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Arupa Ganguly
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Journal Articles

Diazoxide-Unresponsive Congenital Hyperinsulinism in Children With Dominant Mutations of the β-Cell Sulfonylurea Receptor SUR1

Courtney M. MacMullen, Qing Zhou, Kara E. Snider, Paul H. Tewson, Susan A. Becker, Ali Rahim Aziz, Arupa Ganguly, Show-Ling Shyng, Charles A. Stanley
Journal: Diabetes
Diabetes 2011;60(6):1797–1804
https://doi.org/10.2337/db10-1631
Published: 21 May 2011
View article titled, Diazoxide-Unresponsive Congenital Hyperinsulinism in Children With Dominant Mutations of the β-Cell Sulfonylurea Receptor SUR1
Open the PDF for Diazoxide-Unresponsive Congenital Hyperinsulinism in Children With Dominant Mutations of the β-Cell Sulfonylurea Receptor SUR1 in another window
Journal Articles

Congenital Hyperinsulinism–Associated ABCC8 Mutations That Cause Defective Trafficking of ATP-Sensitive K+ Channels: Identification and Rescue

Fei-Fei Yan, Yu-Wen Lin, Courtney MacMullen, Arupa Ganguly, Charles A. Stanley, Show-Ling Shyng
Journal: Diabetes
Diabetes 2007;56(9):2339–2348
https://doi.org/10.2337/db07-0150
Published: 01 September 2007
View article titled, Congenital Hyperinsulinism–Associated <em>ABCC8</em> Mutations That Cause Defective Trafficking of ATP-Sensitive K<sup>+</sup> Channels: <subtitle>Identification and Rescue</subtitle>
Open the PDF for Congenital Hyperinsulinism–Associated <em>ABCC8</em> Mutations That Cause Defective Trafficking of ATP-Sensitive K<sup>+</sup> Channels: <subtitle>Identification and Rescue</subtitle> in another window
Includes: Supplementary data
Journal Articles

Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor

Paul S. Thornton, Courtney MacMullen, Arupa Ganguly, Eduardo Ruchelli, Linda Steinkrauss, Ana Crane, Lydia Aguilar-Bryan, Charles A. Stanley
Journal: Diabetes
Diabetes 2003;52(9):2403–2410
https://doi.org/10.2337/diabetes.52.9.2403
Published: 01 September 2003
View article titled, Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor
Open the PDF for Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor in another window