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

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

There are several proteins associated with the inner nuclear membrane.

A new nuclear membrane forms around the separated daughter chromosomes.

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

There have been identified several integral nuclear membrane proteins of different size and structure.

It is an integral protein within the nuclear membrane.

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

Samp1, is an inner nuclear membrane protein in mammals.

There is no peripheral chromatin on the nuclear membrane.

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

The regulatory functions of inner nuclear membrane proteins strongly suggest this possibility.

Centrosomes are associated with the nuclear membrane during prophase of the cell cycle.

Exactly how the nuclear membrane reforms during telophase of mitosis is debated.

SUN proteins are thought to localize to the inner nuclear membrane.

Required for retaining emerin at the inner nuclear membrane.

Lamin A/C is required for samp1 presence at the inner nuclear membrane.

They link the inner and outer nuclear membranes.

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

The antigens of both antibodies are constituents of the nuclear membrane.

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

The spindle fibers begin to disappear, and a nuclear membrane forms around each set of chromosomes.

"They have circular chromosomes, with no nuclear membranes: They're all prokaryotes.

The outer nuclear membrane is also contiguous with the endoplasmic reticulum.

The nuclear membrane remains intact and the chromosomes do not condense during mitosis.