Papers associated with centromere (and cenpe)

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	Microtubule end conversion mediated by motors and diffusing proteins with no intrinsic microtubule end-binding activity., Chakraborty M., Nat Commun. April 11, 2019; 10 (1): 1673.
	Kinetochore function is controlled by a phospho-dependent coexpansion of inner and outer components., Wynne DJ., J Cell Biol. September 14, 2015; 210 (6): 899-916.
	Preventing farnesylation of the dynein adaptor Spindly contributes to the mitotic defects caused by farnesyltransferase inhibitors., Holland AJ., Mol Biol Cell. May 15, 2015; 26 (10): 1845-56.
	Kinetochore-microtubule attachment throughout mitosis potentiated by the elongated stalk of the kinetochore kinesin CENP-E., Vitre B., Mol Biol Cell. August 1, 2014; 25 (15): 2272-81.
	Multiple domains of human CLASP contribute to microtubule dynamics and organization in vitro and in Xenopus egg extracts., Patel K., Cytoskeleton (Hoboken). March 1, 2012; 69 (3): 155-65.
	In vitro centromere and kinetochore assembly on defined chromatin templates., Guse A., Nature. August 28, 2011; 477 (7364): 354-8.
	CENP-E combines a slow, processive motor and a flexible coiled coil to produce an essential motile kinetochore tether., Kim Y., J Cell Biol. May 5, 2008; 181 (3): 411-9.
	Microtubule capture by CENP-E silences BubR1-dependent mitotic checkpoint signaling., Mao Y., J Cell Biol. September 12, 2005; 170 (6): 873-80.
	Direct observation of microtubule dynamics at kinetochores in Xenopus extract spindles: implications for spindle mechanics., Maddox P., J Cell Biol. August 4, 2003; 162 (3): 377-82.
	Activating and silencing the mitotic checkpoint through CENP-E-dependent activation/inactivation of BubR1., Mao Y., Cell. July 11, 2003; 114 (1): 87-98.

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