<p><b>A</b>. Identification of PEN (shown by red arrow) in the glucosylated human cortical bone samples. <b>B</b>. Identification of PEN (shown by red arrow) in the ribosylated human cortical bone samples. <b>C</b>. The UPLC chromatogram with the peak of ProOH (shown by red arrow) used for determination of collagen contents. Similar amounts of the samples were injected to the column. Notably, the chromatogram obtained from the analysis of the ribosylated sample contains several peaks that are not present in the glucosylated sample.</p
<p>The small vertical bars below the 0 level denote the integration area for each peak, and the majo...
School o f B iotechnology D u b lin C ity U n ive rs ity Under the supervision o
<p>(A) Hydroxyproline (collagen) content (n = 3); (B) Type II collagen content, measured using ELISA...
<p>Insets: MS/MS spectra of standard dihydrocapsaicin (A) and from sample extract (B). Samples were ...
<p>(A) control group, (B) CKD group and (C) CKD + Ergone group. The chromatogram showed identified m...
<p>The chromatogram was acquired from a 200 μL standard solution of 5 μM mastoparan X to which 50 μL...
<p>Eluted peak areas were used for quantification of Pyd, Dpd, and pentosidine.</p
The clinical use of any drug requires a complete understanding of its biotransformation properties. ...
<p>UPLC–MS/MS chromatogram of standard E<sub>1</sub>(E<sub>2</sub>)-9-N-Ade (A, C) and breast tissue...
<p>Fluorescent PEN was quantified in glycated (for 7 days) human cortical (C) and cancellous (T) bon...
Abstract: A method for the determination and quantification of collagen types (I- V) using sample pr...
<p>HPLC chromatogram for (a) <sup>D</sup>Ala substituted imino poor region of type I collagen at 37°...
With a view to facilitating the study of human genetic connective tissue diseases we have developed ...
<p>Chromatograms are shown for A: <i>M. tuberculosis,</i> B: <i>M. avium,</i> C: <i>M. marinum</i>, ...
<p>Chromatograms on the top demonstrate c.3346C>T, p.Q1116X in <i>UACA</i>. Chromatograms on the bot...
<p>The small vertical bars below the 0 level denote the integration area for each peak, and the majo...
School o f B iotechnology D u b lin C ity U n ive rs ity Under the supervision o
<p>(A) Hydroxyproline (collagen) content (n = 3); (B) Type II collagen content, measured using ELISA...
<p>Insets: MS/MS spectra of standard dihydrocapsaicin (A) and from sample extract (B). Samples were ...
<p>(A) control group, (B) CKD group and (C) CKD + Ergone group. The chromatogram showed identified m...
<p>The chromatogram was acquired from a 200 μL standard solution of 5 μM mastoparan X to which 50 μL...
<p>Eluted peak areas were used for quantification of Pyd, Dpd, and pentosidine.</p
The clinical use of any drug requires a complete understanding of its biotransformation properties. ...
<p>UPLC–MS/MS chromatogram of standard E<sub>1</sub>(E<sub>2</sub>)-9-N-Ade (A, C) and breast tissue...
<p>Fluorescent PEN was quantified in glycated (for 7 days) human cortical (C) and cancellous (T) bon...
Abstract: A method for the determination and quantification of collagen types (I- V) using sample pr...
<p>HPLC chromatogram for (a) <sup>D</sup>Ala substituted imino poor region of type I collagen at 37°...
With a view to facilitating the study of human genetic connective tissue diseases we have developed ...
<p>Chromatograms are shown for A: <i>M. tuberculosis,</i> B: <i>M. avium,</i> C: <i>M. marinum</i>, ...
<p>Chromatograms on the top demonstrate c.3346C>T, p.Q1116X in <i>UACA</i>. Chromatograms on the bot...
<p>The small vertical bars below the 0 level denote the integration area for each peak, and the majo...
School o f B iotechnology D u b lin C ity U n ive rs ity Under the supervision o
<p>(A) Hydroxyproline (collagen) content (n = 3); (B) Type II collagen content, measured using ELISA...