M
Martin J. J. Ronis
Researcher at LSU Health Sciences Center New Orleans
Publications - 200
Citations - 8492
Martin J. J. Ronis is an academic researcher from LSU Health Sciences Center New Orleans. The author has contributed to research in topics: Soy protein & Osteoblast. The author has an hindex of 53, co-authored 196 publications receiving 7769 citations. Previous affiliations of Martin J. J. Ronis include University of Arkansas for Medical Sciences & Louisiana State University.
Papers
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Journal ArticleDOI
Feeding Blueberry Diets to Young Rats Dose-Dependently Inhibits Bone Resorption through Suppression of RANKL in Stromal Cells
Jian Zhang,Oxana P. Lazarenko,Jie Kang,Michael L. Blackburn,Martin J. J. Ronis,Thomas M. Badger,Jin-Ran Chen +6 more
TL;DR: Results suggest that inhibition of bone resorption may contribute to increased bone mass during early development after BB consumption.
Journal ArticleDOI
Effects of long-term ethanol administration in a rat total enteral nutrition model of alcoholic liver disease
Martin J. J. Ronis,Leah Hennings,Ben Stewart,Alexei G. Basnakian,Eugene O. Apostolov,Emanuele Albano,Thomas M. Badger,Dennis R. Petersen +7 more
TL;DR: Although the effects of NAC on EtOH-induced fibrosis could not be fully evaluated, NAC had additive effects on hepatocyte proliferation and prevented EtOH -induced oxidative stress and necrosis, despite a failure to reverse hepatic steatosis.
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IL-1 and TNF antagonists prevent inhibition of fracture healing by ethanol in rats.
Daniel S. Perrien,Elizabeth C. Wahl,William R. Hogue,Ulrich Feige,James Aronson,Martin J. J. Ronis,Thomas M. Badger,Charles K. Lumpkin +7 more
TL;DR: The hypothesis that IL-1 and TNF antagonists are capable of protecting fracture healing from the inhibition associated with chronic ethanol consumption is supported for the first time.
Journal ArticleDOI
Altered Expression and Glucocorticoid-Inducibility of Hepatic CYP3A and CYP2B Enzymes in Male Rats Fed Diets Containing Soy Protein Isolate
TL;DR: Potential effects of soy consumption on the metabolism of a wide variety of CYP3A and CYP2B1 substrates are suggested, especially in situations involving coexposure to CYP inducers.
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Matrix effects break the LC behavior rule for analytes in LC-MS/MS analysis of biological samples:
TL;DR: A comprehensive understanding of matrix effects is needed towards improving the use of HPLC and LC- MS/MS techniques for qualitative and quantitative analyses of analytes in pharmacokinetics, proteomics/metabolomics, drug development, and sports drug testing, especially when LC-MS/MS data are analyzed by automation software.