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Thus, mitosis appears critical in the regulation of MELK activity, and conversely MELK may regulate mitotic progression.
These results suggest that CUL3 may regulate mitotic entry.
Thus, CUL3-KLHL18 may regulate mitotic entry through an Aurora-A pathway.
Thus, these results indicate that Cdc5L may regulate mitotic progression through its role in RNA metabolism.
These findings support that KLHL18 forms an E3 ligase with CUL3 and the CUL3-KLHL18 ligase may regulate mitotic entry.
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CYP26B1 activity may also regulate mitotic arrest in male germ cells, as it has been shown in vitro that RA promotes mitosis in cultured gonads [19].
Aur-A may also regulate mitotic spindle orientation by controlling the apical localization of Mud, as Mud is distributed throughout the cell cortex in aur-A mutant neuroblasts [ 28].
Within the retina, CD133+ cells are subject to a complex microenvironment, which is likely to act through cytokines such as LIF and IL-6 and undoubtedly other mitogens that may regulate the mitotic activity and differentitation of these cells into mature cell types.
MELK appears to regulate mitotic cell progression in early embryogenesis [1], in somatic stem cells [15], and in certain cell lineages of the hematopoietic system [6].
Through the use of selective RNAi treatment, we determined that CBP functions to regulate mitotic exit.
Alternatively, FruM may regulate dopamine neuronal activities.
Related(20)
may regulate osteoblast
may regulate cortical
may regulate cellular
may include mitotic
may regulate nuclear
may regulate zebrafish
may regulate early
may regulate primary
may regulate BCLM-associated
may regulate complex
may regulate certain
may regulate fluid
may regulate common
may influence mitotic
may regulate attentional
may regulate neuronal
may increase mitotic
may delay mitotic
may regulate trigeminovascular
may regulate neural
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