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The biological data were confirmed in Phase II of the Anticonvulsant Drug Development Program of the National Institute of Health.
These data were confirmed in other tumor models [31], [32], most recently by Weinberg et al. [33].
These data were confirmed in independent experiments using B cell progenitor cells defined by the expression of B220, CD19, and IgM (Fig. S7B).
These data were confirmed in the small test set of 28 proteins where accurate manual investigation allowed the intrinsic limitations of automatic assessment to be bypassed.
These data were confirmed in freshly thawed mESCs: on soft substrates (Fig. S2C, D), homogenous round and compact colonies corresponded to high expressions of Oct3/4::GFP (Fig. S2C', D'), whereas mESCs plated directly on rigid dishes generated heterogeneous colonies of varying shapes (Fig. S2A, B), corresponding to varying expression levels of Oct3/4::GFP (Fig. S2A', B').
These data were confirmed in this study as the only anti-HDV positive samples found were from these two departments: 8 (8,25%)/97 and 1 (2.5%)/40 among HBsAg and/or anti-HBc positive samples from Amazonas and Magdalena departments, respectively.
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These data are confirmed in twin studies.
This data was confirmed in several studies where even retinoma and retinoblastoma was displayed adjacent to each other in the same eye tumor sample [24].
If these data are confirmed in future studies, the decision to start antipyretic therapy should take into account the baseline ICP value.
If these preliminary data are confirmed in broader testing, RN316 therapy may be particularly useful for treating high risk patients who do not respond adequately to intensive statin therapy.
This data was confirmed in the endothelium of post-mortem lung tissues of SCD patients.
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