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Alternatively, in the absence of such neutralizing antibodies, heterotypic cross-reactive antibodies may form complexes with the virus and the Fc-receptors on these complexed antibodies may attach to mononuclear phagocytes, thus enhancing the efficiency of infection and thereby increasing the number of infected mononuclear phagocytes [ 71– 71].
Proteins may form complexes such as dimers, trimers, etc.
CLR may form complexes with other RAMPs with receptor affinity modulation as a result.
Copper ions may form complexes with both SWCNT functional groups and phenolic and amino molecules in solution, hence acting as bridging agents between CNT and organic contaminants.
It has been noted that optineurin may form complexes with Rab8 and myosin VI [17] [20], mediating the targeting of myosin VI to the Golgi complex and may be involved in organization of the Golgi apparatus [17], [18].
Our data and previous work on HQ [2], [7] suggest that (i) HQ may not be a growth inhibitor at concentrations found in soil but may form complexes with trace elements and (ii) inhibit microbial activity.
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It is not always true because Ag+ may form complex with such electron donors, and for reduction, a reducing agent is required which in turn will be oxidized.
Soils are heterogeneous systems composed of highly diverse microhabitats that may form complex spatial patterns in soil microbial communities.
NATs may form complex regulatory networks in soybean.
Discovery phase analysis identified Fibrinogen chains as bound to Transferrin, indicating that many of these high abundant proteins may form complex with each other in the blood.
These findings also suggest that multiple TCSTs may form complex and highly connected circuits and signaling networks in this important pathogen.
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