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ADCC-independent NK cell functionality was assessed in cytotoxicity assays against K562 cells.
PSII functionality was assessed in vivo by measuring Chl fluorescence using a PAM 100 fluorimeter (Heinz-Walz, Effeltrich, Germany) after a 20′ dark adaptation.
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TEHV in-vivo functionality was assessed using echocardiography as well as angiography.
In vivo functionality was assessed by monitoring growth of 'single-decarboxylase' strains on several amino acids, whose catabolism proceeds via an Ehrlich pathway, as sole nitrogen sources.
Functionality was assessed with the Barthel Index [ 17, 18], in order to explore patients' ability to perform basic activities of daily living (BADL), and the Lawton Scale [ 19, 20] for instrumental daily living activities (IADL).
Microbicide functionality was assessed using an HIV pseudotype virus assay system representing Clade B subtypes.
Six weeks later, lymphatic functionality was assessed by injecting Iodine radiolabeled bovine serum albumin (I-BSA) into prenodal vessels and measuring its recovery in plasma.
To examine the functionality of knob ELP, their uptake was assessed in a hepatocyte cell-line that expresses the receptor for adenovirus serotype 5 fiber and knob, the coxsackievirus and adenovirus receptor (CAR).
Functionality of modulated target genes was assessed in allogeneic mixed leukocyte reaction experiments.
The functionality of the TregPMA cells was assessed in vivo in a mouse model of experimental colitis.
Changes in sporopollenin functionality were assessed using Fourier transform infrared (FTIR) microspectroscopy.
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