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The slides were analysed using the 3-laser ZEISS LSM 510UV Confocal Imager.
The slides were analysed using a fluorescence microscope.
The slides were analysed using confocal laser microscopy (D-Eclipse C1 Nikon, Tokyo, Japan).
The slides were analysed using a fluorescent microscope (LEICA DMIRE2) and a confocal microscope (LEICA TCS-SP2).
The slides were analysed using an Olympus CX31 microscope connected with a Motic MC Camera (2.0 megapixel; MC2001interface, Sterling Heights, MI, USA).
The slides were analysed using an Olympus BX50 fluorescence microscope that was equipped with an Olympus CCD (charge-coupled device) digital chamber Q-Color with refrigeration.
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The stained slides were analysed using the ARIOL SL-50 automated microscope®.
The best slides were analysed using a Leica DMLB microscope and images were captured with a Cohu digital camera using the QFISH software (Leica).
The H&E slides were analysed using a light microscope (Nikon ECLIPSE 80i, Nikon Corporation, Tokyo, Japan), and a score (1 6) was given reflecting the degree of lung inflammation.
Slides were analysed using the Axioplan 2 imaging microscope (Carl Zeiss Light Microscope, Göttingen, Germany).
Glass slides were analysed using a (3D) Zeiss Axioplan II microscope controlled by Axiovision 3.1 software and equipped with Plan-Apochromat 63×/1.4 and Plan-Neofluar 100×/1.30 objectives.
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