Intelligence is known to run in families, but no single genes have yet been identified that can be reliably linked to mental ability.
Many interesting small molecules have been identified that can significantly promote cellular reprogramming (Table 1).
A number of mechanisms have been identified that can lead to (acute) aquatic toxicity.
Structure physical property relationships are identified that can guide future synthetic efforts.
In addition, a conserved water molecule near Thr138 is identified that can serve a functional role in inhibitor binding.
A wide range of hormonal factors have been identified that can alter medullary blood flow under physiological and pathological conditions.
Some design measures have been identified, that can reduce this dose to about 1200 p-mSv/a.
Oxidoreductases, transporters, and regulators have been identified that can increase the tolerance of biocatalysts to inhibitors formed during pretreatment.
In this paper, a right failure prediction criterion is identified that can be used for the Fiber-Tear-Failure load prediction using zone based approach.
So far no SNP or haplotype in the CYP1A2 has yet been identified that can unequivocally be used to predict the metabolic phenotype in any individual patient [47].
MTUS1 (microtubule-associated tumor suppressor 1) has been identified that can function as a tumor suppressor gene in many malignant tumors.
