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Volumn 218, Issue 1, 2005, Pages 79-83
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A fast method to study the secretory activity of neuroendocrine cells at the ultrastructural level
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Author keywords
Cryo FE SEM; Cryo preparation; Cryotransfer system; Field emission scanning electron microscope (FE SEM); Neuroendocrine cells; POMC producing intermediate pituitary melanotrope cells; Secretory activity; Xenopus Jaevis
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Indexed keywords
CELL MEMBRANES;
CYTOLOGY;
ENAMELS;
FIELD EMISSION;
FREEZING;
SCANNING ELECTRON MICROSCOPY;
CRYO-FIELD EMISSION SCANNING ELECTRON MICROSCOPE;
CRYO-PREPARATION;
CRYO-TRANSFER;
CRYOTRANSFER SYSTEM;
FIELD EMISSION SCANNING ELECTRON MICROSCOPE;
FIELD EMISSION SCANNING ELECTRON MICROSCOPES;
NEUROENDOCRINE CELLS;
POMC-PRODUCING INTERMEDIATE PITUITARY MELANOTROPE CELL;
SECRETORY ACTIVITY;
XENOPUS;
XENOPUS JAEVIS;
FIELD EMISSION MICROSCOPES;
GLUTARALDEHYDE;
PROOPIOMELANOCORTIN;
ANIMAL CELL;
ARTICLE;
CELL SECRETION;
CELL ULTRASTRUCTURE;
CONTROLLED STUDY;
CRYO FIELD EMISSION SCANNING ELECTRON MICROSCOPY;
CRYOPRESERVATION;
CRYSTAL STRUCTURE;
FREEZING;
HYPOPHYSIS CELL;
LIGHT;
NEUROSECRETORY CELL;
NONHUMAN;
PRESSURE;
PRIORITY JOURNAL;
SCANNING ELECTRON MICROSCOPY;
TECHNIQUE;
THREE DIMENSIONAL IMAGING;
XENOPUS LAEVIS;
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EID: 17144385455
PISSN: 00222720
EISSN: None
Source Type: Journal
DOI: 10.1111/j.1365-2818.2005.01456.x Document Type: Article |
Times cited : (7)
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References (12)
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