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Produit naturel (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Produit naturel" in French language version.

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53doi.org
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46nih.gov
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14books.google.com
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4harvard.edu
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1thefreedictionary.com
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1naturalproductsfoundation.org
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1semanticscholar.org
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1medilexicon.com
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1archive.org
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1caryinstitute.org
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1eolss.net
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1csiro.au
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1intechopen.com
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1labtimes.org
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1sgm.ac.uk
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1nobelprize.org
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1web.archive.org
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1heathcock.org
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1acs.org
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1sciencehistory.org
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acs.org

archive.org

  • (de) Kossel A, « Ueber die chemische Zusammensetzung der Zelle » [« La Composition chimique de la cellule »], Archiv für Physiologie, Leipzig, Veit & Comp.,‎ , p. 181–186 (lire en ligne)

books.google.com

caryinstitute.org

csiro.au

publish.csiro.au

  • (en) Beekman AM, Barrow RA, « Fungal metabolites as pharmaceuticals », Aust J Chem, vol. 67, no 6,‎ , p. 827–843 (DOI 10.1071/ch13639, lire en ligne)

doi.org

dx.doi.org

  • « All natural », Nature Chemical Biology, vol. 3, no 7,‎ , p. 351 (PMID 17576412, DOI 10.1038/nchembio0707-351) :

    « "The simplest definition for a natural product is a small molecule that is produced by a biological source." »

  • Adriano Rutz, Maria Sorokina, Jakub Galgonek, Daniel Mietchen, Egon Willighagen, Arnaud Gaudry, James G Graham, Ralf Stephan, Roderic Page, Jiří Vondrášek, Christoph Steinbeck, Guido F Pauli, Jean-Luc Wolfender, Jonathan Bisson et Pierre-Marie Allard, « The LOTUS initiative for open knowledge management in natural products research », eLife, vol. 11,‎ , e70780 (PMID 35616633, DOI 10.7554/eLife.70780, S2CID 249064853)
  • (en) János Bérdy, « Bioactive Microbial Metabolites. A Personal View », The Journal of Antibiotics, vol. 58, no 1,‎ , p. 1–26 (DOI 10.1038/ja.2005.1)
  • (en) AA Brakhage, V Schroeckh, « Fungal secondary metabolites - strategies to activate silent gene clusters », Fungal Genet Biol., vol. 48, no 1,‎ , p. 15-22 (DOI 10.1016/j.fgb.2010.04.004)
  • Maplestone RA, Stone MJ, Williams DH, « The evolutionary role of secondary metabolites--a review », Gene, vol. 115, nos 1–2,‎ , p. 151–7 (PMID 1612430, DOI 10.1016/0378-1119(92)90553-2)
  • (en) Hunter P, « Harnessing Nature's wisdom. Turning to Nature for inspiration and avoiding her follies », EMBO Reports, vol. 9, no 9,‎ , p. 838–40 (PMID 18762775, PMCID 2529361, DOI 10.1038/embor.2008.160)
  • (en) Li JW, Vederas JC, « Drug discovery and natural products: end of an era or an endless frontier? », Science, vol. 325, no 5937,‎ , p. 161–5 (PMID 19589993, DOI 10.1126/science.1168243, Bibcode 2009Sci...325..161L)
  • Kliebenstein DJ, « Secondary metabolites and plant/environment interactions: a view through Arabidopsis thaliana tinged glasses », Plant, Cell and Environment, vol. 27, no 6,‎ , p. 675–684 (DOI 10.1111/j.1365-3040.2004.01180.x) :

    « In 1891, following Stahls work on plant biochemistry, Kossel suggested a distinction between basic and secondary metabolism (Stahl 1888). »

  • Karlovsky P, « Secondary metabolites in soil ecology », Soil Biology, vol. 14,‎ , p. 1–19 (ISBN 978-3-540-74542-6, DOI 10.1007/978-3-540-74543-3_1) :

    « The current, generally accepted concept in line with Kossel’s view is that primary metabolites are chemical components of living organisms that are vital for their normal functioning, while secondary metabolites are compounds which are dispensable. »

  • Demain AL, Fang A, « The natural functions of secondary metabolites », Advances in Biochemical Engineering/Biotechnology, vol. 69,‎ , p. 1–39 (ISBN 978-3-540-67793-2, PMID 11036689, DOI 10.1007/3-540-44964-7_1)
  • Williams DH, Stone MJ, Hauck PR, Rahman SK, « Why are secondary metabolites (natural products) biosynthesized? », Journal of Natural Products, vol. 52, no 6,‎ , p. 1189–208 (PMID 2693613, DOI 10.1021/np50066a001)
  • Firn RD, Jones CG, « The evolution of secondary metabolism - a unifying model », Molecular Microbiology, vol. 37, no 5,‎ , p. 989–94 (PMID 10972818, DOI 10.1046/j.1365-2958.2000.02098.x, lire en ligne)
  • Strobel G, Daisy B, « Bioprospecting for microbial endophytes and their natural products », Microbiology and Molecular Biology Reviews, vol. 67, no 4,‎ , p. 491–502 (PMID 14665674, PMCID 309047, DOI 10.1128/MMBR.67.4.491-502.2003)
  • (en) Zaffiri L, Gardner J, Toledo-Pereyra LH, « History of antibiotics. From salvarsan to cephalosporins », Journal of Investigative Surgery, vol. 25, no 2,‎ , p. 67–77 (PMID 22439833, DOI 10.3109/08941939.2012.664099)
  • (en) Procópio RE, Silva IR, Martins MK, Azevedo JL, Araújo JM, « Antibiotics produced by Streptomyces », The Brazilian Journal of Infectious Diseases, vol. 16, no 5,‎ , p. 466–71 (PMID 22975171, DOI 10.1016/j.bjid.2012.08.014)
  • (en) Saxena A, Kumari R, Mukherjee U, Singh P, Lal R, « Draft Genome Sequence of the Rifamycin Producer Amycolatopsis rifamycinica DSM 46095 », Genome Announcements, vol. 2, no 4,‎ , e00662–14 (PMID 24994803, PMCID 4082003, DOI 10.1128/genomeA.00662-14)
  • (en) Hallett M, Albanese A, Dressler D, Segal KR, Simpson DM, Truong D, Jankovic J, « Evidence-based review and assessment of botulinum neurotoxin for the treatment of movement disorders », Toxicon, vol. 67, no June,‎ , p. 94–114 (PMID 23380701, DOI 10.1016/j.toxicon.2012.12.004)
  • (en) Alvin A, Miller KI, Neilan BA, « Exploring the potential of endophytes from medicinal plants as sources of antimycobacterial compounds », Microbiological Research, vol. 169, nos 7–8,‎ , p. 483–95 (PMID 24582778, DOI 10.1016/j.micres.2013.12.009)
  • (en) Wang X, Elshahawi SI, Shaaban KA, Fang L, Ponomareva LV, Zhang Y, Copley GC, Hower JC, Zhan CG, Kharel MK, Thorson JS, « Ruthmycin, a new tetracyclic polyketide from Streptomyces sp. RM-4-15 », Organic Letters, vol. 16, no 2,‎ , p. 456–9 (PMID 24341358, PMCID 3964319, DOI 10.1021/ol4033418)
  • (en) Wang X, Shaaban KA, Elshahawi SI, Ponomareva LV, Sunkara M, Copley GC, Hower JC, Morris AJ, Kharel MK, Thorson JS, « Mullinamides A and B, new cyclopeptides produced by the Ruth Mullins coal mine fire isolate Streptomyces sp. RM-27-46 », The Journal of Antibiotics, vol. 67, no 8,‎ , p. 571–5 (PMID 24713874, PMCID 4146655, DOI 10.1038/ja.2014.37)
  • (en) Akey DL, Gehret JJ, Khare D, Smith JL, « Insights from the sea: structural biology of marine polyketide synthases », Natural Product Reports, vol. 29, no 10,‎ , p. 1038–49 (PMID 22498975, PMCID 3709256, DOI 10.1039/c2np20016c)
  • (en) Thornburg CC, Zabriskie TM, McPhail KL, « Deep-sea hydrothermal vents: potential hot spots for natural products discovery? », Journal of Natural Products, vol. 73, no 3,‎ , p. 489–99 (PMID 20099811, DOI 10.1021/np900662k)
  • (en) Beekman AM, Barrow RA, « Fungal metabolites as pharmaceuticals », Aust J Chem, vol. 67, no 6,‎ , p. 827–843 (DOI 10.1071/ch13639, lire en ligne)
  • (en) Dang L, Van Damme EJ, « Toxic proteins in plants », Phytochemistry, vol. 117,‎ , p. 51–64 (PMID 26057229, DOI 10.1016/j.phytochem.2015.05.020)
  • (en) Kittakoop P, Mahidol C, Ruchirawat S, « Alkaloids as important scaffolds in therapeutic drugs for the treatments of cancer, tuberculosis, and smoking cessation », Current Topics in Medicinal Chemistry, vol. 14, no 2,‎ , p. 239–52 (PMID 24359196, DOI 10.2174/1568026613666131216105049)
  • (en) Russo P, Frustaci A, Del Bufalo A, Fini M, Cesario A, « Multitarget drugs of plants origin acting on Alzheimer's disease », Current Medicinal Chemistry, vol. 20, no 13,‎ , p. 1686–93 (PMID 23410167, DOI 10.2174/0929867311320130008)
  • (en) Dossey AT, « Insects and their chemical weaponry: new potential for drug discovery », Natural Product Reports, vol. 27, no 12,‎ , p. 1737–57 (PMID 20957283, DOI 10.1039/C005319H)
  • (en) Mayer AM, Glaser KB, Cuevas C, Jacobs RS, Kem W, Little RD, McIntosh JM, Newman DJ, Potts BC, Shuster DE, « The odyssey of marine pharmaceuticals: a current pipeline perspective », Trends in Pharmacological Sciences, vol. 31, no 6,‎ , p. 255–65 (PMID 20363514, DOI 10.1016/j.tips.2010.02.005)
  • (en) Bowersox SS, Luther R, « Pharmacotherapeutic potential of omega-conotoxin MVIIA (SNX-111), an N-type neuronal calcium channel blocker found in the venom of Conus magus », Toxicon, vol. 36, no 11,‎ , p. 1651–8 (PMID 9792182, DOI 10.1016/S0041-0101(98)00158-5)
  • (en) Prommer E, « Ziconotide: a new option for refractory pain », Drugs of Today, vol. 42, no 6,‎ , p. 369–78 (PMID 16845440, DOI 10.1358/dot.2006.42.6.973534)
  • (en) Rinehart KL, « Antitumor compounds from tunicates », Medicinal Research Reviews, vol. 20, no 1,‎ , p. 1–27 (PMID 10608919, DOI 10.1002/(SICI)1098-1128(200001)20:1<1::AID-MED1>3.0.CO;2-A)
  • (en) Petek BJ, Loggers ET, Pollack SM, Jones RL, « Trabectedin in soft tissue sarcomas », Marine Drugs, vol. 13, no 2,‎ , p. 974–83 (PMID 25686274, PMCID 4344612, DOI 10.3390/md13020974)
  • (en) Singh R, Sharma M, Joshi P, Rawat DS, « Clinical status of anti-cancer agents derived from marine sources », Anti-Cancer Agents in Medicinal Chemistry, vol. 8, no 6,‎ , p. 603–17 (PMID 18690825, DOI 10.2174/187152008785133074)
  • (en) Beghyn T, Deprez-Poulain R, Willand N, Folleas B, Deprez B, « Natural compounds: leads or ideas? Bioinspired molecules for drug discovery », Chemical Biology & Drug Design, vol. 72, no 1,‎ , p. 3–15 (PMID 18554253, DOI 10.1111/j.1747-0285.2008.00673.x)
  • (en) Koehn FE, Carter GT, « The evolving role of natural products in drug discovery », Nature Reviews. Drug Discovery, vol. 4, no 3,‎ , p. 206–20 (PMID 15729362, DOI 10.1038/nrd1657)
  • (en) Newman DJ, Cragg GM, « Natural products as sources of new drugs over the last 25 years », Journal of Natural Products, vol. 70, no 3,‎ , p. 461–77 (PMID 17309302, DOI 10.1021/np068054v)
  • (en) Atanasov AG, Waltenberger B, Pferschy-Wenzig EM, Linder T, Wawrosch C, Uhrin P, Temml V, Wang L, Schwaiger S, Heiss EH, Rollinger JM, Schuster D, Breuss JM, Bochkov V, Mihovilovic MD, Kopp B, Bauer R, Dirsch VM, Stuppner H, « Discovery and resupply of pharmacologically active plant-derived natural products: A review », Biotechnology Advances, vol. 33, no 8,‎ , p. 1582–614 (PMID 26281720, PMCID 4748402, DOI 10.1016/j.biotechadv.2015.08.001)
  • (en) Lewis RJ, Dutertre S, Vetter I, Christie MJ, « Conus venom peptide pharmacology », Pharmacological Reviews, vol. 64, no 2,‎ , p. 259–98 (PMID 22407615, DOI 10.1124/pr.111.005322)
  • (en) Hartung EF, « History of the use of colchicum and related medicaments in gout; with suggestions for further research », Annals of the Rheumatic Diseases, vol. 13, no 3,‎ , p. 190–200 (PMID 13198053, PMCID 1006735, DOI 10.1136/ard.13.3.190)
  • (en) Gomez-Escribano JP, Alt S, Bibb MJ, « Next Generation Sequencing of Actinobacteria for the Discovery of Novel Natural Products », Marine Drugs, vol. 14, no 4,‎ , p. 78 (PMID 27089350, PMCID 4849082, DOI 10.3390/md14040078)
  • (en) Pawar SV, Ho JC, Yadav GD, Yadav VG, « The Impending Renaissance in Discovery & Development of Natural Products », Current Topics in Medicinal Chemistry, vol. 17, no 2,‎ , p. 251–267 (PMID 27237327, DOI 10.2174/1568026616666160530154649)
  • (en) Blow N, « Metagenomics: exploring unseen communities », Nature, vol. 453, no 7195,‎ , p. 687–90 (PMID 18509446, DOI 10.1038/453687a, Bibcode 2008Natur.453..687B)
  • (en) Hodgkin DC, Kamper J, Mackay M, Pickworth J, Trueblood KN, White JG, « Structure of vitamin B12 », Nature, vol. 178, no 4524,‎ , p. 64–6 (PMID 13348621, DOI 10.1038/178064a0, Bibcode 1956Natur.178...64H)
  • (en) Woodward RB, « The total synthesis of vitamin B 12 », Pure and Applied Chemistry, vol. 33, no 1,‎ , p. 145–77 (PMID 4684454, DOI 10.1351/pac197333010145)
  • (en) Eschenmoser A, « Vitamin B12: Experiments Concerning the Origin of Its Molecular Structure », Angewandte Chemie International Edition in English, vol. 27, no 1,‎ , p. 5–39 (DOI 10.1002/anie.198800051)
  • (en) Heathcock CH, Chemical Synthesis, vol. 320, coll. « NATO ASI Series », , 223–243 p. (DOI 10.1007/978-94-009-0255-8_9, lire en ligne), « As We Head into the 21st Century, Is there Still Value in Total Synthesis of Natural Products as a Research Endeavor? »
  • (en) Nicolaou KC, Vourloumis D, Winssinger N, Baran PS, « The Art and Science of Total Synthesis at the Dawn of the Twenty-First Century », Angewandte Chemie, vol. 39, no 1,‎ , p. 44–122 (PMID 10649349, DOI 10.1002/(SICI)1521-3773(20000103)39:1<44::AID-ANIE44>3.0.CO;2-L)
  • Voloshchuk T, Farina NS, Wauchope OR, Kiprowska M, Haberfield P, Greer A, « Molecular bilateral symmetry of natural products: prediction of selectivity of dimeric molecules by density functional theory and semiempirical calculations », Journal of Natural Products, vol. 67, no 7,‎ , p. 1141–6 (PMID 15270568, DOI 10.1021/np049899e)
  • Glenn WS, Runguphan W, O'Connor SE, « Recent progress in the metabolic engineering of alkaloids in plant systems », Current Opinion in Biotechnology, vol. 24, no 2,‎ , p. 354–65 (PMID 22954587, PMCID 3552043, DOI 10.1016/j.copbio.2012.08.003)
  • (en) Dias DA, Urban S, Roessner U, « A historical overview of natural products in drug discovery », Metabolites, vol. 2, no 4,‎ , p. 303–36 (PMID 24957513, PMCID 3901206, DOI 10.3390/metabo2020303)
  • (de) F Wöhler, « Ueber künstliche Bildung des Harnstoffs » [« About the artificial formation of urea »], Annalen der Physik und Chemie, vol. 88, no 2,‎ , p. 253–256 (DOI 10.1002/andp.18280880206, Bibcode 1828AnP....88..253W)
  • (de) August Kekulé, « Ueber die Constitution und die Metamorphosen der chemischen Verbindungen und über die chemische Natur des Kohlenstoffs » [« Concerning the constitution and the metamorphosis of the chemical compounds and the chemical nature of the carbon »], Annalen der Chemie und Pharmacie, vol. 106, no 2,‎ , p. 129–159 (DOI 10.1002/jlac.18581060202)
  • (de) Justus Liebig, « Ueber Laurent's Theorie der organischen Verbindungen » [« About Laurent 's theory of organic compounds »], Annalen der Pharmacie, vol. 25, no 1,‎ , p. 1–31 (DOI 10.1002/jlac.18380250102)

eolss.net

  • (en) Bertoldo C, Antranikian G, Biotechnology Vol. IX, Paris, Encyclopedia of Life Support Systems (EOLSS), (lire en ligne), « Chapitre 1: Biotechnology of Archaea »

harvard.edu

ui.adsabs.harvard.edu

heathcock.org

  • (en) Heathcock CH, Chemical Synthesis, vol. 320, coll. « NATO ASI Series », , 223–243 p. (DOI 10.1007/978-94-009-0255-8_9, lire en ligne), « As We Head into the 21st Century, Is there Still Value in Total Synthesis of Natural Products as a Research Endeavor? »

intechopen.com

cdn.intechopen.com

  • (en) Fernandes-Pedrosa MF, Félix-Silva J, Menezes YA, An Integrated View of the Molecular Recognition and Toxinology : From Analytical Procedures to Biomedical Applications, InTechOpen, , 23–72 p. (lire en ligne)

labtimes.org

  • (en) Gransalke K, « Mother Nature’s Drug Cabinet », Lab Times, vol. 11, no 1,‎ , p. 16–19 (lire en ligne) :

    « Drug Discovery - Is Mother Nature still the number one source for promising new drugs? »

medilexicon.com

  • « Natural Products », Stedman's Medical Dictionary, Lippincott Williams & Wilkins : « Natural products: naturally occurring compounds that are end products of secondary metabolism; often, they are unique compounds for particular organisms or classes of organisms. »

naturalproductsfoundation.org

  • « About Us », Natural Products Foundation (consulté le ) : « Natural products are represented by a wide array of consumer goods that continue to grow in popularity each year. These products include natural and organic foods, dietary supplements, pet foods, health and beauty products, "green" cleaning supplies and more. Generally, natural products are considered those formulated without artificial ingredients and that are minimally processed. »

nih.gov

ncbi.nlm.nih.gov

  • « All natural », Nature Chemical Biology, vol. 3, no 7,‎ , p. 351 (PMID 17576412, DOI 10.1038/nchembio0707-351) :

    « "The simplest definition for a natural product is a small molecule that is produced by a biological source." »

  • Adriano Rutz, Maria Sorokina, Jakub Galgonek, Daniel Mietchen, Egon Willighagen, Arnaud Gaudry, James G Graham, Ralf Stephan, Roderic Page, Jiří Vondrášek, Christoph Steinbeck, Guido F Pauli, Jean-Luc Wolfender, Jonathan Bisson et Pierre-Marie Allard, « The LOTUS initiative for open knowledge management in natural products research », eLife, vol. 11,‎ , e70780 (PMID 35616633, DOI 10.7554/eLife.70780, S2CID 249064853)
  • Maplestone RA, Stone MJ, Williams DH, « The evolutionary role of secondary metabolites--a review », Gene, vol. 115, nos 1–2,‎ , p. 151–7 (PMID 1612430, DOI 10.1016/0378-1119(92)90553-2)
  • (en) Hunter P, « Harnessing Nature's wisdom. Turning to Nature for inspiration and avoiding her follies », EMBO Reports, vol. 9, no 9,‎ , p. 838–40 (PMID 18762775, PMCID 2529361, DOI 10.1038/embor.2008.160)
  • (en) Li JW, Vederas JC, « Drug discovery and natural products: end of an era or an endless frontier? », Science, vol. 325, no 5937,‎ , p. 161–5 (PMID 19589993, DOI 10.1126/science.1168243, Bibcode 2009Sci...325..161L)
  • Demain AL, Fang A, « The natural functions of secondary metabolites », Advances in Biochemical Engineering/Biotechnology, vol. 69,‎ , p. 1–39 (ISBN 978-3-540-67793-2, PMID 11036689, DOI 10.1007/3-540-44964-7_1)
  • Williams DH, Stone MJ, Hauck PR, Rahman SK, « Why are secondary metabolites (natural products) biosynthesized? », Journal of Natural Products, vol. 52, no 6,‎ , p. 1189–208 (PMID 2693613, DOI 10.1021/np50066a001)
  • Firn RD, Jones CG, « The evolution of secondary metabolism - a unifying model », Molecular Microbiology, vol. 37, no 5,‎ , p. 989–94 (PMID 10972818, DOI 10.1046/j.1365-2958.2000.02098.x, lire en ligne)
  • Strobel G, Daisy B, « Bioprospecting for microbial endophytes and their natural products », Microbiology and Molecular Biology Reviews, vol. 67, no 4,‎ , p. 491–502 (PMID 14665674, PMCID 309047, DOI 10.1128/MMBR.67.4.491-502.2003)
  • (en) Zaffiri L, Gardner J, Toledo-Pereyra LH, « History of antibiotics. From salvarsan to cephalosporins », Journal of Investigative Surgery, vol. 25, no 2,‎ , p. 67–77 (PMID 22439833, DOI 10.3109/08941939.2012.664099)
  • (en) Procópio RE, Silva IR, Martins MK, Azevedo JL, Araújo JM, « Antibiotics produced by Streptomyces », The Brazilian Journal of Infectious Diseases, vol. 16, no 5,‎ , p. 466–71 (PMID 22975171, DOI 10.1016/j.bjid.2012.08.014)
  • (en) Saxena A, Kumari R, Mukherjee U, Singh P, Lal R, « Draft Genome Sequence of the Rifamycin Producer Amycolatopsis rifamycinica DSM 46095 », Genome Announcements, vol. 2, no 4,‎ , e00662–14 (PMID 24994803, PMCID 4082003, DOI 10.1128/genomeA.00662-14)
  • (en) Hallett M, Albanese A, Dressler D, Segal KR, Simpson DM, Truong D, Jankovic J, « Evidence-based review and assessment of botulinum neurotoxin for the treatment of movement disorders », Toxicon, vol. 67, no June,‎ , p. 94–114 (PMID 23380701, DOI 10.1016/j.toxicon.2012.12.004)
  • (en) Alvin A, Miller KI, Neilan BA, « Exploring the potential of endophytes from medicinal plants as sources of antimycobacterial compounds », Microbiological Research, vol. 169, nos 7–8,‎ , p. 483–95 (PMID 24582778, DOI 10.1016/j.micres.2013.12.009)
  • (en) Wang X, Elshahawi SI, Shaaban KA, Fang L, Ponomareva LV, Zhang Y, Copley GC, Hower JC, Zhan CG, Kharel MK, Thorson JS, « Ruthmycin, a new tetracyclic polyketide from Streptomyces sp. RM-4-15 », Organic Letters, vol. 16, no 2,‎ , p. 456–9 (PMID 24341358, PMCID 3964319, DOI 10.1021/ol4033418)
  • (en) Wang X, Shaaban KA, Elshahawi SI, Ponomareva LV, Sunkara M, Copley GC, Hower JC, Morris AJ, Kharel MK, Thorson JS, « Mullinamides A and B, new cyclopeptides produced by the Ruth Mullins coal mine fire isolate Streptomyces sp. RM-27-46 », The Journal of Antibiotics, vol. 67, no 8,‎ , p. 571–5 (PMID 24713874, PMCID 4146655, DOI 10.1038/ja.2014.37)
  • (en) Akey DL, Gehret JJ, Khare D, Smith JL, « Insights from the sea: structural biology of marine polyketide synthases », Natural Product Reports, vol. 29, no 10,‎ , p. 1038–49 (PMID 22498975, PMCID 3709256, DOI 10.1039/c2np20016c)
  • (en) Thornburg CC, Zabriskie TM, McPhail KL, « Deep-sea hydrothermal vents: potential hot spots for natural products discovery? », Journal of Natural Products, vol. 73, no 3,‎ , p. 489–99 (PMID 20099811, DOI 10.1021/np900662k)
  • (en) Dang L, Van Damme EJ, « Toxic proteins in plants », Phytochemistry, vol. 117,‎ , p. 51–64 (PMID 26057229, DOI 10.1016/j.phytochem.2015.05.020)
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