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S Ellard

Showing results (11-20 of 144) with videos related to

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Diabetes Care|June 27, 2000
A severe clinical phenotype results from the co-inheritance of type 2 susceptibility genes and a hepatocyte nuclear factor-1alpha mutationC J Tack, S Ellard, A T Hattersley
Diabetologia|February 26, 2008
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the youngS Ellard, C Bellanné-Chantelot, A T Hattersley, et al.
Journal of Endocrinological Investigation|January 5, 2002
Multiple endocrine neoplasia type 1Burin from Mauritius: a novel MEN1 mutationC Kong, S Ellard, C Johnston, et al.
Clinical Medicine (London, England)|April 10, 2014
Ten years of the national genetic diabetes nurse network: a model for the translation of genetic information into clinical careM Shepherd, K Colclough, S Ellard, et al.
Diabetes Care|November 28, 2001
ACE gene polymorphism as a prognostic indicator in patients with type 2 diabetes and established renal diseaseS Fava, J Azzopardi, S Ellard, et al.
Clinical Endocrinology|January 27, 2005
Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testingS Ellard, A T Hattersley, C M Brewer, et al.
Clinical Genetics|July 15, 2011
JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndromeK Guegan, K Stals, M Day, et al.
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.
Carcinogenesis|December 1, 1993
Cellular and chromosomal hypersensitivity to DNA crosslinking agents and topoisomerase inhibitors in the radiosensitive Chinese hamster irs mutants: phenotypic similarities to ataxia telangiectasia and Fanconi's anaemia cellsN J Jones, S Ellard, R Waters, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|October 14, 2011
Effective treatment of diabetes caused by activating ABCC8/SUR1 mutation with glimepirideB Karges, D Schnur, S Ellard, et al.
Pageof 15

Showing results (11-20 of 144) with videos related to

Sort By:
Pageof 15
Diabetes Care|June 27, 2000
A severe clinical phenotype results from the co-inheritance of type 2 susceptibility genes and a hepatocyte nuclear factor-1alpha mutationC J Tack, S Ellard, A T Hattersley
Diabetologia|February 26, 2008
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the youngS Ellard, C Bellanné-Chantelot, A T Hattersley, et al.
Journal of Endocrinological Investigation|January 5, 2002
Multiple endocrine neoplasia type 1Burin from Mauritius: a novel MEN1 mutationC Kong, S Ellard, C Johnston, et al.
Clinical Medicine (London, England)|April 10, 2014
Ten years of the national genetic diabetes nurse network: a model for the translation of genetic information into clinical careM Shepherd, K Colclough, S Ellard, et al.
Diabetes Care|November 28, 2001
ACE gene polymorphism as a prognostic indicator in patients with type 2 diabetes and established renal diseaseS Fava, J Azzopardi, S Ellard, et al.
Clinical Endocrinology|January 27, 2005
Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testingS Ellard, A T Hattersley, C M Brewer, et al.
Clinical Genetics|July 15, 2011
JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndromeK Guegan, K Stals, M Day, et al.
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.
Carcinogenesis|December 1, 1993
Cellular and chromosomal hypersensitivity to DNA crosslinking agents and topoisomerase inhibitors in the radiosensitive Chinese hamster irs mutants: phenotypic similarities to ataxia telangiectasia and Fanconi's anaemia cellsN J Jones, S Ellard, R Waters, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|October 14, 2011
Effective treatment of diabetes caused by activating ABCC8/SUR1 mutation with glimepirideB Karges, D Schnur, S Ellard, et al.
Pageof 15