However, many questions remain unanswered and, therefore, more data and more models are required to decipher the complex cell wall architecture in bacteria.
Altered B-cell lymphoma 6, a key oncogene in B-cell lymphomagenesis, may be involved in the pathogenesis of preeclampsia, and further investigations are required to decipher the molecular mechanisms.
Future investigations are required to decipher these mechanisms.
Similarly, further studies are required to decipher the mechanisms regulating the survival of newly generated neurons.
Further investigations will be required to decipher the exact mechanisms of the protection we have observed.
Additional experiments are required to decipher the biochemical activity of hSAS-6 and CPAP.
Accurate morphological studies, and new molecular tools, are required to decipher the taxonomy of several genera, including Ectocarpus, Cystoseira, Acrochaetium, Polysiphonia, and Ulva.
However, it has been reported that Culp6 is essentially a cell wall associated protein despite possessing a predicted signal peptide [33] indicating that experimental studies are required to decipher the localization of these hypothetical proteins in M. tuberculosis.
Further in vivo mechanistic/profiling analyses at very early time points following PB exposure, prior to Cyp2b10 transcriptional activation will be required to decipher the sequence of events and epigenetic mechanisms associated with Cyp2b10 activation.
More than likely, locus-specific mutagenesis in B cells depends upon the combinatorial signal generated through multiple histone tail modifications, and further studies are required to decipher the specific histone code assigned to somatic hypermutation.
