1934 - Fellow of the American Association for the Advancement of Science (AAAS)
1915 - Fellow of the Royal Society of Canada
Matrix metalloproteinase, Pathology, Cell biology, Molecular biology and Matrilysin are his primary areas of study. The Matrix metalloproteinase study combines topics in areas such as Wound healing, Immunology, Extracellular matrix and Matrix. William C. Parks studies Chemokine, a branch of Immunology.
William C. Parks interconnects Inflammation, Extracellular and Function in the investigation of issues within Extracellular matrix. The concepts of his Pathology study are interwoven with issues in Gelatinase, Collagenase and In situ hybridization. His research in Cell biology intersects with topics in Tracheal Epithelium, Cadherin, Regulation of gene expression and Anatomy.
William C. Parks mainly focuses on Cell biology, Matrix metalloproteinase, Pathology, Immunology and Extracellular matrix. His study in Cell biology is interdisciplinary in nature, drawing from both Fibrosis, Integrin, Cell migration and Cell adhesion. The concepts of his Matrix metalloproteinase study are interwoven with issues in Wound healing, Matrix and Collagenase.
His Pathology study integrates concerns from other disciplines, such as Pulmonary hypertension, Lung and In situ hybridization. His biological study focuses on Inflammation. His Extracellular matrix study frequently draws connections between adjacent fields such as Function.
The scientist’s investigation covers issues in Immunology, Inflammation, Cell biology, Matrix metalloproteinase and Macrophage. His study in Immunology is interdisciplinary in nature, drawing from both Phenotype, Versican, Gene expression and In vivo. His Inflammation study incorporates themes from Fibrosis, Innate immune system, Immune system and Lung injury.
His Cell biology research is multidisciplinary, relying on both Integrin, Collagenase, MMP1 and Lung disease. His work deals with themes such as Wound healing, Proteolysis, Matrix, Pathology and Extracellular matrix, which intersect with Matrix metalloproteinase. His research integrates issues of ADAMTS and Function in his study of Extracellular matrix.
William C. Parks focuses on Cell biology, Matrix metalloproteinase, Extracellular matrix, Macrophage and Inflammation. His Matrix metalloproteinase study which covers Matrix that intersects with Angiogenesis. His Extracellular matrix research is multidisciplinary, incorporating elements of Morphogen, ADAMTS, Allosteric regulation and Function.
He interconnects Gene expression and Metalloproteinase in the investigation of issues within Function. William C. Parks has researched Macrophage in several fields, including Wound healing and Regeneration. Inflammation is the subject of his research, which falls under Immunology.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Matrix metalloproteinases as modulators of inflammation and innate immunity
William C. Parks;William C. Parks;Carole L. Wilson;Yolanda S. López-Boado.
Nature Reviews Immunology (2004)
Secretion of microbicidal alpha-defensins by intestinal Paneth cells in response to bacteria.
Tokiyoshi Ayabe;Donald P. Satchell;Carole L. Wilson;William C. Parks.
Nature Immunology (2000)
Regulation of Intestinal α-Defensin Activation by the Metalloproteinase Matrilysin in Innate Host Defense
Carole L. Wilson;Andre J. Ouellette;Donald P. Satchell;Tokiyoshi Ayabe.
Induction and evasion of host defenses by type 1-piliated uropathogenic Escherichia coli.
M.A. Mulvey;Y.S. Lopez-Boado;C.L. Wilson;R. Roth.
Matrilysin shedding of syndecan-1 regulates chemokine mobilization and transepithelial efflux of neutrophils in acute lung injury.
Qinglang Li;Pyong Woo Park;Carole L. Wilson;William C. Parks.
The Activity of Collagenase-1 Is Required for Keratinocyte Migration on a Type I Collagen Matrix
Brian K. Pilcher;Jo Ann Dumin;Barry D. Sudbeck;Stephen M. Krane.
Journal of Cell Biology (1997)
Metalloproteinases and their inhibitors: regulators of wound healing.
Sean E. Gill;William C. Parks.
The International Journal of Biochemistry & Cell Biology (2008)
Control of matrix metalloproteinase catalytic activity.
Hyun-Jeong Ra;William C. Parks.
Matrix Biology (2007)
Hypochlorous acid oxygenates the cysteine switch domain of pro-matrilysin (MMP-7). A mechanism for matrix metalloproteinase activation and atherosclerotic plaque rupture by myeloperoxidase.
Xiaoyun Fu;Xiaoyun Fu;Sean Y. Kassim;William C. Parks;Jay W. Heinecke.
Journal of Biological Chemistry (2001)
Production and localization of 92-kilodalton gelatinase in abdominal aortic aneurysms. An elastolytic metalloproteinase expressed by aneurysm-infiltrating macrophages.
R. W. Thompson;D. R. Holmes;R. A. Mertens;Shixiong Liao.
Journal of Clinical Investigation (1995)
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