![]() |
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
|
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 : (103)
|
References (37)
|