KATP channel mutation disrupts hippocampal network activity and nocturnal gamma shifts

KATP channel mutation disrupts hippocampal network activity and nocturnal gamma shifts

ATP-sensitive potassium (KATP) channels couple cell metabolism to cellular electrical activity. Humans affected by severe activating mutations in KATP channels suffer from developmental delay, epilepsy, and neonatal diabetes (DEND syndrome). While the aetiology of diabetes in DEND syndrome is well u...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Burkart, M-E, Kurzke, J, Jacobi, R, Vera, J, Ashcroft, FM, Eilers, J, Lippmann, K
التنسيق:	Journal article
اللغة:	English
منشور في:	Oxford University Press 2024

مواد مشابهة

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منشور في: (2017)

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منشور في: (2000)

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حسب: Ashcroft, FM
منشور في: (2023)

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منشور في: (2015-01-01)

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منشور في: (2024-01-01)

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منشور في: (2006)

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منشور في: (2018-01-01)

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منشور في: (1998)

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منشور في: (2023-03-01)

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حسب: D. Kent Arrell, وآخرون
منشور في: (2022-05-01)

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منشور في: (2021-03-01)

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منشور في: (2024-11-01)

The Structural Basis for the Binding of Repaglinide to the Pancreatic KATP Channel
حسب: Dian Ding, وآخرون
منشور في: (2019-05-01)

Expression of an activating mutation in the gene encoding the KATP channel subunit Kir6.2 in mouse pancreatic beta cells recapitulates neonatal diabetes.
حسب: Girard, C, وآخرون
منشور في: (2009)

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Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetes.
حسب: Männikkö, R, وآخرون
منشور في: (2011)

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حسب: Baukrowitz, T, وآخرون
منشور في: (1999)