The c-Jun NH2-terminal kinase (JNK) is activated when cells are exposed to ultraviolet (UV) radiation. However, the functional consequence of JNK activation in UV-irradiated cells has not been established. It is shown here that JNK is required for UV-induced apoptosis in primary murine embryonic fibroblasts. Fibroblasts with simultaneous targeted disruptions of all the functional Jnk genes were protected against UV-stimulated apoptosis. The absence of JNK caused a defect in the mitochondrial death signaling pathway, including the failure to release cytochrome c. These data indicate that mitochondria are influenced by proapoptotic signal transduction through the JNK pathway
UVB irradiation induced phosphorylation of JNK and subsequent apoptosis in human melanocytes. Deplet...
Entosis is a cell death mechanism that is executed through neighbor cell ingestion and killing that ...
The c-Jun NH(2)-terminal kinase (JNK) has been implicated in both cell death and survival responses ...
The c-Jun NH2-terminal kinase (JNK) is activated when cells are exposed to ultraviolet (UV) radiatio...
Stress-induced JNK activity has been implicated in apoptosis. Gene disruption studies have establi...
UV irradiation and other stress-activated signals activate the Jun N-terminal kinase (JNK, SAPK) pat...
AbstractUV irradiation and other stress-activated signals activate the Jun N-terminal kinase (JNK, S...
The c-Jun NH(2)-terminal kinase (JNK) is activated when cells are exposed to environmental stress, i...
Targeted gene disruption studies have established that the c-Jun NH(2)-terminal kinase (JNK) signali...
UV light (UV-C) is a potent inducer of the c-fos gene. Cells lacking c-Fos are hypersensitive to the...
Irradiation of mammalian cells with ultraviolet-B radiation (UV-B) triggers the activation of a grou...
Activation of c-Jun N-terminal kinase (JNK) signaling pathway is a key event in apoptosis. The cellu...
jun-NH2-terminal kinase (INK) belongs to a family of protein kinases that phosphorylates c-Jun, ATF2...
The nucleotide excision repair (NER) system consists of two subpathways, global genome repair (GGR) ...
Recent studies strongly suggest an active involvement of the c-Jun N-terminal kinase (JNK) signaling...
UVB irradiation induced phosphorylation of JNK and subsequent apoptosis in human melanocytes. Deplet...
Entosis is a cell death mechanism that is executed through neighbor cell ingestion and killing that ...
The c-Jun NH(2)-terminal kinase (JNK) has been implicated in both cell death and survival responses ...
The c-Jun NH2-terminal kinase (JNK) is activated when cells are exposed to ultraviolet (UV) radiatio...
Stress-induced JNK activity has been implicated in apoptosis. Gene disruption studies have establi...
UV irradiation and other stress-activated signals activate the Jun N-terminal kinase (JNK, SAPK) pat...
AbstractUV irradiation and other stress-activated signals activate the Jun N-terminal kinase (JNK, S...
The c-Jun NH(2)-terminal kinase (JNK) is activated when cells are exposed to environmental stress, i...
Targeted gene disruption studies have established that the c-Jun NH(2)-terminal kinase (JNK) signali...
UV light (UV-C) is a potent inducer of the c-fos gene. Cells lacking c-Fos are hypersensitive to the...
Irradiation of mammalian cells with ultraviolet-B radiation (UV-B) triggers the activation of a grou...
Activation of c-Jun N-terminal kinase (JNK) signaling pathway is a key event in apoptosis. The cellu...
jun-NH2-terminal kinase (INK) belongs to a family of protein kinases that phosphorylates c-Jun, ATF2...
The nucleotide excision repair (NER) system consists of two subpathways, global genome repair (GGR) ...
Recent studies strongly suggest an active involvement of the c-Jun N-terminal kinase (JNK) signaling...
UVB irradiation induced phosphorylation of JNK and subsequent apoptosis in human melanocytes. Deplet...
Entosis is a cell death mechanism that is executed through neighbor cell ingestion and killing that ...
The c-Jun NH(2)-terminal kinase (JNK) has been implicated in both cell death and survival responses ...