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Journal Articles

Genetic Variation at the Sulfonylurea Receptor, Type 2 Diabetes, and Coronary Heart Disease

Connor A. Emdin, Derek Klarin, Pradeep Natarajan, CARDIOGRAM Exome Consortium, Jose C. Florez, Sekar Kathiresan, Amit V. Khera

Diabetes 2017;66(8):2310–2315

DOI: https://doi.org/10.2337/db17-0149

Published: 14 April 2017

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Includes: Supplementary data

Journal Articles

Mutations of the Same Conserved Glutamate Residue in NBD2 of the Sulfonylurea Receptor 1 Subunit of the K_ATP Channel Can Result in Either Hyperinsulinism or Neonatal Diabetes

Roope Männikkö, Sarah E. Flanagan, Xiuli Sim, David Segal, Khalid Hussain, Sian Ellard, Andrew T. Hattersley, Frances M. Ashcroft

Diabetes 2011;60(6):1813–1822

DOI: https://doi.org/10.2337/db10-1583

Published: 21 May 2011

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Includes: Supplementary data

Journal Articles

Errata

Diabetes 2008;57(9):2552

DOI: https://doi.org/10.2337/db08-er09

Published: 01 September 2008

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Journal Articles

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence

Maha Abdulhadi-Atwan, Jeremy D. Bushman, Sharona Tornovsky-Babaey, Avital Perry, Abdulsalam Abu-Libdeh, Benjamin Glaser, Show-Ling Shyng, David H. Zangen

Diabetes 2008;57(7):1935–1940

DOI: https://doi.org/10.2337/db08-0159

Published: 01 July 2008

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Journal Articles

The Actions of a Novel Potent Islet β-Cell–Specific ATP-Sensitive K⁺ Channel Opener Can Be Modulated by Syntaxin-1A Acting on Sulfonylurea Receptor 1

Betty Ng, Youhou Kang, Chadwick L. Elias, Yan He, Huanli Xie, John B. Hansen, Philip Wahl, Herbert Y. Gaisano

Diabetes 2007;56(8):2124–2134

DOI: https://doi.org/10.2337/db07-0030

Published: 01 August 2007

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Includes: Supplementary data

Journal Articles

A Mutation in the TMD0-L0 Region of Sulfonylurea Receptor-1 (L225P) Causes Permanent Neonatal Diabetes Mellitus (PNDM)

Ricard Masia, Diva D. De Leon, Courtney MacMullen, Heather McKnight, Charles A. Stanley, Colin G. Nichols

Diabetes 2007;56(5):1357–1362

DOI: https://doi.org/10.2337/db06-1746

Published: 01 May 2007

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Journal Articles

Roles of ATP-Sensitive K+ Channels as Metabolic Sensors: Studies of Kir6.x Null Mice

Kohtaro Minami, Takashi Miki, Takashi Kadowaki, Susumu Seino

Diabetes 2004;53(suppl_3):S176–S180

DOI: https://doi.org/10.2337/diabetes.53.suppl_3.S176

Published: 01 December 2004

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Journal Articles

Toward Linking Structure With Function in ATP-Sensitive K+ Channels

Joseph Bryan, Wanda H. Vila-Carriles, Guiling Zhao, Audrey P. Babenko, Lydia Aguilar-Bryan

Diabetes 2004;53(suppl_3):S104–S112

DOI: https://doi.org/10.2337/diabetes.53.suppl_3.S104

Published: 01 December 2004

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Journal Articles

Effect of Two Amino Acids in TM17 of Sulfonylurea Receptor SUR1 on the Binding of ATP-Sensitive K⁺ Channel Modulators

Annette Hambrock, Tülay Kayar, Demet Stumpp, Hartmut Osswald

Diabetes 2004;53(suppl_3):S128–S134

DOI: https://doi.org/10.2337/diabetes.53.suppl_3.S128

Published: 01 December 2004

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Journal Articles

Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region

Jose C. Florez, Noël Burtt, Paul I.W. de Bakker, Peter Almgren, Tiinamaija Tuomi, Johan Holmkvist, Daniel Gaudet, Thomas J. Hudson, Steve F. Schaffner, Mark J. Daly, Joel N. Hirschhorn, Leif Groop, David Altshuler

Diabetes 2004;53(5):1360–1368

DOI: https://doi.org/10.2337/diabetes.53.5.1360

Published: 01 May 2004

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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

Diabetes 2003;52(9):2403–2410

DOI: https://doi.org/10.2337/diabetes.52.9.2403

Published: 01 September 2003

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Journal Articles

Decreased Fasting and Oral Glucose Stimulated C-peptide in Nondiabetic Subjects With Sequence Variants in the Sulfonylurea Receptor 1 Gene

S. John Weisnagel, Tuomo Rankinen, André Nadeau, D.C. Rao, Yvon C. Chagnon, Louis Pérusse, Claude Bouchard

Diabetes 2001;50(3):697–702

DOI: https://doi.org/10.2337/diabetes.50.3.697

Published: 01 March 2001

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Journal Articles

Dysregulation of Insulin Secretion in Children With Congenital Hyperinsulinism due to Sulfonylurea Receptor Mutations

A. Grimberg, R.J. Ferry, Jr., A. Kelly, S. Koo-McCoy, K. Polonsky, B. Glaser, M.A. Permutt, L. Aguilar-Bryan, D. Stafford, P.S. Thornton, L. Baker, Charles A. Stanley

Diabetes 2001;50(2):322–328

DOI: https://doi.org/10.2337/diabetes.50.2.322

Published: 01 February 2001

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Meeting Abstracts

Sulfonylurea receptor 1 and Kir6.2 expression in the novel human insulin-secreting cell line NES2Y.

W M Macfarlane, R E O'Brien, P D Barnes, R M Shepherd, K E Cosgrove, K J Lindley, A Aynsley-Green, R F James, K Docherty, M J Dunne

Diabetes 2000;49(6):953–960

DOI: https://doi.org/10.2337/diabetes.49.6.953

Published: 01 June 2000

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Meeting Abstracts

Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.

Y Tanizawa, K Matsuda, M Matsuo, Y Ohta, N Ochi, M Adachi, M Koga, S Mizuno, M Kajita, Y Tanaka, K Tachibana, H Inoue, S Furukawa, T Amachi, K Ueda, Y Oka

Diabetes 2000;49(1):114–120

DOI: https://doi.org/10.2337/diabetes.49.1.114

Published: 01 January 2000

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Meeting Abstracts

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

B Glaser, F Ryan, M Donath, H Landau, C A Stanley, L Baker, D E Barton, P S Thornton

Diabetes 1999;48(8):1652–1657

DOI: https://doi.org/10.2337/diabetes.48.8.1652

Published: 01 August 1999

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Meeting Abstracts

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

T Otonkoski, C Ammälä, H Huopio, G J Cote, J Chapman, K Cosgrove, R Ashfield, E Huang, J Komulainen, F M Ashcroft, M J Dunne, J Kere, P M Thomas

Diabetes 1999;48(2):408–415

DOI: https://doi.org/10.2337/diabetes.48.2.408

Published: 01 February 1999

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Journal Articles

Cloning of the Promoters for the β-Cell ATP-Sensitive K-Channel Subunits Kir6.2 and SUR1

Rebecca Ashfield, Stephen J H Ashcroft

Diabetes 1998;47(8):1274–1280

DOI: https://doi.org/10.2337/diab.47.8.1274

Published: 01 August 1998

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Meeting Abstracts

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

S L Shyng, T Ferrigni, J B Shepard, A Nestorowicz, B Glaser, M A Permutt, C G Nichols

Diabetes 1998;47(7):1145–1151

DOI: https://doi.org/10.2337/diabetes.47.7.1145

Published: 01 July 1998

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Meeting Abstracts

Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene.

T Hansen, S M Echwald, L Hansen, A M Møller, K Almind, J O Clausen, S A Urhammer, H Inoue, J Ferrer, J Bryan, L Aguilar-Bryan, M A Permutt, O Pedersen

Diabetes 1998;47(4):598–605

DOI: https://doi.org/10.2337/diabetes.47.4.598

Published: 01 April 1998

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NARROW

Genetic Variation at the Sulfonylurea Receptor, Type 2 Diabetes, and Coronary Heart Disease

Mutations of the Same Conserved Glutamate Residue in NBD2 of the Sulfonylurea Receptor 1 Subunit of the K_ATP Channel Can Result in Either Hyperinsulinism or Neonatal Diabetes

Errata

Novel De Novo Mutation in Sulfonylurea Receptor 1 Presenting as Hyperinsulinism in Infancy Followed by Overt Diabetes in Early Adolescence

The Actions of a Novel Potent Islet β-Cell–Specific ATP-Sensitive K⁺ Channel Opener Can Be Modulated by Syntaxin-1A Acting on Sulfonylurea Receptor 1

A Mutation in the TMD0-L0 Region of Sulfonylurea Receptor-1 (L225P) Causes Permanent Neonatal Diabetes Mellitus (PNDM)

Roles of ATP-Sensitive K+ Channels as Metabolic Sensors: Studies of Kir6.x Null Mice

Toward Linking Structure With Function in ATP-Sensitive K+ Channels

Effect of Two Amino Acids in TM17 of Sulfonylurea Receptor SUR1 on the Binding of ATP-Sensitive K⁺ Channel Modulators

Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region

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

Decreased Fasting and Oral Glucose Stimulated C-peptide in Nondiabetic Subjects With Sequence Variants in the Sulfonylurea Receptor 1 Gene

Dysregulation of Insulin Secretion in Children With Congenital Hyperinsulinism due to Sulfonylurea Receptor Mutations

Sulfonylurea receptor 1 and Kir6.2 expression in the novel human insulin-secreting cell line NES2Y.

Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.

A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

Cloning of the Promoters for the β-Cell ATP-Sensitive K-Channel Subunits Kir6.2 and SUR1

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene.

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