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Our study suggests that GD2 and GD3 can be marker gangliosides for identifying human NSCs.
Similar to these, it is anticipated that GD2 and GD3 confirmed to be expressed in human NSCs in the present study also can be marker molecules available for identifying and isolating NSCs in human brains especially in adulthood; in adult human brains, GM1, GD1a, GD1b and GT1b, but not GD2 and GD3, are predominantly expressed (Svennerholm, 1963).
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These signatures can be markers of a biological response or can help to reveal fundamental biological mechanisms.
In other words, they can be markers for other, more severe problems, which include brain development and heart disease.
This is an important step forward, because it not only supports the idea that there are certain brain regions that can be markers of meditation, but also that we can start to use this information to develop tools to help people practice meditation.
Humans coevolved with their microbiomes [1] [3] and persistent human microbes can be markers of human migrations.
Many nudix-type phosphatases are clinically important enzymes and their overexpression can be markers of disease.
Vitreous levels of HCTL and PON activities can be markers of diabetic retinopathy.
These proteins can be markers of early progression of esophageal cancer.
Thus, vitreous levels of HCTL and PON activity can be markers of diabetic retinopathy.
Of these, 28 and 52 can be markers of indoor air contamination, while the others primarily have dietary sources [ 22].
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