I. McFarlane

发表

Primary iron overload with inappropriate hepcidin expression in V162del ferroportin disease

D. Oxley, T. Ganz, W. Vogel, 2005, Hepatology.

Developmental control of the Nlrp6 inflammasome and a substrate, IL-18, in mammalian intestine.

D. Charnock-Jones, A. Fowden, G. Belteki, 2011, American journal of physiology. Gastrointestinal and liver physiology.

The role of the protein glycosylation state in the control of cellular transport of the amyloid β precursor protein

K. Breen, C. Coughlan, I. McFarlane, 1999, Neuroscience.

Inhibition of N‐glycan processing alters axonal transport of synaptic glycoproteins in vivo

K. Breen, K. Moya, I. McFarlane, 2000, Neuroreport.

Differentiation of mononuclear precursors into osteoclasts on the surface of Si-substituted hydroxyapatite.

W. Bonfield, R. Brooks, N. Rushton, 2006, Journal of biomedical materials research. Part A.

The effect of potassium EDTA on the stability of parathyroid hormone in whole blood

E. English, D. Halsall, I. McFarlane, 2007, Annals of clinical biochemistry.

Potential biomarkers of osteonecrosis in Gaucher disease.

A. Mehta, J. E. Wraith, D. Hughes, 2011, Blood cells, molecules & diseases.

Hepatic steatosis, GH deficiency and the effects of GH replacement: a Liverpool magnetic resonance spectroscopy study.

Jimmy D Bell, G. Kemp, Elizabeth Louise Thomas, 2012, European journal of endocrinology.

Hepatic steatosis, growth hormone deficiency and the effects of growth hormone replacement: a LIVERpool magnetic resonance spectroscopy study.

G. Kemp, Elizabeth Louise Thomas, D. Cuthbertson, 2012 .

Clinical presentation and molecular pathophysiology of autosomal dominant hemochromatosis caused by a novel ferroportin mutation

M. Hermann, W. Griffiths, H. Zoller, 2010, Hepatology.

The Relative Activities of the C 2 GnT 1 and ST 3 GalI Glycosyltransferases Determine O-Glycan Structure and Expression of a Tumor-associated Epitope on MUC 1 *

I. Brockhausen, J. Taylor‐Papadimitriou, M. Dalziel, 2007 .

Individual isoforms of the amyloid βprecursor protein demonstrate differential adhesive potentials to constituents of the extracellular matrix

C. Overly, L. McConlogue, K. Breen, 1997, Journal of neuroscience research.

DACH1, a Zona Glomerulosa Selective Gene in the Human Adrenal, Activates Transforming Growth Factor-β Signaling and Suppresses Aldosterone Secretion

Morris J. Brown, N. Figg, S. Neogi, 2015, Hypertension.

Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case - control study.

N. Wareham, J. Luan, T. Cox, 2003, Human molecular genetics.

The Relative Activities of the C2GnT1 and ST3Gal-I Glycosyltransferases Determine O-Glycan Structure and Expression of a Tumor-associated Epitope on MUC1*

I. Brockhausen, J. Taylor‐Papadimitriou, M. Dalziel, 2001, The Journal of Biological Chemistry.

Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension

James Hadfield, Poul Nissen, Sumedha Garg, 2013, Nature Genetics.

Deletion of the metabolic transcriptional coactivator PGC1β induces cardiac arrhythmia.

C. Lelliott, M. Orešič, A. Grace, 2011, Cardiovascular research.

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease.

P. Deegan, T. Cox, R. Boot, 2005, Blood cells, molecules & diseases.

Familial partial lipodystrophy associated with compound heterozygosity for novel mutations in the LMNA gene

Jimmy D Bell, Elizabeth Louise Thomas, I. Barroso, 2004, Diabetologia.

A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency.

J. Schwabe, V. Chatterjee, R. Bernhardt, 2006, The Journal of clinical endocrinology and metabolism.

Consequences of long-term oral administration of the mitochondria-targeted antioxidant MitoQ to wild-type mice.

D. Rubinsztein, H. M. Cochemé, Robin A. J. Smith, 2010, Free radical biology & medicine.

Lectin analysis of human immunoglobulin G N-glycan sialylation

J. Axford, M. Dalziel, I. McFarlane, 1999, Glycoconjugate Journal.

Identification of novel genes in Hirschsprung disease pathway using whole genome expression study.

A. Loos, I. McFarlane, A. Saeed, 2012, Journal of pediatric surgery.

Identification of mutations in SLC40A1 that affect ferroportin function and phenotype of human ferroportin iron overload.

Martin Hermann, Wolfgang Vogel, Heinz Zoller, 2011, Gastroenterology.