Примери за използване на Binds with high на Английски и техните преводи на Български
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Pasireotide binds with high affinity to four of the five hssts.
Bezlotoxumab is a human monoclonal antitoxin antibody that binds with high affinity to C.
In vitro, this radiopharmaceutical binds with high affinity mainly to SSTR2 but also, to a lesser extent, to SSTR5.
Sodium oxybate is a partial agonist on both GABAA andGABAB receptors and also binds with high affinity to GHB-specific receptors.
Trastuzumab binds with high affinity and specificity to sub-domain IV, a juxta-membrane region of HER2's extracellular domain.
Bezlotoxumab is a human monoclonal antitoxin antibody that binds with high affinity to C. difficile toxin B and neutralizes its activity.
Trastuzumab binds with high affinity and specificity to sub-domain IV, a juxta-membrane region of HER2's extracellular domain.
In vitro data and studies in laboratory animals indicate that 99mTc-depreotide binds with high affinity to somatostatin receptor(SSTR) subtypes 2, 3.
The monoclonal antibody binds with high affinity and selectivity to CD79b, a cell surface component of the B-cell receptor.
Panitumumab is a recombinant,fully human IgG2 monoclonal antibody that binds with high affinity and specificity to the human EGFR.
Pramipexole is a dopamine agonist that binds with high selectivity and specificity to the D2 subfamily of dopamine receptors of which it has a preferential affinity to D3 receptors, and has full intrinsic activity.
In vitro data andstudies in laboratory animals indicate that 99mTc-depreotide binds with high affinity to somatostatin receptor(SSTR) subtypes 2, 3 and 5.
The substance binds with high affinity to the ATP-binding site in such a manner that it is a potent inhibitor of wild-type BCR-ABL and maintains activity against 32/33 imatinib-resistant mutant forms of BCR-ABL.
Alirocumab is a fully human IgG1 monoclonal antibody that binds with high affinity and specificity to proprotein convertase subtilisin kexin type 9(PCSK9).
Canakinumab binds with high affinity specifically to human IL-1 beta and neutralises the biological activity of human IL-1 beta by blocking its interaction with IL-1 receptors, thereby preventing IL-1 beta-induced gene activation and the production of inflammatory mediators.
Pasireotide is a multireceptor targeting somatostatin analog(SSA) that binds with high affinity to four of the five somatostatin receptor subtypes(sst 1, 2, 3 and 5)2.
Basiliximab specifically binds with high affinity(KD-value 0.1 nM) to the CD25 antigen on activated T-lymphocytes expressing the high affinity interleukin-2 receptor(IL2R) and thereby prevents binding of interleukin-2, a critical signal for T-cell proliferation in the cellular immune response involved in allograft rejection.
Mechanism of action Ustekinumab is a fully human IgG1κ monoclonal antibody that binds with high affinity and specificity to the p40 protein subunit of the human cytokines IL-12 and IL-23.
Studies in animals have shown that ioflupane binds with high affinity to the presynaptic dopamine transporter and so radiolabelled ioflupane(123I) can be used as a surrogate marker to examine the integrity of the dopaminergic nigrostriatal neurons.
Ixekizumab is an IgG4 monoclonal antibody that binds with high affinity(< 3 pM) and specificity to interleukin 17A(both IL-17A and IL-17A/F).
Unlike most other anabolic steroids,THG also binds with high affinity to the glucocorticoid receptor, and while this effect may cause additional weight loss, it is also likely to cause extra side effects such as immunosuppression that are not seen with most other steroids.
Studies in animals have shown that ioflupane binds with high affinity to the presynaptic dopamine transporter and so radiolabelled ioflupane.
Denosumab is a human monoclonal antibody(IgG2)that targets and binds with high affinity and specificity to RANKL, preventing the RANKL/RANK interaction from occurring and resulting in reduced osteoclast numbers and function, thereby decreasing bone resorption and cancer-induced bone destruction.
Risankizumab is a humanised immunoglobulin G1(IgG1)monoclonal antibody that selectively binds with high affinity to the p19 subunit of human interleukin 23(IL-23) cytokine without binding to IL12 and inhibits its interaction with the IL-23 receptor complex.
Necitumumab is a recombinant human IgG1 monoclonal antibody that binds with high affinity and specificity to the human epidermal growth factor receptor 1(EGFR) and blocks the ligand binding site, blocking activation by all known ligands and inhibiting relevant biological consequences in vitro.
Denosumab is a human monoclonal antibody(IgG2)that targets and binds with high affinity and specificity to RANKL, preventing activation of its receptor, RANK, on the surface of osteoclast precursors and osteoclasts.
Brodalumab is a recombinant fully human monoclonal immunoglobulin IgG2 antibody that binds with high affinity to human IL-17RA and blocks the biological activities of the pro-inflammatory cytokines IL-17A, IL-17F, IL-17A/F heterodimer, IL-17C and IL-17E(also known as IL-25), resulting in inhibition of the inflammation and clinical symptoms associated with psoriasis.
Vancomycin is a tricyclic glycopeptide antibiotic that inhibits the synthesis of the cell wall in sensitive bacteria by binding with high affinity to the D-alanyl-D-alanine terminus of cell wall precursor units.
Certain GLA mutations can result in the production of abnormally folded and unstable mutant forms of α-Gal A. Migalastat is a pharmacological chaperone that is designed to selectively and reversibly bind with high affinity to the active sites of certain mutant forms of-Gal A, the genotypes of which are referred to as amenable mutations.
It is a tridentate ligand that binds iron with high affinity in a 2:1 ratio.