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  2. CD59 - Wikipedia

    en.wikipedia.org/wiki/CD59

    CD59 glycoprotein, also known as MAC-inhibitory protein (MAC-IP), membrane inhibitor of reactive lysis (MIRL), or protectin, is a protein that in humans is encoded by the CD59 gene. [5] It is an LU domain and belongs to the LY6/uPAR/alpha-neurotoxin protein family. [6] CD59 attaches to host cells via a glycophosphatidylinositol (GPI) anchor.

  3. Complement membrane attack complex - Wikipedia

    en.wikipedia.org/wiki/Complement_membrane_attack...

    Membrane attack complex (Terminal complement complex C5b-9) A membrane attack complex attached to a pathogenic cell The membrane attack complex (MAC) or terminal complement complex (TCC) is a complex of proteins typically formed on the surface of pathogen cell membranes as a result of the activation of the host's complement system, and as such is an effector of the immune system.

  4. BH3 interacting-domain death agonist - Wikipedia

    en.wikipedia.org/wiki/BH3_interacting-domain...

    The BH3 interacting-domain death agonist, or BID, gene is a pro-apoptotic member of the Bcl-2 protein family. [5] Bcl-2 family members share one or more of the four characteristic domains of homology entitled the Bcl-2 homology (BH) domains (named BH1, BH2, BH3 and BH4), and can form hetero- or homodimers.

  5. Threshold potential - Wikipedia

    en.wikipedia.org/wiki/Threshold_potential

    Measuring changes in threshold can indicate changes in membrane potential, axonal properties, and/or the integrity of the myelin sheath. Threshold tracking allows for the strength of a test stimulus to be adjusted by a computer in order to activate a defined fraction of the maximal nerve or muscle potential.

  6. Agonist - Wikipedia

    en.wikipedia.org/wiki/Agonist

    A co-agonist works with other co-agonists to produce the desired effect together. NMDA receptor activation requires the binding of both glutamate, glycine and D-serine co-agonists. Calcium can also act as a co-agonist at the IP3 receptor. A selective agonist is selective for a specific type of receptor. E.g.

  7. S1PR1 - Wikipedia

    en.wikipedia.org/wiki/S1PR1

    S1PR1 like the other members of the GPCR family is composed of seven-transmembrane helices arranged in a structurally conserved bundle. [5] Like other GPCRs, in the extracellular region S1PR1 is composed of three loops: ECL1 between helices II and III, ECL2 between helices IV and V and ECL3 between helices VI and VII.

  8. Agonist-antagonist - Wikipedia

    en.wikipedia.org/wiki/Agonist-antagonist

    Agonist vs. antagonist. In pharmacology the term agonist-antagonist or mixed agonist/antagonist is used to refer to a drug which under some conditions behaves as an agonist (a substance that fully activates the receptor that it binds to) while under other conditions, behaves as an antagonist (a substance that binds to a receptor but does not activate and can block the activity of other agonists).

  9. Cell surface receptor - Wikipedia

    en.wikipedia.org/wiki/Cell_surface_receptor

    Cell surface receptors (membrane receptors, transmembrane receptors) are receptors that are embedded in the plasma membrane of cells. [1] They act in cell signaling by receiving (binding to) extracellular molecules. They are specialized integral membrane proteins that allow communication between the cell and the extracellular space.

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