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Ian McFarlane

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Atif Saeed; Lenka Barreto; Andrea Loos; Ian McFarlane; Sudhesna Guha Neogii; Adil Aslam
Identification of novel genes in Hirschsprung disease pathway using whole genome expression study.
Iman S Gurung; Michael Baker; Mark Campbell; Andrew A Grace; Adrienn Kis; Christopher J Lelliott; Ian McFarlane; Gema Medina-Gomez; Sudeshna Guha Neogi; Matej Oresic; Sergio Rodriguez-Cuenca; Vidya Velagapudi; Antonio Vidal-Puig; Christopher L-H Huang
Deletion of the metabolic transcriptional coactivator PGC1β induces cardiac arrhythmia.
Roman Mayr; William J H Griffiths; Martin Hermann; Ian McFarlane; Halsall David; Armin Finkenstedt; Andrew Douds; Susan E Davies; Andreas R Janecke; Wolfgang Vogel; Timothy M Cox; Heinz Zoller
Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.

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All Publications

2012: Atif Saeed; Lenka Barreto; Andrea Loos; Ian McFarlane; Sudhesna Guha Neogii; Adil Aslam
Identification of novel genes in Hirschsprung disease pathway using whole genome expression study.
Journal of pediatric surgery 2012;47(2):303-7.
2011: Iman S Gurung; Michael Baker; Mark Campbell; Andrew A Grace; Adrienn Kis; Christopher J Lelliott; Ian McFarlane; Gema Medina-Gomez; Sudeshna Guha Neogi; Matej Oresic; Sergio Rodriguez-Cuenca; Vidya Velagapudi; Antonio Vidal-Puig; Christopher L-H Huang
Deletion of the metabolic transcriptional coactivator PGC1β induces cardiac arrhythmia.
Cardiovascular research 2011;92(1):29-38.
2011: Roman Mayr; William J H Griffiths; Martin Hermann; Ian McFarlane; Halsall David; Armin Finkenstedt; Andrew Douds; Susan E Davies; Andreas R Janecke; Wolfgang Vogel; Timothy M Cox; Heinz Zoller
Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.
Gastroenterology 2011;140(7):2056-63, 2063.e1.
2011: Sarah Kempster; Gusztav Belteki; Alison J Forhead; Abigail Fowden; Robert D Catalano; Brian Y Lam; Ian McFarlane; D Stephen Charnock-Jones; Gordon C S Smith
Developmental control of the Nlrp6 inflammasome and a substrate, IL-18, in mammalian intestine.
American journal of physiology. Gastrointestinal and liver physiology 2011;300(2):G253-63.
2011: Elena V Pavlova; Patrick B Deegan; Jane Tindall; Ian McFarlane; Atul Mehta; Derralyn Hughes; J Edmond Wraith; Timothy M Cox
Potential biomarkers of osteonecrosis in Gaucher disease.
Blood cells, molecules & diseases 2011;46(1):27-33.
2010: William J H Griffiths; Roman Mayr; Ian McFarlane; Martin Hermann; Halsall David; Heinz Zoller; Timothy M Cox
Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation.
Hepatology (Baltimore, Md.) 2010;51(3):788-95.
2010: Sergio Rodriguez-Cuenca; Helena M Cochemé; Angela Logan; Irina Abakumova; Tracy A Prime; Claudia Rose; antonio vidal-puig; Anthony C Smith; David C Rubinsztein; Ian M Fearnley; Bruce A Jones; Simon Pope; Simon J R Heales; Brian Y H Lam; Sudeshna Guha Neogi; Ian McFarlane; Andrew M James; Robin A J Smith; Michael P Murphy
Consequences of long-term oral administration of the mitochondria-targeted antioxidant MitoQ to wild-type mice.
Free radical biology & medicine 2010;48(1):161-72.
2009: Kristian Løvås; Ian McFarlane; Huy-Hoang Nguyen; Suzanne Curran; John W R Schwabe; Halsall David; Rita Bernhardt; A Michael Wallace; V Krishna K Chatterjee
A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.
The Journal of clinical endocrinology and metabolism 2009;94(3):914-9.
2007: Emma English; Ian McFarlane; Kevin P Taylor; Halsall David
The effect of potassium EDTA on the stability of parathyroid hormone in whole blood.
Annals of clinical biochemistry 2007;44(Pt 3):297-9.
2005: Patrick B Deegan; Mary Teresa Moran; Ian McFarlane; J Paul Schofield; Rolf G Boot; johannes aerts; Timothy M Cox
Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease.
Blood cells, molecules & diseases 2005;35(2):259-67.
2005: Heinz Zoller; Ian McFarlane; Igor Theurl; Sylvia Stadlmann; Elizabeta Nemeth; David Oxley; Tomas Ganz; Halsall David; Timothy M Cox; Wolfgang Vogel
Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease.
Hepatology (Baltimore, Md.) 2005;42(2):466-72.
2004: David B Savage; Maria A Soos; A Powlson; Stephen O'Rahilly; Ian McFarlane; Halsall David; Inês Barroso; E Louise Thomas; J D Bell; I Scobie; P E Belchetz; W F Kelly; Alan J Schafer
Familial partial lipodystrophy associated with compound heterozygosity for novel mutations in the LMNA gene.
Diabetologia 2004;47(4):753-6.
2004: Elli M Gurnell; Sudheep K Thomas; Ian McFarlane; I Munday; Kottekkattu K Balan; Lawrence H Berman; V Krishna K Chatterjee; Gordon C Wishart
Focused parathyroid surgery with intraoperative parathyroid hormone measurement as a day-case procedure.
The British journal of surgery 2004;91(1):78-82.
2003: Halsall David; Ian McFarlane; Jian'an Luan; Timothy M Cox; Nicholas J Wareham
Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study.
Human molecular genetics 2003;12(12):1361-5.