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PMID |
Sentence |
1 |
9409713
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The beta2 thyroid hormone receptor (TR-beta2) is by far the most abundant isoform in the pituitary, although transcripts of TR-alpha and TR-beta1 genes have been reported in developmental and adult rat pituitary gland.
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2 |
22012613
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Upregulation of TRB2 induced by miR-98 in the early lesions of large artery of type-2 diabetic rat.
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3 |
22012613
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Next, studies using RAOEC cells showed that the TRB2 expression was inhibited by the treatment of miR-98.
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4 |
22012613
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Finally, we validated the changes in TRB2 by studying one of the TRB2's substrates, Akt, in animal models.
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5 |
22012613
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TRB2 plays important roles in the pathogenesis of diabetic-2 large artery complications at early stage, and these effects may be modulated by miR-98.
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6 |
22012613
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Thus, targeting TRB2 and miR-98 could be considered as novel therapeutic strategies for the early large artery deficits in diabetic-2.
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7 |
22012613
|
Upregulation of TRB2 induced by miR-98 in the early lesions of large artery of type-2 diabetic rat.
|
8 |
22012613
|
Next, studies using RAOEC cells showed that the TRB2 expression was inhibited by the treatment of miR-98.
|
9 |
22012613
|
Finally, we validated the changes in TRB2 by studying one of the TRB2's substrates, Akt, in animal models.
|
10 |
22012613
|
TRB2 plays important roles in the pathogenesis of diabetic-2 large artery complications at early stage, and these effects may be modulated by miR-98.
|
11 |
22012613
|
Thus, targeting TRB2 and miR-98 could be considered as novel therapeutic strategies for the early large artery deficits in diabetic-2.
|
12 |
22012613
|
Upregulation of TRB2 induced by miR-98 in the early lesions of large artery of type-2 diabetic rat.
|
13 |
22012613
|
Next, studies using RAOEC cells showed that the TRB2 expression was inhibited by the treatment of miR-98.
|
14 |
22012613
|
Finally, we validated the changes in TRB2 by studying one of the TRB2's substrates, Akt, in animal models.
|
15 |
22012613
|
TRB2 plays important roles in the pathogenesis of diabetic-2 large artery complications at early stage, and these effects may be modulated by miR-98.
|
16 |
22012613
|
Thus, targeting TRB2 and miR-98 could be considered as novel therapeutic strategies for the early large artery deficits in diabetic-2.
|
17 |
22012613
|
Upregulation of TRB2 induced by miR-98 in the early lesions of large artery of type-2 diabetic rat.
|
18 |
22012613
|
Next, studies using RAOEC cells showed that the TRB2 expression was inhibited by the treatment of miR-98.
|
19 |
22012613
|
Finally, we validated the changes in TRB2 by studying one of the TRB2's substrates, Akt, in animal models.
|
20 |
22012613
|
TRB2 plays important roles in the pathogenesis of diabetic-2 large artery complications at early stage, and these effects may be modulated by miR-98.
|
21 |
22012613
|
Thus, targeting TRB2 and miR-98 could be considered as novel therapeutic strategies for the early large artery deficits in diabetic-2.
|
22 |
22012613
|
Upregulation of TRB2 induced by miR-98 in the early lesions of large artery of type-2 diabetic rat.
|
23 |
22012613
|
Next, studies using RAOEC cells showed that the TRB2 expression was inhibited by the treatment of miR-98.
|
24 |
22012613
|
Finally, we validated the changes in TRB2 by studying one of the TRB2's substrates, Akt, in animal models.
|
25 |
22012613
|
TRB2 plays important roles in the pathogenesis of diabetic-2 large artery complications at early stage, and these effects may be modulated by miR-98.
|
26 |
22012613
|
Thus, targeting TRB2 and miR-98 could be considered as novel therapeutic strategies for the early large artery deficits in diabetic-2.
|