Percy MJ - Search Results

1

The myeloproliferative disorder-associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3.

Hookham MB, Elliott J, Suessmuth Y, Staerk J, Ward AC, Vainchenker W, Percy MJ, McMullin MF, Constantinescu SN, Johnston JA. Hookham MB, et al. Among authors: percy mj. Blood. 2007 Jun 1;109(11):4924-9. doi: 10.1182/blood-2006-08-039735. Epub 2007 Feb 22. Blood. 2007. PMID: 17317861 Free article.

2

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. 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.

3

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. 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.

4

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. Mol Cancer. 2003 Sep 9;2:31. doi: 10.1186/1476-4598-2-31. Mol Cancer. 2003. PMID: 14521712 Free PMC article.

5

The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.

Liu E, Percy MJ, Amos CI, Guan Y, Shete S, Stockton DW, McMullin MF, Polyakova LA, Ang SO, Pastore YD, Jedlickova K, Lappin TR, Gordeuk V, Prchal JT. Liu E, et al. Among authors: percy mj. Blood. 2004 Mar 1;103(5):1937-40. doi: 10.1182/blood-2003-07-2550. Epub 2003 Nov 6. Blood. 2004. PMID: 14604959 Free article.

6

The V617F JAK2 mutation and the myeloproliferative disorders.

Percy MJ, McMullin MF. Percy MJ, et al. Hematol Oncol. 2005 Sep-Dec;23(3-4):91-3. doi: 10.1002/hon.761. Hematol Oncol. 2005. PMID: 16285006 Review.

7

Chronic neutrophilic leukemia with an associated V617F JAK2 tyrosine kinase mutation.

Mc Lornan DP, Percy MJ, Jones AV, Cross NC, Mc Mullin MF. Mc Lornan DP, et al. Among authors: percy mj. Haematologica. 2005 Dec;90(12):1696-7. Haematologica. 2005. PMID: 16330446

8

A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis.

Percy MJ, Zhao Q, Flores A, Harrison C, Lappin TR, Maxwell PH, McMullin MF, Lee FS. Percy MJ, et al. Proc Natl Acad Sci U S A. 2006 Jan 17;103(3):654-9. doi: 10.1073/pnas.0508423103. Epub 2006 Jan 9. Proc Natl Acad Sci U S A. 2006. PMID: 16407130 Free PMC article.

9

The incidence of the JAK2 V617F mutation in patients with idiopathic erythrocytosis.

Percy MJ, Jones FG, Green AR, Reilly JT, McMullin MF. Percy MJ, et al. Haematologica. 2006 Mar;91(3):413-4. Epub 2006 Feb 17. Haematologica. 2006. PMID: 16503548

10

Oxygen sensing: recent insights from idiopathic erythrocytosis.

Lee FS, Percy MJ, McMullin MF. Lee FS, et al. Among authors: percy mj. Cell Cycle. 2006 May;5(9):941-5. doi: 10.4161/cc.5.9.2723. Epub 2006 May 1. Cell Cycle. 2006. PMID: 16687917 Free PMC article.

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