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These processes rely on complex signaling networks closely linked to the metabolism.
These processes rely on the reduction of heavy crude oil viscosity by heat to improve its flow from the oil reservoir to the production well.
These processes rely on the reduction of heavy crude oil viscosity by heat to improve its flow from the oil reservoir to the producer well (Nares et al. 2007).
These processes rely on the generation of extremely active OH radicals, which are identified as strong and non-selective oxidants of almost all organic compounds (Li et al. 2006).
As the latter enzymes are cofactor (NADPH) dependent, these processes rely on cofactor recycling which is achieved by whole cell biotransformations, assumingly leading to side products as well as transport limitations depending on the substrate which moreover needs to be N-protected.
These processes rely on the premise that the metabolic pathways associated with a given disease are well delineated, or that groups of proteins with very similar structural or functional design are involved in the disease process.
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Most interesting is that the design of these processes relies on an integrated approach of biocatalyst and process engineering.
The proper execution of these processes relies on a concerted action of multiple proteins.
Nevertheless, whether KDM6 involvement in these processes relies on histone demethylation still remains unclear as most of these studies have relied on complete gene knockdown or deletion approaches.
One qualitative study examined discharge planning ethnographically, drawing conclusions about the processes employed and what these processes relied on [ 14, 15], while two were involved in describing or developing discharge planning models [ 16, 17].
This allowed us, therefore, to dissociate forebrain formation and facial morphogenesis, and demonstrate that these two processes rely on distinct players, namely "early" (2 4ss) and "late" (from 5 6ss) dbx1-expressing subsets respectively.
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