Swanton S - Search Results

1

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders.

Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, Vassiliou GS, Bench AJ, Boyd EM, Curtin N, Scott MA, Erber WN, Green AR; Cancer Genome Project. Baxter EJ, et al. Among authors: swanton s. Lancet. 2005 Mar 19-25;365(9464):1054-61. doi: 10.1016/S0140-6736(05)71142-9. Lancet. 2005. PMID: 15781101

2

An acquired translocation in JAK2 Val617Phe-negative essential thrombocythemia associated with autosomal spread of X-inactivation.

Vassiliou GS, Campbell PJ, Li J, Roberts I, Swanton S, Huntly BJ, Fourouclas N, Baxter EJ, Munro LR, Culligan DA, Scott LM, Green AR. Vassiliou GS, et al. Among authors: swanton s. Haematologica. 2006 Aug;91(8):1100-4. Haematologica. 2006. PMID: 16885051

3

Size matters: the prognostic implications of large and small deletions of the derivative 9 chromosome in chronic myeloid leukemia.

Fourouclas N, Campbell PJ, Bench AJ, Swanton S, Baxter EJ, Huntly BJ, Green AR. Fourouclas N, et al. Among authors: swanton s. Haematologica. 2006 Jul;91(7):952-5. Haematologica. 2006. PMID: 16818283

4

Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG).

Bench AJ, Nacheva EP, Hood TL, Holden JL, French L, Swanton S, Champion KM, Li J, Whittaker P, Stavrides G, Hunt AR, Huntly BJ, Campbell LJ, Bentley DR, Deloukas P, Green AR. Bench AJ, et al. Among authors: swanton s. Oncogene. 2000 Aug 10;19(34):3902-13. doi: 10.1038/sj.onc.1203728. Oncogene. 2000. PMID: 10952764

5

Double Philadelphia masquerading as chromosome 20q deletion--a new recurrent abnormality in chronic myeloid leukaemia blast crisis.

Reid AG, Swanton S, Grace C, Campbell LJ, Green AR, Nacheva EP; United Kingdom Cancer Cytogenetics Group (UKCCG). Reid AG, et al. Among authors: swanton s. Br J Haematol. 2003 Nov;123(3):442-8. doi: 10.1046/j.1365-2141.2003.04606.x. Br J Haematol. 2003. PMID: 14617003 Free article.

6

Myeloid- and lymphoid-specific breakpoint cluster regions in chromosome band 13q14 in acute leukemia.

Coignet LJ, Lima CS, Min T, Streubel B, Swansbury J, Telford N, Swanton S, Bowen A, Nagai M, Catovsky D, Fonatsch C, Dyer MJ. Coignet LJ, et al. Among authors: swanton s. Genes Chromosomes Cancer. 1999 Jul;25(3):222-9. doi: 10.1002/(sici)1098-2264(199907)25:3<222::aid-gcc4>3.0.co;2-c. Genes Chromosomes Cancer. 1999. PMID: 10379868

7

Abnormalities of the ETV6 gene occur in the majority of patients with aberrations of the short arm of chromosome 12: a combined PCR and Southern blotting analysis.

O'Connor HE, Butler TA, Clark R, Swanton S, Harrison CJ, Secker-Walker LM, Foroni L. O'Connor HE, et al. Among authors: swanton s. Leukemia. 1998 Jul;12(7):1099-106. doi: 10.1038/sj.leu.2401070. Leukemia. 1998. PMID: 9665196

8

[2q21-qter trisomy in hepatoblastoma].

Balogh E, Swanton S, Kiss C, Jakab Z, Secker-Walker LM, Oláh E. Balogh E, et al. Among authors: swanton s. Orv Hetil. 1997 Dec 14;138(50):3179-83. Orv Hetil. 1997. PMID: 9446083 Hungarian.

9

Fluorescence in situ hybridization reveals trisomy 2q by insertion into 9p in hepatoblastoma.

Balogh E, Swanton S, Kiss C, Jakab ZS, Secker-Walker LM, Oláh E. Balogh E, et al. Among authors: swanton s. Cancer Genet Cytogenet. 1998 Apr 15;102(2):148-50. doi: 10.1016/s0165-4608(97)00318-x. Cancer Genet Cytogenet. 1998. PMID: 9546070

10

Hematologic malignancies with t(4;11)(q21;q23)--a cytogenetic, morphologic, immunophenotypic and clinical study of 183 cases. European 11q23 Workshop participants.

Johansson B, Moorman AV, Haas OA, Watmore AE, Cheung KL, Swanton S, Secker-Walker LM. Johansson B, et al. Among authors: swanton s. Leukemia. 1998 May;12(5):779-87. doi: 10.1038/sj.leu.2401012. Leukemia. 1998. PMID: 9593281

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