Sentence examples for modification by established from inspiring English sources

We evaluated effect modification by established risk factors for gestational diabetes including age (<35 v ≥35), BMI before pregnancy (<25 v ≥25), family history of diabetes (yes, no), and race (white v non-white) by conducting stratified analyses.

We also investigated effect modification by established breast cancer risk factors that are associated with steroid hormone exposure.

We also examined effect modification by established breast cancer risk factors that are associated with steroid hormone exposure: body mass index (kg/m) among postmenopausal women (≥ 25 vs < 25 kg/m), use of hormone replacement therapy (current vs past vs never user of estrogen or estrogen + progestin) and age at menarche (≤ 12, vs > 12 years).

Transglutaminases (E.C. 2.3.2.13) catalyze the post-translational modification of proteins by establishing ε- γ-glutamyl) lysine isopeptide bonds and by the covalent conjugation of polyamines to endo-glutamyl residues of proteins.

Transglutaminases (TGases, E.C. 2.3.2.13) are intracellular and extracellular enzymes that catalyze the post-translational modification of proteins by establishing ε- γ-glutamyl) lysine isopeptide bonds and the covalent conjugation of polyamines to endo-glutamyl residues of protein substrates (Lorand and Graham 2003; Serafini-Fracassini and Del Duca 2008; Serafini-Fracassini et al. 2009).

Blue-native PAGE (BN-PAGE) and SDS-PAGE were carried out by established methods [ 54] with minor modifications [ 40, 43, 54].

Like Menin and H3K4me3, this modification was established by hkL treatment alone, suggesting that the NF-κB pathway mediates both H2Bub and H3K4me3 modifications.

Transglutaminases (TGases) catalyse post-translational modification of structural proteins by establishing ε- γ-glutamyl) links and covalent conjugation of polyamines.

The specific histone modification established by EZH2 is reversed by the histone demethylases UTX and JMJD3.

Panitumumab F ab' 2 was conjugated with the bifunctional acyclic trans-cyclohexyl-diethylenetriamine-pentaacidic acid (CHX-A -DTPA) CHX-A -DTPAa modifiCHX-A -DTPAstablished methods using fivefold, tenfold, and 20-fold molar exchelate chelate to panitumumabyF(ab')2 [29, 30].

By using this modification, we established a combined analysis of SAGE and real-time quantitative RT PCR, named high-throughput differential screening by SAGE (HDSS).