Both Authors contributed equally to this work.
Longevity effect of IGF-1R+/− mutation depends on genetic background-specific receptor activation
Version of Record online: 11 SEP 2013
© 2013 the Anatomical Society and John Wiley & Sons Ltd
Volume 13, Issue 1, pages 19–28, February 2014
How to Cite
Xu, J., Gontier, G., Chaker, Z., Lacube, P., Dupont, J. and Holzenberger, M. (2014), Longevity effect of IGF-1R+/− mutation depends on genetic background-specific receptor activation. Aging Cell, 13: 19–28. doi: 10.1111/acel.12145
- Issue online: 16 JAN 2014
- Version of Record online: 11 SEP 2013
- Accepted manuscript online: 30 JUL 2013 10:26AM EST
- Manuscript Accepted: 21 JUL 2013
- ANR. Grant Number: NT05-3 42491
- EU NoE. Grant Number: 036894
|acel12145-sup-0001-FigS1.pdf||application/PDF||105K||Fig. S1 Glucose homeostasis in 4- to 6-month-old B6 IGF-1R+/−mice.|
Table S1 Data of Figure 1D and E (lifetime survival).
Table S2 Descriptive statistics of lifespan and survival data from male and female IGF-1R+/− and control mice in B6 genetic background (Data correspond to Figure 1, Panel D and E).
Table S3 Mean lifespan of B6 control mice in recent studies of mouse longevity genes. Highest and lowest means are in bold.
Table S4 Longevity of male and female mice from strains derived from original 129 mice.
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