These two stages are sometimes called early and late anaphase.

The site of cell division is determined before anaphase.

However, most of these errors are detected and corrected before the cell enters in anaphase.

During anaphase, Cdc14 is "uncaged" and spreads to the rest of the cell.

This is because in anaphase I the homologous chromosomes are separated.

Chromosome can bend only at the site of primary constriction during Anaphase.

In nondisjunction, a chromosome may fail to separate during anaphase.

The chiasmata remain on the chromosomes until they are severed in anaphase I.

At the end of anaphase the kinecticore microtubules all degrade.

This occurs just after anaphase and during telophase.

Recently, important advances have been made in our understanding of how the MEN is switched on during anaphase.

Progression from metaphase to anaphase is marked by sister chromatid separation.

During septation at the end of anaphase, Cdr2 localizes to the contractile ring.

By contrast, Cdc14 was released from the nucleolus in the great majority of wild type cells by late anaphase.

The possibility exists that the observed homologue separation may actually reflect anaphase onset.

Furthermore, the breaking of an anaphase bridge could also lead to formation of a micronucleus.

However, the role of TTC39C in anaphase must be confirmed through additional studies.

It is required for two microtubule-dependent processes: nuclear movement prior to anaphase, and chromosome separation.

Hair follicles in anaphase express four different caspases.

When this happens the enzyme complex polyubiquitinates the anaphase inhibitor securin.

Switch-like characteristics are necessary to trigger quick, coordinated chromosomal segregation in anaphase.

The end result is each chromosome is attached to the spindle in the initial stage of anaphase.

The two complexes apparently stay associated with chromosomes after the sister chromatids separate from each other in anaphase.

"Anaphase" falls solidly in the second category.

Indeed, the available data suggested that the signal "wait to enter in anaphase" is produced mostly on or close to unattached kinetochores.