Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Journal of Medical Genetics|June 3, 2005
Mutations in hepatocyte nuclear factor-1beta and their related phenotypesE L Edghill, C Bingham, S Ellard, et al.Diabetic Medicine : a Journal of the British Diabetic Association|November 11, 2009
Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetesO Rubio-Cabezas, E L Edghill, J Argente, et al.Journal of Molecular Biology|July 9, 2004
Structure of the C-terminal RING finger from a RING-IBR-RING/TRIAD motif reveals a novel zinc-binding domain distinct from a RINGAllan D Capili, E L Edghill, Kenneth Wu, et al.Diabetologia|April 13, 2006
Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotypeS E Flanagan, E L Edghill, A L Gloyn, et al.Diabetic Medicine : a Journal of the British Diabetic Association|May 17, 2012
HNF1B deletions in patients with young-onset diabetes but no known renal diseaseE L Edghill, K Stals, R A Oram, et al.Diabetic Medicine : a Journal of the British Diabetic Association|November 23, 2006
Hepatocyte nuclear factor-1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF-1beta in human pancreatic developmentE L Edghill, C Bingham, A S Slingerland, et al.Diabetologia|October 13, 2011
Heterozygous ABCC8 mutations are a cause of MODYP Bowman, S E Flanagan, E L Edghill, et al.Diabetic Medicine : a Journal of the British Diabetic Association|May 17, 2011
Sequencing PDX1 (insulin promoter factor 1) in 1788 UK individuals found 5% had a low frequency coding variant, but these variants are not associated with Type 2 diabetesE L Edghill, A Khamis, M N Weedon, et al.Diabetic Medicine : a Journal of the British Diabetic Association|January 17, 2013
Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiencyE De Franco, C Shaw-Smith, S E Flanagan, et al.Diabetologia|September 11, 2007
Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the youngS Ellard, K Thomas, E L Edghill, et al.Pageof 1