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As we have previously mentioned, studies using HSA as a resuscitation fluid have shown conflicting results in septic and cirrhotic conditions.
In fact, none of the above mentioned studies using either IBC or SIGACT data at a daily resolution confirmed whether they actually feature robust timing signatures.
In contrast to the previously mentioned studies using non-functional FoxP2 alleles, FoxP2 hum influenced ultrasonic vocalization of pups in a specific fashion (Enard et al. 2009).
The two previously mentioned studies using Haem-A-QoL had similar or even worse Cronbach's α (0.6 and 0.13, resp). in the same Haem-A-QoL dimension [ 31, 32].
For the age of Lepidosauria we find no overlap between our deepest credibility interval (251.4 Mya) with the shallowest confidence intervals of Kumazawa [ 37] or Albert et al. [ 38], and in all the above mentioned studies using multidivtime crown-group Squamata is estimated to be Triassic or older.
Another difference between our work and the mentioned studies using the NU-DESC score lies in the fact that in our study the assessment was done by regular nursing staff of the post anesthesia care unit rather than specifically trained psychologists, psychiatrists, or study nurses [ 13].
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Importantly, all the above mentioned studies used mid to late passage hESCs (∼p20 p100), that have been exposed to long term culture effects.
However, none of the mentioned studies used systemic administration where crossing the BBB may constitute a major obstacle to CNTs brain delivery.
However, it should be noted that the above mentioned studies used different definitions of outcome, study population, assessment methods, and confounding factors, thus limiting the feasibility of inter-study comparisons.
Our study is the first to measure muscle cross-sectional area and cognition or brain size; the above mentioned studies used either bioimpedence analysis or DEXA as the measure of muscle bulk.
All mentioned studies used a different dosing schedule (weekly, 3-weekly, daily for 5 days every 3 weeks) and showed that CA4P was safe, well tolerated and lacking haematologic toxicity.
Related(14)
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