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S C Bain

Showing results (61-70 of 109) with videos related to

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Diabetologia|July 1, 1997
A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the youngM P Bulman, M J Dronsfield, T Frayling, et al.
Diabetologia|September 24, 1999
Human leucocyte antigen and insulin gene regions and nephropathy in type I diabetesT A Chowdhury, P H Dyer, C H Mijovic, et al.
Human Molecular Genetics|October 9, 2001
A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteinsF Cucca, R Lampis, M Congia, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 21, 2004
The TGF-beta 1 gene codon 10 polymorphism contributes to the genetic predisposition to nephropathy in Type 1 diabetesA Patel, W R Scott, P A Lympany, et al.
Clinical Chemistry|July 1, 1991
Detection of human apolipoprotein E3, E2, and E4 genotypes by an allele-specific oligonucleotide-primed polymerase chain reaction assay: development and validationE K Green, S C Bain, P J Day, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 18, 2019
Effect of structured self-monitoring of blood glucose, with and without additional TeleCare support, on overall glycaemic control in non-insulin treated Type 2 diabetes: the SMBG Study, a 12-month randomized controlled trialS N Parsons, S D Luzio, J N Harvey, et al.
Diabetes Research and Clinical Practice|August 24, 2010
Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease in diabetes mellitusD A Jones, S L Prior, T S Tang, et al.
Ophthalmology|June 12, 1999
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutationP R Smith, S C Bain, P A Good, et al.
Primary Care Diabetes|July 17, 2009
Use of a patient linked data warehouse to facilitate diabetes trial recruitment from primary careC J Brooks, J W Stephens, D E Price, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 16, 1998
Glomerular filtration rate determination in diabetic patients using iohexol clearance--comparison of single and multiple plasma sampling methodsT A Chowdhury, P H Dyer, W A Bartlett, et al.
Pageof 11

Showing results (61-70 of 109) with videos related to

Sort By:
Pageof 11
Diabetologia|July 1, 1997
A missense mutation in the hepatocyte nuclear factor 4 alpha gene in a UK pedigree with maturity-onset diabetes of the youngM P Bulman, M J Dronsfield, T Frayling, et al.
Diabetologia|September 24, 1999
Human leucocyte antigen and insulin gene regions and nephropathy in type I diabetesT A Chowdhury, P H Dyer, C H Mijovic, et al.
Human Molecular Genetics|October 9, 2001
A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteinsF Cucca, R Lampis, M Congia, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|December 21, 2004
The TGF-beta 1 gene codon 10 polymorphism contributes to the genetic predisposition to nephropathy in Type 1 diabetesA Patel, W R Scott, P A Lympany, et al.
Clinical Chemistry|July 1, 1991
Detection of human apolipoprotein E3, E2, and E4 genotypes by an allele-specific oligonucleotide-primed polymerase chain reaction assay: development and validationE K Green, S C Bain, P J Day, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 18, 2019
Effect of structured self-monitoring of blood glucose, with and without additional TeleCare support, on overall glycaemic control in non-insulin treated Type 2 diabetes: the SMBG Study, a 12-month randomized controlled trialS N Parsons, S D Luzio, J N Harvey, et al.
Diabetes Research and Clinical Practice|August 24, 2010
Association between the rs4880 superoxide dismutase 2 (C>T) gene variant and coronary heart disease in diabetes mellitusD A Jones, S L Prior, T S Tang, et al.
Ophthalmology|June 12, 1999
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutationP R Smith, S C Bain, P A Good, et al.
Primary Care Diabetes|July 17, 2009
Use of a patient linked data warehouse to facilitate diabetes trial recruitment from primary careC J Brooks, J W Stephens, D E Price, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 16, 1998
Glomerular filtration rate determination in diabetic patients using iohexol clearance--comparison of single and multiple plasma sampling methodsT A Chowdhury, P H Dyer, W A Bartlett, et al.
Pageof 11