Results 291 to 300 of about 167,277 (315)
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The mechanism of anaphase spindle elongation
BioEssays, 1989AbstractAt anaphase chromosomes move to the spindle poles (anaphase A) and the spindle poles move apart (anaphase B). In vitro studies using isolated diatom spindles demonstrate that the primary mechano‐chemical event responsible for spindle elongation is the sliding apart of half‐spindle microtubules.
W. Z. Cande, C. J. Hogan
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Chromosome errors at mitotic anaphase
Genome, 1992Errors in mitotic divisions were assayed using various satellite DNAs as probes, hybridized in situ, to show that they included nondisjunction, chromosome and chromatid lagging, chromatid malsegregation, and monopolar segregations. The total rates of error were 1.7, 1.1, and 0.6% for chromosomes X, 17, and 18, respectively. Lagging was the most common
Anthony Correll, Judith H. Ford
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Anaphase Inactivation of the Spindle Checkpoint
Science, 2006The spindle checkpoint delays cell cycle progression until microtubules attach each pair of sister chromosomes to opposite poles of the mitotic spindle. Following sister chromatid separation, however, the checkpoint ignores chromosomes whose kinetochores are attached to only one spindle pole, a state that activates the checkpoint prior to metaphase. We
Janet B. Meehl +4 more
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Cell, 1982
Permeabilized PtK1 cells continue to undergo anaphase chromosome movements provided MgATP is included in the lysis medium. However, chromosome-to-pole movement (anaphase A) and spindle elongation (anaphase B) differ with respect to nucleotide requirements.
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Permeabilized PtK1 cells continue to undergo anaphase chromosome movements provided MgATP is included in the lysis medium. However, chromosome-to-pole movement (anaphase A) and spindle elongation (anaphase B) differ with respect to nucleotide requirements.
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Rephrasing anaphase: separase FEARs shugoshin
Chromosoma, 2005Cleavage of the ring-like cohesin complex by separase triggers segregation of sister chromatids in anaphase. This simplistic model has recently been extended by exciting discoveries on three levels: regulation of anaphase by posttranslational modifications and the cohesin protector shugoshin; non-proteolytic roles of separase; and cohesin-independent ...
Stemmann, Olaf +2 more
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Lactate regulates cell cycle by remodelling the anaphase promoting complex
Nature, 2023Weihai Liu +27 more
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Enzymology of the Anaphase‐Promoting Complex
2005The anaphase-promoting complex (APC) is an ubiquitin-protein ligase that promotes mitotic progression by catalyzing the ubiquitination of numerous proteins, including securin and cyclin. Its complex subunit composition and extensive regulation make the APC an active subject of investigation for both cell biologists and enzymologists.
David O. Morgan, Christopher W. Carroll
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Cohesin and Cdk1: an anaphase barricade
Nature Cell Biology, 2010Separation of sister chromatids at anaphase in metazoan cells requires only the cleavage of the kleisin subunit of centromeric cohesin, but efficient poleward movement of separated sisters requires the associated loss in Cdk1 activity. Activation of the anaphase-promoting complex/cyclosome ensures these events are coordinated.
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?Premature anaphase? in a couple with recurrent miscarriages
Human Genetics, 1993An increased frequency of mitoses with centromere separation affecting all chromosomes was found in lymphocyte cultures from a couple with recurrent spontaneous abortions. The phenomenon was observed in both the wife and husband. The abnormal behaviour of centromeres may predispose the individual to cell division errors, the consequence of which may be
Katalin Bajnóczky, S. Gardó
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Abnormal Anaphases in Regenerating Mouse Livers
Radiation Research, 1968The frequency of anaphase abnormalities (usually presented as bridges, bridges plus fragments, or percentage of normal anaphases) is widely used as a criterion of radiation damage in many materials. Here, the frequency of these three abnormal anaphase categories has been studied in a material frequently used for this purpose, regenerating mouse liver ...
Howard J. Curtis, Alan D. Conger
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