-
1
-
-
33846515640
-
Myelodysplastic syndromes: The complexity of stem-cell diseases
-
DOI 10.1038/nrc2047, PII NRC2047
-
Corey, S. J. et al. Myelodysplastic syndromes: the complexity of stem-cell diseases. Nature Rev. Cancer 7, 118-129 (2007). (Pubitemid 46164747)
-
(2007)
Nature Reviews Cancer
, vol.7
, Issue.2
, pp. 118-129
-
-
Corey, S.J.1
Minden, M.D.2
Barber, D.L.3
Kantarjian, H.4
Wang, J.C.Y.5
Schimmer, A.D.6
-
2
-
-
34247172535
-
Myelodysplastic syndromes: Incidence and survival in the United States
-
DOI 10.1002/cncr.22570
-
Ma, X., Does, M., Raza, A.&Mayne, S. T.Myelodysplastic syndromes: incidence and survival in the United States. Cancer 109, 1536-1542 (2007). (Pubitemid 46595689)
-
(2007)
Cancer
, vol.109
, Issue.8
, pp. 1536-1542
-
-
Ma, X.1
Does, M.2
Raza, A.3
Mayne, S.T.4
-
3
-
-
79952164235
-
Unraveling the molecular pathophysiology of myelodysplastic syndromes
-
Bejar, R., Levine, R. & Ebert, B. L. Unraveling the molecular pathophysiology of myelodysplastic syndromes. J. Clin. Oncol. 29, 504-515 (2011).
-
(2011)
J. Clin. Oncol.
, vol.29
, pp. 504-515
-
-
Bejar, R.1
Levine, R.2
Ebert, B.L.3
-
4
-
-
68949124841
-
Gain-of-function ofmutated C-CBLtumour suppressor inmyeloid neoplasms
-
Sanada, M. et al.Gain-of-function ofmutated C-CBLtumour suppressor inmyeloid neoplasms. Nature 460, 904-908 (2009).
-
(2009)
Nature
, vol.460
, pp. 904-908
-
-
Sanada, M.1
-
5
-
-
44349191457
-
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
-
DOI 10.1038/ng.128, PII NG128
-
Campbell, P. J. et al. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nature Genet. 40, 722-729 (2008). (Pubitemid 351748860)
-
(2008)
Nature Genetics
, vol.40
, Issue.6
, pp. 722-729
-
-
Campbell, P.J.1
Stephens, P.J.2
Pleasance, E.D.3
O'Meara, S.4
Li, H.5
Santarius, T.6
Stebbings, L.A.7
Leroy, C.8
Edkins, S.9
Hardy, C.10
Teague, J.W.11
Menzies, A.12
Goodhead, I.13
Turner, D.J.14
Clee, C.M.15
Quail, M.A.16
Cox, A.17
Brown, C.18
Durbin, R.19
Hurles, M.E.20
Edwards, P.A.W.21
Bignell, G.R.22
Stratton, M.R.23
Futreal, P.A.24
more..
-
6
-
-
79951494668
-
Initial genomesequencingandanalysis ofmultiplemyeloma
-
Chapman, M.A. et al. Initial genomesequencingandanalysis ofmultiplemyeloma. Nature 471, 467-472 (2011).
-
(2011)
Nature
, vol.471
, pp. 467-472
-
-
Chapman, M.A.1
-
7
-
-
77953006634
-
Themutation spectrumrevealed by paired genomesequences froma lung cancer patient
-
Lee, W. et al. Themutation spectrumrevealed by paired genomesequences froma lung cancer patient. Nature 465, 473-477 (2010).
-
(2010)
Nature
, vol.465
, pp. 473-477
-
-
Lee, W.1
-
8
-
-
55549101623
-
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
-
Ley, T. J. et al. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature 456, 66-72 (2008).
-
(2008)
Nature
, vol.456
, pp. 66-72
-
-
Ley, T.J.1
-
9
-
-
72849144434
-
Sequencing technologies - The next generation
-
Metzker, M. L. Sequencing technologies-the next generation. Nature Rev. Genet. 11, 31-46 (2010).
-
(2010)
Nature Rev. Genet.
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
10
-
-
53649106195
-
Next-generation DNA sequencing
-
Shendure, J. & Ji, H. Next-generation DNA sequencing. Nature Biotechnol. 26, 1135-1145 (2008).
-
(2008)
Nature Biotechnol.
, vol.26
, pp. 1135-1145
-
-
Shendure, J.1
Ji, H.2
-
11
-
-
70349969478
-
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
-
Shah, S. P. et al. Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution. Nature 461, 809-813 (2009).
-
(2009)
Nature
, vol.461
, pp. 809-813
-
-
Shah, S.P.1
-
12
-
-
79251635938
-
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma
-
Varela, I. et al. Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma. Nature 469, 539-542 (2011).
-
(2011)
Nature
, vol.469
, pp. 539-542
-
-
Varela, I.1
-
13
-
-
78649906060
-
DNMT3A mutations in acute myeloid leukemia
-
Ley, T. J. et al. DNMT3A mutations in acute myeloid leukemia. N. Engl. J. Med. 363, 2424-2433 (2010).
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 2424-2433
-
-
Ley, T.J.1
-
14
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis, E. R. et al. Recurring mutations found by sequencing an acute myeloid leukemia genome. N. Engl. J. Med. 361, 1058-1066 (2009).
-
(2009)
N. Engl. J. Med.
, vol.361
, pp. 1058-1066
-
-
Mardis, E.R.1
-
15
-
-
79953176952
-
Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia
-
Yan, X. J. et al. Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia. Nature Genet. 43, 309-315 (2011).
-
(2011)
Nature Genet.
, vol.43
, pp. 309-315
-
-
Yan, X.J.1
-
16
-
-
79960036578
-
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
-
Puente, X. S. et al. Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia. Nature 475, 101-105 (2011).
-
(2011)
Nature
, vol.475
, pp. 101-105
-
-
Puente, X.S.1
-
17
-
-
22244453416
-
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
-
DOI 10.1158/0008-5472.CAN-05-0465
-
Nannya, Y. et al. A robust algorithmfor copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res. 65, 6071-6079 (2005). (Pubitemid 40994391)
-
(2005)
Cancer Research
, vol.65
, Issue.14
, pp. 6071-6079
-
-
Nannya, Y.1
Sanada, M.2
Nakazaki, K.3
Hosoya, N.4
Wang, L.5
Hangaishi, A.6
Kurokawa, M.7
Chiba, S.8
Bailey, D.K.9
Kennedy, G.C.10
Ogawa, S.11
-
18
-
-
34347229790
-
Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide- polymorphism genotyping microarrays
-
DOI 10.1086/518809
-
Yamamoto, G. et al. Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of Affymetrix singlenucleotide-polymorphism genotyping microarrays. Am. J. Hum. Genet. 81, 114-126 (2007). (Pubitemid 47001161)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.1
, pp. 114-126
-
-
Yamamoto, G.1
Nannya, Y.2
Kato, M.3
Sanada, M.4
Levine, R.L.5
Kawamata, N.6
Hangaishi, A.7
Kurokawa, M.8
Chiba, S.9
Gilliland, D.G.10
Koeffler, H.P.11
Ogawa, S.12
-
19
-
-
60349104299
-
The spliceosome: Design principles of a dynamic RNP machine
-
Wahl, M. C., Will, C. L. & Luhrmann, R. The spliceosome: design principles of a dynamic RNP machine. Cell 136, 701-718 (2009).
-
(2009)
Cell
, vol.136
, pp. 701-718
-
-
Wahl, M.C.1
Will, C.L.2
Luhrmann, R.3
-
20
-
-
0039769985
-
65 and SR proteins in splicing of pre-mRNA
-
DOI 10.1038/41137
-
Tronchère, H., Wang, J. & Fu, X. D. A protein related to splicing factor U2AF35 that interacts with U2AF65 and SR proteins in splicing of pre-mRNA. Nature 388, 397-400 (1997). (Pubitemid 27334821)
-
(1997)
Nature
, vol.388
, Issue.6640
, pp. 397-400
-
-
Tronchere, H.1
Wang, J.2
Fu, X.-D.3
-
21
-
-
78650825589
-
A population-specific HTR2B stop codon predisposes to severe impulsivity
-
Bevilacqua, L. et al. A population-specific HTR2B stop codon predisposes to severe impulsivity. Nature 468, 1061-1066 (2010).
-
(2010)
Nature
, vol.468
, pp. 1061-1066
-
-
Bevilacqua, L.1
-
22
-
-
77957606541
-
High-throughput,pooledsequencingidentifiesmutations inNUBPL and FOXRED1 in human complex i deficiency
-
Calvo,S.E. et al. High-throughput,pooledsequencingidentifiesmutations inNUBPL and FOXRED1 in human complex I deficiency. Nature Genet. 42, 851-858 (2010).
-
(2010)
Nature Genet.
, vol.42
, pp. 851-858
-
-
Calvos, E.1
-
23
-
-
39649094569
-
New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: Evidence from a core dataset of 2124 patients
-
DOI 10.1182/blood-2007-03-082404
-
Haase, D. et al. New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients. Blood 110, 4385-4395 (2007). (Pubitemid 351377805)
-
(2007)
Blood
, vol.110
, Issue.13
, pp. 4385-4395
-
-
Haase, D.1
Germing, U.2
Schanz, J.3
Pfeilstocker, M.4
Nosslinger, T.5
Hildebrandt, B.6
Kundgen, A.7
Lubbert, M.8
Kunzmann, R.9
Giagounidis, A.A.N.10
Aul, C.11
Trumper, L.12
Krieger, O.13
Stauder, R.14
Muller, T.H.15
Wimazal, F.16
Valent, P.17
Fonatsch, C.18
Steidl, C.19
-
24
-
-
34547190674
-
Splicing regulator SC35 is essential for genomic stability and cell proliferation during mammalian organogenesis
-
DOI 10.1128/MCB.00288-07
-
Xiao, R. et al. Splicing regulator SC35 is essential for genomic stability and cell proliferation during mammalian organogenesis. Mol. Cell. Biol. 27, 5393-5402 (2007). (Pubitemid 47124393)
-
(2007)
Molecular and Cellular Biology
, vol.27
, Issue.15
, pp. 5393-5402
-
-
Xiao, R.1
Sun, Y.2
Ding, J.-H.3
Lin, S.4
Rose, D.W.5
Rosenfeld, M.G.6
Fu, X.-D.7
Li, X.8
-
25
-
-
75749124332
-
Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin
-
Morin, R. D. et al. Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin. Nature Genet. 42, 181-185 (2010).
-
(2010)
Nature Genet.
, vol.42
, pp. 181-185
-
-
Morin, R.D.1
-
26
-
-
27344435774
-
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
-
DOI 10.1073/pnas.0506580102
-
Subramanian, A. et al. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl Acad. Sci. USA 102, 15545-15550 (2005). (Pubitemid 41528093)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.43
, pp. 15545-15550
-
-
Subramanian, A.1
Tamayo, P.2
Mootha, V.K.3
Mukherjee, S.4
Ebert, B.L.5
Gillette, M.A.6
Paulovich, A.7
Pomeroy, S.L.8
Golub, T.R.9
Lander, E.S.10
Mesirov, J.P.11
-
27
-
-
0742323558
-
Nonsense-mediated mRNA decay: Splicing, translation and mRNP dynamics
-
DOI 10.1038/nrm1310
-
Maquat, L. E. Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics. Nature Rev. Mol. Cell Biol. 5, 89-99 (2004). (Pubitemid 38160252)
-
(2004)
Nature Reviews Molecular Cell Biology
, vol.5
, Issue.2
, pp. 89-99
-
-
Maquat, L.E.1
-
28
-
-
34548414281
-
Adult mouse hematopoietic stem cells: Purification and single-cell assays
-
Ema, H. et al. Adult mouse hematopoietic stem cells: purification and single-cell assays. Nature Protocols 1, 2979-2987 (2007).
-
(2007)
Nature Protocols
, vol.1
, pp. 2979-2987
-
-
Ema, H.1
-
29
-
-
70350569286
-
Mechanisms of alternative splicing regulation: Insights frommolecular and genomics approaches
-
Chen, M. & Manley, J. L. Mechanisms of alternative splicing regulation: insights frommolecular and genomics approaches. Nature Rev. Mol. Cell Biol. 10, 741-754 (2009).
-
(2009)
Nature Rev. Mol. Cell Biol.
, vol.10
, pp. 741-754
-
-
Chen, M.1
Manley, J.L.2
-
30
-
-
33947305594
-
Ultraconserved elements are associated with homeostatic control of splicing regulators by alternative splicing and nonsense-mediated decay
-
DOI 10.1101/gad.1525507
-
Ni, J. Z. et al. Ultraconserved elements are associated with homeostatic control of splicing regulators by alternative splicing and nonsense-mediated decay. Genes Dev. 21, 708-718 (2007). (Pubitemid 46440292)
-
(2007)
Genes and Development
, vol.21
, Issue.6
, pp. 708-718
-
-
Ni, J.Z.1
Grate, L.2
Donohue, J.P.3
Preston, C.4
Nobida, N.5
O'Brien, G.6
Shiue, L.7
Clark, T.A.8
Blume, J.E.9
Ares Jr., M.10
-
31
-
-
79953824569
-
Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD i
-
He, H. et al. Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD I. Science 332, 238-240 (2011).
-
(2011)
Science
, vol.332
, pp. 238-240
-
-
He, H.1
-
32
-
-
79953819024
-
Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA
-
Edery, P. et al. Association of TALS developmental disorder with defect in minor splicing component U4atac snRNA. Science 332, 240-243 (2011).
-
(2011)
Science
, vol.332
, pp. 240-243
-
-
Edery, P.1
-
33
-
-
78049416081
-
Alternative pre-mRNA splicing regulation in cancer: Pathways and programs unhinged
-
David, C. J. & Manley, J. L. Alternative pre-mRNA splicing regulation in cancer: pathways and programs unhinged. Genes Dev. 24, 2343-2364 (2010).
-
(2010)
Genes Dev.
, vol.24
, pp. 2343-2364
-
-
David, C.J.1
Manley, J.L.2
-
34
-
-
33947541694
-
Alternative splicing: An emerging topic in molecular and clinical oncology
-
DOI 10.1016/S1470-2045(07)70104-3, PII S1470204507701043
-
Pajares, M. J. et al. Alternative splicing: an emerging topic inmolecular and clinical oncology. Lancet Oncol. 8, 349-357 (2007). (Pubitemid 46464532)
-
(2007)
Lancet Oncology
, vol.8
, Issue.4
, pp. 349-357
-
-
Pajares, M.J.1
Ezponda, T.2
Catena, R.3
Calvo, A.4
Pio, R.5
Montuenga, L.M.6
-
35
-
-
78049446517
-
The U2AF35-related protein Urp contacts the 39 splice site to promoteU12-type intron splicing andthe secondstep of U2-type intron splicing
-
Shen, H., Zheng, X., Luecke, S. & Green, M. R. The U2AF35-related protein Urp contacts the 39 splice site to promoteU12-type intron splicing andthe secondstep of U2-type intron splicing. Genes Dev. 24, 2389-2394 (2010).
-
(2010)
Genes Dev.
, vol.24
, pp. 2389-2394
-
-
Shen, H.1
Zheng, X.2
Luecke, S.3
Green, M.R.4
-
36
-
-
73849128091
-
A p53-dependent mechanismunderlies macrocytic anemia in a mouse model of human 5q2 syndrome
-
Barlow, J. L. et al. A p53-dependent mechanismunderlies macrocytic anemia in a mouse model of human 5q2 syndrome. Nature Med. 16, 59-66 (2010).
-
(2010)
Nature Med.
, vol.16
, pp. 59-66
-
-
Barlow, J.L.1
-
37
-
-
38349088899
-
Identification of RPS14 as a 5q2 syndrome gene by RNA interference screen
-
Ebert, B. L. et al. Identification of RPS14 as a 5q2 syndrome gene by RNA interference screen. Nature 451, 335-339 (2008).
-
(2008)
Nature
, vol.451
, pp. 335-339
-
-
Ebert, B.L.1
|