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Proceedings of the National Academy of Sciences of the United States of America

Volumn 99, Issue 15, 2002, Pages 9852-9857

Association of calnexin with mutant peripheral myelin protein-22 ex vivo: A basis for "gain-of-function" ER diseases

(8) Dickson, K M a Bergeron, J J M a Shames, I a Colby, J a Nguyen, D T a Chevet, E a Thomas, D Y a Snipes, G J a

a MCGILL UNIVERSITY (Canada)

Author keywords

Charcot Marie Tooth disease; Endoplasmic reticulum quality control; Hereditary neuropathy; Myelinopathy; Trembler

Indexed keywords

MUTANT PROTEIN; PERIPHERAL MYELIN PROTEIN 22; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; ENDOPLASMIC RETICULUM; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MOUSE; MUTATION; NEUROPATHOLOGY; NEUROPATHY; NONHUMAN; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; SCIATIC NERVE;

ANIMALS; BASE SEQUENCE; CALCIUM-BINDING PROTEINS; CALNEXIN; CELL LINE; CERCOPITHECUS AETHIOPS; COS CELLS; DNA PRIMERS; HELA CELLS; HUMANS; MEMBRANE PROTEINS; MICE; MYELIN PROTEINS; NERVOUS SYSTEM DISEASES; POLYMERASE CHAIN REACTION; RATS; RECOMBINANT FUSION PROTEINS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SCIATIC NERVE;

ANIMALIA;

EID: 0037162451 PISSN: 00278424 EISSN: None Source Type: Journal
DOI: 10.1073/pnas.152621799 Document Type: Article

Times cited : (97)

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