Parkinson's disease-associated mutations in α-synuclein and UCH-L1 inhibit the unconventional secretion of UCH-L1

Neurochemistry International

Volumn 59, Issue 2, 2011, Pages 251-258

  Konya, Chiho ^a   Hatanaka, Yusuke ^a   Fujiwara, Yuuki ^a,b   Uchida, Kenko ^b   Nagai, Yoshitaka ^a   Wada, Keiji ^a   Kabuta, Tomohiro ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^b WASEDA UNIVERSITY   (Japan)

Author keywords

Synuclein; Parkinson's disease; UCH L1; Unconventional secretion

Indexed keywords

ALPHA SYNUCLEIN; BREFELDIN A; HUNTINGTIN; HYDROLASE; LEUCINE; UBIQUITIN THIOLESTERASE;

ARTICLE; BINDING AFFINITY; CEREBROSPINAL FLUID; ENDOPLASMIC RETICULUM; GENETIC TRANSFECTION; HIPPOCAMPUS; HUMAN; HUMAN CELL; NERVE CELL; OUTCOME ASSESSMENT; PARKINSON DISEASE; PRIORITY JOURNAL; PROTEIN SECRETION; SIGNAL TRANSDUCTION; WESTERN BLOTTING;

ALPHA-SYNUCLEIN; AMINO ACID SEQUENCE; BLOTTING, WESTERN; CELL LINE; ELECTROPHORESIS, POLYACRYLAMIDE GEL; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; PARKINSON DISEASE; UBIQUITIN THIOLESTERASE;

EID: 79960376333     PISSN: 01970186     EISSN: 18729754     Source Type: Journal    
DOI: 10.1016/j.neuint.2011.05.012     Document Type: Article

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