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Microscopic images of tissues were acquired using an E600 upright microscope (Nikon) equipped with a CCD color camera.
Confocal images were acquired using a Zeiss confocal laser scanning unit mounted on an LSM 710 fixed-stage upright microscope.
The sections were air-dried completely and imaged using a Zeiss Axioplan II upright microscope.
Images were obtained using a Zeiss Axioskop 2 upright microscope and AxioVision software.
The scanhead was attached to an upright microscope (ECLIPSE E600FN; Nikon, Tokyo, Japan).
The fluorescence analyses were performed using a BX41 Olympus upright microscope.
Confocal microscope imaging was performed with Leica TCS SP2 AOBS upright microscope.
Neurons were visually identified with infrared videomicroscopy using an upright microscope equipped with a 60x objective.
Morphological changes were photographed with a Nikon 50i series upright microscope equipped with a digital camera.
These neurons were visually identified using an upright microscope with Nomarski optics (Axioscope FS, Zeiss, Germany).
Cortical slices were visualized with an upright microscope (BW51X, Olympus) with infrared differential interference contrast optics.
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