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The frequency of the graft sites along the rigid-rod backbone was found to be the key structural parameter limiting the extent of rod aggregation.
The incorporation of a TT unit on the P BDT-TDDPT) backbone was found to reduce the band gaP BDT-TDDPTV and increase slightly the hole mobackbonef the resulting copolymer, RP2.
Introducing intracellular portions of Ste2p into the Frizzled receptor backbone was found to strongly enhance mating pathway activation as compared to the native Frizzleds, likely by facilitating interaction with the yeast Gα protein Gpa1p.
After 5ns of MD simulations, backbone was found to fluctuate around 5Å which persisted till the end of 15ns simulation.
Furthermore, the incorporation of the arginine residues into the PNA backbone was found to be very effective for avoiding enzymatic degradation, thus further increasing the PNA bioavailability in cellular systems even under extreme conditions.
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The molar mass of the macromolecules generated on the cellulose backbone were found to be similar as the molar mass of the polymers obtained from the CTA free in solution, which allowed a simple analysis of the graft copolymers.
The presence of NaAMPS groups in the copolymer backbone is found to increase the ability of PHPAAm to reduce frictional drag while the vulnerability to mechanical degradation remains unaffected.
Recently, C4′-oxidized (C4-AP) and C5′-oxidized abasic sites (DOB) that are produced following hydrogen atom abstraction from the DNA backbone were found to produce ICLs.
Integration of amide group with pendant hydroxyl or sulfobetaine group in polymer backbones is found to increase their surface hydration of polymer chains and thus to improve their antifouling ability.
Moreover, through the exploitation of a DNA proximity network, a series of conserved "DNA backbones" were found to shape the evolution of the genome structure, with the rest of the genome experiencing rearrangements.
An analytical description of this highly complex but local motion in backbone dihedral space was found to be intractable, but the simple model implemented by the B ACKRUB tool (Davis et al., 2006) very closely approximates the low-energy plasticity thought to actually occur in vivo.
More suggestions(16)
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spine was found to
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