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Publishing research using ab88464? Please let us know so that we can cite the reference in this datasheet.
ab88464 has been referenced in 3 publications.
- Eisch V et al. Progerin impairs chromosome maintenance by depleting CENP-F from metaphase kinetochores in Hutchinson-Gilford progeria fibroblasts. Oncotarget 7:24700-18 (2016).
- Paquet N et al. Néstor-Guillermo Progeria Syndrome: a biochemical insight into Barrier-to-Autointegration Factor 1, alanine 12 threonine mutation. BMC Mol Biol 15:27 (2014).
- Puente XS et al. Exome sequencing and functional analysis identifies BANF1 mutation as the cause of a hereditary progeroid syndrome. Am J Hum Genet 88:650-6 (2011).
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