Transmission electron microscopy was performed as described previously [34 (link)]. The investigator was blinded to group allocation. A whole-mount bright field was obtained using a Nikon SMZ1000 Stereomicroscope. Light and fluorescent microscopic images were obtained by a Nikon Eclipse 90i microscope system, a Nikon confocal microscope system A1+ (Nikon Instruments, Melville, NY, USA), and a ZEISS LSM 980 with Airyscan 2 confocal microscope (Carl Zeiss Microscopy, LLC, White Plains, NY, USA).
Li Q., Han Z., Singh N., Terré B., Fame R.M., Arif U., Page T.D., Zahran T., Abdeltawab A., Huang Y., Cao P., Wang J., Lu H., Lidov H.G., Surendran K., Wu L., Virga J.Q., Zhao Y.T., Schüller U., Wechsler-Reya R.J., Lehtinen M.K., Roy S., Liu Z., Stracker T.H, & Zhao H. (2022). Disruption of GMNC-MCIDAS multiciliogenesis program is critical in choroid plexus carcinoma development. Cell Death and Differentiation, 29(8), 1596-1610.
Corresponding Organization : Center for Cancer Research
Other organizations :
New York Institute of Technology, Institute for Research in Biomedicine, Boston Children's Hospital, Discovery Institute, Sanford Burnham Prebys Medical Discovery Institute, Institute of Molecular and Cell Biology, Sanford Research, China Medical University, Kinderkrebs-Zentrum Hamburg, Universität Hamburg, University Medical Center Hamburg-Eppendorf
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