Fitzgibbon J - Search Results

1

Disease evolution and outcomes in familial AML with germline CEBPA mutations.

Tawana K, Wang J, Renneville A, Bödör C, Hills R, Loveday C, Savic A, Van Delft FW, Treleaven J, Georgiades P, Uglow E, Asou N, Uike N, Debeljak M, Jazbec J, Ancliff P, Gale R, Thomas X, Mialou V, Döhner K, Bullinger L, Mueller B, Pabst T, Stelljes M, Schlegelberger B, Wozniak E, Iqbal S, Okosun J, Araf S, Frank AK, Lauridsen FB, Porse B, Nerlov C, Owen C, Dokal I, Gribben J, Smith M, Preudhomme C, Chelala C, Cavenagh J, Fitzgibbon J. Tawana K, et al. Among authors: fitzgibbon j. Blood. 2015 Sep 3;126(10):1214-23. doi: 10.1182/blood-2015-05-647172. Epub 2015 Jul 10. Blood. 2015. PMID: 26162409 Free article.

2

Mutations of CEBPA in acute myeloid leukemia FAB types M1 and M2.

Snaddon J, Smith ML, Neat M, Cambal-Parrales M, Dixon-McIver A, Arch R, Amess JA, Rohatiner AZ, Lister TA, Fitzgibbon J. Snaddon J, et al. Among authors: fitzgibbon j. Genes Chromosomes Cancer. 2003 May;37(1):72-8. doi: 10.1002/gcc.10185. Genes Chromosomes Cancer. 2003. PMID: 12661007

3

Mutation of CEBPA in familial acute myeloid leukemia.

Smith ML, Cavenagh JD, Lister TA, Fitzgibbon J. Smith ML, et al. Among authors: fitzgibbon j. N Engl J Med. 2004 Dec 2;351(23):2403-7. doi: 10.1056/NEJMoa041331. N Engl J Med. 2004. PMID: 15575056 Free article.

4

Development of a human acute myeloid leukaemia screening panel and consequent identification of novel gene mutation in FLT3 and CCND3.

Smith ML, Arch R, Smith LL, Bainton N, Neat M, Taylor C, Bonnet D, Cavenagh JD, Andrew Lister T, Fitzgibbon J. Smith ML, et al. Among authors: fitzgibbon j. Br J Haematol. 2005 Feb;128(3):318-23. doi: 10.1111/j.1365-2141.2004.05324.x. Br J Haematol. 2005. PMID: 15667533 Free article.

5

A novel K509I mutation of KIT identified in familial mastocytosis-in vitro and in vivo responsiveness to imatinib therapy.

Zhang LY, Smith ML, Schultheis B, Fitzgibbon J, Lister TA, Melo JV, Cross NC, Cavenagh JD. Zhang LY, et al. Among authors: fitzgibbon j. Leuk Res. 2006 Apr;30(4):373-8. doi: 10.1016/j.leukres.2005.08.015. Epub 2005 Sep 22. Leuk Res. 2006. PMID: 16183119

6

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias.

Fitzgibbon J, Smith LL, Raghavan M, Smith ML, Debernardi S, Skoulakis S, Lillington D, Lister TA, Young BD. Fitzgibbon J, et al. Cancer Res. 2005 Oct 15;65(20):9152-4. doi: 10.1158/0008-5472.CAN-05-2017. Cancer Res. 2005. PMID: 16230371

7

Development of a quantitative real-time polymerase chain reaction method for monitoring CEBPA mutations in normal karyotype acute myeloid leukaemia.

Smith LL, Pearce D, Smith ML, Jenner M, Lister TA, Bonnet D, Goff L, Fitzgibbon J. Smith LL, et al. Among authors: fitzgibbon j. Br J Haematol. 2006 Apr;133(1):103-5. doi: 10.1111/j.1365-2141.2006.06001.x. Br J Haematol. 2006. PMID: 16512836 Free article. No abstract available.

8

Genome-wide detection of recurring sites of uniparental disomy in follicular and transformed follicular lymphoma.

Fitzgibbon J, Iqbal S, Davies A, O'shea D, Carlotti E, Chaplin T, Matthews J, Raghavan M, Norton A, Lister TA, Young BD. Fitzgibbon J, et al. Leukemia. 2007 Jul;21(7):1514-20. doi: 10.1038/sj.leu.2404696. Epub 2007 May 10. Leukemia. 2007. PMID: 17495976

9

Familial myelodysplasia and acute myeloid leukaemia--a review.

Owen C, Barnett M, Fitzgibbon J. Owen C, et al. Among authors: fitzgibbon j. Br J Haematol. 2008 Jan;140(2):123-32. doi: 10.1111/j.1365-2141.2007.06909.x. Br J Haematol. 2008. PMID: 18173751 Free article. Review.

10

Segmental uniparental disomy is a commonly acquired genetic event in relapsed acute myeloid leukemia.

Raghavan M, Smith LL, Lillington DM, Chaplin T, Kakkas I, Molloy G, Chelala C, Cazier JB, Cavenagh JD, Fitzgibbon J, Lister TA, Young BD. Raghavan M, et al. Among authors: fitzgibbon j. Blood. 2008 Aug 1;112(3):814-21. doi: 10.1182/blood-2008-01-132431. Epub 2008 May 19. Blood. 2008. PMID: 18490517 Free article.

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