Sentence examples for mouse hearts compared from inspiring English sources

In all cases, there was an excellent linear fit in the time frame of 1.5 to 7.5 min. At baseline, Patlak Ki was reduced 56% in TGmut mouse hearts compared to TGwt mice (Table 3).

In our preliminary experiments, we first determined which E3 ligases were specifically or highly expressed in the mouse hearts compared with other tissues.

We documented decreased serine-473 phosphorylation of Akt/PKB in diabetic WT mouse hearts compared to control WT mouse hearts (P < 0.01).

As shown in Fig. 1E, a significant increase in levels of hyperoxidised Prdx was observed in 2-week-old tg mouse hearts, compared to wt controls, consistent with the production of intracellular H2O2.

Analysis of nuclear extracts prepared from whole heart lysates of mIGF-1 transgenic (Tg) and wild type (WT) mice revealed increased SirT1 protein levels in mIGF-1 Tg mouse hearts compared to wild type littermates.

As shown in Figures  1A and 1B, the interaction of cardiac β2AR with both the PDE4D3 and -D5 isoforms is significantly reduced in βARKct/B1KO mouse hearts compared to control B1KO hearts, an effect that might enable βARKct to enhance cardiac β2AR-dependent pro-contractile signaling in vivo.

The results suggest NF- κB (p65) protein expression was increased in aged mice hearts compared with young mice.

These data were well consistent with the immunoblotting patterns demonstrating lower CD36 protein levels in N-CD36/O-CD36 N-CD36/O-CD36 N-CD36/O-CD36hat of N-mice/O-mock (Fig.  2b).

However, the mitochondrial function remains unchanged in older Sod2+/− mice heart compared to younger Sod2+/− mice heart.

We further show that mitochondrial function decreases in young Sod2+/− mice heart compared to young wildtype mice.

In addition, complex II driven basal (state 2) respiration was significantly decreased in older mice heart compared to younger mice (Fig. 5B D).