Sentence examples for 1 tsc from inspiring English sources

Exact(1)

Other examples are MAPK = 1 combined with mTORC1-activating elements (mTORC1 = 1, TSC = 0, PRAS40 = 0), which restore proliferation to its original level (Proliferationnorm = 0.50) and also lower apoptosis significantly (Apoptosisnorm = 0.13), and FOXO3 = 1 together with MAPK = 2, which blocks apoptosis and restores proliferation (Proliferationnorm = 0.50).

Similar(59)

Those defects are commonly observed by means of DLTS [15, 24, 25] and TSC [26, 27, 29] measurements.

Has mother has a tuberous sclerosis 2 (TSC 2) gene abnormality and a diagnosis of tuberous sclerosis.

Hence, the total score of a TA processor is calculated by Equation 8: TSc = 1 tns 150 × ncb + ncs + 90 × nch − ErS, Open image in new window (8).

As can be seen from Figs. 3 and 4, TSC outperforms the QCP after a power imbalance value of around −6 and −5 dB when (bar {gamma }_{1}=10) dB and (bar {gamma }_{1}=15) dB, respectively.

In the "Context" condition, 12 grasping actions (6 U and 6 T) and 12 simple contact actions (6 Usc and 6 Tsc) were presented, intermixed among them.

As depicted in Figure 7, TSC derived from pediatric gliomas survived significantly better than neural stem cells after both treatments (Student-Newman-Keuls test, p<0.001).

Recent works issued that the tumor suppressor protein tuberous sclerosis complex 2 (TSC 2), an upstream regulator of mTOR, could be phosphorylated by ERK signaling [39], [40], indicating that the phosphorylation of S6K1 may be mediated by ERK signaling.

A putative MrpC binding site located at -140 relative to the predicted cheW4a TSC (-105 relative to that of MXAN_2680; Additional file 3) might mediate the observed up-regulation.

Notably, the TSC line that displayed the near equal maternal-to-paternal expression ratio for H19, TSC line BC.3, was the same line that displayed a maternal expression bias for Igf2 (Table 2).

In a study of 224 TSC patients (74% of whom were under the age of 15), the incidence of renal cysts was 16% in patients with germline TSC1 mutations and 25% in patients with germline TSC2 mutations (9).

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