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Furthermore, an increased µ-opioid receptor binding potential was found in certain brain regions in met/met individuals compared to val/val, which was interpreted as a compensatory mechanism [8].
Estrogen receptor binding potential was found in all pore water samples.
In both whole-brain and regional analysis, increased (R -[C]-PK11195 binding potential was found compaR -[C]-PK11195and sex-matched healthy contR -[C]-PK11195
From these series, increased (R -[C]-PK11195 binding potential was found not only in the ipsilateR -[C]-PK11195n the contR -[C]-PK11195sphere, indicating prolonged and widespread microglia activation after Tbinding
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According to the prediction by the seed complementarity, a potential miR-148b-binding site was found at nt 2135 2142 of NRP1 3′-UTR.
The lower binding site was found more constructive favorable for binding.
The binding constants and binding capacity were calculated, and the nature of binding was found to be noncovalent.
Its potential energy was found.
NET-specific binding was found in the locus coeruleus.
The PTB binding site in DLC1 375–385 was found to match with DLC2 400–410, suggesting a potential role of this region in mediating PTB domain-dependent binding between DLC family members and tensin2 (Fig. 3A).
For receptor/ligand complex with crystal structure, the binding site was defined as the grid points around the ligand which were unoccupied by receptor atoms, whereas for a receptor without crystal complex structure, potential binding sites were found based on the shape of the receptor.
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