Table 1. Targetable phenotypic attributes of leukocytes in vitro/ex vivo/in vivo: an abridged list.

Phenotypic Attribute	Reference
Set A: previously targeted attributes
Characteristic jerky stop and go movement during rolling	[12],[50]
Highly fluctuating rolling velocities	[12],[51]
Larger rolling velocities observed at higher shear rates	[12],[52]
Smaller rolling velocities at higher ligand substrate densities	[12],[52]
Rolling a velocities on pselectin a match reported values	[12],[52]
Small number of bonds within the contact zone, e.g., within 2–20	[12],[53]
Distance-time and velocity-time data for rolling a on a pselectin/vcam1 are indistinguishable from reported data	[12],[50],[51]
Chemokines induce adhesion within seconds	[12],[54]
Set B: currently targeted attributes
LFA-1 and ICAM-1 lateral mobility and diffusion	[55]
LFA-1 nanocluster formation upon binding multivalent ligand	[2]
ICAM-1 spatial configurations in vivo	[33]–[37],[56]
Effect of phosphoinositide 3-kinase inhibitors on adhesion ex vivo	[13]
Effect of phosphoinositide 3-kinase inhibitors on adhesion in vivo	[13]
Set C: future targetable attributes
Induction of LFA-1-dependent neutrophil rolling on ICAM-1 by engagement of E-selectin	[57]
Synergistic effect observed during neutrophil rolling on P- and E-selectin	[58]
Effect of knocking out VAV1/3 guanine nucleotide exchange factors on neutrophil rolling	[20]
Effect of inhibitors to other signaling molecules on cell arrest (pertussis toxin (PTx)-sensitive G proteins, p38 mitogen-activated protein kinase)	[57]

We find that this model accounts for the nonlinear influence of experimentally induced visual motion on human postural behavior both in our data and in previously published results.

^aWe use small caps when referring to the in silico components, features, measurements, and events.