Now showing items 1-20 of 30

    Issue DateTitleAuthor(s)
    1 October 2014RA autoantibodies as predictors of rheumatoid arthritis in non-cystic fibrosis bronchiectasis patients.  Perry, E; Stenton, C; Kelly, C; et al.
    23 January 2017Rab32 connects ER stress to mitochondrial defects in multiple sclerosis  Haile, Y; Deng, X; Ortiz-Sandoval, C; et al.
    1 January 2012Radon and skin cancer in southwest England: an ecologic study  Wheeler, BW; Allen, James; Depledge, MH; et al.
    5 October 2017Random non-fasting C-peptide testing can identify patients with insulin-treated type 2 diabetes at high risk of hypoglycaemia.  Hope, SV; Knight, BA; Shields, BM; et al.
    21 April 2016Random non-fasting C-peptide: bringing robust assessment of endogenous insulin secretion to the clinic  Hope, SV; Knight, BA; Shields, BM; et al.
    19 September 2016Rapid hepatic clearance of full length CCN-2/CTGF: a putative role for LRP1-mediated endocytosis  Gerritsen, KGF; Bovenschen, N; Nguyen, TQ; et al.
    1 February 2017Rare and low-frequency coding variants alter human adult height  Marouli, E; Graff, M; Medina-Gomez, C; et al.
    4 August 2015Rare coding variants and X-linked loci associated with age at menarche  Lunetta, KL; Day, FR; Sulem, P; et al.
    1 October 2015Rates of lateral gene transfer in prokaryotes: high but why?  Vos, Michiel; Hesselman, MC; te Beek, TA; et al.
    1 May 2019Rationale for enteroviral vaccination and antiviral therapies in human type 1 diabetes  Dunne, JL; Richardson, SJ; Atkinson, MA; et al.
    1 June 2016Reactivity to low-flow as a potential determinant for brachial artery flow-mediated vasodilatation  Aizawa, K; Elyas, S; Adingupu, DD; et al.
    12 June 2015Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of WDR73  Jinks, RN; Puffenberger, EG; Baple, Emma Louise; et al.
    21 July 2017Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes  Johnson, MB; De Franco, E; Lango Allen, H; et al.
    1 July 2015Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase Mutation  Chakera, AJ; Steele, AM; Gloyn, Anna L.; et al.
    28 September 2017Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers  Pilling, LC; Atkins, JL; Duff, MO; et al.
    13 September 2018Red cell distribution width and common disease onsets in 240,477 healthy volunteers followed for up to 9 years  Pilling, LC; Atkins, JL; Kuchel, GA; et al.
    5 June 2009Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births.  Slingerland, AS; Shields, BM; Flanagan, SE; et al.
    3 May 2017Regional differences in mitochondrial DNA methylation in human post-mortem brain tissue.  Devall, M; Smith, RG; Jeffries, A; et al.
    22 August 2018Regulation of energy rheostasis by the melanocortin-3 receptor  Ghamari-Langroudi, M; Cakir, I; Lippert, RN; et al.
    2 July 2018Regulation of hepatic glucose production and AMPK by AICAR but not metformin depends on drug uptake through the equilibrative nucleoside transporter 1 (ENT1)  Beall, C; Logie, L; Lees, Z; et al.