SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion (Q57303430)

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3 February 2020

title

SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion (English)

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3 February 2020

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2

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Ariana Kariminejad

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Sian Ellard

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3 February 2020

Andrew Tym Hattersley

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author name string

F H Sansbury

1

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3 February 2020

J A L Houghton

3

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F L Shuixian Shen

4

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A M S Al-Senani

5

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A M Habeb

6

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M Abdullah

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publication date

2 June 2012

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3 February 2020

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3 February 2020

volume

55

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issue

9

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page(s)

2381-2385

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https://scigraph.springernature.com/pub.10.1007/s00125-012-2595-0

3 February 2020

exact match

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cites work

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Human and rat beta cells differ in glucose transporter but not in glucokinase gene expression

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Low levels of glucose transporters and K+ATP channels in human pancreatic beta cells early in development.

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GLUT2 (SLC2A2) is not the principal glucose transporter in human pancreatic beta cells: implications for understanding genetic association signals at this locus

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Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome.

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Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes

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Identification of a novel mutation in the GLUT2 gene in a patient with Fanconi-Bickel syndrome presenting with neonatal diabetes mellitus and galactosaemia

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Defective Glucose Transport across the Blood-Brain Barrier as a Cause of Persistent Hypoglycorrhachia, Seizures, and Developmental Delay

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GLUT-1 deficiency syndrome caused by haploinsufficiency of the blood-brain barrier hexose carrier

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Single-strand conformation polymorphism analysis of the glucose transporter gene GLUT1 in maturity-onset diabetes of the young.

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Transport and metabolism of glucose in an insulin-secreting cell line, beta TC-1.

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GLUT2 mutations, translocation, and receptor function in diet sugar managing

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Glucose transporters: structure, function and consequences of deficiency

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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

21 January 2018

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Detailed physiologic characterization reveals diverse mechanisms for novel genetic Loci regulating glucose and insulin metabolism in humans

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Hyperglycemia and hypoinsulinemia in patients with Fanconi-Bickel syndrome

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12 December 2020

The fanconi syndrome associated with hepatic glycogenosis and abnormal metabolism of galactose

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12 December 2020

Transfection of AtT-20ins cells with GLUT-2 but not GLUT-1 confers glucose-stimulated insulin secretion. Relationship to glucose metabolism

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Fanconi-Bickel syndrome

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Glucose uptake, utilization, and signaling in GLUT2-null islets

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Liver glucose transporter: a basolateral protein in hepatocytes and intestine and kidney cells

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Incidence, genetics, and clinical phenotype of permanent neonatal diabetes mellitus in northwest Saudi Arabia

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10.1007/S00125-012-2595-0

Identifiers

DOI

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3 February 2020

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