Results 41 to 50 of about 18,904 (232)

CDC20 maintains tumor initiating cells

open access: yesOncotarget, 2015
Glioblastoma is the most prevalent and lethal primary intrinsic brain tumor. Glioblastoma displays hierarchical arrangement with a population of self-renewing and tumorigenic glioma tumor initiating cells (TICs), or cancer stem cells. While non-neoplastic neural stem cells are generally quiescent, glioblastoma TICs are often proliferative with mitotic ...
Xie, Qi   +9 more
openaire   +3 more sources

A novel strategy to block mitotic progression for targeted therapyResarch in context

open access: yesEBioMedicine, 2019
Background: Blockade of mitotic progression is an ideal approach to induce mitotic catastrophe that suppresses cancer cell expansion. Cdc20 is a critical mitotic factor governing anaphase initiation and the exit from mitosis through recruiting substrates
Junlong (Jack) Chi   +11 more
doaj   +1 more source

A quantitative model of the initiation of DNA replication in Saccharomyces cerevisiae predicts the effects of system perturbations. [PDF]

open access: yes, 2012
BackgroundEukaryotic cell proliferation involves DNA replication, a tightly regulated process mediated by a multitude of protein factors. In budding yeast, the initiation of replication is facilitated by the heterohexameric origin recognition complex ...
DaSilva, Lance F   +6 more
core   +3 more sources

Phosphorylation of MCPH1 isoforms during mitosis followed by isoform‐specific degradation by APC/C‐CDH1 [PDF]

open access: yes, 2019
Microcephalin‐1 (MCPH1) exists as 2 isoforms that regulate cyclin‐dependent kinase‐1 activation and chromosome condensation during mitosis, with MCPH1 mutations causing primary microcephaly.
Blain, Peter G.   +5 more
core   +2 more sources

Cell division cycle 20 (CDC20) drives prostate cancer progression via stabilization of β-catenin in cancer stem-like cellsResearch in context

open access: yesEBioMedicine, 2019
Background: Cell division cycle 20 (CDC20) is frequently overexpressed in malignant tumours and involved in the differentiation process of hematopoietic stem cells.
Qin Zhang   +9 more
doaj   +1 more source

Active Transport Can Greatly Enhance Cdc20:Mad2 Formation [PDF]

open access: yesInternational Journal of Molecular Sciences, 2014
To guarantee genomic integrity and viability, the cell must ensure proper distribution of the replicated chromosomes among the two daughter cells in mitosis. The mitotic spindle assembly checkpoint (SAC) is a central regulatory mechanism to achieve this goal.
Bashar Ibrahim, Richard Henze
openaire   +2 more sources

Increased CDC20 expression is associated with pancreatic ductal adenocarcinoma differentiation and progression

open access: yesJournal of Hematology & Oncology, 2012
Purpose Cell division cycle 20 (CDC20) homolog is an anaphase-promoting complex activator that is essential for cell division, but whether its expression in pancreatic ductal adenocarcinoma (PDAC) is significant is unknown.
Chang David Z   +7 more
doaj   +1 more source

Implications of alternative routes to APC/C inhibition by the mitotic checkpoint complex. [PDF]

open access: yesPLoS Computational Biology, 2018
The mitotic checkpoint (also called spindle assembly checkpoint) is a signaling pathway that ensures faithful chromosome segregation. Mitotic checkpoint proteins inhibit the anaphase-promoting complex (APC/C) and its activator Cdc20 to prevent precocious
Fridolin Gross   +3 more
doaj   +1 more source

Pan-cancer noncoding genomic analysis identifies functional CDC20 promoter mutation hotspots

open access: yesiScience, 2021
Summary: Noncoding DNA sequences occupy more than 98% of the human genome; however, few cancer noncoding drivers have been identified compared with cancer coding drivers, probably because cancer noncoding drivers have a distinct mutation pattern due to ...
Zaoke He   +9 more
doaj   +1 more source

Novel regulation of mitotic exit by the Cdc42 effectors Gic1 and Gic2 [PDF]

open access: yes, 2004
Copyright @ The Rockefeller University PressThe guanine nucleotide exchange factor Cdc24, the GTPase Cdc42, and the Cdc42 effectors Cla4 and Ste20, two p21-activated kinases, form a signal transduction cascade that promotes mitotic exit in yeast.
Höfken, T, Schiebel, E
core   +2 more sources

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