Integrated analysis of copy number alterations and gene expression: A bivariate assessment of equally directed abnormalities
-
M Schafer 2009 Integrated analysis of copy number alterations and gene expression: a bivariate assessment of equally directed abnormalities Bioinformatics 25 3228 3235
-
(2009)
Bioinformatics
, vol.25
, pp. 3228-3235
-
-
Schafer, M.1
-
32
-
-
33744474290
-
Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21
-
DOI 10.1073/pnas.0602360103
-
JC Strefford 2006 Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21 Proc Natl Acad Sci U S A 103 8167 8172 (Pubitemid 43801070)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.21
, pp. 8167-8172
-
-
Strefford, J.C.1
Van Delft, F.W.2
Robinson, H.M.3
Worley, H.4
Yiannikouris, O.5
Selzer, R.6
Richmond, T.7
Hann, I.8
Bellotti, T.9
Raghavan, M.10
Young, B.D.11
Saha, V.12
Harrison, C.J.13
-
33
-
-
59449093453
-
A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups
-
S Sulong 2009 A comprehensive analysis of the CDKN2A gene in childhood acute lymphoblastic leukemia reveals genomic deletion, copy number neutral loss of heterozygosity, and association with specific cytogenetic subgroups Blood 113 100 107
-
(2009)
Blood
, vol.113
, pp. 100-107
-
-
Sulong, S.1
-
34
-
-
67650653451
-
Copy-number variation: The end of the human genome?
-
PH Dear 2009 Copy-number variation: the end of the human genome? Trends Biotechnol 27 448 454
-
(2009)
Trends Biotechnol
, vol.27
, pp. 448-454
-
-
Dear, P.H.1
-
35
-
-
49649110984
-
Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome
-
A Shlien 2008 Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome Proc Natl Acad Sci U S A 105 11264 11269
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 11264-11269
-
-
Shlien, A.1
-
36
-
-
33745210559
-
Genetic variation in human gene expression
-
ET Dermitzakis BE Stranger 2006 Genetic variation in human gene expression Mamm Genome 17 503 508
-
(2006)
Mamm Genome
, vol.17
, pp. 503-508
-
-
Dermitzakis, E.T.1
Stranger, B.E.2
-
38
-
-
42649117472
-
Distribution and functional impact of DNA copy number variation in the rat
-
DOI 10.1038/ng.141, PII NG141
-
V Guryev 2008 Distribution and functional impact of DNA copy number variation in the rat Nat Genet 40 538 545 (Pubitemid 351601223)
-
(2008)
Nature Genetics
, vol.40
, Issue.5
, pp. 538-545
-
-
Guryev, V.1
Saar, K.2
Adamovic, T.3
Verheul, M.4
Van Heesch, S.A.A.C.5
Cook, S.6
Pravenec, M.7
Aitman, T.8
Jacob, H.9
Shull, J.D.10
Hubner, N.11
Cuppen, E.12
-
39
-
-
63449117467
-
Segmental copy number variation shapes tissue transcriptomes
-
CN Henrichsen 2009 Segmental copy number variation shapes tissue transcriptomes Nat Genet 41 424 429
-
(2009)
Nat Genet
, vol.41
, pp. 424-429
-
-
Henrichsen, C.N.1
-
40
-
-
35648930913
-
The role of transcription factories in large-scale structure and dynamics of interphase chromatin
-
DOI 10.1016/j.semcdb.2007.08.008, PII S1084952107001231, Membrane Lipid Microdomains: Roles in Signalling and Disease and 3D Chromatin
-
T Sexton D Umlauf S Kurukuti P Fraser 2007 The role of transcription factories in large-scale structure and dynamics of interphase chromatin Semin Cell Dev Biol 18 691 697 (Pubitemid 350026432)
-
(2007)
Seminars in Cell and Developmental Biology
, vol.18
, Issue.5
, pp. 691-697
-
-
Sexton, T.1
Umlauf, D.2
Kurukuti, S.3
Fraser, P.4
|