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Studies with archival human prostate specimens were approved by the Biomedical Research Ethics Board of the MUHC-Montreal General Hospital.
All procedures for informed consent and collecting human specimens were approved by the Ethics Committee of National Research Institute for Family Planning, China.
The FHCI specimens were approved for research purposes by the NCI Office of Human Subjects Research.
All studies concerning human specimens were approved by the Institutional Review Board of the National Defense Medical College.
Experiments using human specimens were approved by the Schepens Eye Research Institute Institutional Review Board (IRB 2011-027).
The collection and use of human IVD specimens were approved by the ethics committee of Kobe University Hospital.
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Collection of the human specimens was approved by the ethics committee of the National Research Centre (Giza, Egypt), and Institutional Animal Care and Use Committee approval for collection of animal samples was obtained from St Jude Children's Research Hospital (Memphis, TN, USA).
This study using patient serum specimens was approved by the Ethics Committee of Fujita Health University School of Medicine.
Written informed consent was obtained from each patient and the use of these human specimens was approved by the Keio University Ethics Committee.
The MERIT study, including written informed consent for stored specimens, was approved by the Institutional Review Boards (IRB) or Independent Ethics Committees (IEC) of all participating sites.
The collection of the specimens was approved by the New York University Institution Review Board.
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