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The intercellular bridge is severed or resolved, resulting in separation of the two daughter cells.
First, the intercellular bridge was modeled as the difference between the inner and outer cylinders.
The furrow ingresses until a small intercellular bridge forms.
A cell junction (or intercellular bridge) is a type of structure that exists within the tissue of some multicellular organisms, such as animals.
During telophase, the proteins are located within the midbody in the intercellular bridge, where they are discarded after cytokinesis.
During the final phase of mitosis, telophase, the furrow forms an intercellular bridge using mitotic spindle fibers.
The small fraction of this volume where the intercellular bridge intersects the spherical caps was subtracted from the furrow cortex volume.
Histopathology will reveal prominent intercellular bridges and nuclear changes such as pleomorphism, hyperchromatism and prominent nucleoli.
Refers to a carcinoma with observable features and characteristics indicative of squamous differentiation (intercellular bridges, keratinization, squamous pearls).
During Drosophila oogenesis, filamin localizes to the ring canals, which are membrane-associated actin cytoskeletal structures that create intercellular bridges between germline cells.
This might happen for some clumps of primordial germ cells are known to form intercellular bridges so that they exist as a syncytium (fused cells, sharing several nuclei).
This may include the production of one or more forms of cytokeratin or other intermediate filaments, intercellular bridge structures, keratin pearls, and/or tissue architectural motifs such as stratification or pseudo-stratification.
The portion of the furrow cortex flanking the intercellular bridge, which extend upwards to the flexion point of the curvature of the main cell body, was modeled as a difference of inner and outer spherical caps.
For example, both filamin and fwd are involved in the function of ring canals, which are membrane-associated actin cytoskeletal structures that create intercellular bridges between germline cells during early mitotic divisions [ 38, 39, 40].
In routinely stained sections, the keratinizing form exhibits equally clear-cut evidence of squamous differentiation in the form of intercellular bridges and/or squamous pearls, while the nonkeratinizing form lacks obvious signs of keratinization.
To do this, we modeled the cell in three shapes: a sphere at early anaphase, a cylinder with two spherical caps at late anaphase, and a dumbbell with spherical cap domains connected by a cylindrical intercellular bridge.
In the case of Bas-SqCC, it is essential that both evidence of squamous differentiation (i.e., intercellular bridges, production of keratin, tonofilament bundles) and basaloid architecture (i.e. prominent peripheral palisading of cell nuclei, organoid/lobular structures) are identified to make a correct diagosis.