Sentence examples for most commonly released from inspiring English sources

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What are the most commonly released toxins?

Angiosperms pollen is most commonly released as single pollen grains or monads [ 4] which represent the basic angiosperm pollen-unit.

As the cytotoxin is most commonly released in the lysosome following cleavage of the linker molecule, it is important to ensure that the cytotoxin remains stable in low pH environments and has the capacity to move into the cytosolic or nuclear compartments of the cell within which it takes effect.

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In 2004 Jawbone, as the company was most commonly called, released its first headset, a Bluetooth-driven device created by chief designer Yves Béhar to hang on the wearer's ear and communicate with the wearer's mobile phone.

Patients with ADHD intended for treatment with Equasym XL®, either previously treatment-naive, receiving treatment with other MPH formulations (immediate-release or long-acting, most commonly immediate-release Medikinet® and Medikinet® retard, respectively), receiving a different pharmacological therapy or receiving non-pharmacological therapy were observed for 6 12 weeks in routine care.

The average age of individuals misusing ADHD stimulant medication in a US National Survey on Drug Use and Health was 19.5 years [ 5] and, of 1,025 students in a US university, 16 % had abused or misused medication, most commonly immediate-release methylphenidate (MPH) [ 4].

Despite its name, sucrose synthase (SUS) most commonly degrades sucrose to release uridine diphosphate glucose (UDP -glucose and frUDP -glucoseterotrophic cells [ 65].

As expected, we found that phthalates were most commonly used in modified-release RX drug formulations that provided timed-release and targeted-release of active ingredients.

Over a 1-year period the most commonly dispensed antineoplastics were gonadotropin-releasing hormone analogues, such as goserelin, and pyrimidine analogues, such as capecitabine, reflecting the high rates of prostate and colorectal cancers (table 4).

In bacteria, chain release is most commonly effected by a thioesterase (TE) domain [ 18], which releases the peptide by either hydrolysis or internal cyclization [ 16, 17, 19].

The aims of this study were to construct electrospun PLA scaffolds that are able to release the two most commonly used ascorbic acid derivatives (AA and A2P), to evaluate the comparative effectives of the two in terms of collagen production and finally to assess the impact of the AA and A2P on the mechanical properties of the electrospun scaffolds.

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