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Jayne A L Minton

Showing results (1-10 of 9) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation surveyor: software for DNA sequence analysisJayne A L Minton, Sarah E Flanagan, Sian Ellard
Reviews in Endocrine & Metabolic Disorders|March 6, 2003
Wolfram syndromeJayne A L Minton, Lynne A Rainbow, Christopher Ricketts, et al.
Diabetes|June 25, 2010
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalitiesOscar Rubio-Cabezas, Jayne A L Minton, Iren Kantor, et al.
Diabetes|March 28, 2002
Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populationsJayne A L Minton, Andrew T Hattersley, Katharine Owen, et al.
The Review of Diabetic Studies : RDS|May 10, 2007
The impact of the angiotensin-converting enzyme insertion/deletion polymorphism on severe hypoglycemia in Type 2 diabetesRachel M Freathy, Kathryn F Lonnen, Anna M Steele, et al.
Biochemical Pharmacology|March 29, 2003
Pharmacological characterisation of a cell line expressing GABA B1b and GABA B2 receptor subunitsWarren D Hirst, Adam J Babbs, Andrew Green, et al.
Diabetes Care|October 22, 2008
Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetesOscar Rubio-Cabezas, Jayne A L Minton, Richard Caswell, et al.
JOP : Journal of the Pancreas|January 13, 2010
Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiologyEmma L Edghill, Jayne A L Minton, Christopher J Groves, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous familiesOscar Rubio-Cabezas, Ann-Marie Patch, Jayne A L Minton, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Methods in Molecular Biology (Clifton, N.J.)|October 13, 2010
Mutation surveyor: software for DNA sequence analysisJayne A L Minton, Sarah E Flanagan, Sian Ellard
Reviews in Endocrine & Metabolic Disorders|March 6, 2003
Wolfram syndromeJayne A L Minton, Lynne A Rainbow, Christopher Ricketts, et al.
Diabetes|June 25, 2010
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalitiesOscar Rubio-Cabezas, Jayne A L Minton, Iren Kantor, et al.
Diabetes|March 28, 2002
Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populationsJayne A L Minton, Andrew T Hattersley, Katharine Owen, et al.
The Review of Diabetic Studies : RDS|May 10, 2007
The impact of the angiotensin-converting enzyme insertion/deletion polymorphism on severe hypoglycemia in Type 2 diabetesRachel M Freathy, Kathryn F Lonnen, Anna M Steele, et al.
Biochemical Pharmacology|March 29, 2003
Pharmacological characterisation of a cell line expressing GABA B1b and GABA B2 receptor subunitsWarren D Hirst, Adam J Babbs, Andrew Green, et al.
Diabetes Care|October 22, 2008
Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetesOscar Rubio-Cabezas, Jayne A L Minton, Richard Caswell, et al.
JOP : Journal of the Pancreas|January 13, 2010
Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiologyEmma L Edghill, Jayne A L Minton, Christopher J Groves, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous familiesOscar Rubio-Cabezas, Ann-Marie Patch, Jayne A L Minton, et al.
Pageof 1