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It has been shown that functional mitochondria are required for all cell processes due to common energetic requirements [24].
It has previously been shown that functional instances of protein motifs tend to lie in intrinsically disordered regions of protein sequence [12], [13], [14].
It has been shown that functional secretion machinery is required for full expression and secretion of Yops through this feedback regulatory mechanism [11], [37].
In addition, it has been shown that functional TFBSs tend to be evolutionary constrained [ 33, 34].
Furthermore, it has been shown that functional and expression similarity between orthologs is (virtually) independent of the protein sequence identity.
It has also been shown that functional Rho GTPases are required for Ras-dependent transformation (Qiu et al, 1995).
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Finally, it was shown that functional groups formed by H2O2-treatment (mostly non-phenolic OH groups) are more thermally stable than those formed by O3-treatment.
It is shown that functional measures associated with the Pv- or the Albeverio-Høegh-Krohn models in Euclidean quantum field theories are dimensionally reducible, so that functional integrals with respect to them can be approximated by one dimensional integrals.
It is shown that functional degradation of aged FeNiCoAlTa, containing fine dispersed γ′-particles ∼5 8 nm in diameter is caused by the interaction of different martensite variants under cyclic loading in tension.
Recently it was shown that functional reverse cholesterol transport critically depends on biliary sterol secretion [24].
Very recently, it was shown that functional Yap and induction of CTGF are required for cardiac precursor migration.
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been argued that functional
been observed that functional
been shown that non-western
been shown that photonic
been proved that functional
been reported that functional
been shown that activated
been shown that adaptive
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