Exact(1)
At the centrosomes, Pcnt serves as a multifunctional scaffold for various proteins and protein complexes and has important functions in microtubule organization, cell division, cell cycle progression, assembly of cilia and probably in various other fundamental cellular processes.
Similar(59)
In this paper, engineering change progression of assembly tooling is modeled as a decrease of impact on affected tasks, which implies that the duration of certain changed task reduces gradually.
The centrosomes then progressively move away during spindle assembly progression.
Also CCT may mediate the folding of 1000 2000 other proteins that play diverse and critical functions in the cell, as, for example, cell cycle progression, chromatin remodeling, assembly of nuclear pore complex and protein degradation [35], [36].
This data was collected as described in the methods section where thioflavin S fluorescence as shown in Figure 2C is integrated to measure tau progression into an assembly competent intermediate or polymer that is also observed in filamentous tau lesions in tauopathies [20], [21].
Centrosomal proteins control cell cycle progression and spindle kinetochore assembly (Kumar et al., 2013).
The coupling of replication fork progression and nucleosome assembly might compensate for short-term fluctuations in histone availability (Mejlvang et al., 2014).
The release of these factors from pre-60S particles ensures their recycling and likely triggers conformational changes that are critical determinants for the progression of ribosome assembly, e.g. promoting export or subunit-joining competence.
More specifically, the protein complexes containing Sm-like domains of the Scd6p family are predicted to regulate the stability of mRNA encoding proteins involved in cell cycle progression and vesicular assembly.
This suggests that a TFIID-TFIIB-DNA sub-complex is likely the most susceptible substrate for inhibition, while the presence of other core promoter factors may facilitate the progression of PIC assembly and reduce the time interval of this vulnerable stage.
The latter review highlighted the ways in which HDAC inhibitors lead to impaired mitotic progression, defects in kinetochore assembly, and aberrations in spindle assembly checkpoint controls, resulting in premature exit from mitosis.
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