LLNI Funded Publications
A childhood acute lymphoblastic leukemia genome-wide association study identifies novel sex-specific risk variants.
Author:Singh SK
Other Authors: Lupo PJ, Scheurer ME, Saxena A, Kennedy AE, Ibrahimou B, Barbieri MA, Mills KI, McCauley JL, Okcu MF, Dorak MT,
Last Updated:07/11/2019
Source:PubMed
Original Source:PubMed
Type:Journal Article
DOI:10.1097/MD.0000000000005300
Journal:Medicine
Volume:95
Issue:46
Pages:e5300
Date: November 2016
Link:https://insights.ovid.com/article/00005792-201611150-00027
A common polymorphism in the oxygen-dependent degradation (ODD) domain of hypoxia inducible factor-1alpha (HIF-1alpha) does not impair Pro-564 hydroxylation.
Author:Percy MJ
Other Authors: Mooney SM, McMullin MF, Flores A, Lappin TR, Lee FS,
Journal:Mol Cancer
Date: September 2003
A comparison of∞ —L-fucosidose activity in normal and chronic lymphocytic leukaemic lymphocytes
Author:Crockard A D
Other Authors: Bridges J M, Lewis M H R,
Journal:Biochem Soc Tran5
Date: 1980
A compound combination screening approach with potential to identify new treatment options for paediatric acute myeloid leukaemia
Author:Lappin K
Other Authors: Davies L, Matchett K, Ge Y, Mills K, Blayney J,
Last Updated:20/10/2022
Source:PubMed
Original Source:PubMed
Type:Journal Article
DOI:10.1038/s41598-020-75453-3
Journal:Scientific reports
Date: October 2020
A critical appraisal of tools available for monitoring epigenetic changes in clinical samples from patients with myeloid malignancies
Author:Gronbaek K
Other Authors: Muller-Tidow C, Perini G, Lehmann S, Bach Treppendahl M, Mills K, Plass C, Schlegelberger B,
Journal:Haematologica
Date: 2012
A derivative chromosome 14 resulting in partial trisomy of chromosome 12 in B-cell Chronic Lymphocytic Leukemia
Author:McManus A P
Other Authors: Bailie K E M, Jess H, Desai Z R,
Journal:Cer Genet. Cytogenet
Date: 1994
A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis.
Author:Percy MJ
Other Authors: Zhao Q, Flores A, Harrison C, Lappin TR, Maxwell PH, McMullin MF, Lee FS,
Journal:Proc Natl Acad Sci U S A
Date: January 2006
A gain-of-function mutation in the HIF2A gene in familial erythrocytosis
Author:Percy MJ
Other Authors: Furlow PW, Lucas GS, Li X, Lappin TR, McMullin MF, Lee FS,
Journal:N Engl J Med
Date: January 2008
A molecular signature of dormancy in CD34CD38 acute myeloid leukaemia cells.
Author:Al-Asadi MG
Other Authors: Brindle G, Castellanos M, May ST, Mills KI, Russell NH, Seedhouse CH, Pallis M,
Last Updated:22/10/2019
Source:PubMed
Original Source:PubMed
Type:Journal Article
DOI:10.18632/oncotarget.22808
Journal:Oncotarget
Volume:8
Issue:67
Pages:111405-111418
Date: December 2017
A new polycythaemia vera-associated SOCS3 SH2 mutant (SOCS3F136L) cannot regulate erythropoietin responses
Author:Suessmuth Y
Other Authors: Elliott J, Percy MJ, Inami M, Attal H, Harrison CN, Inokuchi K, McMullin MF, Johnston JA,
Journal:Br J Haematol
Date: November 2009
A nonsynonymous LNK polymorphism associated with idiopathic erythrocytosis
Author:McMullin M F
Other Authors: Wu C, Percy M J, Tong W,
Journal:Am J Hematol
Date: 2011
Link:https://onlinelibrary.wiley.com/doi/full/10.1002/ajh.22154
A Novel Base Change Leading to Hb Vanderbilt [beta89(F5)Ser–>Arg, AGT>AGA].
Author:Goodyer M J
Other Authors: Elhassadi E I, Percy M J, McMullin M F,
Journal:Hemoglobin
Date: 2011
Link:https://www.tandfonline.com/doi/abs/10.3109/03630269.2011.594137?journalCode=ihem20
