Relevant bibliographies by topics / Chemical profiling

Academic literature on the topic 'Chemical profiling'

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Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Chemical profiling"

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Piotrowski, Jeff S., Chuek Hei Ho, and Charles Boone. "The Awesome Power of Synergy from Chemical-Chemical Profiling." Chemistry & Biology 17, no. 8 (August 2010): 789–90. http://dx.doi.org/10.1016/j.chembiol.2010.08.002.

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Imran, Ali, Masood Sadiq Butt, Mian Kamran Sha, and Javed Iqbal Sult. "Chemical Profiling of Black Tea Polyphenols." Pakistan Journal of Nutrition 12, no. 3 (February 15, 2013): 261–67. http://dx.doi.org/10.3923/pjn.2013.261.267.

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Lewis, Melissa M., Yi Yang, Ewa Wasilewski, Hance A. Clarke, and Lakshmi P. Kotra. "Chemical Profiling of Medical Cannabis Extracts." ACS Omega 2, no. 9 (September 22, 2017): 6091–103. http://dx.doi.org/10.1021/acsomega.7b00996.

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Mazák, Károly, Sándor Hosztafi, Márta Kraszni, and Béla Noszál. "Physico-chemical profiling of semisynthetic opioids." Journal of Pharmaceutical and Biomedical Analysis 135 (February 2017): 97–105. http://dx.doi.org/10.1016/j.jpba.2016.12.014.

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Horning, Benjamin D., Radu M. Suciu, Darian A. Ghadiri, Olesya A. Ulanovskaya, Megan L. Matthews, Kenneth M. Lum, Keriann M. Backus, Steven J. Brown, Hugh Rosen, and Benjamin F. Cravatt. "Chemical Proteomic Profiling of Human Methyltransferases." Journal of the American Chemical Society 138, no. 40 (September 30, 2016): 13335–43. http://dx.doi.org/10.1021/jacs.6b07830.

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Martin, Brent R. "Chemical approaches for profiling dynamic palmitoylation." Biochemical Society Transactions 41, no. 1 (January 29, 2013): 43–49. http://dx.doi.org/10.1042/bst20120271.

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Protein palmitoylation is a critical post-translational modification important for membrane compartmentalization, trafficking and regulation of many key signalling proteins. Recent non-radioactive chemo-proteomic labelling methods have enabled a new focus on this emerging regulatory modification. Palmitoylated proteins can now be profiled in complex biological systems by MS for direct annotation and quantification. Based on these analyses, palmitoylation is clearly widespread and broadly influences the function of many cellular pathways. The recent introduction of selective chemical labelling approaches has opened new opportunities to revisit long-held questions about the enzymatic regulation of this widespread post-translational modification. In the present review, we discuss the impact of new chemical labelling approaches and future challenges for the dynamic global analysis of protein palmitoylation.
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THORNTON, JOHN I. "DNA Profiling." Chemical & Engineering News 67, no. 47 (November 20, 1989): 18–30. http://dx.doi.org/10.1021/cen-v067n047.p018.

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Badea, Georgiana Ileana, Ioana Diaconu, and Gabriel Lucian Radu. "Organic Acids Chemical Profiling in Food Items." Revista de Chimie 68, no. 6 (July 15, 2017): 1147–52. http://dx.doi.org/10.37358/rc.17.6.5631.

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A fast separation method for simultaneous determination of eleven organic acids was validated and applied to different commercial food items to evaluate their organic acids content. The present method gives detection limits between 0.04 and 4.65 mg mL-1, recovery values in real samples between 78.2 and 97.3% and relative standard deviation values for precision lower than 5%. All validation data were in acceptable range and prove the method�s fit for purpose. The advantages of the method are the short runtime analysis (15 min), no preparation step for the samples before the injection combined with good sensitivity which recommends it for routine control analysis in food industries. Moreover, this methodology has high potential in drinks industry but can by further extended to other types of food items.
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Lagurin, L. G., M. O. Galingana, J. D. J. Magsalin, J. E. S. Escaño, and F. M. Dayrit. "Chemical profiling of Philippine Moringa oleifera leaves." Acta Horticulturae, no. 1158 (April 2017): 257–68. http://dx.doi.org/10.17660/actahortic.2017.1158.29.

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Imran, Muhammad, Masood Sadiq Butt, Faqir Muhammad Anjum, and Javed Iqbal Sultan. "Chemical Profiling of Different Mango Peel Varieties." Pakistan Journal of Nutrition 12, no. 10 (September 15, 2013): 934–42. http://dx.doi.org/10.3923/pjn.2013.934.942.

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Dissertations / Theses on the topic "Chemical profiling"

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Ogunleye, Olatokumbo Olajumi Luca. "Chemical Inducers of Dimerization for Profiling Protein Kinases." Diss., The University of Arizona, 2015. http://hdl.handle.net/10150/579019.

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Chemical inducers of dimerization (CID) represent an important tool that has been implemented in numerous biological applications namely protein functions, protein stability, signal transduction, gene transcription, etc. Most generally CIDs are defined as bivalent molecules capable of inducing proximity between two targeted proteins. This proximity can in turn promote or disfavor a certain biological activity. Cell permeable small molecules in particular represent a very effective method to induce precise temporal and spatial control over a specific biological target. Our lab has devoted much effort in studying and elucidating the activity and functions of protein kinases, which represent a very attractive therapeutic target for the treatment of cancer and many other disorders. Towards this goal we have developed a general CID enabled three-hybrid split-luciferase methodology for the investigation of kinase-inhibitor interactions in vitro. We demonstrate that by modulating the kinase-ligand affinity of the CID we are able to successfully profile many structurally non-related protein kinases. We also investigate the use of weaker affinity kinase ligands to allow competitive displacement of CID by the selected inhibitor. In addition we report the design, synthesis and applications of novel CID's for the profiling of kinase inhibitors in mammalian cells and we demonstrate the feasibility of the assay to be used as a new platform for the discovery of cell permeable kinase inhibitors. Finally, we report a new ligand-gated split-kinase that can be selectively activated by photocleavable inducers of dimerization. We further prove how the activity of split-proteins can be deactivated with temporal control with use of non DNA damaging UV radiation.
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PUNZALAN, LOUVY LYNN CALVELO. "Chemoproteomic Profiling of a Pharmacophore-Focused Chemical Library." Kyoto University, 2020. http://hdl.handle.net/2433/259001.

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Peterson, Vanessa M. (Vanessa Marie). "Detecting and molecular profiling cancer cells in patients." Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/86863.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemical Engineering, 2013.
"September 2013." Page 173 blank. Cataloged from PDF version of thesis.
Includes bibliographical references (pages 152-163).
Although tumor cells obtained from human patients by surgical biopsy, image-guided intervention, blood draws or fluid drainage (paracentesis, thoracentesis) are a valuable source for analyzing tumor cells, conventional means of proteomic analysis are limited. Highly sensitive and quantitative technologies for point-of-care and multiplexed analysis on small sample sizes are in great demand. To this end, we developed three technologies to improve our understanding of the molecular signatures of cancer in clinical samples. In the first section, we describe a diagnostic magnetic resonance (DMR) device that was developed for point-of-care analyses of human tumors. We optimized a magnetic nanoparticle assay to improve sensitivity and robustness of the DMR approach. The DMR device was tested by analyzing samples from 50 patients. The results were then validated in an independent cohort of 20 additional patients. DMR enabled quantification of multiple protein markers in all patients. Using a four-protein signature enabled us to achieve 96% accuracy for establishing cancer diagnosis, surpassing conventional clinical analysis by immunohistochemistry. Results also show that protein expression patterns decay with time, underscoring the temporal need for rapid sampling and diagnoses. Also, a surprising degree of heterogeneity in protein expression both across different patient samples and even within the same tumor was observed, which has important implications for molecular diagnostics and therapeutic drug targeting. In the second section we molecularly profiled tumor cells in ascites - peritoneal fluid frequently drained for symptomatic relief in advanced ovarian cancer (OvCA) patients. First, we profiled a comprehensive panel of 85 biomarkers in ovarian cancer and benign cell lines. From this data set, 31 markers were identified and profiled in a training set of human ascites samples (n=1 8). We identified an ascites-derived tumor signature termed ATCdx containing four markers which was then validated in a cohort of 47 patients (33 ovarian cancer and 14 control) and correctly identified all 33 ovarian cancer patients. Serial samples were obtained from a subset of patients' serial samples (n=7) and profiled, demonstrating that ATCs can be used to measure treatment response and differentiate responders from non-responders. Finally, we specifically designed a novel microfluidic enrichment chip that allows rapid visualization of cancer cells in heterogeneous ascites fluid. This chip requires small sample volumes (< 1 mL) and has single cell detection sensitivity. Furthermore, it is inexpensive to construct and can be easily fabricated using soft lithographic techniques, providing a point-of-care method that could potentially find widespread use for ATC analyses and diagnosis. In the final section, a multiplexed proteomic assay using a photocleavable DNA barcoding method was developed to multiplex protein detection in single cells. We tested 94 antibodies against common cancer markers to examine different treatment responses and heterogeneity at the single cell level. We then extended our analysis to human clinical samples to demonstrate the potential of protein-based measurements to assist in monitoring cancer therapy through differential changes before and after treatment. We show that protein based tumor profiles can provide sufficient information to predict treatment response. Finally, we examined interpatient variability and intratumoral heterogeneity of single cells with this highly sensitive assay. Together, these technologies can help overcome current clinical limitations and expedite advancements in cancer treatment.
by Vanessa M. Peterson.
Ph. D.
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Kabbani, Nazir. "Chemical-genetic profiling of platelet-activating factor in yeast." Thesis, University of Ottawa (Canada), 2009. http://hdl.handle.net/10393/28189.

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The basic biological processes between the yeast Saccharomyces cerevisiae and mammals are highly conserved. Yeast posses many genes that are implicated in human diseases and have been successfully used as a model for the study of neurodegeneration. Platelet-Activating Factor (C16:0 PAF) causes neuronal cell death independent of its receptor and has been implicated in Alzheimer's disease. I hypothesized that yeast could be used as a model system for deciphering PAF receptor-independent signalling and have utilized genome-wide chemical genomic screening in yeast to further characterize the molecular mechanism of PAF toxicity. Two complementary screens implicate PAF in many cellular processes, some of which parallel results obtained in mammalian studies. I have found that PAF challenge is cytotoxic, delays cell cycle progression, and affects actin stability leading to spindle misorientation and bi-nucleate mother cells.
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Goudsmits, E. "Chemical profiling of ballistic materials : analysis of organic gunshot residue." Thesis, Liverpool John Moores University, 2018. http://researchonline.ljmu.ac.uk/8454/.

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Gunshot residue (GSR) is a complex chemical mixture that is created during the discharge of a firearm. Its detection and interpretation play a crucial role in the investigation of firearm incidents. Current GSR analysis is limited to inorganic GSR (IGSR), however, the evidential value could be strengthened by inclusion of organic GSR (OGSR). The present study aims to address this potential by proposing a categorisation system for relevant OGSR compounds and developing a methodology for the collection, extraction and analysis of both organic and inorganic GSR from a single sample. The organic composition of more than 50 propellant powders has been determined and compared against more than 200 propellant compositions reported in the literature. This work has resulted in a three-tier categorisation system for OGSR compounds, which together with the current IGSR classification will provide unequivocal identification of GSR materials with the possibility of discriminating between GSR from different ammunition types. Evaluation of MonoTrap extraction showed that this is an effective pre-concentration technique for the characterisation of propellants. Solid-phase microextraction (SPME), however, was the superior method for the extraction of OGSR compounds from various sampling media, including swabs and stubs. The optimised methodology involves GSR collection using carbon adhesive stubs followed by SPME gas chromatography – mass spectrometry (GC-MS) analysis of OGSR and subsequent scanning electron microscopy – energy-dispersive X-ray spectrometry (SEM-EDX) analysis for IGSR. This protocol has resulted in the detection of both characteristic IGSR and categorised organic compounds, demonstrating the ability to obtain a full chemical profile from a single sample. Detection of both first and second tier organic compounds provides complementary compositional information that could be used to discriminate between samples. Furthermore, this methodology requires no changes to the current sampling and IGSR analysis protocols and addresses the limited storage time of OGSR. Since GC-MS instruments are readily available in most analytical laboratories, implementation of the proposed protocol is feasible.
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Chen, Zewei. "Authentication of Complex Botanical Materials by Chemometrics and Chemical Profiling." Ohio University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1617010785195628.

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Charlton, Thomas. "Chemical proteomic profiling to investigate lipoprotein biogenesis in Clostridium difficile." Thesis, Imperial College London, 2015. http://hdl.handle.net/10044/1/29661.

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Bacterial lipoproteins feature an N-terminal Type II signal peptide, containing a lipobox motif which targets these proteins for post-translational lipidation. Following secretion, pre-prolipoprotein diacylglyceryl transferase (Lgt) catalyses the addition of an S-diacylglyceryl moiety to the lipobox cysteine thiol. The signal peptide sequence is then cleaved by a lipoprotein signal peptidase (Lsp), leaving the modified cysteine as the N-terminal residue of the mature Gram-positive lipoprotein. Lipoproteins are surface exposed and play an important role at the host-pathogen interface, as well as being implicated in nutrient uptake, sporulation and antibiotic resistance. Clostridium difficile is a Gram-positive, spore forming, obligate anaerobe which causes severe gastrointestinal disease in humans. Spores are the transmissible agent of C. difficile, with infection typically occurring via the faecal-oral route. Lipoproteins of C. difficile are known to function in nutrient uptake and adhesion and the lipoproteome is likely to be important in transmission and colonisation. Bacterial lipidation is difficult to study by traditional methods, however, metabolic tagging with bioothogonally-tagged lipid analogues has recently emerged as a powerful method to study lipidated proteins. This thesis describes the development and optimisation of metabolic tagging and quantitative chemical proteomics to investigate lipidation in C. difficile. The application of this approach to profile the lipoproteomes of 630 Δerm and the clinically relevant 'hypervirulent' strain R20291 is described. This work includes the use of these probes, in combination with genetic and chemical inactivation of lgt, lspA and lspA2, to investigate lipoprotein biogenesis in C. difficile and to demonstrate the presence of two active Lsps. A combination of quantitative proteomics and phenotypic analysis has identified new functions for the C. difficile lipoproteome, including a role in the regulation of flagella and toxin production and in the initiation of sporulation.
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Silva, Saliya Sudharshana 1976. "Transcriptional profiling and flux measurements of polyhydroxybutyrate production in Synechocystis." Thesis, Massachusetts Institute of Technology, 2004. http://hdl.handle.net/1721.1/28657.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2004.
Includes bibliographical references (leaves 39-41).
(cont.) to determine the CO₂ uptake rates and PHB production rates of strains engineered for enhanced CO₂ fixation and PHB production respectively.
The metabolism of Synechocystis PCC6803 cells has been investigated using full-genome DNA micro-arrays and C14 tracer techniques. Full-genome (3169 genes) DNA micro-arrays were used to probe transcript levels of Synechocystis cells grown under a variety of medium conditions. Canonical discriminant analysis was used to identify transcript levels that allowed discrimination between growth media conditions, and allowed predictions of polyhydroxybutyrate (PHB) levels. Phosphate-related genes were found to alter in response to phosphate limitation and were found to include differentially regulated multi-gene families. Nitrogen-related genes were not found to be substantially reflective of nitrogen limitation under the conditions studied. Finally, transcription of PHA biosynthetic pathway genes were found to reflect the media conditions of greatest PHB accumulation, suggesting that constitutive over-expression of the PHA biosynthetic genes may lead to greater PHB accumulation levels. A methodology using C14 tracers was developed for the accurate measurement of CO₂ uptake rates and the partitioning of the fixed carbon into different biosynthetic fractions. These techniques were applied to the characterization of WT Synechocystis cells in late exponential phase. A stoichiometric model of Synechocystis metabolism was used to determine constraints between the measurements. A balance on C14 counts was obtained and significant levels of secreted compounds were not detected. The measured carbon fixation rates were found to be consistent with the observed growth rates, but inconsistent with measurements of oxygen evolution in the light and uptake in the dark made using a Clarke Electrode apparatus. These techniques may be used in future studies
by Saliya Sudharshana Silva.
S.M.
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Kates, Lisa Natasha. "Chemical profiling and environmental modelling of waste from clandestine methylamphetamine laboratories." Thesis, University of Strathclyde, 2013. http://oleg.lib.strath.ac.uk:80/R/?func=dbin-jump-full&object_id=22542.

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Methylamphetamine (MA) is an illicit drug abused by millions of people worldwide. MA can be manufactured easily using a variety of household chemicals and several different methods. The illicit manufacture of MA produces large amounts of waste: one kilogram of MA produces five to seven kilograms of toxic waste, which is illegally disposed of in a number of different ways, creating a source of pollution. MA waste contains many harmful components, however it has never been characterised. In this work, MA was synthesised following three different synthetic routes. The waste were collected and subject to chemical profiling using gas chromatography-mass spectrometry. Key marker compounds of the waste were identified which may aid in the detection and prosecution of an illicit dumpsite. Those key marker compounds include MA, 1-phenyl-2-propanone, Nformylmethylamphetamine, and 2,6-di-tert-butylphenol. Environmental partition coefficients were measured experimentally for several of the i dentified waste components. The octanol-water partition coefficient (KOW) and the organic carbon partition coefficient (KOC) were measured following standard methods. The KOW values were found to be in accordance with computer estimated values produced from the environmental modelling programme, EPI SuiteTM, while the KOC values were calculated as a function of organic carbon content from collected sediment samples. Using the measured KOW values and calculated KOC values, a fugacity model of the waste was generated using EPI SuiteTM to predict the distribution of the waste once it enters the environment. It was determined that the majority of the waste components will partition predominantly into the water compartment. This study encompasses the first research on waste generated from the illicit manufacture of MA, with the aim to provide information to law enforcement personnel and environment agencies to allow clandestine manufacturers to be prosecuted under environmental legislation in addition to drugs legislation.
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Taylor, Michael. "To F-SIMS/XPS chemical depth profiling of synthetic polymer hydrogels." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/38755/.

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Over the last decade the beneficial properties of hydrogels as artificial cell culture supports have been extensively investigated. Certain synthetic hydrogels have been proposed to be similar in composition and structure to the native extracellular matrix of the stem cell niche, their in vivo cell habitat, which is a powerful component in controlling stem cell fate. The stem cell differentiation pathway taken is influenced by many factors. When culturing cells within or upon hydrogels the choice can be strongly dependent on the underlying 3D hydrogel chemistry which strongly influences hydrogel-cell interactions. The interrelationship between hydrogel chemistry and that of biomolecules in controlling cellular response ideally requires analysis methods to characterise the chemistry without labels and normally in 3D. Time-of-flight secondary ion mass spectrometry (ToF SIMS) has the potential to be utilised for through thickness characterisation of hydrogels. The frozen-hydrated sample format is well suited to minimise changes associated with dehydration or the complication of chemical ‘fixation’. There is however significant challenges associated with this sample format. Frost formation occurs on cold samples in the ambient atmosphere affecting the quality of chemical information acquired from depth profiling frozen hydrogel samples. We develop a simple method to remove this frost by blowing with gas prior to entry into the instrument which is shown to produce remarkably good profiles on a poly(2-hydroxyethyl methacrylate) (pHEMA) hydrogel film where a model protein, lysozyme, is incorporated to demonstrated how biomolecule distribution within hydrogels can be determined. A comparison of lysozyme incorporation is made between the situation where the protein is present in the polymer dip coating solution and lysozyme is a component of the incubation medium. It is shown that protonated water clusters H(H2O)n+ where n=5-11 that are indicative of ice are detected through the entire thickness of the pHEMA and the lysozyme distribution through the pHEMA hydrogel films can be determined using the intensity of characteristic fragment secondary ions. Quantitative TOF-SIMS analysis is highly desirable in biomaterial analysis as the amount and type of molecule in the material analysed may be determined. This has significant interest in hydrogel chemical analysis as cellular development on or within hydrogels may be highly influenced by the concentration and type of soluble molecule. Unfortunately, the matrix effect in SIMS changes the measured signal intensity of the analyte, preventing accurate quantitation. For this reason, we apply X-Ray Photoelectron Spectroscopy (XPS) on the equivalent samples as the ToF-SIMS in an attempt to correlate molecular ion yields to exact elemental concentrations. Similarly to ToF-SIMS the frozen-hydrated format in XPS is however still relatively unexplored. We apply the developed preparatory procedure in 3D XPS analysis of pHEMA/lysozyme hydrogel films in a hydrated state. We show that this format is suitable for alternative high vacuum analysis techniques. Furthermore, we show that lysozyme ingression and concentration can be determined through XPS. This work describes the first example of the characterisation of a hydrogel by ToF-SIMS and XPS in a frozen hydrated format, characterising hydrogels in a format most reflecting its native hydrated state at culture conditions. The described procedure allows for the mapping of biomolecules in a label free manner in 3D, furthermore allowing quantitative determination of biomolecule concentrations in hydrogels.
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Books on the topic "Chemical profiling"

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Instrument Development for Atmospheric Research and Monitoring: Lidar Profiling, Doas and Tunable Diode Laser Spectroscopy (Transport and Chemical Transformation ... of Pollutants in the Troposphere, V. 8). Springer, 1997.

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Jones, Rebecca. Green Harvest. CSIRO Publishing, 2010. http://dx.doi.org/10.1071/9780643101074.

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Green Harvest explores the ideas and practices that have shaped organic farming and gardening in Australia from the interwar years to the present day. It reveals that Australian organic farming and gardening societies were amongst the first in the world, being active as early as the 1940s. In what way does human health depend upon the natural environment? Green Harvest traces this idea through four themes of Australian organic farming and gardening – soil, chemical free, ecological well-being and back to the land – each illustrated with a case study profiling an Australian organic farmer or gardener. Personalities in Australian organic gardening, such as Jackie French and Peter Bennett, talk about organic growing. The book also features extracts from early organic magazines and interviews with current organic growers, including banana and macadamia farmers, managers of outback sheep stations, dairy farmers and self-sufficiency gardeners. All of these tell the story of Australian organic farming and gardening: past, present and future.
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Book chapters on the topic "Chemical profiling"

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Bastasz, R. "Hydrogen Profiling in Titanium." In Springer Series in Chemical Physics, 397–99. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_106.

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Shepherd, F. R., W. Vandervorst, W. M. Lau, W. H. Robinson, and A. J. SpringThorpe. "SIMS Depth Profiling of Si in GaAs." In Springer Series in Chemical Physics, 350–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_93.

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Huber, Kilian V. M., and Giulio Superti-Furga. "Profiling of Small Molecules by Chemical Proteomics." In Methods in Molecular Biology, 211–18. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-3341-9_15.

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v. Criegern, R., and I. Weitzel. "SIMS Depth Profiling with Oblique Primary Beam Incidence." In Springer Series in Chemical Physics, 319–22. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_84.

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Robinson, W. H., and J. D. Brown. "Depth Profiling of Dopants in Aluminum Gallium Arsenide." In Springer Series in Chemical Physics, 357–59. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_95.

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Hannoush, Rami N. "Profiling Cellular Myristoylation and Palmitoylation Using ω-Alkynyl Fatty Acids." In Chemical Genomics and Proteomics, 85–94. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-349-3_7.

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Sułkowska-Ziaja, Katarzyna, Katarzyna Kała, Jan Lazur, and Bożena Muszyńska. "Chemical and Bioactive Profiling of Wild Edible Mushrooms." In Fungal Biology, 129–57. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-02622-6_6.

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Bryan, S. R., D. P. Griffis, R. W. Linton, and W. J. Hamilton. "Digital Slit Imaging for High-Resolution SIMS Depth Profiling." In Springer Series in Chemical Physics, 239–41. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_63.

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Boudewijn, P. R., and H. W. Werner. "Quantitative SIMS Depth Profiling of Semiconductor Materials and Devices." In Springer Series in Chemical Physics, 270–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_71.

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Schulte, F., and M. Maier. "Temperature Dependent Broadening Effects in Oxygen SIMS Depth Profiling." In Springer Series in Chemical Physics, 285–87. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82724-2_74.

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Conference papers on the topic "Chemical profiling"

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Moremi, P., GP Kamatou, W. Chen, and A. Viljoen. "Chemical profiling of Croton gratissimus Burch." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399752.

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Han, Ju, Seema Singh, Lan Sun, Blake Simmons, Manfred Auer, and Bahram Parvin. "Chemical profiling of the plant cellwall through Raman microspectroscopy." In 2010 IEEE International Symposium on Biomedical Imaging: From Nano to Macro. IEEE, 2010. http://dx.doi.org/10.1109/isbi.2010.5490228.

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Wang, Huijun, Francisco Garcia, An Chi, Ivan Cornella Taracido, Anne Mai Wasssermann, and Andy Liaw. "Profiling Diverse Chemical Space to Map the Druggable Proteome." In BCB '18: 9th ACM International Conference on Bioinformatics, Computational Biology and Health Informatics. New York, NY, USA: ACM, 2018. http://dx.doi.org/10.1145/3233547.3233624.

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Lin, Chiao-Chi, Peter J. Krommenhoek, Stephanie S. Watson, and Xiaohong Gu. "Chemical depth profiling of photovoltaic backsheets after accelerated laboratory weathering." In SPIE Solar Energy + Technology, edited by Neelkanth G. Dhere, John H. Wohlgemuth, and Rebecca Jones-Albertus. SPIE, 2014. http://dx.doi.org/10.1117/12.2066400.

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Bawase, Moqtik, Yogesh Sathe, Suhail Mulla, and Sukrut S. Thipse. "Chemical Profiling of Exhaust Particulate Matter from Indian In-Service Vehicles." In Symposium on International Automotive Technology. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2021. http://dx.doi.org/10.4271/2021-26-0192.

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Bittner, M., A. Springer, R. Schenk, and MF Melzig. "Cultivation of Black Cohosh: Non-targeted Chemical Profiling and Comparison to Wild." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608500.

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Fikry, SM, NH Khalil, and OM Salama. "Chemical profiling, biostatic and biocidal dynamics of Origanum vulgare L. essential oil." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399870.

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Gu, Xiaohong, Chiao-Chi Lin, Peter J. Krommenhoek, Yadong Lyu, Jae Hyun Kim, Li-Chieh Yu, Tinh Nguyen, and Stephanie S. Watson. "Depth profiling of chemical and mechanical degradation of UV-exposed PV backsheets." In 2016 IEEE 43rd Photovoltaic Specialists Conference (PVSC). IEEE, 2016. http://dx.doi.org/10.1109/pvsc.2016.7749560.

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Guo, Baoshan, Cheng Lei, Takuro Ito, Yiyue Jiang, Yasuyuki Ozeki, and Keisuke Goda. "High-throughput optofluidic profiling of Euglena gracilis with morphological and chemical specificity." In SPIE/COS Photonics Asia, edited by Ming Li, Bahram Jalali, Keisuke Goda, and Kevin K. Tsia. SPIE, 2016. http://dx.doi.org/10.1117/12.2245836.

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Muenmuang, Chotika, Monpilai Narasingha, Theerawut Phusantisampan, and Malinee Sriariyanun. "Chemical Profiling of Morinda Citrifolia Extract From Solvent and Soxhlet Extraction Method." In ICBBS '17: 6th International Conference on Bioinformatics and Biomedical Science. New York, NY, USA: ACM, 2017. http://dx.doi.org/10.1145/3121138.3121194.

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Reports on the topic "Chemical profiling"

1

Tuncay Aktosun. Chemical Depth Profiling from Neutron Reflectometry. Office of Scientific and Technical Information (OSTI), March 2006. http://dx.doi.org/10.2172/877659.

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Hanson, Alfred K., Percy L. Donaghay, Casey Moore, and Richard Arrieta. Transitioning Submersible Chemical Analyzer Technologies for Sustained, Autonomous Observations from Profiling Moorings, Gliders and other AUVs. Fort Belvoir, VA: Defense Technical Information Center, January 2008. http://dx.doi.org/10.21236/ada496460.

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Michel Bonin, Tom Harvill, Jared Hoog, Don Holve, Alan Alsing, Bob Clark, and Steve Hrivnak. "A High Speed Laser Profiling Device for Refractory Lininig Thickness Measurements In a Gasifier with Cross-Cut to the Metals, Forest Products, Chemical and Power Generation Industries". Office of Scientific and Technical Information (OSTI), November 2007. http://dx.doi.org/10.2172/963420.

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