-
1
-
-
79959829264
-
Cytogenetic and molecular genetic characterization of the 'high hyperdiploid' B-cell precursor acute lymphoblastic leukaemia cell line MHH-CALL-2 reveals a near-haploid origin
-
Aburawi HE, Biloglav A, Johansson B, Paulsson K. 2011. Cytogenetic and molecular genetic characterization of the 'high hyperdiploid' B-cell precursor acute lymphoblastic leukaemia cell line MHH-CALL-2 reveals a near-haploid origin. Br J Haematol 154: 275-277.
-
(2011)
Br J Haematol
, vol.154
, pp. 275-277
-
-
Aburawi, H.E.1
Biloglav, A.2
Johansson, B.3
Paulsson, K.4
-
2
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR. 2010. A method and server for predicting damaging missense mutations. Nat Methods 7: 248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
3
-
-
59149099298
-
Emerging paradigms in cancer genetics: Some important findings from high-density single nucleotide polymorphism array studies
-
Bacolod MD, Schemmann GS, Giardina SF, Paty P, Notterman DA, Barany F. 2009. Emerging paradigms in cancer genetics: Some important findings from high-density single nucleotide polymorphism array studies. Cancer Res 69: 723-727.
-
(2009)
Cancer Res
, vol.69
, pp. 723-727
-
-
Bacolod, M.D.1
Schemmann, G.S.2
Giardina, S.F.3
Paty, P.4
Notterman, D.A.5
Barany, F.6
-
4
-
-
78651430230
-
Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization
-
Boeva V, Zinovyev A, Bleakley K, Vert JP, Janoueix-Lerosey I, Delattre O, Barillot E. 2011. Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization. Bioinformatics 27: 268-269.
-
(2011)
Bioinformatics
, vol.27
, pp. 268-269
-
-
Boeva, V.1
Zinovyev, A.2
Bleakley, K.3
Vert, J.P.4
Janoueix-Lerosey, I.5
Delattre, O.6
Barillot, E.7
-
5
-
-
0035207819
-
Adaptive evolution in LINE-1 retrotransposons
-
Boissinot S, Furano AV. 2001. Adaptive evolution in LINE-1 retrotransposons. Mol Biol Evol 18: 2186-2194.
-
(2001)
Mol Biol Evol
, vol.18
, pp. 2186-2194
-
-
Boissinot, S.1
Furano, A.V.2
-
6
-
-
0019445146
-
Near-haploid acute lymphoblastic leukemia: a unique subgroup with a poor prognosis?
-
Brodeur GM, Williams DL, Look AT, Bowman WP, Kalwinsky DK. 1981. Near-haploid acute lymphoblastic leukemia: a unique subgroup with a poor prognosis? Blood 58: 14-19.
-
(1981)
Blood
, vol.58
, pp. 14-19
-
-
Brodeur, G.M.1
Williams, D.L.2
Look, A.T.3
Bowman, W.P.4
Kalwinsky, D.K.5
-
7
-
-
33750735356
-
DNA repair and PARP in aging
-
Burkle A. 2006. DNA repair and PARP in aging. Free Radic Res 40: 1295-1302.
-
(2006)
Free Radic Res
, vol.40
, pp. 1295-1302
-
-
Burkle, A.1
-
8
-
-
0032566526
-
Identification of Nck family genes, chromosomal localization, expression, and signaling specificity
-
Chen M, She H, Davis EM, Spicer CM, Kim L, Ren R, Le Beau MM, Li W. 1998. Identification of Nck family genes, chromosomal localization, expression, and signaling specificity. J Biol Chem 273: 25171-25178.
-
(1998)
J Biol Chem
, vol.273
, pp. 25171-25178
-
-
Chen, M.1
She, H.2
Davis, E.M.3
Spicer, C.M.4
Kim, L.5
Ren, R.6
Le Beau, M.M.7
Li, W.8
-
9
-
-
0033053010
-
High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes
-
Chudoba I, Plesch A, Lorch T, Lemke J, Claussen U, Senger G. 1999. High resolution multicolor-banding: A new technique for refined FISH analysis of human chromosomes. Cytogenet Cell Genet 84: 156-160.
-
(1999)
Cytogenet Cell Genet
, vol.84
, pp. 156-160
-
-
Chudoba, I.1
Plesch, A.2
Lorch, T.3
Lemke, J.4
Claussen, U.5
Senger, G.6
-
10
-
-
84859910490
-
DBIRD complex integrates alternative mRNA splicing with RNA polymerase II transcript elongation
-
Close P, East P, Dirac-Svejstrup AB, Hartmann H, Heron M, Maslen S, Chariot A, Soding J, Skehel M, Svejstrup JQ. 2012. DBIRD complex integrates alternative mRNA splicing with RNA polymerase II transcript elongation. Nature 484: 386-389.
-
(2012)
Nature
, vol.484
, pp. 386-389
-
-
Close, P.1
East, P.2
Dirac-Svejstrup, A.B.3
Hartmann, H.4
Heron, M.5
Maslen, S.6
Chariot, A.7
Soding, J.8
Skehel, M.9
Svejstrup, J.Q.10
-
11
-
-
0003228073
-
Identification and utilization of arbitrary correlations in models of recombination signal sequences
-
RESEARCH0072
-
Cowell LG, Davila M, Kepler TB, Kelsoe G. 2002. Identification and utilization of arbitrary correlations in models of recombination signal sequences. Genome Biol 3:RESEARCH0072.
-
(2002)
Genome Biol
, vol.3
-
-
Cowell, L.G.1
Davila, M.2
Kepler, T.B.3
Kelsoe, G.4
-
12
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, Kernytsky AM, Sivachenko AY, Cibulskis K, Gabriel SB, Altshuler D, Daly MJ. 2011. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 43: 491-498.
-
(2011)
Nat Genet
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
Philippakis, A.A.7
del Angel, G.8
Rivas, M.A.9
Hanna, M.10
McKenna, A.11
Fennell, T.J.12
Kernytsky, A.M.13
Sivachenko, A.Y.14
Cibulskis, K.15
Gabriel, S.B.16
Altshuler, D.17
Daly, M.J.18
-
13
-
-
77952967459
-
mTORC1-mediated cell proliferation, but not cell growth, controlled by the 4E-BPs
-
Dowling RJ, Topisirovic I, Alain T, Bidinosti M, Fonseca BD, Petroulakis E, Wang X, Larsson O, Selvaraj A, Liu Y, Kozma SC, Thomas G, Sonenberg N. 2010. mTORC1-mediated cell proliferation, but not cell growth, controlled by the 4E-BPs. Science 328: 1172-1176.
-
(2010)
Science
, vol.328
, pp. 1172-1176
-
-
Dowling, R.J.1
Topisirovic, I.2
Alain, T.3
Bidinosti, M.4
Fonseca, B.D.5
Petroulakis, E.6
Wang, X.7
Larsson, O.8
Selvaraj, A.9
Liu, Y.10
Kozma, S.C.11
Thomas, G.12
Sonenberg, N.13
-
14
-
-
84870322656
-
Genome-wide methylation screen in low-grade breast cancer identifies novel epigenetically altered genes as potential biomarkers for tumor diagnosis
-
Faryna M, Konermann C, Aulmann S, Bermejo JL, Brugger M, Diederichs S, Rom J, Weichenhan D, Claus R, Rehli M, Schirmacher P, Sinn HP, Plass C, Gerhauser C. 2012. Genome-wide methylation screen in low-grade breast cancer identifies novel epigenetically altered genes as potential biomarkers for tumor diagnosis. FASEB J 26: 4937-4950.
-
(2012)
FASEB J
, vol.26
, pp. 4937-4950
-
-
Faryna, M.1
Konermann, C.2
Aulmann, S.3
Bermejo, J.L.4
Brugger, M.5
Diederichs, S.6
Rom, J.7
Weichenhan, D.8
Claus, R.9
Rehli, M.10
Schirmacher, P.11
Sinn, H.P.12
Plass, C.13
Gerhauser, C.14
-
15
-
-
84858221706
-
Ensembl 2012
-
Flicek P, Amode MR, Barrell D, Beal K, Brent S, Carvalho-Silva D, Clapham P, Coates G, Fairley S, Fitzgerald S, Gil L, Gordon L, Hendrix M, Hourlier T, Johnson N, Kahari AK, Keefe D, Keenan S, Kinsella R, Komorowska M, Koscielny G, Kulesha E, Larsson P, Longden I, McLaren W, Muffato M, Overduin B, Pignatelli M, Pritchard B, Riat HS, Ritchie GR, Ruffier M, Schuster M, Sobral D, Tang YA, Taylor K, Trevanion S, Vandrovcova J, White S, Wilson M, Wilder SP, Aken BL, Birney E, Cunningham F, Dunham I, Durbin R, Fernandez-Suarez XM, Harrow J, Herrero J, Hubbard TJ, Parker A, Proctor G, Spudich G, Vogel J, Yates A, Zadissa A, Searle SM. 2012. Ensembl 2012. Nucleic Acids Res 40: D84-90.
-
(2012)
Nucleic Acids Res
, vol.40
-
-
Flicek, P.1
Amode, M.R.2
Barrell, D.3
Beal, K.4
Brent, S.5
Carvalho-Silva, D.6
Clapham, P.7
Coates, G.8
Fairley, S.9
Fitzgerald, S.10
Gil, L.11
Gordon, L.12
Hendrix, M.13
Hourlier, T.14
Johnson, N.15
Kahari, A.K.16
Keefe, D.17
Keenan, S.18
Kinsella, R.19
Komorowska, M.20
Koscielny, G.21
Kulesha, E.22
Larsson, P.23
Longden, I.24
McLaren, W.25
Muffato, M.26
Overduin, B.27
Pignatelli, M.28
Pritchard, B.29
Riat, H.S.30
Ritchie, G.R.31
Ruffier, M.32
Schuster, M.33
Sobral, D.34
Tang, Y.A.35
Taylor, K.36
Trevanion, S.37
Vandrovcova, J.38
White, S.39
Wilson, M.40
Wilder, S.P.41
Aken, B.L.42
Birney, E.43
Cunningham, F.44
Dunham, I.45
Durbin, R.46
Fernandez-Suarez, X.M.47
Harrow, J.48
Herrero, J.49
Hubbard, T.J.50
Parker, A.51
Proctor, G.52
Spudich, G.53
Vogel, J.54
Yates, A.55
Zadissa, A.56
Searle, S.M.57
more..
-
16
-
-
0038746982
-
Peculiar structure and location of 9p21 homozygous deletion breakpoints in human cancer cells
-
Florl AR, Schulz WA. 2003. Peculiar structure and location of 9p21 homozygous deletion breakpoints in human cancer cells. Genes Chromosomes Cancer 37: 141-148.
-
(2003)
Genes Chromosomes Cancer
, vol.37
, pp. 141-148
-
-
Florl, A.R.1
Schulz, W.A.2
-
17
-
-
75549087826
-
COSMIC (the Catalogue of Somatic Mutations in Cancer): A resource to investigate acquired mutations in human cancer
-
Forbes SA, Tang G, Bindal N, Bamford S, Dawson E, Cole C, Kok CY, Jia M, Ewing R, Menzies A and others. 2010. COSMIC (the Catalogue of Somatic Mutations in Cancer): A resource to investigate acquired mutations in human cancer. Nucleic Acids Res 38: D652-657.
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Forbes, S.A.1
Tang, G.2
Bindal, N.3
Bamford, S.4
Dawson, E.5
Cole, C.6
Kok, C.Y.7
Jia, M.8
Ewing, R.9
Menzies, A.10
-
18
-
-
60849103086
-
hnRNP K interacts with RNA binding motif protein 42 and functions in the maintenance of cellular ATP level during stress conditions
-
Fukuda T, Naiki T, Saito M, Irie K. 2009. hnRNP K interacts with RNA binding motif protein 42 and functions in the maintenance of cellular ATP level during stress conditions. Genes Cells 14: 113-128.
-
(2009)
Genes Cells
, vol.14
, pp. 113-128
-
-
Fukuda, T.1
Naiki, T.2
Saito, M.3
Irie, K.4
-
19
-
-
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
-
20
-
-
0026094623
-
Near haploid acute lymphoblastic leukemia: Seven new cases and a review of the literature
-
Gibbons B, MacCallum P, Watts E, Rohatiner AZS, Webb D, Katz FE, Secker-Walker LM, Temperley IJ, Harrison CJ, Campbell RHA, Nash R, Broadbent V, Chessells JM. 1991. Near haploid acute lymphoblastic leukemia: Seven new cases and a review of the literature. Leukemia 5: 738-743.
-
(1991)
Leukemia
, vol.5
, pp. 738-743
-
-
Gibbons, B.1
MacCallum, P.2
Watts, E.3
Rohatiner, A.Z.S.4
Webb, D.5
Katz, F.E.6
Secker-Walker, L.M.7
Temperley, I.J.8
Harrison, C.J.9
Campbell, R.H.A.10
Nash, R.11
Broadbent, V.12
Chessells, J.M.13
-
21
-
-
79953715693
-
Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel
-
Gonzalez-Perez A, Lopez-Bigas N. 2011. Improving the assessment of the outcome of nonsynonymous SNVs with a consensus deleteriousness score, Condel. Am J Hum Genet 88: 440-449.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 440-449
-
-
Gonzalez-Perez, A.1
Lopez-Bigas, N.2
-
22
-
-
77957571905
-
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
-
Goode EL, Chenevix-Trench G, Song H, Ramus SJ, Notaridou M, Lawrenson K, Widschwendter M, Vierkant RA, Larson MC, Kjaer SK, Birrer MJ, Berchuck A, Schildkraut J, Tomlinson I, Kiemeney LA, Cook LS, Gronwald J, Garcia-Closas M, Gore ME, Campbell I, Whittemore AS, Sutphen R, Phelan C, Anton-Culver H, Pearce CL, Lambrechts D, Rossing MA, Chang-Claude J, Moysich KB, Goodman MT, Dork T, Nevanlinna H, Ness RB, Rafnar T, Hogdall C, Hogdall E, Fridley BL, Cunningham JM, Sieh W, McGuire V, Godwin AK, Cramer DW, Hernandez D, Levine D, Lu K, Iversen ES, Palmieri RT, Houlston R, van Altena AM, Aben KK, Massuger LF, Brooks-Wilson A, Kelemen LE, Le ND, Jakubowska A, Lubinski J, Medrek K, Stafford A, Easton DF, Tyrer J, Bolton KL, Harrington P, Eccles D, Chen A, Molina AN, Davila B N, Arango H, Tsai YY, Chen Z, Risch HA, McLaughlin J, Narod SA, Ziogas A, Brewster W, Gentry-Maharaj A, Menon U, Wu AH, Stram DO, Pike MC, Beesley J, Webb PM, Chen X, Ekici AB, Thiel FC, Beckmann MW, Yang H, Wentzensen N, Lissowska J, Fasching PA, Despierre E, Amant F, Vergote I, Doherty J, Hein R, Wang-Gohrke S, Lurie G, Carney ME, Thompson PJ, Runnebaum I, Hillemanns P, Durst M, Antonenkova N, Bogdanova N, Leminen A, Butzow R, Heikkinen T, Stefansson K, Sulem P, Besenbacher S, Sellers TA, Gayther SA, Pharoah PD. 2010. A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. Nat Genet 42: 874-879.
-
(2010)
Nat Genet
, vol.42
, pp. 874-879
-
-
Goode, E.L.1
Chenevix-Trench, G.2
Song, H.3
Ramus, S.J.4
Notaridou, M.5
Lawrenson, K.6
Widschwendter, M.7
Vierkant, R.A.8
Larson, M.C.9
Kjaer, S.K.10
Birrer, M.J.11
Berchuck, A.12
Schildkraut, J.13
Tomlinson, I.14
Kiemeney, L.A.15
Cook, L.S.16
Gronwald, J.17
Garcia-Closas, M.18
Gore, M.E.19
Campbell, I.20
Whittemore, A.S.21
Sutphen, R.22
Phelan, C.23
Anton-Culver, H.24
Pearce, C.L.25
Lambrechts, D.26
Rossing, M.A.27
Chang-Claude, J.28
Moysich, K.B.29
Goodman, M.T.30
Dork, T.31
Nevanlinna, H.32
Ness, R.B.33
Rafnar, T.34
Hogdall, C.35
Hogdall, E.36
Fridley, B.L.37
Cunningham, J.M.38
Sieh, W.39
McGuire, V.40
Godwin, A.K.41
Cramer, D.W.42
Hernandez, D.43
Levine, D.44
Lu, K.45
Iversen, E.S.46
Palmieri, R.T.47
Houlston, R.48
Van Altena, A.M.49
Aben, K.K.50
Massuger, L.F.51
Brooks-Wilson, A.52
Kelemen, L.E.53
Le, N.D.54
Jakubowska, A.55
Lubinski, J.56
Medrek, K.57
Stafford, A.58
Easton, D.F.59
Tyrer, J.60
Bolton, K.L.61
Harrington, P.62
Eccles, D.63
Chen, A.64
Molina, A.N.65
Davila, B.N.66
Arango, H.67
Tsai, Y.Y.68
Chen, Z.69
Risch, H.A.70
McLaughlin, J.71
Narod, S.A.72
Ziogas, A.73
Brewster, W.74
Gentry-Maharaj, A.75
Menon, U.76
Wu, A.H.77
Stram, D.O.78
Pike, M.C.79
Beesley, J.80
Webb, P.M.81
Chen, X.82
Ekici, A.B.83
Thiel, F.C.84
Beckmann, M.W.85
Yang, H.86
Wentzensen, N.87
Lissowska, J.88
Fasching, P.A.89
Despierre, E.90
Amant, F.91
Vergote, I.92
Doherty, J.93
Hein, R.94
Wang-Gohrke, S.95
Lurie, G.96
Carney, M.E.97
Thompson, P.J.98
Runnebaum, I.99
Hillemanns, P.100
Durst, M.101
Antonenkova, N.102
Bogdanova, N.103
Leminen, A.104
Butzow, R.105
Heikkinen, T.106
Stefansson, K.107
Sulem, P.108
Besenbacher, S.109
Sellers, T.A.110
Gayther, S.A.111
Pharoah, P.D.112
more..
-
23
-
-
79961182320
-
In-depth annotation of SNPs arising from resequencing projects using NGS-SNP
-
Grant JR, Arantes AS, Liao X, Stothard P. 2011. In-depth annotation of SNPs arising from resequencing projects using NGS-SNP. Bioinformatics 27: 2300-2301.
-
(2011)
Bioinformatics
, vol.27
, pp. 2300-2301
-
-
Grant, J.R.1
Arantes, A.S.2
Liao, X.3
Stothard, P.4
-
24
-
-
84863495094
-
The hallmarks of cancer. A long non-coding RNA point of view
-
Gutschner T, Diederichs S. 2012. The hallmarks of cancer. A long non-coding RNA point of view. RNA Biology 9: 703-719.
-
(2012)
RNA Biology
, vol.9
, pp. 703-719
-
-
Gutschner, T.1
Diederichs, S.2
-
25
-
-
84555191727
-
Scpliceosome mutations in hematopoietic malignancies
-
Hahn CN, Scott HS. 2011. Scpliceosome mutations in hematopoietic malignancies. Nat. Genet. 44: 9-10.
-
(2011)
Nat. Genet.
, vol.44
, pp. 9-10
-
-
Hahn, C.N.1
Scott, H.S.2
-
26
-
-
84886341242
-
Acute lymphoblastic leukemia
-
Heim S, Mitelman F, editors., 3rd ed. New Jersey: Wiley-Blackwell
-
Harrison CJ, Johansson B. 2009. Acute lymphoblastic leukemia. In: Heim S, Mitelman F, editors. Cancer Cytogenetics, 3rd ed. New Jersey: Wiley-Blackwell, pp. 233-296.
-
(2009)
Cancer Cytogenetics
, pp. 233-296
-
-
Harrison, C.J.1
Johansson, B.2
-
27
-
-
2942563738
-
Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia
-
Harrison CJ, Moorman AV, Broadfield ZJ, Cheung KL, Harris RL, Reza Jalali G, Robinson HM, Barber KE, Richards SM, Mitchell CD, Eden TO, Hann IM, Hill FG, Kinsey SE, Gibson BE, Lilleyman J, Vora A, Goldstone AH, Franklin IM, Durrant J, Martineau, M. 2004. Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia. Br J Haematol 125: 552-559.
-
(2004)
Br J Haematol
, vol.125
, pp. 552-559
-
-
Harrison, C.J.1
Moorman, A.V.2
Broadfield, Z.J.3
Cheung, K.L.4
Harris, R.L.5
Reza Jalali, G.6
Robinson, H.M.7
Barber, K.E.8
Richards, S.M.9
Mitchell, C.D.10
Eden, T.O.11
Hann, I.M.12
Hill, F.G.13
Kinsey, S.E.14
Gibson, B.E.15
Lilleyman, J.16
Vora, A.17
Goldstone, A.H.18
Franklin, I.M.19
Durrant, J.20
Martineau, M.21
more..
-
28
-
-
79251609962
-
Epigenetic regulations in hematopoietic Hox code
-
He H, Hua X, Yan J. 2011a. Epigenetic regulations in hematopoietic Hox code. Oncogene 30: 379-388.
-
(2011)
Oncogene
, vol.30
, pp. 379-388
-
-
He, H.1
Hua, X.2
Yan, J.3
-
29
-
-
80052495940
-
Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA
-
He YF, Li BZ, Li Z, Liu P, Wang Y, Tang Q, Ding J, Jia Y, Chen Z, Li L, Sun Y, Li X, Dai Q, Song CX, Zhang K, He C, Xu GL. 2011b. Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA. Science 333: 1303-1307.
-
(2011)
Science
, vol.333
, pp. 1303-1307
-
-
He, Y.F.1
Li, B.Z.2
Li, Z.3
Liu, P.4
Wang, Y.5
Tang, Q.6
Ding, J.7
Jia, Y.8
Chen, Z.9
Li, L.10
Sun, Y.11
Li, X.12
Dai, Q.13
Song, C.X.14
Zhang, K.15
He, C.16
Xu, G.L.17
-
30
-
-
13044264463
-
Hypodiploidy with less than 45 chromosomes confers adverse risk in childhood acute lymphoblastic leukemia: a report from the children's cancer group
-
Heerema NA, Nachman JB, Sather HN, Sensel MG, Lee MK, Hutchinson R, Lange BJ, Steinherz PG, Bostrom B, Gaynon PS, Uckun F. 1999. Hypodiploidy with less than 45 chromosomes confers adverse risk in childhood acute lymphoblastic leukemia: a report from the children's cancer group. Blood 94: 4036-4045.
-
(1999)
Blood
, vol.94
, pp. 4036-4045
-
-
Heerema, N.A.1
Nachman, J.B.2
Sather, H.N.3
Sensel, M.G.4
Lee, M.K.5
Hutchinson, R.6
Lange, B.J.7
Steinherz, P.G.8
Bostrom, B.9
Gaynon, P.S.10
Uckun, F.11
-
31
-
-
80052461558
-
Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine
-
Ito S, Shen L, Dai Q, Wu SC, Collins LB, Swenberg JA, He C, Zhang Y. 2011. Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine. Science 333: 1300-1303.
-
(2011)
Science
, vol.333
, pp. 1300-1303
-
-
Ito, S.1
Shen, L.2
Dai, Q.3
Wu, S.C.4
Collins, L.B.5
Swenberg, J.A.6
He, C.7
Zhang, Y.8
-
32
-
-
84863797091
-
Biomarkers for detection and prognosis of breast cancer identified by a functional hypermethylome screen
-
Jeschke J, Van Neste L, Glockner SC, Dhir M, Calmon MF, Deregowski V, Van Criekinge W, Vlassenbroeck I, Koch A, Chan TA, Cope L, Hooker CM, Schuebel KE, Gabrielson E, Winterpacht A, Baylin SB, Herman JG, Ahuja N. 2012. Biomarkers for detection and prognosis of breast cancer identified by a functional hypermethylome screen. Epigenetics 7: 701-709.
-
(2012)
Epigenetics
, vol.7
, pp. 701-709
-
-
Jeschke, J.1
Van Neste, L.2
Glockner, S.C.3
Dhir, M.4
Calmon, M.F.5
Deregowski, V.6
Van Criekinge, W.7
Vlassenbroeck, I.8
Koch, A.9
Chan, T.A.10
Cope, L.11
Hooker, C.M.12
Schuebel, K.E.13
Gabrielson, E.14
Winterpacht, A.15
Baylin, S.B.16
Herman, J.G.17
Ahuja, N.18
-
33
-
-
38349177862
-
Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray
-
Kawamata N, Ogawa S, Zimmermann M, Kato M, Sanada M, Hemminki K, Yamatomo G, Nannya Y, Koehler R, Flohr T, Miller CW, Harbott J, Ludwig WD, Stanulla M, Schrappe M, Bartram CR, Koeffler HP. 2008. Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray. Blood 111: 776-784.
-
(2008)
Blood
, vol.111
, pp. 776-784
-
-
Kawamata, N.1
Ogawa, S.2
Zimmermann, M.3
Kato, M.4
Sanada, M.5
Hemminki, K.6
Yamatomo, G.7
Nannya, Y.8
Koehler, R.9
Flohr, T.10
Miller, C.W.11
Harbott, J.12
Ludwig, W.D.13
Stanulla, M.14
Schrappe, M.15
Bartram, C.R.16
Koeffler, H.P.17
-
34
-
-
0016750782
-
[A cell-line with 27 chromosomes in a human acute leukemia (author's transl)]
-
Kessous A, Corberand J, Grozdea J, Colombies P. 1975. [A cell-line with 27 chromosomes in a human acute leukemia (author's transl)]. Nouv Rev Fr Hematol 15: 73-81.
-
(1975)
Nouv Rev Fr Hematol
, vol.15
, pp. 73-81
-
-
Kessous, A.1
Corberand, J.2
Grozdea, J.3
Colombies, P.4
-
35
-
-
33747875631
-
Molecular processes of chromosome 9p21 deletions causing inactivation of the p16 tumor suppressor gene in human cancer: deduction from structural analysis of breakpoints for deletions
-
Kohno T, Yokota J. 2006. Molecular processes of chromosome 9p21 deletions causing inactivation of the p16 tumor suppressor gene in human cancer: deduction from structural analysis of breakpoints for deletions. DNA Repair (Amst) 5: 1273-1281.
-
(2006)
DNA Repair (Amst)
, vol.5
, pp. 1273-1281
-
-
Kohno, T.1
Yokota, J.2
-
36
-
-
79955468280
-
Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene
-
Kotake Y, Nakagawa T, Kitagawa K, Suzuki S, Liu N, Kitagawa M, Xiong Y. 2010. Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene. Oncogene 30: 1956-1962.
-
(2010)
Oncogene
, vol.30
, pp. 1956-1962
-
-
Kotake, Y.1
Nakagawa, T.2
Kitagawa, K.3
Suzuki, S.4
Liu, N.5
Kitagawa, M.6
Xiong, Y.7
-
37
-
-
34548289288
-
Septins regulate actin organization and cell-cycle arrest through nuclear accumulation of NCK mediated by SOCS7
-
Kremer BE, Adang LA, Macara IG. 2007. Septins regulate actin organization and cell-cycle arrest through nuclear accumulation of NCK mediated by SOCS7. Cell 130: 837-850.
-
(2007)
Cell
, vol.130
, pp. 837-850
-
-
Kremer, B.E.1
Adang, L.A.2
Macara, I.G.3
-
38
-
-
69649109364
-
Circos: An information aesthetic for comparative genomics
-
Krzywinski M, Schein J, Birol I, Connors J, Gascoyne R, Horsman D, Jones SJ, Marra MA. 2009. Circos: An information aesthetic for comparative genomics. Genome Res 19: 1639-1645.
-
(2009)
Genome Res
, vol.19
, pp. 1639-1645
-
-
Krzywinski, M.1
Schein, J.2
Birol, I.3
Connors, J.4
Gascoyne, R.5
Horsman, D.6
Jones, S.J.7
Marra, M.A.8
-
39
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
Kumar P, Henikoff S, Ng PC. 2009. Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc 4: 1073-1081.
-
(2009)
Nat Protoc
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
40
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, Kann L, Lehoczky J, LeVine R, McEwan P, McKernan K, Meldrim J, Mesirov JP, Miranda C, Morris W, Naylor J, Raymond C, Rosetti M, Santos R, Sheridan A, Sougnez C, Stange-Thomann N, Stojanovic N, Subramanian A, Wyman D, Rogers J, Sulston J, Ainscough R, Beck S, Bentley D, Burton J, Clee C, Carter N, Coulson A, Deadman R, Deloukas P, Dunham A, Dunham I, Durbin R, French L, Grafham D, Gregory S, Hubbard T, Humphray S, Hunt A, Jones M, Lloyd C, McMurray A, Matthews L, Mercer S, Milne S, Mullikin JC, Mungall A, Plumb R, Ross M, Shownkeen R, Sims S, Waterston RH, Wilson RK, Hillier LW, McPherson JD, Marra MA, Mardis ER, Fulton LA, Chinwalla A T, Pepin KH, Gish WR, Chissoe SL, Wendl MC, Delehaunty KD, Miner TL, Delehaunty A, Kramer JB, Cook LL, Fulton RS, Johnson DL, Minx PJ, Clifton SW, Hawkins T, Branscomb E, Predki P, Richardson P, Wenning S, Slezak T, Doggett N, Cheng JF, Olsen A, Lucas S, Elkin C, Uberbacher E, Frazier M, Gibbs RA, Muzny DM, Scherer SE, Bouck JB, Sodergren EJ, Worley KC, Rives CM, Gorrell JH, Metzker ML, Naylor SL, Kucherlapati RS, Nelson DL, Weinstock GM, Sakaki Y, Fujiyama A, Hattori M, Yada T, Toyoda A, Itoh T, Kawagoe C, Watanabe H, Totoki Y, Taylor T, Weissenbach J, Heilig R, Saurin W, Artiguenave F, Brottier P, Bruls T, Pelletier E, Robert C, Wincker P, Smith DR, Doucette-Stamm L, Rubenfield M, Weinstock K, Lee HM, Dubois J, Rosenthal A, Platzer M, Nyakatura G, Taudien S, Rump A, Yang H, Yu J, Wang J, Huang G, Gu J, Hood L, Rowen L, Madan A, Qin S, Davis RW, Federspiel NA, Abola AP, Proctor MJ, Myers RM, Schmutz J, Dickson M, Grimwood J, Cox DR, Olson MV, Kaul R, Raymond C, Shimizu N, Kawasaki K, Minoshima S, Evans GA, Athanasiou M, Schultz R, Roe BA, Chen F, Pan H, Ramser J, Lehrach H, Reinhardt R, McCombie WR, de la Bastide M, Dedhia N, Blocker H, Hornischer K, Nordsiek G, Agarwala R, Aravind L, Bailey JA, Bateman A, Batzoglou S, Birney E, Bork P, Brown DG, Burge CB, Cerutti L, Chen HC, Church D, Clamp M, Copley RR, Doerks T, Eddy SR, Eichler E E, Furey TS, Galagan J, Gilbert JG, Harmon C, Hayashizaki Y, Haussler D, Hermjakob H, Hokamp K, Jang W, Johnson LS, Jones TA, Kasif S, Kaspryzk A, Kennedy S, Kent WJ, Kitts P, Koonin EV, Korf I, Kulp D, Lancet D, Lowe T M, McLysaght A, Mikkelsen T, Moran JV, Mulder N, Pollara VJ, Ponting CP, Schuler G, Schultz J, Slater G, Smit AF, Stupka E, Szustakowski J, Thierry-Mieg D, Thierry-Mieg J, Wagner L, Wallis J, Wheeler R, Williams A, Wolf YI, Wolfe KH, Yang SP, Yeh RF, Collins F, Guyer MS, Peterson J, Felsenfeld A, Wetterstrand KA, Patrinos A, Morgan MJ, de Jong P, Catanese JJ, Osoegawa K, Shizuya H, Choi S, Chen YJ. 2001. Initial sequencing and analysis of the human genome. Nature 409: 860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
Devon, K.7
Dewar, K.8
Doyle, M.9
FitzHugh, W.10
Funke, R.11
Gage, D.12
Harris, K.13
Heaford, A.14
Howland, J.15
Kann, L.16
Lehoczky, J.17
LeVine, R.18
McEwan, P.19
McKernan, K.20
Meldrim, J.21
Mesirov, J.P.22
Miranda, C.23
Morris, W.24
Naylor, J.25
Raymond, C.26
Rosetti, M.27
Santos, R.28
Sheridan, A.29
Sougnez, C.30
Stange-Thomann, N.31
Stojanovic, N.32
Subramanian, A.33
Wyman, D.34
Rogers, J.35
Sulston, J.36
Ainscough, R.37
Beck, S.38
Bentley, D.39
Burton, J.40
Clee, C.41
Carter, N.42
Coulson, A.43
Deadman, R.44
Deloukas, P.45
Dunham, A.46
Dunham, I.47
Durbin, R.48
French, L.49
Grafham, D.50
Gregory, S.51
Hubbard, T.52
Humphray, S.53
Hunt, A.54
Jones, M.55
Lloyd, C.56
McMurray, A.57
Matthews, L.58
Mercer, S.59
Milne, S.60
Mullikin, J.C.61
Mungall, A.62
Plumb, R.63
Ross, M.64
Shownkeen, R.65
Sims, S.66
Waterston, R.H.67
Wilson, R.K.68
Hillier, L.W.69
McPherson, J.D.70
Marra, M.A.71
Mardis, E.R.72
Fulton, L.A.73
Chinwalla, A.T.74
Pepin, K.H.75
Gish, W.R.76
Chissoe, S.L.77
Wendl, M.C.78
Delehaunty, K.D.79
Miner, T.L.80
Delehaunty, A.81
Kramer, J.B.82
Cook, L.L.83
Fulton, R.S.84
Johnson, D.L.85
Minx, P.J.86
Clifton, S.W.87
Hawkins, T.88
Branscomb, E.89
Predki, P.90
Richardson, P.91
Wenning, S.92
Slezak, T.93
Doggett, N.94
Cheng, J.F.95
Olsen, A.96
Lucas, S.97
Elkin, C.98
Uberbacher, E.99
Frazier, M.100
Gibbs, R.A.101
Muzny, D.M.102
Scherer, S.E.103
Bouck, J.B.104
Sodergren, E.J.105
Worley, K.C.106
Rives, C.M.107
Gorrell, J.H.108
Metzker, M.L.109
Naylor, S.L.110
Kucherlapati, R.S.111
Nelson, D.L.112
Weinstock, G.M.113
Sakaki, Y.114
Fujiyama, A.115
Hattori, M.116
Yada, T.117
Toyoda, A.118
Itoh, T.119
Kawagoe, C.120
Watanabe, H.121
Totoki, Y.122
Taylor, T.123
Weissenbach, J.124
Heilig, R.125
Saurin, W.126
Artiguenave, F.127
Brottier, P.128
Bruls, T.129
Pelletier, E.130
Robert, C.131
Wincker, P.132
Smith, D.R.133
Doucette-Stamm, L.134
Rubenfield, M.135
Weinstock, K.136
Lee, H.M.137
Dubois, J.138
Rosenthal, A.139
Platzer, M.140
Nyakatura, G.141
Taudien, S.142
Rump, A.143
Yang, H.144
Yu, J.145
Wang, J.146
Huang, G.147
Gu, J.148
Hood, L.149
Rowen, L.150
Madan, A.151
Qin, S.152
Davis, R.W.153
Federspiel, N.A.154
Abola, A.P.155
Proctor, M.J.156
Myers, R.M.157
Schmutz, J.158
Dickson, M.159
Grimwood, J.160
Cox, D.R.161
Olson, M.V.162
Kaul, R.163
Raymond, C.164
Shimizu, N.165
Kawasaki, K.166
Minoshima, S.167
Evans, G.A.168
Athanasiou, M.169
Schultz, R.170
Roe, B.A.171
Chen, F.172
Pan, H.173
Ramser, J.174
Lehrach, H.175
Reinhardt, R.176
McCombie, W.R.177
De La Bastide, M.178
Dedhia, N.179
Blocker, H.180
Hornischer, K.181
Nordsiek, G.182
Agarwala, R.183
Aravind, L.184
Bailey, J.A.185
Bateman, A.186
Batzoglou, S.187
Birney, E.188
Bork, P.189
Brown, D.G.190
Burge, C.B.191
Cerutti, L.192
Chen, H.C.193
Church, D.194
Clamp, M.195
Copley, R.R.196
Doerks, T.197
Eddy, S.R.198
Eichler, E.E.199
Furey, T.S.200
Galagan, J.201
Gilbert, J.G.202
Harmon, C.203
Hayashizaki, Y.204
Haussler, D.205
Hermjakob, H.206
Hokamp, K.207
Jang, W.208
Johnson, L.S.209
Jones, T.A.210
Kasif, S.211
Kaspryzk, A.212
Kennedy, S.213
Kent, W.J.214
Kitts, P.215
Koonin, E.V.216
Korf, I.217
Kulp, D.218
Lancet, D.219
Lowe, T.M.220
McLysaght, A.221
Mikkelsen, T.222
Moran, J.V.223
Mulder, N.224
Pollara, V.J.225
Ponting, C.P.226
Schuler, G.227
Schultz, J.228
Slater, G.229
Smit, A.F.230
Stupka, E.231
Szustakowski, J.232
Thierry-Mieg, D.233
Thierry-Mieg, J.234
Wagner, L.235
Wallis, J.236
Wheeler, R.237
Williams, A.238
Wolf, Y.I.239
Wolfe, K.H.240
Yang, S.P.241
Yeh, R.F.242
Collins, F.243
Guyer, M.S.244
Peterson, J.245
Felsenfeld, A.246
Wetterstrand, K.A.247
Patrinos, A.248
Morgan, M.J.249
De Jong, P.250
Catanese, J.J.251
Osoegawa, K.252
Shizuya, H.253
Choi, S.254
Chen, Y.J.255
more..
-
41
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H, Durbin R. 2009. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
42
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R. 2009. The sequence alignment/map format and SAMtools. Bioinformatics 25: 2078-2079.
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
Marth, G.7
Abecasis, G.8
Durbin, R.9
-
43
-
-
0037350661
-
TET1, a member of a novel protein family, is fused to MLL in acute myeloid leukemia containing the t(10;11)(q22;q23)
-
Lorsbach RB, Moore J, Mathew S, Raimondi SC, Mukatira ST, Downing JR. 2003. TET1, a member of a novel protein family, is fused to MLL in acute myeloid leukemia containing the t(10;11)(q22;q23). Leukemia 17: 637-641.
-
(2003)
Leukemia
, vol.17
, pp. 637-641
-
-
Lorsbach, R.B.1
Moore, J.2
Mathew, S.3
Raimondi, S.C.4
Mukatira, S.T.5
Downing, J.R.6
-
44
-
-
0031729221
-
Near-haploid common acute lymphoblastic leukaemia of childhood with a second hyperdiploid line: a DNA ploidy and fluorescence in-situ hybridization study
-
Ma SK, Chan GC, Wan TS, Lam CK, Ha SY, Lau YL, Chan LC. 1998. Near-haploid common acute lymphoblastic leukaemia of childhood with a second hyperdiploid line: a DNA ploidy and fluorescence in-situ hybridization study. Br J Haematol 103: 750-755.
-
(1998)
Br J Haematol
, vol.103
, pp. 750-755
-
-
Ma, S.K.1
Chan, G.C.2
Wan, T.S.3
Lam, C.K.4
Ha, S.Y.5
Lau, Y.L.6
Chan, L.C.7
-
45
-
-
76249101323
-
PML-RARalpha/RXR alters the epigenetic landscape in acute promyelocytic leukemia
-
Martens JH, Brinkman AB, Simmer F, Francoijs KJ, Nebbioso A, Ferrara F, Altucci L, Stunnenberg HG. 2010. PML-RARalpha/RXR alters the epigenetic landscape in acute promyelocytic leukemia. Cancer Cell 17: 173-185.
-
(2010)
Cancer Cell
, vol.17
, pp. 173-185
-
-
Martens, J.H.1
Brinkman, A.B.2
Simmer, F.3
Francoijs, K.J.4
Nebbioso, A.5
Ferrara, F.6
Altucci, L.7
Stunnenberg, H.G.8
-
46
-
-
0031581073
-
A novel ligand for an SH3 domain of the adaptor protein Nck bears an SH2 domain and nuclear signaling motifs
-
Matuoka K, Miki H, Takahashi K, Takenawa T. 1997. A novel ligand for an SH3 domain of the adaptor protein Nck bears an SH2 domain and nuclear signaling motifs. Biochem Biophys Res Commun 239: 488-492.
-
(1997)
Biochem Biophys Res Commun
, vol.239
, pp. 488-492
-
-
Matuoka, K.1
Miki, H.2
Takahashi, K.3
Takenawa, T.4
-
47
-
-
28444495985
-
Identification of novel argonaute-associated proteins
-
Meister G, Landthaler M, Peters L, Chen PY, Urlaub H, Luhrmann R, Tuschl T. 2005. Identification of novel argonaute-associated proteins. Curr Biol 15: 2149-2155.
-
(2005)
Curr Biol
, vol.15
, pp. 2149-2155
-
-
Meister, G.1
Landthaler, M.2
Peters, L.3
Chen, P.Y.4
Urlaub, H.5
Luhrmann, R.6
Tuschl, T.7
-
48
-
-
84876451223
-
-
Mitelman database of chromosome aberrations and fusion genes in cancer. Available at:
-
Mitelman F, Johansson B, Mertens F. 2013. Mitelman database of chromosome aberrations and fusion genes in cancer. Available at: http:/cgap.nci.nih.gov/Chromosomes/Mitelman.
-
(2013)
-
-
Mitelman, F.1
Johansson, B.2
Mertens, F.3
-
49
-
-
84868664680
-
A central role for long non-coding RNA in cancer
-
Mitra SA, Mitra AP, Triche TJ. 2012. A central role for long non-coding RNA in cancer. Front Genet 3: 17.
-
(2012)
Front Genet
, vol.3
, pp. 17
-
-
Mitra, S.A.1
Mitra, A.P.2
Triche, T.J.3
-
50
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan CG, Goorha S, Radtke I, Miller CB, Coustan-Smith E, Dalton JD, Girtman K, Mathew S, Ma J, Pounds SB, Su X, Pui CH, Relling MV, Evans WE, Shurtleff SA, Downing JR. 2007. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature 446: 758-764.
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, S.2
Radtke, I.3
Miller, C.B.4
Coustan-Smith, E.5
Dalton, J.D.6
Girtman, K.7
Mathew, S.8
Ma, J.9
Pounds, S.B.10
Su, X.11
Pui, C.H.12
Relling, M.V.13
Evans, W.E.14
Shurtleff, S.A.15
Downing, J.R.16
-
51
-
-
0033973587
-
Active repression of methylated genes by the chromosomal protein MBD1
-
Ng HH, Jeppesen P, Bird A. 2000. Active repression of methylated genes by the chromosomal protein MBD1. Mol Cell Biol 20: 1394-1406.
-
(2000)
Mol Cell Biol
, vol.20
, pp. 1394-1406
-
-
Ng, H.H.1
Jeppesen, P.2
Bird, A.3
-
52
-
-
0026755913
-
Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia
-
Onodera N, McCabe NR, Nachman JB, Johnson FL, Le Beau MM, Rowley JD, Rubin CM. 1992a. Hyperdiploidy arising from near-haploidy in childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer 4: 331-336.
-
(1992)
Genes Chromosomes Cancer
, vol.4
, pp. 331-336
-
-
Onodera, N.1
McCabe, N.R.2
Nachman, J.B.3
Johnson, F.L.4
Le Beau, M.M.5
Rowley, J.D.6
Rubin, C.M.7
-
53
-
-
0026748638
-
Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia
-
Onodera N, McCabe NR, Rubin CM. 1992b. Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia. Blood 80: 203-208.
-
(1992)
Blood
, vol.80
, pp. 203-208
-
-
Onodera, N.1
McCabe, N.R.2
Rubin, C.M.3
-
54
-
-
0017659027
-
Chromosomes and causation of human cancer and leukemia. XXIII. Near-haploidy in acute leukemia
-
Oshimura M, Freeman AI, Sandberg AA. 1977. Chromosomes and causation of human cancer and leukemia. XXIII. Near-haploidy in acute leukemia. Cancer 40: 1143-1148.
-
(1977)
Cancer
, vol.40
, pp. 1143-1148
-
-
Oshimura, M.1
Freeman, A.I.2
Sandberg, A.A.3
-
55
-
-
0141992996
-
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Panagopoulos I, Knuutila S, Jee KJ, Garwicz S, Fioretos T, Mitelman F, Johansson B. 2003. Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia. Blood 102: 3010-3015.
-
(2003)
Blood
, vol.102
, pp. 3010-3015
-
-
Paulsson, K.1
Panagopoulos, I.2
Knuutila, S.3
Jee, K.J.4
Garwicz, S.5
Fioretos, T.6
Mitelman, F.7
Johansson, B.8
-
56
-
-
24944520140
-
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Morse H, Fioretos T, Behrendtz M, Strombeck B, Johansson B. 2005. Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer 44: 113-122.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 113-122
-
-
Paulsson, K.1
Morse, H.2
Fioretos, T.3
Behrendtz, M.4
Strombeck, B.5
Johansson, B.6
-
57
-
-
78650745577
-
Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Forestier E, Lilljebjorn H, Heldrup J, Behrendtz M, Young BD, Johansson B. 2010. Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia. Proc Natl Acad Sci USA 107: 21719-21724.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 21719-21724
-
-
Paulsson, K.1
Forestier, E.2
Lilljebjorn, H.3
Heldrup, J.4
Behrendtz, M.5
Young, B.D.6
Johansson, B.7
-
58
-
-
0025234883
-
Clinical presentation, karyotypic characterization, and treatment outcome of childhood acute lymphoblastic leukemia with a near-haploid or hypodiploid less than 45 line
-
Pui CH, Carroll AJ, Raimondi SC, Land VJ, Crist WM, Shuster JJ, Williams DL, Pullen DJ, Borowitz MJ, Behm FG, Look AT. 1990. Clinical presentation, karyotypic characterization, and treatment outcome of childhood acute lymphoblastic leukemia with a near-haploid or hypodiploid less than 45 line. Blood 75: 1170-1177.
-
(1990)
Blood
, vol.75
, pp. 1170-1177
-
-
Pui, C.H.1
Carroll, A.J.2
Raimondi, S.C.3
Land, V.J.4
Crist, W.M.5
Shuster, J.J.6
Williams, D.L.7
Pullen, D.J.8
Borowitz, M.J.9
Behm, F.G.10
Look, A.T.11
-
59
-
-
0023260072
-
Hypodiploidy is associated with a poor prognosis in childhood acute lymphoblastic leukemia
-
Pui CH, Williams DL, Raimondi SC, Rivera GK, Look AT, Dodge RK, George SL, Behm FG, Crist WM, Murphy SB. 1987. Hypodiploidy is associated with a poor prognosis in childhood acute lymphoblastic leukemia. Blood 70: 247-253.
-
(1987)
Blood
, vol.70
, pp. 247-253
-
-
Pui, C.H.1
Williams, D.L.2
Raimondi, S.C.3
Rivera, G.K.4
Look, A.T.5
Dodge, R.K.6
George, S.L.7
Behm, F.G.8
Crist, W.M.9
Murphy, S.B.10
-
60
-
-
0345529967
-
Reassessment of the prognostic significance of hypodiploidy in pediatric patients with acute lymphoblastic leukemia
-
Raimondi SC, Zhou Y, Mathew S, Shurtleff SA, Sandlund JT, Rivera GK, Behm FG, Pui CH. 2003. Reassessment of the prognostic significance of hypodiploidy in pediatric patients with acute lymphoblastic leukemia. Cancer 98: 2715-2722.
-
(2003)
Cancer
, vol.98
, pp. 2715-2722
-
-
Raimondi, S.C.1
Zhou, Y.2
Mathew, S.3
Shurtleff, S.A.4
Sandlund, J.T.5
Rivera, G.K.6
Behm, F.G.7
Pui, C.H.8
-
62
-
-
0035057686
-
Tumorigenesis in neurofibromatosis: New insights and potential therapies
-
Reed N, Gutmann DH. 2001. Tumorigenesis in neurofibromatosis: New insights and potential therapies. Trends Mol Med 7: 157-162.
-
(2001)
Trends Mol Med
, vol.7
, pp. 157-162
-
-
Reed, N.1
Gutmann, D.H.2
-
63
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Rozen S, Skaletsky H. 2000. Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 132: 365-386.
-
(2000)
Methods Mol Biol
, vol.132
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
-
64
-
-
84873566348
-
Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia
-
Safavi S, Forestier E, Golovleva I, Barbany G, Nord KH, Moorman AV, Harrison CJ, Johansson B, Paulsson K. 2012. Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia. Leukemia 27: 248-250.
-
(2012)
Leukemia
, vol.27
, pp. 248-250
-
-
Safavi, S.1
Forestier, E.2
Golovleva, I.3
Barbany, G.4
Nord, K.H.5
Moorman, A.V.6
Harrison, C.J.7
Johansson, B.8
Paulsson, K.9
-
65
-
-
84856758666
-
MicroRNAs in acute leukemia: From biological players to clinical contributors
-
Schotte D, Pieters R, Den Boer ML. 2012. MicroRNAs in acute leukemia: From biological players to clinical contributors. Leukemia 26: 1-12.
-
(2012)
Leukemia
, vol.26
, pp. 1-12
-
-
Schotte, D.1
Pieters, R.2
Den Boer, M.L.3
-
67
-
-
0034142337
-
Adaptor proteins CRK and CRKL associate with the serine/threonine protein kinase GCKR promoting GCKR and SAPK activation
-
Shi CS, Tuscano J, Kehrl JH. 2000. Adaptor proteins CRK and CRKL associate with the serine/threonine protein kinase GCKR promoting GCKR and SAPK activation. Blood 95: 776-782.
-
(2000)
Blood
, vol.95
, pp. 776-782
-
-
Shi, C.S.1
Tuscano, J.2
Kehrl, J.H.3
-
68
-
-
33751100684
-
RNPC1, an RNA-binding protein and a target of the p53 family, is required for maintaining the stability of the basal and stress-induced p21 transcript
-
Shu L, Yan W, Chen X. 2006. RNPC1, an RNA-binding protein and a target of the p53 family, is required for maintaining the stability of the basal and stress-induced p21 transcript. Genes Dev 20: 2961-2972.
-
(2006)
Genes Dev
, vol.20
, pp. 2961-2972
-
-
Shu, L.1
Yan, W.2
Chen, X.3
-
69
-
-
66349083341
-
A geometric approach for classification and comparison of structural variants
-
Sindi S, Helman E, Bashir A, Raphael BJ. 2009. A geometric approach for classification and comparison of structural variants. Bioinformatics 25: i222-230.
-
(2009)
Bioinformatics
, vol.25
-
-
Sindi, S.1
Helman, E.2
Bashir, A.3
Raphael, B.J.4
-
70
-
-
19944431331
-
Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway
-
Soulier J, Leblanc T, Larghero J, Dastot H, Shimamura A, Guardiola P, Esperou H, Ferry C, Jubert C, Feugeas JP, Henri A, Toubert A, Socie G, Baruchel A, Sigaux F, D'Andrea AD, Gluckman E. 2005. Detection of somatic mosaicism and classification of Fanconi anemia patients by analysis of the FA/BRCA pathway. Blood 105: 1329-1336.
-
(2005)
Blood
, vol.105
, pp. 1329-1336
-
-
Soulier, J.1
Leblanc, T.2
Larghero, J.3
Dastot, H.4
Shimamura, A.5
Guardiola, P.6
Esperou, H.7
Ferry, C.8
Jubert, C.9
Feugeas, J.P.10
Henri, A.11
Toubert, A.12
Socie, G.13
Baruchel, A.14
Sigaux, F.15
D'Andrea, A.D.16
Gluckman, E.17
-
71
-
-
0035878530
-
Near haploid childhood acute lymphoblastic leukemia masked by hyperdiploid line: Detection by fluorescence in situ hybridization
-
Stark B, Jeison M, Gobuzov R, Krug H, Glaser-Gabay L, Luria D, El-Hasid R, Harush MB, Avrahami G, Fisher S, Stein J, Zaizov R, Yaniv I. 2001. Near haploid childhood acute lymphoblastic leukemia masked by hyperdiploid line: Detection by fluorescence in situ hybridization. Cancer Genet Cytogenet 128: 108-113.
-
(2001)
Cancer Genet Cytogenet
, vol.128
, pp. 108-113
-
-
Stark, B.1
Jeison, M.2
Gobuzov, R.3
Krug, H.4
Glaser-Gabay, L.5
Luria, D.6
El-Hasid, R.7
Harush, M.B.8
Avrahami, G.9
Fisher, S.10
Stein, J.11
Zaizov, R.12
Yaniv, I.13
-
73
-
-
84865706330
-
CCR10 and its ligands in regulation of epithelial immunity and diseases
-
Xiong N, Fu Y, Hu S, Xia M, Yang J. 2012. CCR10 and its ligands in regulation of epithelial immunity and diseases. Protein Cell 3: 571-580.
-
(2012)
Protein Cell
, vol.3
, pp. 571-580
-
-
Xiong, N.1
Fu, Y.2
Hu, S.3
Xia, M.4
Yang, J.5
-
74
-
-
77953096072
-
Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a
-
Yap KL, Li S, Munoz-Cabello AM, Raguz S, Zeng L, Mujtaba S, Gil J, Walsh MJ, Zhou MM. 2010. Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a. Mol Cell 38: 662-674.
-
(2010)
Mol Cell
, vol.38
, pp. 662-674
-
-
Yap, K.L.1
Li, S.2
Munoz-Cabello, A.M.3
Raguz, S.4
Zeng, L.5
Mujtaba, S.6
Gil, J.7
Walsh, M.J.8
Zhou, M.M.9
-
75
-
-
16844364661
-
A second human Dbf4/ASK-related protein, Drf1/ASKL1, is required for efficient progression of S and M phases
-
Yoshizawa-Sugata N, Ishii A, Taniyama C, Matsui E, Arai K, Masai H. 2005. A second human Dbf4/ASK-related protein, Drf1/ASKL1, is required for efficient progression of S and M phases. J Biol Chem 280: 13062-13070.
-
(2005)
J Biol Chem
, vol.280
, pp. 13062-13070
-
-
Yoshizawa-Sugata, N.1
Ishii, A.2
Taniyama, C.3
Matsui, E.4
Arai, K.5
Masai, H.6
-
76
-
-
33751527925
-
Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome
-
Zhang J, Feuk L, Duggan GE, Khaja R, Scherer SW. 2006. Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome. Cytogenet Genome Res 115: 205-214.
-
(2006)
Cytogenet Genome Res
, vol.115
, pp. 205-214
-
-
Zhang, J.1
Feuk, L.2
Duggan, G.E.3
Khaja, R.4
Scherer, S.W.5
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