Correction for Adon et al., "Cdk2 and Cdk4 Regulate the Centrosome Cycle and Are Critical Mediators of Centrosome Amplification in p53-Null Cells". [PDF]
Mol Cell Biol, 2020 Adon AM +6 more
europepmc +1 more source
Phosphorylation of Centrin during the Cell Cycle and Its Role in Centriole Separation Preceding Centrosome Duplication [PDF]
, 2001 W Lütz +4 more
openalex +1 more source
Synthetic trap‐peptides identify a TOM complex phosphatase – PP2A dephosphorylates Tom6
The FEBS Journal, Volume 293, Issue 1, Page 271-294, January 2026.Synthetic trap‐peptides facilitate the identification of complete holoenzymes that bind to the target sequence remarkably close to the phosphorylation site. PP4 bound to, but did not dephosphorylate, the peptide substrate taken from yeast Tom6 pSer16, showing that proximity alone does not induce phosphatase activity.
Laura Scheinost +7 more
wiley +1 more source
RhoD participates in the regulation of cell-cycle progression and centrosome duplication [PDF]
, 2012 Athena Kyrkou +9 more
openalex +1 more source
Mechanosensing in Dendritic Cells
Immunological Reviews, Volume 337, Issue 1, January 2026.ABSTRACT Since their discovery, dendritic cells have been recognized for their unusual capacity to sense and respond to physical stimuli within their environment. However, it took nearly two decades—and the advent of mechanobiology—to elucidate the underlying mechanisms and functional implications of this mechanical hypersensitivity. In this review, we
Vincent Calmettes +5 more
wiley +1 more source
HeliyonThe centrosome is a major microtubule organizing center in animal cells. The position of the centrosomes inside the cell is important for cell functions such as cell cycle, and thus should be tightly regulated.
Shohei Tada +7 more
doaj +1 more source
“It Takes Two to Tango”: understanding how centrosome duplication is regulated throughout the cell cycle [PDF]
, 2001 Edward H. Hinchcliffe, Greenfield Sluder
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A fluorescence lifetime separation approach for FLIM live‐cell imaging
Journal of Microscopy, Volume 301, Issue 1, Page 91-106, January 2026.Abstract Fluorescence lifetime imaging microscopy (FLIM) translates the duration of excited states of fluorophores into lifetime information as an additional source of contrast in images of biological samples. This offers the possibility to separate fluorophores particularly beneficial in case of similar excitation spectra.
Cornelia Wetzker +8 more
wiley +1 more source
Molecular Mechanisms that Restrict Yeast Centrosome Duplication to One Event per Cell Cycle [PDF]
, 2014 Menattallah Elserafy +7 more
openalex +1 more source