McMullin MF - Search Results

1

JAK2 V617F: a single mutation in the myeloproliferative group of disorders.

McLornan D, Percy M, McMullin MF. McLornan D, et al. Among authors: mcmullin mf. Ulster Med J. 2006 May;75(2):112-9. Ulster Med J. 2006. PMID: 16755940 Free PMC article. Review. No abstract available.

2

Retroviral-mediated gene transfer of the human erythropoietin gene into a factor-dependent cell line, TF-1.

Percy MJ, Winter PC, Lappin TR, McMullin MF. Percy MJ, et al. Among authors: mcmullin mf. Leukemia. 1995 Oct;9 Suppl 1:S66-9. Leukemia. 1995. PMID: 7475317

3

Selective block in erythropoietin-induced differentiation of growth factor-independent retrovirally-infected TF-1 cells.

Percy MJ, Lappin TR, Buckley OM, McMullin MF. Percy MJ, et al. Among authors: mcmullin mf. Leuk Res. 1997 Jul;21(7):657-66. doi: 10.1016/s0145-2126(97)00032-5. Leuk Res. 1997. PMID: 9301687

4

Sequence analysis of the 3' hypoxia-responsive element of the human erythropoietin gene in patients with erythrocytosis.

Percy MJ, McMullin MF, Lappin TR. Percy MJ, et al. Among authors: mcmullin mf. Biochem Mol Med. 1997 Oct;62(1):132-4. doi: 10.1006/bmme.1997.2627. Biochem Mol Med. 1997. PMID: 9367810

5

Erythrocytosis due to a mutation in the erythropoietin receptor gene.

Percy MJ, McMullin MF, Roques AW, Westwood NB, Acharya J, Hughes AE, Lappin TR, Pearson TC. Percy MJ, et al. Among authors: mcmullin mf. Br J Haematol. 1998 Feb;100(2):407-10. doi: 10.1046/j.1365-2141.1998.00550.x. Br J Haematol. 1998. PMID: 9488636 Free article.

6

Erythropoietin receptor and hematological disease.

McMullin MF, Percy MJ. McMullin MF, et al. Am J Hematol. 1999 Jan;60(1):55-60. doi: 10.1002/(sici)1096-8652(199901)60:1<55::aid-ajh9>3.0.co;2-v. Am J Hematol. 1999. PMID: 9883806 Free article. Review.

7

Familial idiopathic methemoglobinemia revisited: original cases reveal 2 novel mutations in NADH-cytochrome b5 reductase.

Percy MJ, Gillespie MJ, Savage G, Hughes AE, McMullin MF, Lappin TR. Percy MJ, et al. Among authors: mcmullin mf. Blood. 2002 Nov 15;100(10):3447-9. doi: 10.1182/blood-2002-05-1405. Epub 2002 Jul 5. Blood. 2002. PMID: 12393396 Free article.

8

Chuvash-type congenital polycythemia in 4 families of Asian and Western European ancestry.

Percy MJ, McMullin MF, Jowitt SN, Potter M, Treacy M, Watson WH, Lappin TR. Percy MJ, et al. Among authors: mcmullin mf. Blood. 2003 Aug 1;102(3):1097-9. doi: 10.1182/blood-2002-10-3246. Epub 2003 Apr 17. Blood. 2003. PMID: 12702509 Free article.

9

A common polymorphism in the oxygen-dependent degradation (ODD) domain of hypoxia inducible factor-1alpha (HIF-1alpha) does not impair Pro-564 hydroxylation.

Percy MJ, Mooney SM, McMullin MF, Flores A, Lappin TR, Lee FS. Percy MJ, et al. Among authors: mcmullin mf. Mol Cancer. 2003 Sep 9;2:31. doi: 10.1186/1476-4598-2-31. Mol Cancer. 2003. PMID: 14521712 Free PMC article.

10

Recessive congenital methaemoglobinaemia: functional characterization of the novel D239G mutation in the NADH-binding lobe of cytochrome b5 reductase.

Percy MJ, Crowley LJ, Davis CA, McMullin MF, Savage G, Hughes J, McMahon C, Quinn RJ, Smith O, Barber MJ, Lappin TR. Percy MJ, et al. Among authors: mcmullin mf. Br J Haematol. 2005 Jun;129(6):847-53. doi: 10.1111/j.1365-2141.2005.05526.x. Br J Haematol. 2005. PMID: 15953014 Free article.

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