In addition to the regulation of apoptosis and necroptosis, cFLIP is known to be a negative regulator of autophagy.
An alternatively spliced variant of MyD88, called MyD88 short (MyD88s), has been identified to be a negative regulator of inflammatory signaling pathways.
PKCα has been shown to be a negative regulator of contractility and PKCα gene deletion in mice protected against heart failure.
A zinc finger type transcription factor, AJ18, is thought to be a negative regulator of osteoblast differentiation, but its expression mechanism is not fully understood.
OsMKP1 has been shown to be a negative regulator of the wound response in rice.
These studies also indicated that SUB1A-1 might be a negative regulator of OsSUB1C.
CAM-1 is considered to be a negative regulator of canonical Wnt signaling; excess EGL-20, a canonical Wnt ligand, mirrors the neuronal phenotype of CAM-1 mutants.
AMPK has been documented to be a negative regulator of cap-dependent translation [15].
Recently, optineurin has been shown to be a negative regulator of NF-κB [14].
IRF-8 has been shown to be a negative regulator of osteoclastogenesis.
