Percy MJ - Search Results

1

Erythropoietin receptor and hematological disease.

McMullin MF, Percy MJ. McMullin MF, et al. Among authors: percy mj. 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.

2

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. Biochem Mol Med. 1997 Oct;62(1):132-4. doi: 10.1006/bmme.1997.2627. Biochem Mol Med. 1997. PMID: 9367810

3

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. 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.

4

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. Leukemia. 1995 Oct;9 Suppl 1:S66-9. Leukemia. 1995. PMID: 7475317

5

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. Leuk Res. 1997 Jul;21(7):657-66. doi: 10.1016/s0145-2126(97)00032-5. Leuk Res. 1997. PMID: 9301687

6

The prevalence of CALR mutations in a cohort of patients with myeloproliferative neoplasms.

Grinsztejn E, Percy MJ, McClenaghan D, Quintana M, Cuthbert RJ, McMullin MF. Grinsztejn E, et al. Among authors: percy mj. Int J Lab Hematol. 2016 Feb;38(1):102-6. doi: 10.1111/ijlh.12447. Epub 2015 Nov 11. Int J Lab Hematol. 2016. PMID: 26555437

7

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

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

8

Genetic basis of congenital erythrocytosis: mutation update and online databases.

Bento C, Percy MJ, Gardie B, Maia TM, van Wijk R, Perrotta S, Della Ragione F, Almeida H, Rossi C, Girodon F, Aström M, Neumann D, Schnittger S, Landin B, Minkov M, Randi ML, Richard S, Casadevall N, Vainchenker W, Rives S, Hermouet S, Ribeiro ML, McMullin MF, Cario H; ECE-Consortium; Chauveau A, Gimenez-Roqueplo AP, Bressac-de-Paillerets B, Altindirek D, Lorenzo F, Lambert F, Dan H, Gad-Lapiteau S, Catarina Oliveira A, Rossi C, Fraga C, Taradin G, Martin-Nuñez G, Vitória H, Diaz Aguado H, Palmblad J, Vidán J, Relvas L, Ribeiro ML, Luigi Larocca M, Luigia Randi M, Pedro Silveira M, Percy M, Gross M, Marques da Costa R, Beshara S, Ben-Ami T, Ugo V; ECE-Consortium. Bento C, et al. Among authors: percy mj, percy m. Hum Mutat. 2014 Jan;35(1):15-26. doi: 10.1002/humu.22448. Epub 2013 Oct 22. Hum Mutat. 2014. PMID: 24115288

9

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. 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.

10

Novel and Mediterranean beta thalassemia mutations in the indigenous Northern Ireland population.

Knott M, Ramadan KM, Savage G, Jones FG, El-Agnaf M, McMullin MF, Percy MJ. Knott M, et al. Among authors: percy mj. Blood Cells Mol Dis. 2006 Mar-Apr;36(2):265-8. doi: 10.1016/j.bcmd.2005.12.005. Epub 2006 Feb 8. Blood Cells Mol Dis. 2006. PMID: 16466947

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