The mammalian FOXO (forkhead box, O subclass) proteins, FOXO1A, FOXO3A, FOXO4, and FOXO6, are a family of transcription factors with complex and incompletely understood functional profiles [ 1- 3].
Because EpCAM function is incompletely characterized, and the functional activities of dendritic cells are best studied in vivo, we sought to explore the function of this molecule in EpCAM-deficient mice.
The rules determining whether a consensus motif is functional remain incompletely understood.
However, the physiological role of GRP in cardioventilatory regulation is incompletely understood since most functional studies have been carried out using bombesin rather than GRP.
Thus far, the precise role of colXI α1 in proliferation and invasion remains incompletely understood, and few functional data have been reported.
Much has been learned regarding the molecular and cellular cues that promote NKT cell development, yet how these cells are maintained in the thymus and the periphery and how they acquire functional competence are incompletely understood.
However, this functional dichotomy is incompletely understood, particularly regulation of p38-dependent survival.
Because the Ciona intestinalis genome is incompletely annotated, we computationally assigned functional descriptions to the sequences.
The reasons and mechanisms for these differences in rate of gene loss among different functional groups remain incompletely understood, but current theories propose a link of equimolar amounts of different regulatory genes (gene balance hypothesis) [ 48].
Head incompletely preserved; antennae faint; incomplete.
However, the functional architecture of these circuits remains incompletely understood.
