(Q40791919)

English

Identification and pharmacological correction of a membrane trafficking defect associated with a mutation in the sulfonylurea receptor causing familial hyperinsulinism

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Identification and pharmacological correction of a membrane trafficking defect associated with a mutation in the sulfonylurea receptor causing familial hyperinsulinism (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

author name string

Partridge CJ

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Beech DJ

2

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Sivaprasadarao A

3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

language of work or name

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publication date

16 July 2001

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

276

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

38

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

35947-35952

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Adenosine diphosphate as an intracellular regulator of insulin secretion.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

ATP-sensitive K+ channels and insulin secretion: their role in health and disease.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Octameric stoichiometry of the KATP channel complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

ATP-sensitive potassium channels: a model of heteromultimeric potassium channel/receptor assemblies

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Truncation of Kir6.2 produces ATP-sensitive K+ channels in the absence of the sulphonylurea receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

ATP binding properties of the nucleotide-binding folds of SUR1.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Cooperative binding of ATP and MgADP in the sulfonylurea receptor is modulated by glibenclamide

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

The Manganese Cation Disrupts Membrane Dynamics along the Secretory Pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Identification of molecular regions responsible for the membrane trafficking of Kir6.2.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Rapid and efficient site-specific mutagenesis without phenotypic selection

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Misfolding of membrane proteins in health and disease: the lady or the tiger?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Correction of defective protein trafficking of a mutant HERG potassium channel in human long QT syndrome. Pharmacological and temperature effects

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Pharmacological chaperones: a new twist on receptor folding.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Chloride Conductance Expressed by ΔF508 and Other Mutant CFTRs In Xenopus Oocytes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Missense mutation (G480C) in the CFTR gene associated with protein mislocalization but normal chloride channel activity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Neurotensin inhibition of the hyperpolarization-activated cation current (Ih) in the rat substantia nigra pars compacta implicates the protein kinase C pathway.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

The Hsc70 co-chaperone CHIP targets immature CFTR for proteasomal degradation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Biosynthetic transport of the asialoglycoprotein receptor H1 to the cell surface occurs via endosomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Newly synthesized transferrin receptors can be detected in the endosome before they appear on the cell surface.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Crystal structure of the ATP-binding subunit of an ABC transporter

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Structural biology of Rad50 ATPase: ATP-driven conformational control in DNA double-strand break repair and the ABC-ATPase superfamily

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Functional Analysis of a Mutant Sulfonylurea Receptor, SUR1-R1420C, That Is Responsible for Persistent Hyperinsulinemic Hypoglycemia of Infancy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Direct Photoaffinity Labeling of the Kir6.2 Subunit of the ATP-sensitive K+Channel by 8-Azido-ATP

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M104762200

21 January 2018

Identifiers

10.1074/JBC.M104762200

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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