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S Ellard

Showing results (101-110 of 144) with videos related to

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Diabetes|May 22, 2016
Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 DiabetesK A Patel, R A Oram, S E Flanagan, et al.
Diabetes|August 28, 2001
The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuriaC Bingham, S Ellard, A J Nicholls, et al.
Diabetes|March 29, 2001
beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutationsE R Pearson, G Velho, P Clark, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|July 29, 2011
A pathway to insulin independence in newborns and infants with diabetesS Shahawy, N K Chan, S Ellard, et al.
American Journal of Human Genetics|December 31, 2005
Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotypeD B Sparrow, G Chapman, M A Wouters, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2000
The mutated human gene encoding hepatocyte nuclear factor 1beta inhibits kidney formation in developing Xenopus embryosW Wild, E Pogge von Strandmann, A Nastos, et al.
Nature Genetics|March 31, 2000
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosisM P Bulman, K Kusumi, T M Frayling, et al.
Diabetologia|June 6, 2009
Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live birthsA S Slingerland, B M Shields, S E Flanagan, et al.
Diabetes|March 29, 2001
beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factorsT M Frayling, J C Evans, M P Bulman, et al.
Diabetologia|June 16, 2011
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutationsR R Kapoor, S E Flanagan, C T James, et al.
Pageof 15

Showing results (101-110 of 144) with videos related to

Sort By:
Pageof 15
Diabetes|May 22, 2016
Type 1 Diabetes Genetic Risk Score: A Novel Tool to Discriminate Monogenic and Type 1 DiabetesK A Patel, R A Oram, S E Flanagan, et al.
Diabetes|August 28, 2001
The generalized aminoaciduria seen in patients with hepatocyte nuclear factor-1alpha mutations is a feature of all patients with diabetes and is associated with glucosuriaC Bingham, S Ellard, A J Nicholls, et al.
Diabetes|March 29, 2001
beta-cell genes and diabetes: quantitative and qualitative differences in the pathophysiology of hepatic nuclear factor-1alpha and glucokinase mutationsE R Pearson, G Velho, P Clark, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|July 29, 2011
A pathway to insulin independence in newborns and infants with diabetesS Shahawy, N K Chan, S Ellard, et al.
American Journal of Human Genetics|December 31, 2005
Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotypeD B Sparrow, G Chapman, M A Wouters, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2000
The mutated human gene encoding hepatocyte nuclear factor 1beta inhibits kidney formation in developing Xenopus embryosW Wild, E Pogge von Strandmann, A Nastos, et al.
Nature Genetics|March 31, 2000
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosisM P Bulman, K Kusumi, T M Frayling, et al.
Diabetologia|June 6, 2009
Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live birthsA S Slingerland, B M Shields, S E Flanagan, et al.
Diabetes|March 29, 2001
beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factorsT M Frayling, J C Evans, M P Bulman, et al.
Diabetologia|June 16, 2011
Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutationsR R Kapoor, S E Flanagan, C T James, et al.
Pageof 15