Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinism

Human Molecular Genetics

Volumn 18, Issue 13, 2009, Pages 2400-2413

  Taneja, Tarvinder K ^a   Mankouri, Jamel ^a   Karnik, Rucha ^a   Kannan, Soundarapandian ^a   Smith, Andrew J ^a   Munsey, Tim ^a   Christesen, Henrik B T ^b   Beech, David J ^a   Sivaprasadarao, Asipu ^a  

^a UNIVERSITY OF LEEDS   (United Kingdom)

^b ODENSE UNIVERSITY HOSPITAL   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM); INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; SULFONYLUREA RECEPTOR 1;

ARTICLE; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CELL COMPARTMENTALIZATION; CELL MEMBRANE TRANSPORT; CELL MIGRATION; CELL SURFACE; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; GENE EXPRESSION; GENE FUNCTION; GENE LOCATION; GENE MUTATION; GOLGI COMPLEX; HUMAN; HUMAN CELL; HYPERINSULINISM; INSULIN RELEASE; PANCREAS ISLET BETA CELL; PRIORITY JOURNAL; PROTEIN INTERACTION;

AMINO ACID MOTIFS; AMINO ACID SEQUENCE; CELL LINE; ENDOPLASMIC RETICULUM; HUMANS; INSULIN; KATP CHANNELS; MOLECULAR SEQUENCE DATA; MONOMERIC GTP-BINDING PROTEINS; MUTATION, MISSENSE; PERSISTENT HYPERINSULINEMIA HYPOGLYCEMIA OF INFANCY; POTASSIUM CHANNELS, INWARDLY RECTIFYING; PROTEIN BINDING; PROTEIN TRANSPORT; SEQUENCE ALIGNMENT;

EID: 67249102334     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddp179     Document Type: Article

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