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Diabetes
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February 11, 2021
The <i>KCNJ11-E23K</i> Gene Variant Hastens Diabetes Progression by Impairing Glucose-Induced Insulin Secretion
Gregor Sachse, Elizabeth Haythorne, Thomas Hill, et al.
Structure (London, England : 1993)
|
December 5, 2024
Structures of TASK-1 and TASK-3 K2P channels provide insight into their gating and dysfunction in disease
Peter Rory Hall, Thibault Jouen-Tachoire, Marcus Schewe, et al.
Diabetes
|
October 19, 2007
Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy
Julian P H Shield, Sarah E Flanagan, Deborah J Mackay, et al.
EMBO Reports
|
May 24, 2008
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes
Heidi de Wet, Peter Proks, Mathilde Lafond, et al.
Diabetes
|
May 30, 2006
Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects
Kenju Shimomura, Christophe A J Girard, Peter Proks, et al.
Diabetes
|
August 2, 2013
A mouse model of human hyperinsulinism produced by the E1506K mutation in the sulphonylurea receptor SUR1
Kenju Shimomura, Maija Tusa, Michaela Iberl, et al.
Clinical Case Reports
|
October 29, 2015
The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutation
Susan M O'Connell, Peter Proks, Holger Kramer, et al.
Nature Structural & Molecular Biology
|
February 26, 2025
Cryo-EM structure of the human THIK-1 K2P K<sup>+</sup> channel reveals a lower Y gate regulated by lipids and anesthetics
Karin E J Rödström, Bisher Eymsh, Peter Proks, et al.
Nature Communications
|
August 23, 2014
Reversible changes in pancreatic islet structure and function produced by elevated blood glucose
Melissa F Brereton, Michaela Iberl, Kenju Shimomura, et al.
Human Molecular Genetics
|
February 19, 2005
Relapsing diabetes can result from moderately activating mutations in KCNJ11
Anna L Gloyn, Frank Reimann, Christophe Girard, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 55) with videos related to
Sort By:
Page
of 6
Diabetes
|
February 11, 2021
The <i>KCNJ11-E23K</i> Gene Variant Hastens Diabetes Progression by Impairing Glucose-Induced Insulin Secretion
Gregor Sachse, Elizabeth Haythorne, Thomas Hill, et al.
Structure (London, England : 1993)
|
December 5, 2024
Structures of TASK-1 and TASK-3 K2P channels provide insight into their gating and dysfunction in disease
Peter Rory Hall, Thibault Jouen-Tachoire, Marcus Schewe, et al.
Diabetes
|
October 19, 2007
Mosaic paternal uniparental isodisomy and an ABCC8 gene mutation in a patient with permanent neonatal diabetes and hemihypertrophy
Julian P H Shield, Sarah E Flanagan, Deborah J Mackay, et al.
EMBO Reports
|
May 24, 2008
A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes
Heidi de Wet, Peter Proks, Mathilde Lafond, et al.
Diabetes
|
May 30, 2006
Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects
Kenju Shimomura, Christophe A J Girard, Peter Proks, et al.
Diabetes
|
August 2, 2013
A mouse model of human hyperinsulinism produced by the E1506K mutation in the sulphonylurea receptor SUR1
Kenju Shimomura, Maija Tusa, Michaela Iberl, et al.
Clinical Case Reports
|
October 29, 2015
The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutation
Susan M O'Connell, Peter Proks, Holger Kramer, et al.
Nature Structural & Molecular Biology
|
February 26, 2025
Cryo-EM structure of the human THIK-1 K2P K<sup>+</sup> channel reveals a lower Y gate regulated by lipids and anesthetics
Karin E J Rödström, Bisher Eymsh, Peter Proks, et al.
Nature Communications
|
August 23, 2014
Reversible changes in pancreatic islet structure and function produced by elevated blood glucose
Melissa F Brereton, Michaela Iberl, Kenju Shimomura, et al.
Human Molecular Genetics
|
February 19, 2005
Relapsing diabetes can result from moderately activating mutations in KCNJ11
Anna L Gloyn, Frank Reimann, Christophe Girard, et al.
Page
of 6