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Courtney MacMullen

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

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Diabetes|August 28, 2003
Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptorPaul S Thornton, Courtney MacMullen, Arupa Ganguly, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptorSheela N Magge, Show-Ling Shyng, Courtney MacMullen, et al.
The Journal of Biological Chemistry|February 6, 2008
Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinismYu-Wen Lin, Jeremy D Bushman, Fei-Fei Yan, et al.
The Journal of Clinical Investigation|July 4, 2008
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutationsSara E Pinney, Courtney MacMullen, Susan Becker, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2004
Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulationCharles A Stanley, Paul S Thornton, Arupa Ganguly, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2016
Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin EffectTricia R Bhatti, Karthik Ganapathy, Alison R Huppmann, et al.
Hormone Research in Paediatrics|July 18, 2013
Dominant form of congenital hyperinsulinism maps to HK1 region on 10qSara E Pinney, Karthik Ganapathy, Jonathan Bradfield, et al.
The Journal of Clinical Endocrinology and Metabolism|September 27, 2007
Accuracy of [18F]fluorodopa positron emission tomography for diagnosing and localizing focal congenital hyperinsulinismOlga T Hardy, Miguel Hernandez-Pampaloni, Janet R Saffer, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
Pharmacological rescue of mitochondrial dysfunction, neurite degeneration, and premature death of ALS and AD iPSC-derived neuronsNeelam Shahani, Rupkatha Banerjee, Courtney MacMullen, et al.
The Journal of Biological Chemistry|April 1, 2006
Effects of a GTP-insensitive mutation of glutamate dehydrogenase on insulin secretion in transgenic miceChanghong Li, Andrea Matter, Andrea Kelly, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Diabetes|August 28, 2003
Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptorPaul S Thornton, Courtney MacMullen, Arupa Ganguly, et al.
The Journal of Clinical Endocrinology and Metabolism|September 10, 2004
Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptorSheela N Magge, Show-Ling Shyng, Courtney MacMullen, et al.
The Journal of Biological Chemistry|February 6, 2008
Destabilization of ATP-sensitive potassium channel activity by novel KCNJ11 mutations identified in congenital hyperinsulinismYu-Wen Lin, Jeremy D Bushman, Fei-Fei Yan, et al.
The Journal of Clinical Investigation|July 4, 2008
Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutationsSara E Pinney, Courtney MacMullen, Susan Becker, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2004
Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulationCharles A Stanley, Paul S Thornton, Arupa Ganguly, et al.
The Journal of Clinical Endocrinology and Metabolism|January 13, 2016
Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin EffectTricia R Bhatti, Karthik Ganapathy, Alison R Huppmann, et al.
Hormone Research in Paediatrics|July 18, 2013
Dominant form of congenital hyperinsulinism maps to HK1 region on 10qSara E Pinney, Karthik Ganapathy, Jonathan Bradfield, et al.
The Journal of Clinical Endocrinology and Metabolism|September 27, 2007
Accuracy of [18F]fluorodopa positron emission tomography for diagnosing and localizing focal congenital hyperinsulinismOlga T Hardy, Miguel Hernandez-Pampaloni, Janet R Saffer, et al.
Biorxiv : the Preprint Server for Biology|May 18, 2026
Pharmacological rescue of mitochondrial dysfunction, neurite degeneration, and premature death of ALS and AD iPSC-derived neuronsNeelam Shahani, Rupkatha Banerjee, Courtney MacMullen, et al.
The Journal of Biological Chemistry|April 1, 2006
Effects of a GTP-insensitive mutation of glutamate dehydrogenase on insulin secretion in transgenic miceChanghong Li, Andrea Matter, Andrea Kelly, et al.
Pageof 2