Modeling protein misfolding in Charcot-Marie-Tooth disease

Advances in Experimental Medicine and Biology

Volumn 820, Issue , 2015, Pages 91-102

  Theocharopoulou, Georgia ^a   Vlamos, Panayiotis ^a  

^a Ionian University   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATING TRANSCRIPTION FACTOR 4; GROWTH ARREST AND DNA DAMAGE INDUCIBLE PROTEIN 153; INITIATION FACTOR 2; PROTEIN;

ARTICLE; AUTOPHAGY; CONCEPTUAL FRAMEWORK; DEMYELINATION; ENDOPLASMIC RETICULUM; GENE MUTATION; GENETIC ASSOCIATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MOLECULAR DYNAMICS; MUSCLE ACTION POTENTIAL; MYELIN SHEATH; NERVE CELL PLASTICITY; NERVE CONDUCTION; NERVE POTENTIAL; OLIGOMERIZATION; PATHOGENESIS; PERIPHERAL NEUROPATHY; PROTEIN AGGREGATION; PROTEIN CLEAVAGE; PROTEIN DEGRADATION; PROTEIN FOLDING; PROTEIN PHOSPHORYLATION; SCHWANN CELL; SIGNAL TRANSDUCTION; UBIQUITINATION; UNFOLDED PROTEIN RESPONSE; BIOLOGICAL MODEL; CHARCOT-MARIE-TOOTH DISEASE; CHEMISTRY; DEMYELINATING DISEASES; GENE EXPRESSION; GENETICS; PERIPHERAL NERVOUS SYSTEM DISEASES;

CHARCOT-MARIE-TOOTH DISEASE; DEMYELINATING DISEASES; GENE EXPRESSION; HUMANS; MODELS, GENETIC; PERIPHERAL NERVOUS SYSTEM DISEASES; PROTEIN FOLDING; PROTEINS; SIGNAL TRANSDUCTION;

EID: 84912061824     PISSN: 00652598     EISSN: 22148019     Source Type: Book Series    
DOI: 10.1007/978-3-319-09012-2_7     Document Type: Article

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