In all behavioral examinations there was a clear difference to
age matched wt - controls which increased with age.
Not exact matches
(A) Isolated islets from 3 - wk - old, female, Tg - hIAPP mice were cultured in presence of different concentrations of islet extracts (IE) from old Tg - hIAPP mice, with overt diabetic pathology and
age -
matched WT mice.
Groups of male Tg - hIAPP mice were injected i.p. at 3 wk of
age with 10 % pancreas homogenate from either 12 - mo - old, male, IAPP Tg mice bearing substantial islet amyloid aggregates (as shown in Fig. 1) or from
age -
matched, male,
WT mice not expressing hIAPP.
(E) Body weights of developing XpdTTD / TTD and XpdTTD / † XPCS mice after weaning plotted as a percentage of the weight of
age -
matched control
wt and heterozygote (hz) littermates (set at 100 %).
Methods: R6 / 2 CAG 240 (peak training at 11 weeks of
age), zQ175 knock in (KI) HET (peak training at 27 weeks of
age) and BAC HD (peak training at 48 weeks of
age), as well as respective
age -
matched wild type (
WT) control mice, were trained on the peak interval task (20 s interval) in which response rates during unreinforced peak trials were examined.
The Effect of Acetyl - L - carnitine and R - alpha - lipoic acid Treatment in ApoE4 Mouse as a Model of Human Alzheimer's Disease J Neurol Sci 2009 (Mar 31)[Epub ahead of print] We measured
age - dependent effects of human ApoE4 on cerebral blood flow (CBF) using ApoE4 transgenic mice compared to
age -
matched wild - type (
WT) mice by use of -LSB-(14) C] iodoantipyrene autoradiography.