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S Ellard

Showing results (41-50 of 144) with videos related to

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Human Genetics|January 24, 1998
A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetesT M Frayling, M P Bulman, M Appleton, et al.
Mutagenesis|November 1, 1996
A comparison of conventional metaphase analysis of Giemsa-stained chromosomes with multi-colour fluorescence in situ hybridization analysis to detect chromosome aberrations induced by daunomycinS Ellard, S Toper, G Stemp, et al.
QJM : Monthly Journal of the Association of Physicians|July 19, 2011
Pseudohypoaldosteronism type 2 presenting with hypertension and hyperkalaemia due to a novel mutation in the WNK4 geneA M Brooks, M Owens, J A Sayer, et al.
Archives of Disease in Childhood|February 6, 2009
Hyperinsulinaemic hypoglycaemiaR R Kapoor, S E Flanagan, C James, et al.
Archives of Disease in Childhood|August 26, 1998
Genetic testing for maturity onset diabetes of the young in childhood hyperglycaemiaK A Matyka, F Beards, M Appleton, et al.
Diabetologia|April 16, 2004
Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndromeL W Harries, S Ellard, R W A Jones, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 29, 2007
Low prevalence of mitochondrial DNA 3243A>G point mutation in Caucasians with unexplained renal diseaseR Singh, E Edghill, C Bingham, 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.
QJM : Monthly Journal of the Association of Physicians|March 20, 2019
Juvenile diabetes and visual impairment: Wolfram syndromeA K Annamalai, S Ellard, M Shanmugam, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 5, 2013
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin responseV B Arya, S Rahman, S Senniappan, et al.
Pageof 15

Showing results (41-50 of 144) with videos related to

Sort By:
Pageof 15
Human Genetics|January 24, 1998
A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetesT M Frayling, M P Bulman, M Appleton, et al.
Mutagenesis|November 1, 1996
A comparison of conventional metaphase analysis of Giemsa-stained chromosomes with multi-colour fluorescence in situ hybridization analysis to detect chromosome aberrations induced by daunomycinS Ellard, S Toper, G Stemp, et al.
QJM : Monthly Journal of the Association of Physicians|July 19, 2011
Pseudohypoaldosteronism type 2 presenting with hypertension and hyperkalaemia due to a novel mutation in the WNK4 geneA M Brooks, M Owens, J A Sayer, et al.
Archives of Disease in Childhood|February 6, 2009
Hyperinsulinaemic hypoglycaemiaR R Kapoor, S E Flanagan, C James, et al.
Archives of Disease in Childhood|August 26, 1998
Genetic testing for maturity onset diabetes of the young in childhood hyperglycaemiaK A Matyka, F Beards, M Appleton, et al.
Diabetologia|April 16, 2004
Abnormal splicing of hepatocyte nuclear factor-1 beta in the renal cysts and diabetes syndromeL W Harries, S Ellard, R W A Jones, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 29, 2007
Low prevalence of mitochondrial DNA 3243A>G point mutation in Caucasians with unexplained renal diseaseR Singh, E Edghill, C Bingham, 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.
QJM : Monthly Journal of the Association of Physicians|March 20, 2019
Juvenile diabetes and visual impairment: Wolfram syndromeA K Annamalai, S Ellard, M Shanmugam, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 5, 2013
HNF4A mutation: switch from hyperinsulinaemic hypoglycaemia to maturity-onset diabetes of the young, and incretin responseV B Arya, S Rahman, S Senniappan, et al.
Pageof 15