Examples of 'receptor subtype' in a sentence

Meaning of "receptor subtype"

In biology and medicine, the phrase 'receptor subtype' refers to specific variations or types of receptors found on cell surfaces or in the body. These subtypes have slightly different structures and functions, allowing them to interact with specific molecules or transmit signals in unique ways. The phrase is commonly used in the field of pharmacology when discussing drug interactions and targeting specific receptor subtypes

How to use "receptor subtype" in a sentence

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receptor subtype
A third receptor subtype is expressed in normal human liver.
Binding assay using expression cell of prostanoids receptor subtype.
Binds to one receptor subtype as an agonist and to another as an antagonist.
Increased cell proliferation mediated through one receptor subtype.
The exact receptor subtype profile required is however not known.
Binding assay using expression cell of the prostanoide receptor subtype.
Each receptor subtype generally is associated with different biological activities.
Editing is also thought to function in cell surface expression of the receptor subtype.
Stimulation of this receptor subtype is also associated with growth hormone secretion.
The effect seems to depend on both the gal administration site as involved receptor subtype.
The exact receptor subtype profile required is however not believed to be known.
This compound preferentially binds one tachykinin receptor subtype compared to other such receptors.
Each receptor subtype is involved in a different serotonin function and has different properties.
These compounds preferentially bind one tachykinin receptor subtype compared to other such receptors.
Serotonic receptor subtype selective agents may find utility in the treatment of such disorders.

See also

All of the reference prior art compounds tested demonstrated low affinity for this receptor subtype.
Unfortunately we do not know which receptor subtype is responsible for the antidepressant activities.
Four to eight oocytes were tested for every compound and NMDA receptor subtype.
Each NPY receptor subtype is generally associated to a different biological activity.
This is the most abundant GABAA receptor subtype.
Stimulation of this receptor subtype lowers the intracellular cyclic AMP concentration in adipocytes.
Romifidine acts as an agonist at the α2 adrenergic receptor subtype.
An exception is the ACPD receptor subtype which has the properties of a metabotropic receptor.
However, they do not necessarily bind with a homogeneous receptor subtype.
Somatostatin receptor subtype 2 is expressed on a wide variety of tumor types.
The compound of the invention show a pronounced nicotinic acetylcholine a7 receptor subtype selectivity.
Each a1 receptor subtype exhibits its own pharmacologic and tissue specificities.
Heretofore conformationally constrained backbone cyclized somatostatin analogs had selectivity predominantly to receptor subtype 5.
It was hypothesized that this receptor subtype is of importance for the action of anti-psychotics.
Compounds of the invention, like buspirone, exhibited potent affinity for this serotonin receptor subtype.
Several compounds having such a7 receptor subtype selectivity have been reported in the literature.
These diseases can develop from the presence of antibodies against the muscarinic receptor subtype m2 m2achr.
It was hypothesised that this receptor subtype is of importance for the action of anti-psychotics.
They act preferentially on the human NK2A receptor subtype.
Each a2 receptor subtype appears to exhibit its own pharmacological and tissue specificities.
This response is at least in part due to the activation of the A1 receptor subtype.
Each alpha-2 receptor subtype appears to exhibit its own pharmacological and tissue specificities.
Rabbit vas deferens has been found to have predominantly the a 2A receptor subtype.
Each receptor subtype couples to a second messenger system through an intervening G-protein.
Apparent binding constants for compound 5c at each receptor subtype are listed in Table 3.
The dopamine D1 receptor subtype has been shown to occur in at least two discrete forms.
There is no disclosure or suggestion of the sequence for the human EP3 receptor subtype.
The glutamate receptor subtype NMDA is well known for its role in causing excito-neurotoxicity.
Cells were transiently transfected with rat muscarinic receptor subtype 1 DNA by the DEAE-dextran method.
The muscarinic M2 receptor subtype serves to control presynaptic acetylcholine release.
BK and kallidin act as equipotent agonists at the B2 bradykinin receptor subtype.
Particularly, selectivity over SST receptor subtype 2 avoids influences on glucagon secretion K.
Potent adenosine receptor antagonists that are selective for the A1 receptor subtype.
The 5-HT2c receptor subtype is transcribed and expressed in hypothalamic structures associated with appetite regulation.
The antilipolytic activity of adenosine is mediated through activation of the A1 receptor subtype.

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