Search Results - "Bonilla, Leo"

Refine Results
  1. 1

    Absolute Quantification of the G Protein-Coupled Receptor Rhodopsin by LC/MS/MS Using Proteolysis Product Peptides and Synthetic Peptide Standards by Barnidge, David R, Dratz, Edward A, Martin, Therese, Bonilla, Leo E, Moran, Liam B, Lindall, Arnold

    Published in Analytical chemistry (Washington) (01-02-2003)
    “…Methods for the absolute quantification of a membrane protein are described using isotopically labeled or unlabeled synthetic peptides as standards. Synthetic…”
    Get full text
    Journal Article
  2. 2

    24-Hour Lock Mass Protection by Lee, Kimberly A, Farnsworth, Chris, Yu, Wen, Bonilla, Leo E

    Published in Journal of proteome research (04-02-2011)
    “…The positive role and application of highly accurate mass measurements in proteomics is well documented. The new generation of hybrid FTMS and Q-TOF…”
    Get full text
    Journal Article
  3. 3

    Maximizing the sensitivity and reliability of peptide identification in large-scale proteomic experiments by harnessing multiple search engines by Yu, Wen, Taylor, J. Alex, Davis, Michael T, Bonilla, Leo E, Lee, Kimberly A, Auger, Paul L, Farnsworth, Chris C, Welcher, Andrew A, Patterson, Scott D

    Published in Proteomics (Weinheim) (01-03-2010)
    “…Despite recent advances in qualitative proteomics, the automatic identification of peptides with optimal sensitivity and accuracy remains a difficult goal. To…”
    Get full text
    Journal Article
  4. 4

    Free and total biotherapeutic evaluation in chromatographic assays: interference from targets and immunogenicity by White, Joleen T, Bonilla, Leo E

    Published in Bioanalysis (01-10-2012)
    “…Measurement of drug concentrations is critical during drug development, supporting evaluation of safety and efficacy in the context of pharmacokinetics…”
    Get more information
    Journal Article
  5. 5

    The evolution of tools for protein phosphorylation site analysis: from discovery to clinical application by Bonilla, Leo, Means, Gary, Lee, Kimberly, Patterson, Scott

    Published in BioTechniques (01-04-2008)
    “…The importance of the analysis of signaling pathways has been proven for many years by the elucidation of key signaling molecules. However, in most cases these…”
    Get full text
    Journal Article
  6. 6
  7. 7

    Quantitation of 4-Oxo-4-(3-pyridyl)butanoic Acid and Enantiomers of 4-Hydroxy-4-(3-pyridyl)butanoic Acid in Human Urine:  A Substantial Pathway of Nicotine Metabolism by Hecht, Stephen S, Hatsukami, Dorothy K, Bonilla, Leo E, Hochalter, J. Bradley

    Published in Chemical research in toxicology (01-02-1999)
    “…A liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry (LC-APCI-MS/MS) method was developed to analyze human urine for…”
    Get full text
    Journal Article
  8. 8

    Intra-specific variability of feverfew: correlations between parthenolide, morphological traits and seed origin by Cutlan, A R, Bonilla, L E, Simon, J E, Erwin, J E

    Published in Planta medica (01-10-2000)
    “…Parthenolide, a biologically active sesquiterpene lactone found in feverfew [Tanacetum parthenium (L.) Schultz Bip., Asteraceae], has been indirectly linked to…”
    Get more information
    Journal Article
  9. 9

    Systems toxicology by Hartung, Thomas, van Vliet, Erwin, Jaworska, Joanna, Bonilla, Leo, Skinner, Nigel, Thomas, Russell

    “…The need for a more mechanistic understanding of the ways in which chemicals modulate biological pathways is urgent if we are to identify and better assess…”
    Get full text
    Journal Article
  10. 10

    Lactols in Hydrolysates of DNA Treated with α-Acetoxy-N-nitrosopyrrolidine or Crotonaldehyde by Wang, Mingyao, Upadhyaya, Pramod, Dinh, Trieu T, Bonilla, Leo E, Hecht, Stephen S

    Published in Chemical research in toxicology (01-12-1998)
    “…α-Acetoxy-N-nitrosopyrrolidine (α-acetoxyNPYR) is a stable precursor to α-hydroxyNPYR, the initial product of metabolism and proposed proximate carcinogen of…”
    Get full text
    Journal Article
  11. 11

    Eosinophil Peroxidase Oxidation of Thiocyanate by Arlandson, Mary, Decker, Troy, Roongta, Vikram A., Bonilla, Leo, Mayo, Kevin H., MacPherson, Jennifer C., Hazen, Stanley L., Slungaard, Arne

    Published in The Journal of biological chemistry (05-01-2001)
    “…Although the pseudohalide thiocyanate (SCN−) is the preferred substrate for eosinophil peroxidase (EPO) in fluids of physiologic halide composition, the…”
    Get full text
    Journal Article
  12. 12

    Heme from Alzheimer's brain inhibits muscarinic receptor binding via thiyl radical generation by Venters, Homer D, Bonilla, Leo E, Jensen, Tara, Garner, Hart P, Bordayo, Elizabeth Z, Najarian, Melissa M, Ala, Thomas A, Mason, Ronald P, Frey, William H

    Published in Brain research (01-08-1997)
    “…An endogenous inhibitor (<3500 Da) of antagonist binding to the muscarinic acetylcholine receptor (mAChR) has been reported to be elevated 3-fold in…”
    Get full text
    Journal Article
  13. 13

    A study of glycoproteins in human serum and plasma reference standards (HUPO) using multilectin affinity chromatography coupled with RPLC-MS/MS by Yang, Ziping, Hancock, William S., Chew, Tori Richmond, Bonilla, Leo

    Published in Proteomics (Weinheim) (01-08-2005)
    “…The glycoproteome is a major subproteome present in human plasma. In this study, we isolated and characterized approximately 150 glycoproteins from the human…”
    Get full text
    Journal Article
  14. 14

    Eosinophil peroxidase oxidation of thiocyanate. Characterization of major reaction products and a potential sulfhydryl-targeted cytotoxicity system by Arlandson, M, Decker, T, Roongta, V A, Bonilla, L, Mayo, K H, MacPherson, J C, Hazen, S L, Slungaard, A

    Published in The Journal of biological chemistry (05-01-2001)
    “…Although the pseudohalide thiocyanate (SCN(-)) is the preferred substrate for eosinophil peroxidase (EPO) in fluids of physiologic halide composition, the…”
    Get full text
    Journal Article
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20