LLNI Funded Publications

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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

Link:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3436239/

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

Link:http://www.oncotarget.com/index.php?journal=oncotarget&page=article&op=view&path%5b%5d=22808&path%5b%5d=72005

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

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