Aberrant disulphide bonding contributes to the ER retention of alpha1-antitrypsin deficiency variants

Human Molecular Genetics

Volumn 25, Issue 4, 2016, Pages 642-650

  Ronzoni, Riccardo ^a   Berardelli, Romina ^a   Medicina, Daniela ^b   Sitia, Roberto ^c   Gooptu, Bibek ^d,e   Fra, Anna Maria ^a  

^a UNIVERSITY OF BRESCIA   (Italy)

^b SPEDALI CIVILI   (Italy)

^c VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^d UNIVERSITY OF LONDON   (United Kingdom)

^e KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTEINE; HOMODIMER; POLYMER; ALPHA 1 ANTITRYPSIN; DISULFIDE;

ALPHA 1 ANTITRYPSIN DEFICIENCY; ARTICLE; BINDING AFFINITY; CELL ADHESION; COVALENT BOND; DISULFIDE BOND; ENDOPLASMIC RETICULUM; LIVER CELL; PRIORITY JOURNAL; ANIMAL; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; MOUSE; MUTATION; POLYMERIZATION; TUMOR CELL LINE;

ALPHA 1-ANTITRYPSIN; ALPHA 1-ANTITRYPSIN DEFICIENCY; ANIMALS; CELL LINE, TUMOR; DISULFIDES; ENDOPLASMIC RETICULUM; GENOTYPE; HEPATOCYTES; HUMANS; MALE; MICE; MUTATION; POLYMERIZATION;

EID: 84983680204     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddv501     Document Type: Article

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