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Cells from four aggregate-positive L1E-R4 clones visualized by fluorescence microscopy are indicated by asterisks.
Cells from four aggregate-negative L1C-R4 clones visualized by fluorescence microscopy are indicated by asterisks.
Cells from four aggregate-positive R1 wild-type clones visualized by fluorescence microscopy are indicated by asterisks.
Cells from four aggregate-negative R1 wild-type clones visualized by fluorescence microscopy are indicated by asterisks.
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Time after start of microscopy is indicated (top left).
Nomarski contrasted, bright-field microscopy pictures are indicated as BF.
For electron microscopy, statistical analyses are indicated in the Supplemental Experimental Procedures.
Representative images taken using SIM (A) and STED (B) microscopy are shown and filopodia are indicated by white arrowheads.
Nuclear abnormalities were scored by immunofluorescence microscopy, numbers of scored cells are indicated within each bar.
Even a classic clinical presentation and typical colours of grains in mycetoma does not reliably distinguish actinomycetoma from implantation mycosis, so laboratory investigations, including microscopy, histology and extended cultures are indicated.
The core for IF was divided into two parts if electron microscopy (EM) was indicated.
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