-
1
-
-
84865572873
-
Treatment and outcome of Wilms' tumour patients: An analysis of all cases registered in the UKW3 trial
-
Pritchard-Jones, K. et al. Treatment and outcome of Wilms' tumour patients: an analysis of all cases registered in the UKW3 trial. Ann. Oncol. 23, 2457-2463 (2012).
-
(2012)
Ann. Oncol.
, vol.23
, pp. 2457-2463
-
-
Pritchard-Jones, K.1
-
2
-
-
33749266701
-
Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour
-
DOI 10.1136/jmg.2006.041723
-
Scott, R. H., Stiller, C. A., Walker, L. & Rahman, N. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J. Med. Genet. 43, 705-715 (2006). (Pubitemid 44483912)
-
(2006)
Journal of Medical Genetics
, vol.43
, Issue.9
, pp. 705-715
-
-
Scott, R.H.1
Stiller, C.A.2
Walker, L.3
Rahman, N.4
-
3
-
-
0030017174
-
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12- q21
-
DOI 10.1038/ng0896-461
-
Rahman, N. et al. Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21. Nat. Genet. 13, 461-463 (1996). (Pubitemid 26256621)
-
(1996)
Nature Genetics
, vol.13
, Issue.4
, pp. 461-463
-
-
Rahman, N.1
Arbour, L.2
Tonin, P.3
Renshaw, J.4
Pelletier, J.5
Baruchel, S.6
Pritchard-Jones, K.7
Stratton, M.R.8
Narod, S.A.9
-
4
-
-
0032053822
-
Linkage of familial Wilms' tumor predisposition to two-locus model for the etiology of familial tumors
-
McDonald, J. M. et al. Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors. Cancer Res. 58, 1387-1390 (1998). (Pubitemid 28193596)
-
(1998)
Cancer Research
, vol.58
, Issue.7
, pp. 1387-1390
-
-
McDonald, J.M.1
Douglass, E.C.2
Fisher, R.3
Geiser, C.F.4
Krill, C.E.5
Strong, L.C.6
Virshup, D.7
Huff, V.8
-
5
-
-
0034131510
-
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2
-
Rapley, E. A. et al. Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2. Br. J. Cancer 83, 177-183 (2000). (Pubitemid 30411714)
-
(2000)
British Journal of Cancer
, vol.83
, Issue.2
, pp. 177-183
-
-
Rapley, E.A.1
Barfoot, R.2
Bonaiti-Pellie, C.3
Chompret, A.4
Foulkes, W.5
Perusinghe, N.6
Reeve, A.7
Royer-Pokora, B.8
Schumacher, V.9
Shelling, A.10
Skeen, J.11
De Tourreil, S.12
Weirich, A.13
Pritchard-Jones, K.14
Stratton, M.R.15
Rahman, N.16
-
6
-
-
84872621246
-
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
-
Ruark, E. et al. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer. Nature 493, 406-410 (2013).
-
(2013)
Nature
, vol.493
, pp. 406-410
-
-
Ruark, E.1
-
7
-
-
77953277032
-
The Paf1 complex: Platform or player in RNA polymerase II transcription? Biochim
-
Jaehning, J. A. The Paf1 complex: platform or player in RNA polymerase II transcription? Biochim. Biophys. Acta 1799, 379-388 (2010).
-
(2010)
Biophys. Acta
, vol.1799
, pp. 379-388
-
-
Jaehning, J.A.1
-
8
-
-
84875056702
-
The many roles of the conserved eukaryotic Paf1 complex in regulating transcription, histone modifications, and disease states
-
Tomson, B. N. & Arndt, K. M. The many roles of the conserved eukaryotic Paf1 complex in regulating transcription, histone modifications, and disease states. Biochim. Biophys. Acta 1829, 116-126 (2013).
-
(1829)
Biochim. Biophys. Acta
, pp. 116-126
-
-
Tomson, B.N.1
Arndt, K.M.2
-
9
-
-
80052491229
-
Versatile TPR domains accommodate different modes of target protein recognition and function
-
Allan, R. K. & Ratajczak, T. Versatile TPR domains accommodate different modes of target protein recognition and function. Cell Stress Chaperones 16, 353-367 (2011).
-
(2011)
Cell Stress Chaperones
, vol.16
, pp. 353-367
-
-
Allan, R.K.1
Ratajczak, T.2
-
10
-
-
0036123253
-
Ctr9, Rtf1, and Leo1 are components of the Paf1/RNA polymerase II complex
-
DOI 10.1128/MCB.22.7.1971-1980.2002
-
Mueller, C. L. & Jaehning, J. A. Ctr9, Rtf1, and Leo1 are components of the Paf1/RNA polymerase II complex. Mol. Cell. Biol. 22, 1971-1980 (2002). (Pubitemid 34224606)
-
(2002)
Molecular and Cellular Biology
, vol.22
, Issue.7
, pp. 1971-1980
-
-
Mueller, C.L.1
Jaehning, J.A.2
-
11
-
-
35548950642
-
Paf1 complex homologues are required for Notch-regulated transcription during somite segmentation
-
DOI 10.1038/sj.embor.7401045, PII 7401045
-
Akanuma, T., Koshida, S., Kawamura, A., Kishimoto, Y. & Takada, S. Paf1 complex homologues are required for Notch-regulated transcription during somite segmentation. EMBO Rep. 8, 858-863 (2007). (Pubitemid 350001430)
-
(2007)
EMBO Reports
, vol.8
, Issue.9
, pp. 858-863
-
-
Akanuma, T.1
Koshida, S.2
Kawamura, A.3
Kishimoto, Y.4
Takada, S.5
-
12
-
-
65349123354
-
A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity
-
Ding, L. et al. A genome-scale RNAi screen for Oct4 modulators defines a role of the Paf1 complex for embryonic stem cell identity. Cell Stem Cell 4, 403-415 (2009).
-
(2009)
Cell Stem Cell
, vol.4
, pp. 403-415
-
-
Ding, L.1
-
13
-
-
18744385803
-
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
-
DOI 10.1038/ng1048
-
Carpten, J. D. et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat. Genet. 32, 676-680 (2002). (Pubitemid 35435184)
-
(2002)
Nature Genetics
, vol.32
, Issue.4
, pp. 676-680
-
-
Carpten, J.D.1
Robbins, C.M.2
Villablanca, A.3
Forsberg, L.4
Presciuttini, S.5
Bailey-Wilsons, J.6
Simonds, W.F.7
Gillanders, E.M.8
Kennedy, A.M.9
Chen, J.D.10
Agarwal, S.K.11
Sood, R.12
Jones, M.P.13
Moses, T.Y.14
Haven, C.15
Petillo, D.16
Leotlela, P.D.17
Harding, B.18
Cameron, D.19
Pannett, A.A.20
Hoog, A.21
Heath III, H.22
James-Newton, L.A.23
Robinson, B.24
Zarbo, R.J.25
Cavaco, B.M.26
Wassif, W.27
Perrier, N.D.28
Rosen, I.B.29
Kristoffersson, U.30
Turnpenny, P.D.31
Farnebo, L.-O.32
Besser, G.M.33
Jackson, C.E.34
Morreau, H.35
Trent, J.M.36
Thakker, R.V.37
Marx, S.J.38
Teh, B.T.39
Larsson, C.40
Hobbs, M.R.41
more..
-
14
-
-
84855843599
-
-
University of Washington updated 2012
-
Rich, T. A. GeneReviews (University of Washington, 2008; updated 2012).
-
(2008)
GeneReviews
-
-
Rich, T.A.1
-
15
-
-
79956307251
-
Stampy: A statistical algorithm for sensitive and fast mapping of Illumina sequence reads
-
Lunter, G. & Goodson, M. Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads. Genome Res. 21, 936-939 (2011).
-
(2011)
Genome Res.
, vol.21
, pp. 936-939
-
-
Lunter, G.1
Goodson, M.2
-
16
-
-
84949211439
-
Integrating mapping-, assemblyand haplotype-based approaches for calling variants in clinical sequencing application
-
WGS500 Consortium
-
Rimmer, A., Phan, H., Mathieson, I., Zamin, I., Twigg, S. R. F., WGS500 Consortium, Wilkie, A. O. M. & McVean, G. Integrating mapping-, assemblyand haplotype-based approaches for calling variants in clinical sequencing applications. Nat. Genet. (2012).
-
(2012)
Nat. Genet.
-
-
Rimmer, A.1
Phan, H.2
Mathieson, I.3
Zamin, I.4
Twigg, S.R.F.5
Wilkie, A.O.M.6
McVean, G.7
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