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. 2014 Oct 3;2:144. doi: 10.1186/s40478-014-0144-4

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© Kreft et al.; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Kif21b expression in the grey matter does not change during physiological ageing, but is significantly increased in young Alzheimer patients. Kif21b expression was stratified according to the age at death into three categories based on age at death of the NDC (<25^th percentile represents <62 yrs, between 25-75^th percentile equals 62-72 yrs or >75^th percentile is >72 yrs). Kif21b was compared between the three age categories in A) NDC, B) MS and C) AD.