These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Merotelic kinetochore orientation occurs frequently during early mitosis in mammalian tissue cells and error correction is achieved by two different mechanisms. Cimini D; Moree B; Canman JC; Salmon ED J Cell Sci; 2003 Oct; 116(Pt 20):4213-25. PubMed ID: 12953065 [TBL] [Abstract][Full Text] [Related]
5. Kinetochore recruitment of two nucleolar proteins is required for homolog segregation in meiosis I. Rabitsch KP; Petronczki M; Javerzat JP; Genier S; Chwalla B; Schleiffer A; Tanaka TU; Nasmyth K Dev Cell; 2003 Apr; 4(4):535-48. PubMed ID: 12689592 [TBL] [Abstract][Full Text] [Related]
6. Merotelic kinetochores in mammalian tissue cells. Salmon ED; Cimini D; Cameron LA; DeLuca JG Philos Trans R Soc Lond B Biol Sci; 2005 Mar; 360(1455):553-68. PubMed ID: 15897180 [TBL] [Abstract][Full Text] [Related]
8. The monopolin complex crosslinks kinetochore components to regulate chromosome-microtubule attachments. Corbett KD; Yip CK; Ee LS; Walz T; Amon A; Harrison SC Cell; 2010 Aug; 142(4):556-67. PubMed ID: 20723757 [TBL] [Abstract][Full Text] [Related]
9. Condensin association with histone H2A shapes mitotic chromosomes. Tada K; Susumu H; Sakuno T; Watanabe Y Nature; 2011 Jun; 474(7352):477-83. PubMed ID: 21633354 [TBL] [Abstract][Full Text] [Related]
10. Two fission yeast homologs of Drosophila Mei-S332 are required for chromosome segregation during meiosis I and II. Rabitsch KP; Gregan J; Schleiffer A; Javerzat JP; Eisenhaber F; Nasmyth K Curr Biol; 2004 Feb; 14(4):287-301. PubMed ID: 14972679 [TBL] [Abstract][Full Text] [Related]
11. Spo13 maintains centromeric cohesion and kinetochore coorientation during meiosis I. Lee BH; Kiburz BM; Amon A Curr Biol; 2004 Dec; 14(24):2168-82. PubMed ID: 15620644 [TBL] [Abstract][Full Text] [Related]
13. Kinetochore and heterochromatin domains of the fission yeast centromere. Pidoux AL; Allshire RC Chromosome Res; 2004; 12(6):521-34. PubMed ID: 15289660 [TBL] [Abstract][Full Text] [Related]
14. A role for metaphase spindle elongation forces in correction of merotelic kinetochore attachments. Choi SH; McCollum D Curr Biol; 2012 Feb; 22(3):225-30. PubMed ID: 22264609 [TBL] [Abstract][Full Text] [Related]
15. Control of Shugoshin function during fission-yeast meiosis. Vaur S; Cubizolles F; Plane G; Genier S; Rabitsch PK; Gregan J; Nasmyth K; Vanoosthuyse V; Hardwick KG; Javerzat JP Curr Biol; 2005 Dec; 15(24):2263-70. PubMed ID: 16360688 [TBL] [Abstract][Full Text] [Related]
17. Chromosome segregation: clamping down on deviant orientations. Pidoux A; Allshire R Curr Biol; 2003 May; 13(10):R385-7. PubMed ID: 12747847 [TBL] [Abstract][Full Text] [Related]
18. Cohesins determine the attachment manner of kinetochores to spindle microtubules at meiosis I in fission yeast. Yokobayashi S; Yamamoto M; Watanabe Y Mol Cell Biol; 2003 Jun; 23(11):3965-73. PubMed ID: 12748297 [TBL] [Abstract][Full Text] [Related]
19. Studies of meiosis disclose distinct roles of cohesion in the core centromere and pericentromeric regions. Sakuno T; Watanabe Y Chromosome Res; 2009; 17(2):239-49. PubMed ID: 19308704 [TBL] [Abstract][Full Text] [Related]
20. Aurora controls sister kinetochore mono-orientation and homolog bi-orientation in meiosis-I. Hauf S; Biswas A; Langegger M; Kawashima SA; Tsukahara T; Watanabe Y EMBO J; 2007 Oct; 26(21):4475-86. PubMed ID: 17932486 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]