In recent years human model systems have emerged to study cellular aging to overcome this drawback, for example premature aging syndromes associated with the LMNA gene [ 42- 44].
Powerful high throughput sequence-driven metagenomic approaches have emerged to study the genetic potential of complex gut microbial communities [ 2, 3].
RNA-seq has emerged to be a valuable tool for studying transcriptomic changes that occur in response to microbial invasion in host cells although studies using RNA-seq on fish are limited.
With advancements in TB immunobiology, a host of studies has emerged to show that IFNγ+CD4+ T cells are directly or indirectly involved in TB pathogenesis.
This applies especially to plasma/serum, and therefore techniques have emerged to enrich and study subproteomes to reduce the complexity and to be able to detect low abundant proteins [ 89, 90].
With the developments in physical mapping and sequencing activities, new databases have emerged to integrate outputs from studies on wheat and barley.
Recent studies have emerged to show the importance of macrophages in the formation and progression of atherosclerosis[9, 10], and the high macrophage content is one of the principal factors associated with plaque instability[11].
It's taken 25 years, but a growing number of studies have emerged to support criticality, starting with findings that show evidence of it in neuronal activity.
