Effects of neuropathic and non-neuropathic isomers of tricresyl phosphate and their microsomal activation on the production of axon-like processes by differentiating mouse N2a neuroblastoma cells

Journal of Neurochemistry

Volumn 76, Issue 3, 2001, Pages 671-678

  Fowler, Maxine J ^a   Flaskos, John ^b   Graham McLean, W ^c   Hargreaves, Alan J ^a  

^a NOTTINGHAM TRENT UNIVERSITY   (United Kingdom)

^b ARISTOTLE UNIVERSITY OF THESSALONIKI   (Greece)

^c UNIVERSITY OF LIVERPOOL   (United Kingdom)

Author keywords

Axon outgrowth; Neurofilament heavy chain; Tricresyl phosphate and metabolic activation

Indexed keywords

ANTIBODY; CYTOSKELETON PROTEIN; NEUROFILAMENT PROTEIN; ORGANOPHOSPHATE; TRICRESYL PHOSPHATE;

ANIMAL CELL; ARTICLE; BRAIN MICROSOME; CELL VIABILITY; CONTROLLED STUDY; GROWTH INHIBITION; ISOMER; METABOLIC ACTIVATION; MOUSE; NERVE CELL DIFFERENTIATION; NERVE DEGENERATION; NERVE FIBER GROWTH; NEUROBLASTOMA CELL; NEUROPATHY; NEUROTOXICITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; WESTERN BLOTTING;

ANIMALS; AXONS; CELL DIFFERENTIATION; CELL SURVIVAL; CYTOSKELETAL PROTEINS; DOSE-RESPONSE RELATIONSHIP, DRUG; GAP-43 PROTEIN; MICE; MICROSOMES; NEURAL INHIBITION; NEUROBLASTOMA; NEUROFILAMENT PROTEINS; TIME FACTORS; TRITOLYL PHOSPHATES; TUBULIN; TUMOR CELLS, CULTURED;

ANIMALIA;

EID: 0035156116     PISSN: 00223042     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1471-4159.2001.00020.x     Document Type: Article

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