Acknowledgement Statement Clause Samples

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Acknowledgement Statement. The results published here are in whole or part based upon data generated by The Cancer Genome Atlas managed by the NCI and NHGRI. Information about TCGA can be found at ▇▇▇▇://▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇.▇▇▇.
Acknowledgement Statement. The Genotype-Tissue Expression (GTEx) Project was supported by the Common Fund of the Office of the Director of the National Institutes of Health (▇▇▇▇▇▇▇▇▇▇.▇▇▇.▇▇▇/▇▇▇▇). Additional funds were provided by the NCI, NHGRI, NHLBI, NIDA, NIMH, and NINDS. Donors were enrolled at Biospecimen Source Sites funded by NCI\Leidos Biomedical Research, Inc. subcontracts to the National Disease Research Interchange (10XS170), Roswell Park Cancer Institute (10XS171), and Science Care, Inc. (X10S172). The Laboratory, Data Analysis, and Coordinating Center (LDACC) was funded through a contract (HHSN268201000029C) to the The Broad Institute, Inc. Biorepository operations were funded through a Leidos Biomedical Research, Inc. subcontract to ▇▇▇ ▇▇▇▇▇ Research Institute (10ST1035). Additional data repository and project management were provided by Leidos Biomedical Research, Inc.(HHSN261200800001E). The Brain Bank was supported supplements to University of Miami grant DA006227. Statistical Methods development grants were made to the University of Geneva (MH090941 & MH101814), the University of Chicago (MH090951,MH090937, MH101825, & MH101820), the
Acknowledgement Statement. I , acknowledge that I have been instructed and shown how to use the time clock and understand how to correctly claim tips and change job codes if necessary. I also understand that it is my responsibility to claim 100% of any gratuities I receive (charge, cash or otherwise) according to tax law. I also understand that failure to correctly claim tips or correctly change job codes can lead to corrective action up to and including suspension and/ or termination.
Acknowledgement Statement. As a visiting student, I will abide by Lehigh University’s policies and regulations. I understand that Lehigh University and the State of Pennsylvania’s policies and laws prohibit the use of illegal drugs and forbid any person less than 21 years of age the use or possession of any alcoholic beverages. I acknowledge that any Diversity Overnight Program participant who disobeys the policies on alcohol and/or drug use and/or possession will not be allowed to further participate in the program and will be asked to terminate the visit, leaving campus as soon as travel arrangements are finalized. I also understand that any violations of the university policies may disqualify my acceptance of admission to Lehigh University.
Acknowledgement Statement. All published scientific findings derived from tissues and/or data obtained through the NeuroBioBank must acknowledge the “NIH NeuroBioBank” as the source. NIH NeuroBioBank must be notified of any publications so that the publication can be linked to the tissues or data. Data Release Principles and Standards. Data from NeuroBioBank tissues are expected to be shared in an easily accessible format so as to increase the value of the significant public investment.
Acknowledgement Statement. This research was supported by the Intramural Research Program of the NIMH(NCT00001260, 900142).
Acknowledgement Statement. I acknowledge that I have read, understand, and will comply with the above terms, conditions and usage requirements. Electronic Device Provided to User: Microsoft Surface Go
Acknowledgement Statement. Supported by a SWLA Convention & Visitors Bureau Tourism Marketing Grant from Visit Lake ▇▇▇▇▇▇▇ (the Lake ▇▇▇▇▇▇▇/SWLA Convention & Visitors Bureau) as administered by the Arts & Humanities Council of SWLA.
Acknowledgement Statement. ☐ By checking this box, I acknowledge that I have carefully read and understand the expectations in Section Two. I agree to uphold it to the best of my ability.
Acknowledgement Statement. This study is funded by the Intramural program at the NHGRI/NIH. The study dataset was created using two human samples and 20 daughter lines which were established clonally to compare mutation frequencies among samples. One human sample is obtained from a patient with blood disorder (▇▇▇▇▇▇▇▇ ▇▇, Blood, 2014) and one human sample is obtained from a collaborator, ▇▇. ▇▇▇▇▇ ▇▇▇▇▇▇, at the NHLBI (CTRL-1 from ▇▇▇▇▇▇ T, JCI, 2013). Whole exome sequencing and targeted deep sequencing was performed in addition to SNP arrays to detect variations among the samples.