This results in the accumulation of farnesyl-prelamin A at the nuclear membrane.

These are supported by small bundles of microtubules that arise near a point on the nuclear membrane.

There is no peripheral chromatin on the nuclear membrane.

At this late stage the nuclear membrane disappears and a spindle forms.

Gp-210 anchors the pore complex to the nuclear membrane.

In mammals, the nuclear membrane can break down within minutes, following a set of steps.

There are several proteins associated with the inner nuclear membrane.

It is an integral protein within the nuclear membrane.

In contrast to the nucleus of a eukaryotic cell, it is not surrounded by a nuclear membrane.

This is important for controlling processes on either side of the nuclear membrane.

The nuclear envelope has things sticking out of it that look like tubes and sheets.

Once introduced within a plant host cell, virions migrate to the nuclear envelope.

Nucleoporin p62 (p62) is a protein complex associated with the nuclear envelope.

Cytokinesis usually occurs at the same time that the nuclear envelope is reforming, yet they are distinct processes.

Another important function of the cyclin B1-Cdk1 complex is to break down the nuclear envelope.

The nuclear envelopes of their cells are notable for remaining intact throughout mitosis.

Proteins gain entry into the nucleus through the nuclear envelope.

The first sign is a clear, actin-free zone appearing around the nuclear envelope.

Antibodies against this protein can be used to identify the nuclear envelope in immunofluorescence experiments.

The nuclear envelope allows the nucleus to control its contents, and separate them from the rest of the cytoplasm where necessary.