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PMID |
Sentence |
1 |
30862678
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Dual specificity phosphatases (DUSPs) are a family of phosphatases mainly responsible for MAPK inhibition.
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2 |
30862678
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Diabetes-induced DUSP4 reduction enhanced p38 and c-Jun N-terminal kinase (JNK) activity and podocyte dysfunction.
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3 |
30862678
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The overexpression of DUSP4 prevented the activation of p38, JNK, caspase 3/7 activity, and NADPH oxidase 4 expression induced by high glucose level exposure.
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4 |
30862678
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These morphological changes were associated with profound podocyte foot process effacement, cell death, and sustained p38 and JNK activation.
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5 |
30862678
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Moreover, inhibition of protein kinase C-δ prevented DUSP4 expression decline and p38/JNK activation in the podocytes and renal cortex of diabetic mice.
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6 |
30862678
|
Dual specificity phosphatases (DUSPs) are a family of phosphatases mainly responsible for MAPK inhibition.
|
7 |
30862678
|
Diabetes-induced DUSP4 reduction enhanced p38 and c-Jun N-terminal kinase (JNK) activity and podocyte dysfunction.
|
8 |
30862678
|
The overexpression of DUSP4 prevented the activation of p38, JNK, caspase 3/7 activity, and NADPH oxidase 4 expression induced by high glucose level exposure.
|
9 |
30862678
|
These morphological changes were associated with profound podocyte foot process effacement, cell death, and sustained p38 and JNK activation.
|
10 |
30862678
|
Moreover, inhibition of protein kinase C-δ prevented DUSP4 expression decline and p38/JNK activation in the podocytes and renal cortex of diabetic mice.
|
11 |
30862678
|
Dual specificity phosphatases (DUSPs) are a family of phosphatases mainly responsible for MAPK inhibition.
|
12 |
30862678
|
Diabetes-induced DUSP4 reduction enhanced p38 and c-Jun N-terminal kinase (JNK) activity and podocyte dysfunction.
|
13 |
30862678
|
The overexpression of DUSP4 prevented the activation of p38, JNK, caspase 3/7 activity, and NADPH oxidase 4 expression induced by high glucose level exposure.
|
14 |
30862678
|
These morphological changes were associated with profound podocyte foot process effacement, cell death, and sustained p38 and JNK activation.
|
15 |
30862678
|
Moreover, inhibition of protein kinase C-δ prevented DUSP4 expression decline and p38/JNK activation in the podocytes and renal cortex of diabetic mice.
|