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Sarah E Flanagan

Showing results (1-10 of 229) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channelSarah E Flanagan, Sian Ellard
Indian Pediatrics|July 17, 2012
Permanent neonatal diabetes caused by a novel mutationVandana Jain, Sarah E Flanagan, Sian Ellard
Genetic Testing and Molecular Biomarkers|July 21, 2010
Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutationsSarah E Flanagan, Ann-Marie Patch, Sian Ellard
Reviews in Endocrine & Metabolic Disorders|October 6, 2010
Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11Emma L Edghill, Sarah E Flanagan, Sian Ellard
Seminars in Pediatric Surgery|December 28, 2010
Genetics of congenital hyperinsulinemic hypoglycemiaSarah E Flanagan, Ritika R Kapoor, Khalid Hussain
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
Frontiers in Endocrinology|July 25, 2022
Congenital Hyperinsulinism: Current Laboratory-Based Approaches to the Genetic Diagnosis of a Heterogeneous DiseaseThomas I Hewat, Matthew B Johnson, Sarah E Flanagan
The Lancet. Diabetes & Endocrinology|July 31, 2016
Monogenic autoimmune diseases of the endocrine systemMatthew B Johnson, Andrew T Hattersley, Sarah E Flanagan
Nature Reviews. Endocrinology|April 16, 2026
The effect of hypoglycaemia on neurodevelopment: insights from congenital hyperinsulinismPamela Bowman, Jonna M E Männistö, Sarah E Flanagan
Indian Pediatrics|October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two SiblingsAmit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.
Pageof 23

Showing results (1-10 of 229) with videos related to

Sort By:
Pageof 23
Methods in Molecular Biology (Clifton, N.J.)|November 11, 2008
Identification of mutations in the Kir6.2 subunit of the K(ATP) channelSarah E Flanagan, Sian Ellard
Indian Pediatrics|July 17, 2012
Permanent neonatal diabetes caused by a novel mutationVandana Jain, Sarah E Flanagan, Sian Ellard
Genetic Testing and Molecular Biomarkers|July 21, 2010
Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutationsSarah E Flanagan, Ann-Marie Patch, Sian Ellard
Reviews in Endocrine & Metabolic Disorders|October 6, 2010
Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11Emma L Edghill, Sarah E Flanagan, Sian Ellard
Seminars in Pediatric Surgery|December 28, 2010
Genetics of congenital hyperinsulinemic hypoglycemiaSarah E Flanagan, Ritika R Kapoor, Khalid Hussain
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
Frontiers in Endocrinology|July 25, 2022
Congenital Hyperinsulinism: Current Laboratory-Based Approaches to the Genetic Diagnosis of a Heterogeneous DiseaseThomas I Hewat, Matthew B Johnson, Sarah E Flanagan
The Lancet. Diabetes & Endocrinology|July 31, 2016
Monogenic autoimmune diseases of the endocrine systemMatthew B Johnson, Andrew T Hattersley, Sarah E Flanagan
Nature Reviews. Endocrinology|April 16, 2026
The effect of hypoglycaemia on neurodevelopment: insights from congenital hyperinsulinismPamela Bowman, Jonna M E Männistö, Sarah E Flanagan
Indian Pediatrics|October 25, 2016
Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two SiblingsAmit Kumar Satapathy, Vandana Jain, Sian Ellard, et al.
Pageof 23