Functional analysis of a mutant sulphonylurea receptor associated with a mild form of persistent hyperinsulinaemic hypoglycaemia of infancy

Functional analysis of a mutant sulphonylurea receptor associated with a mild form of persistent hyperinsulinaemic hypoglycaemia of infancy

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Trapp, S, Jones, P, Matsuo, M, Amachi, T, Ueda, K, Tanizawa, Y, Oka, Y, Ashcroft, F
التنسيق:	Journal article
منشور في:	2000

مواد مشابهة

Functional analysis of a mutant sulfonylurea receptor, SUR1-R1420C, that is responsible for persistent hyperinsulinemic hypoglycemia of infancy.
حسب: Matsuo, M, وآخرون
منشور في: (2000)

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Asymptomatic Hyperinsulinaemic Hypoglycaemia
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Sulphonylureas and hypoglycaemia.
حسب: Ferner, R, وآخرون
منشور في: (1988)

Varied presentation of hyperinsulinaemic hypoglycaemia
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The diagnosis and management of hyperinsulinaemic hypoglycaemia
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Hyperinsulinaemic Hypoglycaemia - The Molecular Mechanisms
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Familial persistent hyperinsulinaemic hypoglycaemia of infancy due to a novel glucokinase (GCK) activating mutation G68V
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Somatostatin analogues for the treatment of hyperinsulinaemic hypoglycaemia
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NEM modification prevents high-affinity ATP binding to the first nucleotide binding fold of the sulphonylurea receptor, SUR1.
حسب: Matsuo, M, وآخرون
منشور في: (1999)

Heterogeneity in disease severity in a family with a novel G68V GCK activating mutation causing persistent hyperinsulinaemic hypoglycaemia of infancy.
حسب: Wabitsch, M, وآخرون
منشور في: (2007)

Diazoxide-responsive hyperinsulinaemic hypoglycaemia in tyrosinaemia type 1
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منشور في: (2021-01-01)

Phenotypic heterogeneity in a family with a novel activating glucokinase (GCK) mutation (G68V) causing familial persistent hyperinsulinaemic hypoglycaemia of infancy
حسب: Gloyn, A, وآخرون
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Longitudinal Auxological recovery in a cohort of children with Hyperinsulinaemic Hypoglycaemia
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Adult-onset hyperinsulinaemic hypoglycaemia in clinical practice: diagnosis, aetiology and management
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A tale of two sisters – delayed diagnosis of genetic hyperinsulinaemic hypoglycaemia
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An Evaluation of Growth Hormone and IGF-1 Responses in Neonates with Hyperinsulinaemic Hypoglycaemia
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Hyperinsulinaemic hypoglycaemia: A rare association of vanishing white matter disease
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منشور في: (2020-01-01)

Sirolimus therapy in a child with partially diazoxide-responsive hyperinsulinaemic hypoglycaemia
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منشور في: (2016-10-01)

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene.
حسب: Ewan R Pearson, وآخرون
منشور في: (2007-04-01)

Hyperinsulinaemic hypoglycaemia - a diagnostic challenge. A report of two atypical cases.
حسب: Renata Baronaite Hansen, وآخرون
منشور في: (2015-07-01)

Clinical presentation of 54 patients with endogenous hyperinsulinaemic hypoglycaemia: a neurological chameleon (observational study)
حسب: Luca G. Valente, وآخرون
منشور في: (2018-11-01)

Accuracy and impact on quality of life of real-time continuous glucose monitoring in children with hyperinsulinaemic hypoglycaemia
حسب: Madhini Sivasubramanian, وآخرون
منشور في: (2023-09-01)

Exceptional diazoxide sensitivity in hyperinsulinaemic hypoglycaemia due to a novel HNF4A mutation
حسب: Ved Bhushan Arya, وآخرون
منشور في: (2019-05-01)

Diazoxide use for neonatal hyperinsulinaemic hypoglycaemia in a low-resource setting: A Case Report
حسب: Adekoya AO, وآخرون
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Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase
حسب: Heslegrave Amanda J, وآخرون
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Paternal uniparental isodisomy of chromosome 11p15.5 within the pancreas causes isolated hyperinsulinaemic hypoglycaemia
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Hyperinsulinaemic hypoglycaemia in non-anaesthetized Göttingen minipigs induces a counter-regulatory endocrine response and electrocardiographic changes
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Chronic Hyperinsulinaemic Hypoglycaemia in Rats Is Accompanied by Increased Body Weight, Hyperleptinaemia, and Decreased Neuronal Glucose Transporter Levels in the Brain
حسب: Vivi F. H. Jensen, وآخرون
منشور في: (2017-01-01)

Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor.
حسب: Tucker, S, وآخرون
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Trends in Presentation and Management of Endogenous Hyperinsulinaemic Hypoglycaemia Over the Last Three Decades at a Tertiary Care Centre (1992–2022)
حسب: Setu Gupta, وآخرون
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New uses for old drugs: neonatal diabetes and sulphonylureas.
حسب: Ashcroft, F
منشور في: (2010)

Congenital Hyperinsulinemic Hypoglycaemia of Infancy- A Case Report
حسب: Mani Raj, وآخرون
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Characterization of two novel forms of the rat sulphonylurea receptor SUR1A2 and SUR1BDelta31.
حسب: Gros, L, وآخرون
منشور في: (2002)

Effects of protein phosphorylation on the sulphonylurea receptor of the pancreatic beta-cell.
حسب: Niki, I, وآخرون
منشور في: (1997)

Interactions between nicorandil and sulphonylureas: a structural basis.
حسب: Reimann, F, وآخرون
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Binding of sulphonylureas to plasma proteins – a KATP channel perspective
حسب: Proks, P, وآخرون
منشور في: (2018)

Binding of sulphonylureas to plasma proteins - A KATP channel perspective.
حسب: Peter Proks, وآخرون
منشور في: (2018-01-01)

Involvement of the n-terminus of Kir6.2 in coupling to the sulphonylurea receptor.
حسب: Reimann, F, وآخرون
منشور في: (1999)

Promiscuous coupling between the sulphonylurea receptor and inwardly rectifying potassium channels.
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منشور في: (1996)