Sentence examples for selective medicines from inspiring English sources

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It is critical to understand the information that can be derived from this wealth of data to not just identify the chemical, biological and/or genetic markers/patterns of a particular disease but also to utilize this knowledge to design more potent and selective medicines.

This multigenesis view of cancer should also lead to an expanded perspective on cancer therapy which may result in the development of more selective medicines that are not only cancer subtype-specific and thus more effective but also less damaging to non-cancer cells.

Similar(58)

Thus, there is no single breakthrough in oncology but rather many individual steps of developing personalised and selective cancer medicines.

Incorporating new technologies such as designer genetic engineering, nanotechnology, and bio-selective nuclear medicine tracers into study designs helps to gain important insights into OA pathophysiology.

This paper describes the development, implementation, and evaluation of an integrated selective in sleep medicine for fourth-year medical students.

The most commonly used psychotropic medicines were selective serotonin reuptake inhibitors (5.1%) and benzodiazepine or benzodiazepine-like medicines (3.9%).

The most commonly used psychotropic medicines are selective serotonin reuptake inhibitors and benzodiazepine or benzodiazepine-like medicines.

These medicines included selective oestrogen reuptake inhibitors (tamoxifen 2109B, 2110C and toremifene 8216K), aromatase inhibitors (anastrozole 8179L, exemestane 8506Q, letrozole 8245Y); and other breast cancer therapies (goserelin 1452M; trastuzumab 4632T, 4639E, 4650R, 4703M, 7264H, 7265J, 7266K, 7267L; lapatinib 9148L; 500 mg preparations of medroxyprogesterone 2728N) [ 22].

Read important information (continued from previous side) Especially tell your healthcare provider if you take antidepressant medicines called:    selective serotonin reuptake inhibitors (SSRIs), or serotonin norepinephrine reuptake inhibitors (SNRIs) , or tricyclic antidepressants (TCAs), or  monoamine oxidase inhibitors (MAOIs).

Previous evidence showed the potential use of the NTSR1 as a biomarker for cancer progression and as a component of personalized medicine in selective cancers [ 24], and this is consistent with our present result.

Given both its specific expression in tumors compared to corresponding healthy tissues and its proximity to tumor blood vessels (making it accessible via the bloodstream) we propose TNW as a good candidate for selective delivery of anticancer medicine.

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