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.
285 related articles for article (PubMed ID: 26858254)
1. Degradation of the Separase-cleaved Rec8, a Meiotic Cohesin Subunit, by the N-end Rule Pathway. Liu YJ; Liu C; Chang Z; Wadas B; Brower CS; Song ZH; Xu ZL; Shang YL; Liu WX; Wang LN; Dong W; Varshavsky A; Hu RG; Li W J Biol Chem; 2016 Apr; 291(14):7426-38. PubMed ID: 26858254 [TBL] [Abstract][Full Text] [Related]
2. Analyzing N-terminal Arginylation through the Use of Peptide Arrays and Degradation Assays. Wadas B; Piatkov KI; Brower CS; Varshavsky A J Biol Chem; 2016 Sep; 291(40):20976-20992. PubMed ID: 27510035 [TBL] [Abstract][Full Text] [Related]
3. Role of cleavage by separase of the Rec8 kleisin subunit of cohesin during mammalian meiosis I. Kudo NR; Anger M; Peters AH; Stemmann O; Theussl HC; Helmhart W; Kudo H; Heyting C; Nasmyth K J Cell Sci; 2009 Aug; 122(Pt 15):2686-98. PubMed ID: 19625504 [TBL] [Abstract][Full Text] [Related]
4. Degradation of a cohesin subunit by the N-end rule pathway is essential for chromosome stability. Rao H; Uhlmann F; Nasmyth K; Varshavsky A Nature; 2001 Apr; 410(6831):955-9. PubMed ID: 11309624 [TBL] [Abstract][Full Text] [Related]
5. Degradation of securin in mouse and pig oocytes is dependent on ubiquitin-proteasome pathway and is required for proteolysis of the cohesion subunit, Rec8, at the metaphase-to-anaphase transition. Huo LJ; Zhong ZS; Liang CG; Wang Q; Yin S; Ai JS; Yu LZ; Chen DY; Schatten H; Sun QY Front Biosci; 2006 Sep; 11():2193-202. PubMed ID: 16720305 [TBL] [Abstract][Full Text] [Related]
6. Crystal structure of the Ate1 arginyl-tRNA-protein transferase and arginylation of N-degron substrates. Kim BH; Kim MK; Oh SJ; Nguyen KT; Kim JH; Varshavsky A; Hwang CS; Song HK Proc Natl Acad Sci U S A; 2022 Aug; 119(31):e2209597119. PubMed ID: 35878037 [TBL] [Abstract][Full Text] [Related]
7. Temporally and spatially selective loss of Rec8 protein from meiotic chromosomes during mammalian meiosis. Lee J; Iwai T; Yokota T; Yamashita M J Cell Sci; 2003 Jul; 116(Pt 13):2781-90. PubMed ID: 12759374 [TBL] [Abstract][Full Text] [Related]
8. N-terminal arginylation generates a bimodal degron that modulates autophagic proteolysis. Yoo YD; Mun SR; Ji CH; Sung KW; Kang KY; Heo AJ; Lee SH; An JY; Hwang J; Xie XQ; Ciechanover A; Kim BY; Kwon YT Proc Natl Acad Sci U S A; 2018 Mar; 115(12):E2716-E2724. PubMed ID: 29507222 [TBL] [Abstract][Full Text] [Related]
9. Characterization of arginylation branch of N-end rule pathway in G-protein-mediated proliferation and signaling of cardiomyocytes. Lee MJ; Kim DE; Zakrzewska A; Yoo YD; Kim SH; Kim ST; Seo JW; Lee YS; Dorn GW; Oh U; Kim BY; Kwon YT J Biol Chem; 2012 Jul; 287(28):24043-52. PubMed ID: 22577142 [TBL] [Abstract][Full Text] [Related]
10. Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L. Ward A; Hopkins J; Mckay M; Murray S; Jordan PW G3 (Bethesda); 2016 Jun; 6(6):1713-24. PubMed ID: 27172213 [TBL] [Abstract][Full Text] [Related]
11. Ablation of arginylation in the mouse N-end rule pathway: loss of fat, higher metabolic rate, damaged spermatogenesis, and neurological perturbations. Brower CS; Varshavsky A PLoS One; 2009 Nov; 4(11):e7757. PubMed ID: 19915679 [TBL] [Abstract][Full Text] [Related]
12. RGS4 and RGS5 are in vivo substrates of the N-end rule pathway. Lee MJ; Tasaki T; Moroi K; An JY; Kimura S; Davydov IV; Kwon YT Proc Natl Acad Sci U S A; 2005 Oct; 102(42):15030-5. PubMed ID: 16217033 [TBL] [Abstract][Full Text] [Related]
13. Studying meiotic cohesin in somatic cells reveals that Rec8-containing cohesin requires Stag3 to function and is regulated by Wapl and sororin. Wolf PG; Cuba Ramos A; Kenzel J; Neumann B; Stemmann O J Cell Sci; 2018 Jun; 131(11):. PubMed ID: 29724914 [TBL] [Abstract][Full Text] [Related]
14. Liat1, an arginyltransferase-binding protein whose evolution among primates involved changes in the numbers of its 10-residue repeats. Brower CS; Rosen CE; Jones RH; Wadas BC; Piatkov KI; Varshavsky A Proc Natl Acad Sci U S A; 2014 Nov; 111(46):E4936-45. PubMed ID: 25369936 [TBL] [Abstract][Full Text] [Related]
15. Arginyltransferase, its specificity, putative substrates, bidirectional promoter, and splicing-derived isoforms. Hu RG; Brower CS; Wang H; Davydov IV; Sheng J; Zhou J; Kwon YT; Varshavsky A J Biol Chem; 2006 Oct; 281(43):32559-73. PubMed ID: 16943202 [TBL] [Abstract][Full Text] [Related]
16. Meiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1beta and SMC3. Eijpe M; Offenberg H; Jessberger R; Revenkova E; Heyting C J Cell Biol; 2003 Mar; 160(5):657-70. PubMed ID: 12615909 [TBL] [Abstract][Full Text] [Related]
17. Analysis of absolute amounts of two meiotic cohesin subunits, RAD21L and REC8, in mouse spermatocytes. Taniuchi Y; Hiraide K; Su R; Ijuin K; Wei X; Horii T; Hatada I; Lee J J Reprod Dev; 2023 Apr; 69(2):78-86. PubMed ID: 36740274 [TBL] [Abstract][Full Text] [Related]
18. Resolution of chiasmata in oocytes requires separase-mediated proteolysis. Kudo NR; Wassmann K; Anger M; Schuh M; Wirth KG; Xu H; Helmhart W; Kudo H; McKay M; Maro B; Ellenberg J; de Boer P; Nasmyth K Cell; 2006 Jul; 126(1):135-46. PubMed ID: 16839882 [TBL] [Abstract][Full Text] [Related]
19. Essential role of Ubr11, but not Ubr1, as an N-end rule ubiquitin ligase in Schizosaccharomyces pombe. Fujiwara H; Tanaka N; Yamashita I; Kitamura K Yeast; 2013 Jan; 30(1):1-11. PubMed ID: 23348717 [TBL] [Abstract][Full Text] [Related]