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本文引用的文献
1
The C-terminal region of A-kinase anchor protein 350 (AKAP350A) enables formation of microtubule-nucleation centers and interacts with pericentriolar proteins.
J Biol Chem. 2017 Dec 15;292(50):20394-20409. doi: 10.1074/jbc.M117.806018. Epub 2017 Oct 20.
2
Degradation of Cep68 and PCNT cleavage mediate Cep215 removal from the PCM to allow centriole separation, disengagement and licensing.
Nat Cell Biol. 2015 Jan;17(1):31-43. doi: 10.1038/ncb3076. Epub 2014 Dec 15.
3
Amorphous no more: subdiffraction view of the pericentriolar material architecture.
Trends Cell Biol. 2014 Mar;24(3):188-97. doi: 10.1016/j.tcb.2013.10.001. Epub 2013 Nov 19.
4
Disconnecting the Golgi ribbon from the centrosome prevents directional cell migration and ciliogenesis.
J Cell Biol. 2011 May 30;193(5):917-33. doi: 10.1083/jcb.201011014. Epub 2011 May 23.
5
Microtubule nucleation at the cis-side of the Golgi apparatus requires AKAP450 and GM130.
EMBO J. 2009 Apr 22;28(8):1016-28. doi: 10.1038/emboj.2009.47. Epub 2009 Feb 26.
6
Centrosomal proteins CG-NAP and kendrin provide microtubule nucleation sites by anchoring gamma-tubulin ring complex.
Mol Biol Cell. 2002 Sep;13(9):3235-45. doi: 10.1091/mbc.e02-02-0112.
7
AKAP350 at the Golgi apparatus. I. Identification of a distinct Golgi apparatus targeting motif in AKAP350.
J Biol Chem. 2002 Oct 25;277(43):40967-72. doi: 10.1074/jbc.M203307200. Epub 2002 Aug 5.
8
CDK1-mediated phosphorylation of the RIIalpha regulatory subunit of PKA works as a molecular switch that promotes dissociation of RIIalpha from centrosomes at mitosis.
J Cell Sci. 2001 Sep;114(Pt 18):3243-54. doi: 10.1242/jcs.114.18.3243.
9
The PACT domain, a conserved centrosomal targeting motif in the coiled-coil proteins AKAP450 and pericentrin.
EMBO Rep. 2000 Dec;1(6):524-9. doi: 10.1093/embo-reports/kvd105.
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