Shelby

Robert G. Emmet, Peter Harriott, Tim Laros, Wallace Leung, Shelby A. Miller,... 

Shelby A. Miller, David K Schmalzer, Anthony G. Fonseca, Vincent Conrad,... 

Shelby A. Miller, Ph.D., P.E., Resident Retired Senior Engineer, Argonne National Laboratory American Association for the Advancement of Science (Fellow), American Chemical Society, American Institute of Chemical Engineers (Fellow), American Institutes of Chemists (Fellow), Filtration Society, New York Academy of Sciences, Society of Chemical Industry (Section 18, Liquid-Solid Operations and Equipment Section 27, Energy Resources, Conversion, and Utilization)... 

The test system was considerably less sensitive to endosulfan when mouse ER, rather than human ER, was used to mediate (3-gal activity (Ramamoorthy et al. 1997). In similar assays, endosulfan at 10 jM had no effect on (3-gal activity in yeast Saccharomyces) transfected with either the human or rainbow trout ER (Andersen et al. 1999). In addition, no effect was observed on transcriptional activation of HeLa cells transfected with plasmids containing an estrogen receptor as a responsive element (Shelby et al. 1996). Endosulfan also did not induce transient reporter gene expression in MCF-7 human breast cancer cells at an incubation concentration of 2.5 pM (Andersen et al. 1999). Maximum endosulfan-induced ER-mediated luciferase reporter gene expression occurred in vitro in a T47D human breast adenocarcinoma cell line at approximately 10 pM, while 50% expression of luciferase occurred at about 5.9 pM the maximum expression was approximately 59% of the effect from exposure to 0.03 nM estradiol (0.00003 pM) (Legler et al. 1999). Luciferase expression from combined treatment with endosulfan and dieldrin was additive over concentrations ranging from 3 to 8 pM. 

Shelby MD, Newbold RR, Tully DB, etal. 1996. Assessing environmental chemicals for estrogenicity using a combination of in vitro and in vivo assays. Environ Health Perspect 104(12) 1296-1300. 

Figures 2, 3, and 4 present the data on segments F-1, F-2, and F-3, respectively Because of reslstence encountered at F-2 and F-3, It was not possible to complete sampling down to the 4-foot depths by auger and Shelby Tube ...

A6. Araneo, B. A., Shelby, J Li, G. Z., Ku, W and Daynes, R. A., Administration of dehy-droepiandrosterone to burned mice preserves normal immunologic competence. Arch. Surg. 128,318-325 (1993). 

Shelby, J. E. (1997), Introduction to Glass Science and Technology, Royal Society of Chemistry, Cambridge. 

Volume 152. Guide to Molecular Cloning Techniques Edited by Shelby L. Berger and Alan R. Kimmel... 

Rapp, D.B. and J.E. Shelby, Photo-induced hydrogen outgassing of glass.. Non-Crystalline Solids, 349, 254-259,2004. 

Schmitt, M.L., J.E. Shelby and M.M. Hall, Preparation of hollow glass microspheres from sol-gel derived glass for application in hydrogen gas storage. /. Non-Crystalline Solids, 352, 626-631,2006. 

Prof. Robert M. Metzger Department of Chemistry The University of Alabama Room 1088B, Shelby Hall Tuscaloosa, AL 35487-0336 USA... 

Milliron, D. I Raoux, S. Shelby, R. M. Jordan-Sweet, J. 2007. Solution-phase deposition and nanopatterning of GeSbSe phase-change materials. Nature Mater. 6 352-356. 

When setting the maximum test concentration, it is important to test into the mg plate-1 range where possible (Gatehouse et al., 1990), as some mutagens are only detectable when tested at high concentrations. However, for nontoxic, soluble mutagens an upper limit of 5 mg plate-1 is recommended (DeSerres and Shelby, 1979). For less soluble compounds at least one dose exhibiting precipitation should be included. 

DeSerres, F.J. and Shelby, M.D. (1979). Recommendations on datas production and analysis using the Salmonella/microsome mutagenicity assay. Mutation Res. 64 159-165. 

Tennant, R.W., Margolin, B.H., Shelby, M.D., Zeiger, E., Haseman, J.K., Spalding, J., Caspary, W., Resnick, M., Stasiewicz, S., Anderson, B. and Minor, R. (1987). Prediction of chemical carcinogenicity in rodents from in vitro genetic toxicity assays. Science 236 933-941. 

Continuous dry coring (without water or mud) of the interval immediately above and below the mobile LNAPL layer seems an obvious way of determining the mobile LNAPL thickness. Standard split-spoon samples are commonly used for this purpose. The use of clear acrylic shelby tubes have also been used with favorable results. However, several problems are associated with coring which results in overestimating the actual thickness of the product. These factors include ... 

The test pit method consists of excavating a pit using a backhoe to a depth where hydrocarbon pools in the bottom of the pit. Soil samples are subsequently obtained above and below the hydrocarbon-affected zone using hand-driven tubes (acrylic small-diameter shelby tubes). Problems associated with this method include ... 

Shelby, M.K., Cherrington, N.J., Vansell, N.R. and Klaassen, C.D. (2003) Tissue mRNA expression of the rat UDP-glucuronosyltransferase gene family. Drug Metabolism and Disposition, 31, 326-333. 

Tennant RW, Margolin BH, Shelby MD, et al. 1987. Prediction of chemical carcinogenicity in rodents from in vitro genetic toxicity assays. Science 236 933-941. 

ZeitUn SG, Shelby RD, Sullivan KF (2001) CENP-A is phosphorylated by Aurora B kinase and plays an unexpected role in completion of cytokinesis. J Cell Biol 155(7) 1147-1157 Zhang Y, Griffin K, Mondal N, Parvin JD (2004) Phosphorylation of histone H2A inhibits transcription on chromatin templates. J Biol Chem 279(21) 21866-21872... 

The contributions of the late Dr. Shelby A. Miller and Dr. John D. Bacha to the seventh edition are gratefully acknowledged. 

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