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Gene Information

Gene symbol: DUSP4

Gene name: dual specificity phosphatase 4

HGNC ID: 3070

Synonyms: HVH2, MKP-2, TYP

Related Genes

# Gene Symbol Number of hits
1 CASP3 1 hits
2 JUN 1 hits
3 MAPK1 1 hits
4 MAPK8 1 hits
5 NOX4 1 hits
6 PRKCA 1 hits

Related Sentences

# PMID Sentence
1 30862678 Dual specificity phosphatases (DUSPs) are a family of phosphatases mainly responsible for MAPK inhibition.
2 30862678 Diabetes-induced DUSP4 reduction enhanced p38 and c-Jun N-terminal kinase (JNK) activity and podocyte dysfunction.
3 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.
4 30862678 These morphological changes were associated with profound podocyte foot process effacement, cell death, and sustained p38 and JNK activation.
5 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.
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.