All terms in GO

Label Id Description
obsolete smooth muscle fiber development GO_0048746 [OBSOLETE. The process whose specific outcome is the progression of smooth muscle fiber over time, from its formation to the mature structure.]
response to oscillatory fluid shear stress GO_0097702 [Any response to fluid shear stress where the fluid is moving across a solid surface with an oscillatory flow. Disturbed flow patterns at the arterial bifurcations and curvatures may cause endothelial dysfunction, which initiates atherosclerosis.]
L-altrarate dehydratase activity GO_1990594 [Catalysis of the reaction: L-altrarate = 5-dehydro-4-deoxy-D-glucarate + H2O.]
GO_0048747 GO_0048747
cellular response to pulsatile fluid shear stress GO_0097703 [Any response to pulsatile fluid shear stress that occurs at the level of a cell.]
cellular response to fluid shear stress GO_0071498 [Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a fluid shear stress stimulus. Fluid shear stress is the force acting on an object in a system where the fluid is moving across a solid surface.]
mast cell secretagogue receptor activity GO_1990595 [Combining with basic secretagogues to initiate pseudo-allergic reactions in mast cells.]
negative regulation of skeletal muscle fiber development GO_0048744 [Any process that stops, prevents, or reduces the frequency, rate or extent of skeletal muscle fiber development. Muscle fibers are formed by the maturation of myotubes. They can be classed as slow, intermediate/fast or fast.]
cellular response to oscillatory fluid shear stress GO_0097704 [Any response to oscillatory fluid shear stress that occurs at the level of a cell.]
protein K69-linked ufmylation GO_1990592 [A protein ufmylation process in which a polymer of the ubiquitin-like protein UFM1 is formed by linkages between lysine residues at position 69 of the UFM1 monomers, is added to a protein.]
protein polyufmylation GO_1990564 [Covalent attachment of the ubiquitin-like protein UFM1 to a protein, forming an UFM1 chain.]
smooth muscle tissue development GO_0048745 [The process whose specific outcome is the progression of smooth muscle over time, from its formation to the mature structure.]
muscle tissue development GO_0060537 [The progression of muscle tissue over time, from its initial formation to its mature state. Muscle tissue is a contractile tissue made up of actin and myosin fibers.]
vascular endothelial cell response to pulsatile fluid shear stress GO_0097705 [Any response to pulsatile fluid shear stress that occurs in a vascular endothelial cell.]
nascent polypeptide-associated complex binding GO_1990593 [Binding to nascent polypeptide-associated complex, a heterodimeric protein complex that can reversibly bind to ribosomes and is located in direct proximity to newly synthesized polypeptide chains as they emerge from the ribosome.]
purine deoxyribonucleoside monophosphate metabolic process GO_0009170 [The chemical reactions and pathways involving purine deoxyribonucleoside monophosphate, a compound consisting of a purine base linked to a deoxyribose sugar esterified with phosphate on the sugar.]
vascular endothelial cell response to oscillatory fluid shear stress GO_0097706 [Any response to oscillatory fluid shear stress that occurs in a vascular endothelial cell.]
ATF1-ATF4 transcription factor complex GO_1990590 [Transcription factor complex consisting of ATF1 and ATF4 subunits that is capable of binding to cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3') of the GRP78 (HSPA5) promoter. Involved in the ER stress response pathway.]
purine deoxyribonucleoside monophosphate biosynthetic process GO_0009171 [The chemical reactions and pathways resulting in the formation of purine deoxyribonucleoside monophosphate, a compound consisting of a purine base linked to a deoxyribose sugar esterified with phosphate on the sugar.]
ferroptosis GO_0097707 [A programmed cell death characterized morphologically by the presence of smaller than normal mitochondria with condensed mitochondrial membrane densities, reduction or vanishing of mitochondria crista, and outer mitochondrial membrane rupture. Activation of mitochondrial voltage-dependent anion channels and mitogen-activated protein kinases, upregulation of endoplasmic reticulum stress, and inhibition of cystine/glutamate antiporter are involved in the induction of ferroptosis. This process is characterized by the accumulation of lipid peroxidation products and lethal reactive oxygen species (ROS) derived from iron metabolism. Glutathione peroxidase 4 (GPX4), heat shock protein beta-1, and nuclear factor erythroid 2-related factor 2 function as negative regulators of ferroptosis by limiting ROS production and reducing cellular iron uptake, respectively. In contrast, NADPH oxidase and p53 act as positive regulators of ferroptosis by promotion of ROS production and inhibition of expression of SLC7A11 (a specific light-chain subunit of the cystine/glutamate antiporter), respectively. Misregulated ferroptosis has been implicated in multiple physiological and pathological processes.]