Moreover, we demonstrated for the first time successful gene transfer in living animals with a single-component peptide vector.
However, we demonstrated for the first time that an affibody targeting intracellular signal transduction molecules could inhibit cell proliferation and the production of inflammatory mediators.
As we demonstrated for the previous scenario, Spin Images descriptors appear to be more sensitive to holes than our own, and these results confirm it.
In this study, we demonstrated, for the first time, the correlation between the expression levels of monacolin K biosynthetic genes and monacolin K production in Monascus.
In addition, we demonstrated for the first time that small differences in surface potential maps associated with organic thiol patterns can be resolved by KPFM in mV range.
We demonstrated for the first time that rodents can be trained to use tools.
All together, we demonstrated for the first time, that NT α-Syn modifications circumvent immunological tolerance.
We demonstrated for the first time that AAV transgene expression via the stress-inducible GFAP-promoter allows endogenous modulation.
In this study, we demonstrated for the first time that hES cells could be differentiated into hepatic progenitor cells.
We demonstrated for the first time the presence of Ufm1 modification pathway and the protein targets in the mitochondria.
We demonstrated for the first time a cellular compartment-specifc regulation process of GSK-3β activity upon MPP+-treatment.
