Janet E. Saunders
Medical University of South Carolina
5 Papers
28 Citations
Janet E. Saunders is an academic researcher from Medical University of South Carolina. The author has contributed to research in topics: Chemistry & Extracellular matrix. The author has an hindex of 2, co-authored 3 publications.
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Papers
Characterization of functionally distinct mitochondrial subpopulations
TL;DR: The results demonstrate that flow cytometry can be used to identify mitochondrial subpopulations based on high, mid and low NAO content and/or volume/complexity and that side scatter was a better indicator of volume and that as side scatter (SSC) decreased mitochondrial volume increased.
25
Defining the Tumor Microenvironment by Integration of Immunohistochemistry and Extracellular Matrix Targeted Imaging Mass Spectrometry.
Denys Rujchanarong,Julia E. Lefler,Janet E. Saunders,Sarah Pippin,Laura Spruill,Jennifer R. Bethard,Lauren E. Ball,Anand Mehta,Richard R. Drake,Michael C. Ostrowski,Peggi M. Angel +10 more
TL;DR: In this paper, a targeted approach for investigating collagen and other extracellular matrix proteins from formalin-fixed, paraffin-embedded (FFPE) tissues was proposed.
20
Differential Protease Specificity by Collagenase as a Novel Approach to Serum Proteomics That Includes Identification of Extracellular Matrix Proteins without Enrichment.
Jade K Macdonald,Cassandra L. Clift,Janet E. Saunders,Stephen Zambrzycki,Anand Mehta,Richard R. Drake,Peggi M. Angel +6 more
TL;DR: The potential for serum biomarker research using differential protease specificity (DPS) using alternate protease specificity as a targeting mechanism to selectively digest circulating ECM protein serum proteins is investigated.
2
Perspectives on pediatric congenital aortic valve stenosis: Extracellular matrix proteins, post translational modifications, and proteomic strategies
TL;DR: In this paper , the authors summarize current knowledge regarding ECM proteins and their post translational modifications (PTMs) during aortic valve development and disease and contributing factors to ECM dysregulation in CAVS.
A Rapid Array-Based Approach to N-Glycan Profiling of Cultured Cells.
Peggi M. Angel,Janet E. Saunders,Cassandra L. Clift,Shai White-Gilbertson,Christina Voelkel-Johnson,Elizabeth S. Yeh,Anand Mehta,Richard R. Drake +7 more
TL;DR: A rapid array-based workflow for profiling N-glycan signatures from cells, adapted from imaging mass spectrometry used for on-tissue N- Glycosylation studies, is reported, requiring as few as 3000 cells per replicate with a 3-20% coefficient of variation to capture label-free profiles of N- glycans.