Academic literature on the topic 'Natural products'
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Journal articles on the topic "Natural products"
ANB, Singab. "Bioavailability of Natural Products." Bioequivalence & Bioavailability International Journal 3, no. 1 (January 4, 2019): 1–2. http://dx.doi.org/10.23880/beba-16000137.
Full textFirst Komen, Ivana, and Nina Grgurić Čop. "Naturally traditional or traditionally natural – exploring the concepts natural and traditional in marketing research." Zbornik radova Ekonomskog fakulteta u Rijeci: časopis za ekonomsku teoriju i praksu/Proceedings of Rijeka Faculty of Economics: Journal of Economics and Business 40, no. 1 (June 30, 2022): 225–46. http://dx.doi.org/10.18045/zbefri.2022.1.225.
Full textHamann, Mark. "Natural Products and Climate Change." Tropical Journal of Natural Product Reseach 1, no. 2 (August 9, 2017): 47–48. http://dx.doi.org/10.26538/tjnpr/v1i2.1.
Full textHelmi, Yousif Alfarra, and Nor Omar Muhammad. "Microbial Transformation of Natural Products." Greener Journal of Biological Sciences 3, no. 10 (December 13, 2013): 357–64. http://dx.doi.org/10.15580/gjbs.2013.10.112913995.
Full textGoldman, Ran D., Alex L. Rogovik, David Lai, and Sunita Vohra. "Potential Interactions of Drug–Natural Health Products and Natural Health Products–Natural Health Products among Children." Journal of Pediatrics 152, no. 4 (April 2008): 521–26. http://dx.doi.org/10.1016/j.jpeds.2007.09.026.
Full textCarroll, Anthony R., Brent R. Copp, Rohan A. Davis, Robert A. Keyzers, and Michèle R. Prinsep. "Marine natural products." Natural Product Reports 38, no. 2 (2021): 362–413. http://dx.doi.org/10.1039/d0np00089b.
Full textSherman, Carol, and Allen Sherman. "Natural Products Industry." Business Ethics: The Magazine of Corporate Responsibility 11, no. 2 (1997): 20–21. http://dx.doi.org/10.5840/bemag199711225.
Full textHeard, Stephanie C., Guangwei Wu, and Jaclyn M. Winter. "Antifungal natural products." Current Opinion in Biotechnology 69 (June 2021): 232–41. http://dx.doi.org/10.1016/j.copbio.2021.02.001.
Full textNogueira, Cláudio R., and Lucia M. X. Lopes. "Antiplasmodial Natural Products." Molecules 16, no. 3 (March 4, 2011): 2146–90. http://dx.doi.org/10.3390/molecules16032146.
Full textEldahshan, Omayma. "Hepatoprotective Natural Products." Archives of Pharmaceutical Sciences Ain Shams University 1, no. 2 (July 1, 2017): 46–47. http://dx.doi.org/10.21608/aps.2017.11027.
Full textDissertations / Theses on the topic "Natural products"
Bringans, Scott D. "Studies on natural product derivatives : HIV therapies incorporating marine natural products." Thesis, University of Canterbury. Chemistry, 2001. http://hdl.handle.net/10092/6699.
Full textAguilar, Aguinaga Rodrigo, Torres Alexander César Enrique Alva, Esquivel Karla Paola Bernedo, Deza Jhoselyn Lucia Nicole Gomez, and Melgarejo Michael Richard Ganoza. "Shampoo Sólido Natural: Pashoo." Bachelor's thesis, Universidad Peruana de Ciencias Aplicadas (UPC), 2019. http://hdl.handle.net/10757/651789.
Full textPashoo is a company that was created thanks to the idea of five students who are studying the tenth cycle at the Universidad Peruana de Ciencias Aplicadas (UPC), which is oriented to the beauty and health care industry through manufacturing and marketing 100% natural bar shampoo based on selected ingredients according to their nutritional values that they provide to the hair. We have shampoos of different scents and for all types of hair such as jojoba oil, coconut, almond, argan and avocado shampoo combined with natural essences that give the client a feeling of relaxation. On the other hand, we have segmented our customers so that our product can solve their problems. For this project, we are looking at women who have problems with hair loss and irritation on the scalp and who are looking for organic and natural products that are aware of the care of the environment. We will distribute our products through fairs and by delivery using social media and our webpage as communication channels where customers can find necessary information about us and our products. In the same way, show the validations of the business model, the development of the business, the financial and marketing plan, as well as the operations that were carried out throughout this project, finally leaving our conclusions and recommendations for the completion of the project of business.
Trabajo de investigación
Woods, Katherine B. "Bioactive natural products." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/26234.
Full textDesjardine, Kelsey Lorne. "Bioactive marine natural products." Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/31286.
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Chemistry, Department of
Graduate
Dagli, Selma. "Studies in natural products." Thesis, University of Glasgow, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.392427.
Full textTele, Chhagan Godha. "Studies in natural products." Thesis, University of Aberdeen, 1987. http://digitool.abdn.ac.uk/R?func=search-advanced-go&find_code1=WSN&request1=AAIU539757.
Full textLaguna, Egea Juan Carlos. "Acción farmacológica a nivel hepático de los derivados polifenólicos de Cynara scolymus L." Doctoral thesis, Universitat de Barcelona, 1986. http://hdl.handle.net/10803/673012.
Full textDorel, Bruscas Ruth. "New annulation strategies: from polycyclic aromatic hydrocarbons to natural products." Doctoral thesis, Universitat Rovira i Virgili, 2017. http://hdl.handle.net/10803/401589.
Full textEsta Tesis Doctoral cubre tres campos de la química orgánica sintética dedicados a la síntesis de nuevos materiales basados en hidrocarburos aromáticos policíclicos (HAPs), el desarrollo de nuevas metodologías sintéticas catalizadas por complejos metálicos, y la síntesis de derivados de productos naturales. El desarrollo de nuevas estrategias para la síntesis de nuevos fragmentos de grafeno con estructuras bien definidas es un campo de gran interés dada su potencial implementación en dispositivos de electrónica molecular. Los fragmentos de grafeno con estructuras circulares resultan particularmente interesantes debido a sus extraordinarias propiedades optoelectrónicas y de autoensamblaje. En este contexto se desarrolló la síntesis un nuevo fragmento circular de grafeno de elevada simetría C54H20, tetrabenzocircumpireno, cuyas propiedades electrónicas fueron examinadas mediante microscopía de efecto túnel (STM). Los acenos están constituidos por anillos de benceno fusionados en línea, y representan otra atractiva clase de HAPs debido a sus propiedades semiconductoras. Sin embargo, su aplicación en dispositivos electrónicos está limitada por su baja solubilidad y su inherente inestabilidad. Una posible solución para salvar estas limitaciones es preparar derivados parcialmente saturados más estables, los cuales pueden usarse como precursores de los sistemas conjugados. Así, se estableció un nuevo método para la preparación de acenos parcialmente saturados, el cual está basado en una ciclación catalizada por oro(I) de 1,7-eninos que derivan de un precursor común. Este método resultó ser general y permitió la preparación de diversos dihidrotetracenos funcionalizados, así como de hidroacenos con hasta nueve anillos linealmente fusionados.
This PhD covers three fields of synthetic organic chemistry devoted to the synthesis of new materials based on polycyclic aromatic hydrocarbons (PAHs), the development of new metal-catalyzed synthetic methodology, and the synthesis of natural product derivatives. The development of new strategies for the precise synthesis of structurally well-defined novel graphene cutouts is a field of great interest due to their potential implementation in molecular electronic devices. Particularly interesting PAHs are disc-shaped fragments of graphene because of their unique optoelectronic and self-assembly properties, which are predicted to be enhanced for expanded systems. In this context, an efficient synthesis of a new discotic highly symmetric C54H20 graphene fragment – tetrabenzocircumpyrene – was developed and the electronic properties of this new graphene fragment were examined by scanning tunneling microscopy (STM). Acenes consist of planar sets of linearly fused benzene rings and represent another appealing class of PAHs due to their semiconducting properties. Nonetheless, their applicability in electronic devices is limited by their poor solubility and their inherent instability. One approach to circumvent these limitations is the preparation of more stable partially saturated derivatives, which can be used as precursors of the conjugated systems. Thus, a selective method for the preparation of partially saturated acenes under mild reaction conditions was developed based on a gold(I)-catalyzed cyclization of suitable 1,7-enynes that were assembled from a common precursor. The method proved to be general and allowed the preparation of functionalized dihydrotetracenes, as well as larger hydroacenes with up to nine linearly fused rings. The outstanding ability of gold(I) complexes to construct complex polycyclic frameworks was also examined in the context of the synthesis of natural products. Thus, the gold(I)-catalyzed alkoxycyclization of cyclopropyl-tethered 1,6-enynes allowed the ready assembly of the [3,5,5,7] tetracyclic skeleton of Echinopines, which opened an entry for the preparation of functionalized derivatives of these natural products.
Azzouz, Mariam. "Enantioselective synthesis of natural products." Doctoral thesis, Universitat Rovira i Virgili, 2013. http://hdl.handle.net/10803/365571.
Full textThe present thesis deals with the development of methodology for the syntheses of several organic molecules that were selected by their interesting biological properties: the antibiotic AT2433-A1, the glycosidase inhibidor nectrisine and analogs of the anti-viral Cidofovir (Figure 1.1) . Although apparently structurally unrelated, they were envisaged to be synthesized through common high-efficient key steps that involve metal-catalyzed process. Enantioselective Synthesis of nectrisine We explore an enantioselective synthesis of nectrisine based on Pd-catalyzed asymmetric allylic amination, cross-metathesis and dihydroxylation as key steps. Scheme 1 shows the retrosynthesis proposed, where the key synthon is the allylamine 4 which is obtained in high enantiomeric purity by a deracemization process using Pd/DACH as a catalytic system. Cross-metathesis will allow increasing the chain length, and at the same time would provide the aldehyde functionality necessary for formation of the cyclic imine moiety in the final nectrisine. Besides, configuration of double bond resulting from cross-metathesis must be E in order to provide the correct configuration of hydroxyl groups in 2 after the dihydroxylation reaction. The stereoselectivity of this reaction will be controlled by the stereocenter in the molecule, which could be also be enhanced by chiral ligands in a matched double stereodifferentiation process. The asymmetric allylic amination from racemic butadiene monoepoxide using (η3-C3H5)PdCl/DACH-naphtyl system and t-Butyl-benzoyl-imido carboxylate as a N-nucleophile proceeded with excellent yield (98%) and enantioselectivity (97%) to obtain the chiral allylic amine synthon 4. Elongation of the chain of the key chiral allylic imide with ethyl acrylate through cross metathesis using Hoveyda-Grubbs catalyst (5 mol %), proceeded quatitatively to obtain the trans alkene intermediates 3. The installation of the syn diol moiety via dihydroxylation of the alkene proceeded with high yield and good diastereoselectivity with OsO4/TMEDA. Hydrolysis of benzoate group in 2 with LiOH and in situ cyclization led to the lactam. Whose hydroxyl functionalities were fully protected by treatment with TBSCl. Subsequent protection with di-t-butyl dicarbonate (Boc) 2O and Et3N in CH2Cl2 gave desired product in 50% yield. The increased carbonyl electrophilicity resulting from NBoc protection should facilitate the smooth reduction of the lactam, which proceeded by reaction with Super Hydride® at −78°C to give lactol. Enantioselective Synthesis of Cidofovir Analogues In this context, the retrosynthetic proposal is shown in Scheme 2. Cidofovir (HPMPC) analogues could be obtained by double bond reduction of product 7 followed by protecting group cleavage on compound 11. Compound 7 in turn can be synthesized from compound 6 via chain elongation mediated by cross-metathesis reaction. Lastly, chiral synthon 6 could be obtained by a palladium-catalyzed dynamic kinetic asymmetric transformation (DYKAT) from racemic butadiene monoepoxide (5). The asymmetric allylic amination of racemic butadiene monoepoxide with cytosine as N-nucleophile was carried out with (η3-C3H5)PdCl/DACH-naphtyl system to obtain chiral allylic cytosine in 85% yield and 72% ee. The reaction was successfully expanded to other pyrimidine and purine bases, among which adenine afforded chiral allyl adenine in 90% yield and 92% ee. Chain elongation via Ru-cross metathesis of key allylic nucleobases and diethyl allylphosphonate with second generation Grubbs catalyst (5 mol%), produced desired compounds in 92% and 90% yield, respectively. Deprotection of all protecting groups with TMSBr afforded the desired unsaturated acyclic nucleosides 8 and 9 in good yields. Hydrogenation with (H2, /Pd/C) at 3 bar rendered the saturated Cidifovir analogues 10. Approaches to the Enantioselective Synthesis of AT2433-A1 The objective of this work was to explore a new enantioselective method to obtain AT2433-A1 with special focus on the synthesis of the 2, 4-dideoxy-4-amino-xyloside moiety. The retrosynthetic proposal is shown in Scheme 5.6. The aminodeoxysugar (19) could be obtained from 16 by eletrophile-induced cyclization. A key point is the selection of group X, since it must control the regioselectivity of the cyclization to an endo-mode and eventually must behave as a leaving group in a future glycosylation reaction. Amino alcohol 16 could be prepared from allylic amine 13 by dihydroxylation, sulphate formation and elimination. Compound 13 can be synthesized from allyl amine 12 via chain elongation mediated by cross-metathesis reaction. Lastly, chiral allyl amine 12 could be obtained, similarly to the previous chapters, by a palladium-catalyzed dynamic kinetic asymmetric transformation (DYKAT) from the racemic butadiene monoepoxide 5. On the other hand, the intermediate 15 could be also obtained by addition to the Garner aldehyde (18) followed by deprotection of the protecting groups in 17. The asymmetric allylic amination from racemic butadiene monoepoxide using (η3-C3H5)PdCl/DACH-naphtyl system and imide as a nitrogen nucleophile proceeded with good yield (96%) and enantioselectivity (90%). Chain elongation of key chiral allylic amine 12 was carried out by cross metathesis with allyl phenyl sulphide with Hoveyda-Grubbs catalyst (5 mol%) to obtain the corresponding trans alkene 13 in 80% yield. The installation of the diol moiety with OsO4 was unsuccesful, due to the competitive oxidation of sulfur, preventing the completion of the synthesis.
Al-Zereini, Wael. "Natural products from marine bacteria." [S.l.] : [s.n.], 2006. http://deposit.ddb.de/cgi-bin/dokserv?idn=982197985.
Full textBooks on the topic "Natural products"
Zhang, Lixin, and Arnold L. Demain, eds. Natural Products. Totowa, NJ: Humana Press, 2005. http://dx.doi.org/10.1007/978-1-59259-976-9.
Full textOsbourn, Anne, Rebecca J. Goss, and Guy T. Carter, eds. Natural Products. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118794623.
Full textA, Beutler John, DerMarderosian Ara, and Facts and Comparisons (Firm), eds. Natural products. St. Louis, Mo: Facts and Comparisons, 2002.
Find full textNag, Moupriya, Dibyajit Lahiri, Jaideep Banerjee, and Taniya Roy Chowdhury. Natural Products. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003300557.
Full textP, Cannell Richard J., ed. Natural products isolation. Totowa, N.J: Humana Press, 1998.
Find full textJ, Cutler Stephen, and Cutler Horace G. 1932-, eds. Biologically active natural products: Pharmaceuticals. Boca Raton, FL: CRC Press, 2000.
Find full textSarker, Satyajit D., Zahid Latif, and Alexander I. Gray, eds. Natural Products Isolation. Totowa, NJ: Humana Press, 2005. http://dx.doi.org/10.1385/1592599559.
Full textKiyota, Hiromasa, ed. Marine Natural Products. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4637-9.
Full textKinghorn, A. Douglas, Heinz Falk, Simon Gibbons, Yoshinori Asakawa, Ji-Kai Liu, and Verena M. Dirsch, eds. Antimalarial Natural Products. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-89873-1.
Full textSarker, Satyajit D., and Lutfun Nahar, eds. Natural Products Isolation. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-624-1.
Full textBook chapters on the topic "Natural products"
Cooper, Rose. "Natural Products." In Russell, Hugo & Ayliffe's, 550–64. Oxford, UK: Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781118425831.ch22a.
Full textKinghorn, A. Douglas, P. Annécie Benatrehina, and Garima Agarwal. "Natural Products." In Encyclopedia of Cancer, 1–4. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-27841-9_3977-3.
Full textSpainhour, Charles B. "Natural Products." In Drug Discovery Handbook, 11–72. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471728780.ch1.
Full textBuckingham, J. "Natural Products." In Chemical Nomenclature, 162–207. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-4958-7_7.
Full textPetrzilka, Martin, and Charles Ehret. "Natural Products." In Perfumes, 499–531. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-3826-0_19.
Full textKinghorn, A. Douglas, P. Annécie Benatrehina, and Garima Agarwal. "Natural Products." In Encyclopedia of Cancer, 3025–28. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-46875-3_3977.
Full textChin, Young-Won, and A. Douglas Kinghorn. "Natural Products." In Encyclopedia of Cancer, 2465–67. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-16483-5_3977.
Full textTimbrell, John, and Frank A. Barile. "Natural Products." In Introduction to Toxicology, 189–200. 4th ed. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003188575-13.
Full textZoeller, Jerome. "Natural Products." In Synthetic Sequences in Organic Chemistry, 53–90. Boca Raton: CRC Press, 2023. http://dx.doi.org/10.1201/9781003397816-3.
Full textSingh, Sheo B. "Pharmaceuticals: Natural Products and Natural Product Models." In Natural Products in Chemical Biology, 287–324. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118391815.ch12.
Full textConference papers on the topic "Natural products"
Luković, Milica, and Jovan Nićiforović. "NATURE AND NATURAL FOOD PRODUCTS IN FUTURE TOURIST’S PERSPECTIVE." In Tourism International Scientific Conference Vrnjačka Banja - TISC. FACULTY OF HOTEL MANAGEMENT AND TOURISM IN VRNJAČKA BANJA UNIVERSITY OF KRAGUJEVAC, 2022. http://dx.doi.org/10.52370/tisc22467ml.
Full textPachlatko, J. "Natural Products in Crop Protection." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01701.
Full textGarten, Daniel, Katharina Anding, Steffen Lerm, Gerhard Linss, and Peter Brückner. "Image analysis of natural products." In OCM 2013 - Optical Characterization of Materials. KIT Scientific Publishing, 2013. http://dx.doi.org/10.58895/ksp/1000032143-15.
Full textNurmi, Petteri, Eemil Lagerspetz, Wray Buntine, Patrik Floréen, Joonas Kukkonen, and Peter Peltonen. "Natural language retrieval of grocery products." In Proceeding of the 17th ACM conference. New York, New York, USA: ACM Press, 2008. http://dx.doi.org/10.1145/1458082.1458308.
Full textOzalp, Nesrin. "Energy, Environment, and Economical Advantages of Solar Thermal Cracking of Natural Gas." In ASME 2012 31st International Conference on Ocean, Offshore and Arctic Engineering. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/omae2012-84222.
Full textSchmidt, S., S. Bereswill, MM Heimesaat, and MF Melzig. "Natural products as modifiers of antibiotic resistance." 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-0039-3400064.
Full text"In Silico Drug Discovery using Natural Products." In INTERNATIONAL CONFERENCE ON BIOLOGICAL RESEARCH AND APPLIED SCIENCE. Jinnah University for Women, 2024. http://dx.doi.org/10.37962/ibras/2024/14.
Full textGrinberga, Juta, and Ilze Beitane. "A review: alternatives to substitute fructose in food products for patients with diabetes." In Research for Rural Development 2023 : annual 29th international scientific conference proceedings. Latvia University of Life Sciences and Technologies, 2023. http://dx.doi.org/10.22616/rrd.29.2023.008.
Full textHilton, Peter J., and Richard P. Gabric. "Multiple-image acquisition for inspection of natural products." In Photonics for Industrial Applications, edited by George E. Meyer and James A. DeShazer. SPIE, 1995. http://dx.doi.org/10.1117/12.198869.
Full textCheng, Xian, Liangwu Bi, Zhendong Zhao, and Yuxiang Chen. "Advances in Enzyme Assisted Extraction of Natural Products." In 3rd International Conference on Material, Mechanical and Manufacturing Engineering (IC3ME 2015). Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/ic3me-15.2015.72.
Full textReports on the topic "Natural products"
Nguyen, Tuan Hoang. Synthesis of Polycyclic Natural Products. Office of Scientific and Technical Information (OSTI), January 2003. http://dx.doi.org/10.2172/815761.
Full textLyle A. Johnson. Value-Added Products from Remote Natural Gas. Office of Scientific and Technical Information (OSTI), March 2002. http://dx.doi.org/10.2172/910125.
Full textJeon, Insik. New Synthetic Methods for Hypericum Natural Products. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/897366.
Full textFallis, Kathleen, Katherine Harper, and Rich Ford. Control of Biofouling using Biodegradable Natural Products. Fort Belvoir, VA: Defense Technical Information Center, October 2002. http://dx.doi.org/10.21236/ada603755.
Full textDeMordaunt, Austin, Smriti Sharma, Merril Stypula, Corinne Charlton, and ShangMin Lin. Market Analysis: Upcycling Natural Gas Into Solid Carbon Products. Office of Scientific and Technical Information (OSTI), January 2022. http://dx.doi.org/10.2172/1838316.
Full textKuchler, Fred, Megan Sweitzer, and Carolyn Chelius. prevalence of the "natural" claim on food product packaging. Washington, D.C.: USDA Economic Research Service, May 2023. http://dx.doi.org/10.32747/2023.8023700.ers.
Full textOmelianenko, B. I., B. S. Niconov, B. I. Ryzhov, and N. D. Shikina. Weathering products of basic rocks as sorptive materials of natural radionuclides. Office of Scientific and Technical Information (OSTI), June 1994. http://dx.doi.org/10.2172/87335.
Full textScience, Fera. Analysis of CBD Products. Food Standards Agency, November 2022. http://dx.doi.org/10.46756/sci.fsa.cis490.
Full textDavis, Matthew C. New Ionic Liquids from Natural Products for Environmentally Benign Aircraft Deicing and Anti-Icing. Fort Belvoir, VA: Defense Technical Information Center, December 2010. http://dx.doi.org/10.21236/ada580819.
Full textWeaver, J., J. Wilson, D. Kampbell, and M. Randolph. Field-derived transformation rates for modeling natural bioattenuation of trichloroethene and its degradation products. Office of Scientific and Technical Information (OSTI), January 1996. http://dx.doi.org/10.2172/210807.
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