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In contrast, cell surface expression of αVβ3 or mRNA for the β1, β3 or β5 subunits did not appear to contribute to sensitivity of cells to FMDV.
General factors that contribute to sensitivity are developmental periods, genetic conditions, nutritional deficiencies, predisposing diseases and personal habits.
This proves that positions other than the GGLG and YF motifs can also contribute to sensitivity or robustness.
Thus, small kidney size may contribute to sensitivity to acute injury, even though baseline kidney function as estimated by steady state BUN levels is equivalent.
As oxidative base damage and strand breaks induced by ionising radiation are repaired mainly by these two pathways, defective repair activities might contribute to sensitivity to and improved survival following radiotherapy.
H1993 showed higher expression than H2073 of certain histone variants and chromatin factors, targets that may specifically contribute to sensitivity to depsipeptide and may be downregulated by chemotherapy (Supplementary Table 1; Supplementary Figure 4).
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We conclude from this that collagen-binding significantly contributes to sensitivity to NET-dependent killing, most likely by promoting attachment of Y. enterocolitica to NETs.
Also, importantly, the articulatory motor cortex contributed to sensitivity, independently of response bias in our study.
We conclude that reduced LHC content, although likely contributing to sensitivity, cannot be the only reason for the extreme phenotype of chy1chy2lut2lut5.
The increased sensitivity at nonjoint sites (sternum and anterior tibia), as well as over joints, indicates that central mechanisms may contribute to pain sensitivity in RA.
Limited exposure to antigens in utero and the lack of preexisting immunological memory contribute to this sensitivity [3].
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