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Under additional conditions on Φ, we further show that:.
We further show that goal direction shares a common neural representation with facing direction.
In addition we further show that DN1-DN3 transition controls thymic epithelium morphogenesis [25], [26].
We further show that these bounds are the best possible.
We further show that the first cell fate decision was disrupted in Pk2 embryos.
We further show that the knowledge learned on the synthetic dataset generalizes to constrained real images.
We further show that a Thsp modified peptide cannot be degraded by proteasomes in vitro.
We further show that succession planning affects the nature of learning about the incoming CEO's ability.
We further show that the increased ATP largely comes from non-mitochondrial sources.
We further show that MVBs promote the competence of RISCs in loading small RNAs.
We further show that basic structural features of these stromal components are preserved during ageing.
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