Quantitative microscopy reveals 3D organization and kinetics of endocytosis in rat hepatocytes

Microscopy Research and Technique

Volumn 69, Issue 9, 2006, Pages 693-707

  Marbet, Permsin ^a   Rahner, Christoph ^a,c   Stieger, Bruno ^b   Landmann, Lukas ^a  

^a UNIVERSITY OF BASEL   (Switzerland)

^b UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^c YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Colocalization; Confocal microscopy; Electron microscopy; Image restoration

Indexed keywords

CELL MEMBRANES; COMPLEXATION; ELECTRON MICROSCOPES; ELECTRON MICROSCOPY; LIGANDS; MOLECULAR BIOLOGY; RATS;

3D ORGANIZATIONS; COLOCALIZATION; ENDOSOMES; HEPATOCYTES; MEMBRANE AREA; POWER; QUANTITATIVE MICROSCOPY; RAT HEPATOCYTES; SHORT TERM; TIME INTERVAL;

IMAGE RECONSTRUCTION;

ASIALOGLYCOPROTEIN; DEXTRAN; HORSERADISH PEROXIDASE; RAB PROTEIN; RAB11 PROTEIN; RAB7 PROTEIN; SECRETORY COMPONENT; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CONFOCAL LASER MICROSCOPY; CONTROLLED STUDY; ELECTRON MICROSCOPY; ENDOCYTOSIS; ENDOSOME; IMAGE PROCESSING; IMAGE RECONSTRUCTION; IMMUNOFLUORESCENCE; INTERNALIZATION; LIVER CELL; LYSOSOME; NONHUMAN; PRIORITY JOURNAL; RAT; TRANSCYTOSIS;

EID: 33748628805     PISSN: 1059910X     EISSN: 10970029     Source Type: Journal    
DOI: 10.1002/jemt.20337     Document Type: Article

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