Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes

Human Molecular Genetics

Volumn 9, Issue 15, 2000, Pages 2251-2261

  Ganesh, Subramaniam ^a   Lal Agarwala, Kishan ^a   Ueda, Kazunori ^a   Akagi, Takumi ^b   Shoda, Keiko ^a   Usui, Takeo ^a   Hashikawa, Tsutomu ^b   Osada, Hiroyuki ^a   Delgado Escueta, Antonio V ^c   Yamakawa, Kazuhiro ^a  

^a INST OF PHYS AND CHEMICAL RESEARCH   (Japan)

^b RIKEN BRAIN SCIENCE INSTITUTE   (Japan)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CYTOPLASM PROTEIN; GENE PRODUCT; LAFORIN; MUTANT PROTEIN; PHOSPHOSERINE; PHOSPHOTHREONINE; PHOSPHOTYROSINE; PROTEIN TYROSINE PHOSPHATASE; RECOMBINANT ENZYME; UBIQUITIN; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; ELECTRON MICROSCOPY; ENZYME DEFECT; ENZYME SPECIFICITY; ENZYME SUBSTRATE; GENETIC TRANSFECTION; HELA CELL; HUMAN; HUMAN CELL; HYDROLYSIS; IMMUNOFLUORESCENCE; MISSENSE MUTATION; MOLECULAR CLONING; MYOCLONUS EPILEPSY; NUCLEOTIDE SEQUENCE; POLYSOME; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN DEGRADATION; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN PROTEIN INTERACTION; PROTEIN TARGETING; RNA TRANSLATION; TRANSLATION REGULATION;

EID: 0034703182     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/oxfordjournals.hmg.a018916     Document Type: Article

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