Certain myositis autoantibodies are markers for distinct overlap syndromes and predict therapeutic outcomes.
Of course, additional studies are necessary to identify the most suitable combinations of cell surface markers for distinct subpopulations from early to late developmental stages.
Moreover, certain myositis autoantibodies such as anti-Jo-1, anti-fibrillarin, and anti-U1RNP are markers for distinct overlap syndromes, irrespective of their current classification as MSAs or MAAs.
Furthermore, we incorporated a number of markers for distinct differentiation pathways (e.g. hematopoietic and pancreatic) and cell types (e.g. cancer subtypes and a range of normal cell types) to serve as essential controls.
Thus, it was not unexpected to find that CD4+ T cells in patients with SCCHN were characterised by the loss of CCR7 and L-selectin surface molecules, which are functionally associated with cell migration into tissues and serve as phenotypic markers for distinct stages of lymphocyte differentiation, respectively.
In this study, we demonstrated the usefulness of a molecular marker for a distinct type of RGC for studying development.
In this study, we identify Lrp12/Mig13a, a mammalian gene related to mig-13, as a novel marker for a distinct subpopulation of preplate neurons.
The single intervening histidine (His, H) is relevant to our findings and is a convenient marker for naming distinct opa configurations even when they share the same number of repeats.
A host of publications have revealed the great value of this Ca-binding protein as a neuronal marker for identifying distinct neuronal subpopulations (reviews by Braun et al. 1991; Heizmann and Braun 1992; Braun 1990; Celio 1990).
Therefore, this study represents a report of LIN28A as a highly specific and sensitive diagnostic marker for the distinct pathological verification of ETMR and, correspondingly, as a new important diagnostic tool to be routinely applied in all malignant childhood brain tumors where ETMR may be considered a possible diagnosis.
