Magnetic nanoparticles (MNPs) with special morphology were commonly used as biomaterials, while morphological effects of non-targeted biomolecule-modified MNPs on biological behaviors were still unclear.
However, cell shape changes related to nanofiber morphology are commonly associated with order of magnitude differences in fiber diameter, and cell shape changes associated with the differentiation path appear to be quite noticeable in the literature [ 26– 28].
Centrioles displaying these two types of appendages, along with their characteristic morphology, were commonly found in the normal human astrocytes however, abnormal appendage structures in the astrocytoma/glioblastoma cell lines were particularly common in T98G and U-87 MG cell lines.
Mitochondrial membrane potential varies, depending on energy demand, subcellular location, and morphology and is commonly used as an indicator of mitochondrial functional status.
Augmentation of CBX7 by knockdown of miR-182 expression, in turn, positively regulated the expression of E-cadherin, a key protein involved in maintaining normal epithelial cell morphology, which is commonly lost during neoplastic progression.
Because the morphology of leaves is commonly used for plant identification, the studies shown in Table 1 have examined the shape and morphological description for plant leaves.
Similarly, the nucleoli of cancer cells are enlarged and increased in number, and thus the morphology of nucleoli is commonly used as a diagnostic marker for transformed cells clinically corresponding to adverse prognosis [ 172, 173].
Lacking tools for fast, reliable and efficient analysis however, fungal morphology is still commonly tackled by empirical trial-and-error techniques during strain selection and process development procedures.
