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1 in meiotic chromosome cohesion, as a spindle checkpoint component.
2 her B-type cyclins in the absence of spindle checkpoint components.
3 fferential genetic interactions with spindle checkpoint components.
4 or by inactivating a subset of recombination checkpoint components.
5 netochores and the subsequent recruitment of checkpoint components.
6 ts cells in metaphase independently of other checkpoint components.
7 cell division and death by associating with checkpoint components, although their mode of regulation
9 sion is reduced in the absence of DNA damage checkpoint components and nonhomologous end-joining (NHE
11 and a portion of Mad2, all essential mitotic-checkpoint components, are stably bound elements of unat
12 d kinetochore; consequently, accumulation of checkpoint components at spindle poles increases markedl
13 -CIN) we down-regulated the spindle assembly checkpoint component BUB1 and the mitotic cohesin SMC1A,
14 isolated a Xenopus homologue of the spindle checkpoint component Bub1, and investigated its role in
15 ion, kinetochore localization of the spindle checkpoint components BubR1, Mad2, and Cenp-E is diminis
16 that PP1(Dis2)-mediated dephosphorylation of checkpoint components forms a novel spindle checkpoint s
22 asm, yet kinetochore localization of spindle checkpoint components is required for proper recovery fr
23 mitotic arrest by dominant-negative spindle checkpoint components led to a failure in completion of
28 ) mice by reducing levels of another mitotic checkpoint component, Mad2, is now shown to result in el
30 synthesis of proteins including the mitotic checkpoint component MAD2L1 was negatively regulated.
31 r data indicate that some well-characterized checkpoint components maintain minisatellite stability i
32 lacking functional SAN-1 or a second spindle checkpoint component, MDF-2, failed to arrest the cell c
33 he function of ribonucleotide reductase as a checkpoint component of S progression was studied in yea
36 estore the checkpoint, suggesting that other checkpoint component(s) were depleted from the extract t
38 Experimental observations have shown that checkpoint components stream from attached kinetochores
39 5CDC/hCdc20, a protein known to link spindle checkpoint components such as MAD2 to anaphase promoting
42 controlled specifically by Bub2p, one of the checkpoint components that is conserved in fission yeast
44 hat hPer2 directly acts on the hp53 node, as checkpoint components upstream of hp53 remained active i
45 /Rad17/Mec3 complex and Rad24 are DNA damage checkpoint components with limited homology to replicati
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