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Thus far, the p24 proteins have been mainly implicated in the selection and packaging of secretory cargo proteins (cargo receptor model; reviewed in [2]).
In the following, we focus on those proteins that have been mainly implicated in FasL reverse signalling and trafficking.
These receptors have been mainly implicated in non-apoptotic processes including cellular activation, differentiation and survival [ 1], but they might also be involved in other forms of cell death, e.g. programmed necrosis as in the case of TNFR-2 [ 2].
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Stimulation of postsynaptic 5HT1A and 5HT2A receptors has been mainly implicated in the development of the syndrome.
Indeed, precuneus has been mainly implicated in subjective experience and conscious self-representation [ 31, 41].
GS1 isoenzymes are involved in nitrogen assimilation and recycling derived from several different physiological processes (reviewed in [ 6]), whereas GS2 has been mainly implicated in the reassimilation of the ammonia released during photorespiration [ 7, 8].
It has been mainly unused since.
It has been suggested that GlyT2 is mainly implicated in the control of inhibitory neurotransmission via GlyRs, whereas GlyT1 is considered to regulate the glycine level in both inhibitory neuron and excitatory neurons [4 8].
However, it has been suggested that Top2β is mainly implicated in the induction of DSB, while Top2α is essential for citotoxicity [30].
In contrast, the under-abundant proteins were mainly implicated in transport, TCA cycle and respiration.
SOX7 is mainly implicated in parietal endoderm differentiation [ 19].
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