Examples of using Binding affinity in English and their translations into Norwegian
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Despite very low binding affinity with the androgen receptor,
Lurasidone binds strongly to dopaminergic D2- and to serotonergic 5-HT2A and 5-HT7- receptors with high binding affinity of 0.994, 0.47 and 0.495 nM, respectively.
Despite very low binding affinity with the androgen receptor,
Regardless of extremely low binding affinity with the androgen receptor,
Despite very low binding affinity with the androgen receptor,
The information in this section is based on binding affinity between sugammadex and other medicinal products,
For toremifene, which has a relatively high binding affinity for sugammadex and for which relatively high plasma concentrations might be present,
Click here to buy Trenbolone in Blagoevgrad Bulgaria Trenbolone offer for sale in Blagoevgrad Bulgaria Trenbolone has an exceptionally solid binding affinity for the androgen receptor too,
Even though oxymetholone possesses very low binding affinity when it comes to the androgen receptor,
Aripiprazole exhibited high binding affinity in vitro for dopamine D2
Click here to buy Trenbolone in Bat Yam Israel Trenbolone available in Bat Yam Israel Trenbolone has an extremely strong binding affinity for the androgen receptor also,
Aripiprazole exhibits high binding affinity in vitro for dopamine D2
also enjoys a significantly lower binding affinity for the IGF binding proteins that were discussed earlier.
especially when we note that in its initial state Oxymetholone has a notably low binding affinity for the androgen receptor.
Click here to buy Trenbolone in Saint Catharines-Niagara Canada Trenbolone available in Saint Catharines-Niagara Canada Trenbolone has an exceptionally solid binding affinity for the androgen receptor also,
However, they have different binding affinities for receptors in different parts of the body.
as peptides consisting of the individual peptide loop structures have been found to have binding affinities for N-type voltage sensitive calcium channels that are several orders of magnitude lower than that of the parent(ziconotide) compound.
Interestingly, the modifications allow IGF-1 DES to enjoy a lowered binding affinity for the IGF binding proteins that were discussed earlier,
This is possible due to its binding affinity for SHBG.
Despite really low binding affinity with the androgen receptor,