المؤلفون: Monsalve Escudero, Laura, Loaiza Cano, Vanessa, Pajaro Gonzalez, Yina, Oliveros Diaz, Andres, Diaz Castillo, Fredyc, Quiñones, Wiston, Robledo, Sara, Martínez Gutiérrez, Marlen

المصدر: National Center for Emerging and Zoonotic Infectious Diseases [https://www.cdc.gov/ncezid/dvbd/about.htmlTest]. ; Carrillo-Hernández MY, Ruiz-Saenz J, Villamizar LJ, Gómez-Rangel SY, Martínez-Gutierrez M. Co-circulation and simultaneous co-infection of dengue, chikungunya, and zika viruses in patients with febrile syndrome at the Colombian-Venezuelan border. BMC Infect Dis. 2018;18(1):61. https://doi.org/10.1186/s12879-018-2976-1Test. ; Mercado M, Acosta-Reyes J, Parra E, Pardo L, Rico A, Campo A, et al. Clinical and histopathological features of fatal cases with dengue and chikungunya virus co-infection in Colombia, 2014 to 2015. Eurosurveillance. 2016;21(22):30244. ; Strauss JH, Strauss EG. The alphaviruses: gene expression, replication, and evolution. Microbiol Mol Biol Rev. 1994;58(3):491–562. ; Halstead SB. ....

مصطلحات موضوعية: Zika virus, Chikungunya virus, Indole alkaloids, Molecular docking, Antiviral

وصف الملف: application/pdf

العلاقة: BMC Complementary Medicine and Therapies; https://bmccomplementmedtherapies.biomedcentral.com/articles/10.1186/s12906-021-03386-zTest; http://hdl.handle.net/20.500.12494/43636Test; Monsalve-Escudero, L.M., Loaiza-Cano, V., Pájaro-González, Y. et al. (2021) Indole alkaloids inhibit zika and chikungunya virus infection in different cell lines. BMC Complement Med Ther 21, 216 (2021). https://doi.org/10.1186/s12906-021-03386-zTest

الإتاحة: https://doi.org/20.500.12494/43636Test
https://doi.org/10.1186/s12879-018-2976-1Test
https://doi.org/10.3201/eid2104.141723Test
https://doi.org/10.1371/journal.pntd.0000389Test
https://doi.org/10.1016/j.trstmh.2010.01.011Test
https://doi.org/10.1007/s00705-006-0903-zTest
https://doi.org/10.1016/j.jneuroim.2017.03.001Test
https://doi.org/10.1056/NEJMoa1600651Test
https://doi.org/10.1056/NEJMoa1605564Test
https://doi.org/10.1099/vir.0.057422-0Test

المؤلفون: Monsalve Escudero, Laura, Loaiza Cano, Vanessa, Pajaro Gonzalez, Yina, Oliveros Diaz, Andres, Diaz Castillo, Fredyc, Quiñones, Wiston, Robledo, Sara, Martínez Gutiérrez, Marlén

مصطلحات موضوعية: Zika virus, Chikungunya virus, Indole alkaloids, Molecular docking, Antiviral

وصف الملف: application/pdf

العلاقة: https://bmccomplementmedtherapies.biomedcentral.com/articles/10.1186/s12906-021-03386-zTest; BMC Complementary Medicine and Therapies; National Center for Emerging and Zoonotic Infectious Diseases [https://www.cdc.gov/ncezid/dvbd/about.htmlTest].; Carrillo-Hernández MY, Ruiz-Saenz J, Villamizar LJ, Gómez-Rangel SY, Martínez-Gutierrez M. Co-circulation and simultaneous co-infection of dengue, chikungunya, and zika viruses in patients with febrile syndrome at the Colombian-Venezuelan border. BMC Infect Dis. 2018;18(1):61. https://doi.org/10.1186/s12879-018-2976-1Test.; Mercado M, Acosta-Reyes J, Parra E, Pardo L, Rico A, Campo A, et al. Clinical and histopathological features of fatal cases with dengue and chikungunya virus co-infection in Colombia, 2014 to 2015. Eurosurveillance. 2016;21(22):30244.; Strauss JH, Strauss EG. The alphaviruses: gene expression, replication, and evolution. Microbiol Mol Biol Rev. 1994;58(3):491–562.; Halstead SB. 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BMC Complement Med Ther 21, 216 (2021). https://doi.org/10.1186/s12906-021-03386-zTest

الإتاحة: https://doi.org/20.500.12494/43636Test
https://doi.org/10.1186/s12879-018-2976-1Test
https://doi.org/10.3201/eid2104.141723Test
https://doi.org/10.1371/journal.pntd.0000389Test
https://doi.org/10.1016/j.trstmh.2010.01.011Test
https://doi.org/10.1007/s00705-006-0903-zTest
https://doi.org/10.1016/j.jneuroim.2017.03.001Test
https://doi.org/10.1056/NEJMoa1600651Test
https://doi.org/10.1056/NEJMoa1605564Test
https://doi.org/10.1099/vir.0.057422-0Test

المؤلفون: Martínez Gutiérrez, Marlén, Ruiz Saenz, Julian

مصطلحات موضوعية: Canine distemper virus, Hemagglutinin gene, Genotype, Genome evolution

وصف الملف: application/pdf

العلاقة: https://www.frontiersin.org/articles/10.3389/fmicb.2019.01982/fullTest; Front Microbiol.; https://hdl.handle.net/20.500.12494/15090Test; Quintero-Gil D, Rendon-Marin S, Martinez-Gutierrez M, Ruiz-Saenz J. Origin of canine distemper virus: consolidating evidence to understand potential zoonoses. Front Microbiol. 2019 Aug 28;10:1982.

الإتاحة: https://doi.org/20.500.12494/15090Test
https://doi.org/10.3389/fmicb.2019.01982Test
https://hdl.handle.net/20.500.12494/15090Test

المؤلفون: Ruiz-Saenz, Julian, Martinez-Gutierrez, Marlen

مصطلحات موضوعية: distemper, evolution, measle, morbillivirus, Zoonotic disease

وصف الملف: application/pdf

العلاقة: https://www.frontiersin.org/articles/10.3389/fmicb.2019.01982/fullTest; Front Microbiol.; Abdullah N., Kelly J. T., Graham S. C., Birch J., Goncalves-Carneiro D., Mitchell T., et al. . (2018). Structure-guided identification of a nonhuman morbillivirus with zoonotic potential. J. Virol. 92:e01248–18. 10.1128/JVI.01248-18; Baker J. A., Sheffy B. E., Robson D. S., Gilmartin J. (1966). Response to measles virus by puppies with maternally transferred distemper antibodies. Cornell Vet. 56:588. [PubMed] [Google Scholar] Behura S. K., Severson D. W. (2013). Codon usage bias: causative factors, quantification methods and genome-wide patterns: with emphasis on insect genomes. Biol. Rev. 88, 49–61. 10.1111/j.1469-185X.2012.00242.x; Bieringer M., Han J. W., Kendl S., Khosravi M., Plattet P., Schneider-Schaulies J. (2013). Experimental adaptation of wild-type canine distemper virus (CDV) to the human entry receptor CD150. PLoS ONE 8:e57488. 10.1371/journal.pone.0057488; Blancou J. (2004). Dog distemper: imported into Europe from South America? Hist. Med. Vet. 29, 35−41.; Brown A. L., Mccarthy R. E. (1974). Relationship between measles and canine distemper viruses determined by delayed type hypersensitivity reactions in dogs. Nature 248, 344–345. 10.1038/248344a0; Brown A. L., Vitamvas J. A., Merry D. L., Beckenhauer W. H. (1972). Immune response of pups to modified live-virus canine distemper-measles vaccine. Am. J. Vet. Res. 33, 1447–1456.; Christe K. L., Salyards G. W., Houghton S. D., Ardeshir A., Yee J. L. (2019). Modified dose efficacy trial of a canine distemper-measles vaccine for use in Rhesus Macaques (Macaca mulatta). J. Am. Assoc. Lab. Anim. Sci. 58, 397–405. 10.30802/AALAS-JAALAS-18-000091; Cosby S. L., Weir L. (2018). Measles vaccination: threat from related veterinary viruses and need for continued vaccination post measles eradication. Hum. Vaccin. Immunother. 14, 229–233. 10.1080/21645515.2017.1403677; De Vries R. D., Duprex W. P., De Swart R. L. (2015). Morbillivirus infections: an introduction. Viruses 7, 699–706. 10.3390/v7020699; De Vries R. D., Ludlow M., Verburgh R. J., Van Amerongen G., Yuksel S., Nguyen D. T., et al. . (2014). Measles vaccination of nonhuman primates provides partial protection against infection with canine distemper virus. J. Virol. 88, 4423–4433. 10.1128/JVI.03676-13; Di Paola N., De Melo Freire C. C., De Andrade Zanotto P. M. (2018). Does adaptation to vertebrate codon usage relate to flavivirus emergence potential? PLoS ONE 13:e0191652. 10.1371/journal.pone.0191652; Drexler J. F., Corman V. M., Muller M. A., Maganga G. D., Vallo P., Binger T., et al. . (2012). Bats host major mammalian paramyxoviruses. Nat. Commun. 3:796. 10.1038/ncomms1796; Duque-valencia J., Sarute N., Olarte-Castillo X. A., Ruíz-Sáenz J. (2019). Evolution and interspecies transmission of canine distemper virus-an outlook of the diverse evolutionary landscapes of a multi-host virus. Viruses 11:E582. 10.3390/v11070582; Emerman M., Malik H. S. (2010). Paleovirology–modern consequences of ancient viruses. PLoS Biol. 8:e1000301. 10.1371/journal.pbio.1000301; Freire C. C. M., Palmisano G., Braconi C. T., Cugola F. R., Russo F. B., Beltrão-Braga P. C., et al. . (2018). NS1 codon usage adaptation to humans in pandemic Zika virus. Mem. Inst. Oswaldo Cruz 113:e170385. 10.1590/0074-02760170385; Furuse Y., Suzuki A., Oshitani H. (2010). Origin of measles virus: divergence from rinderpest virus between the 11th and 12th centuries. Virol. J. 7:52. 10.1186/1743-422X-7-52; Goni N., Iriarte A., Comas V., Sonora M., Moreno P., Moratorio G., et al. . (2012). Pandemic influenza A virus codon usage revisited: biases, adaptation and implications for vaccine strain development. Virol. J. 9:263. 10.1186/1743-422X-9-263; Haralambieva I. H., Kennedy R. B., Ovsyannikova I. G., Whitaker J. A., Poland G. A. (2015). Variability in humoral immunity to measles vaccine: new developments. Trends Mol. Med. 21, 789–801. 10.1016/j.molmed.2015.10.005; Holzmann H., Hengel H., Tenbusch M., Doerr H. W. (2016). Eradication of measles: remaining challenges. Med. Microbiol. Immunol. 205, 201–208. 10.1007/s00430-016-0451-4; https://hdl.handle.net/20.500.12494/15172Test; Quintero-Gil D, Rendon-Marin S, Martinez-Gutierrez M, Ruiz-Saenz J. Origin of canine distemper virus: consolidating evidence to understand potential zoonoses. Front Microbiol. 2019 Aug 28;10:1982. doi:10.3389/fmicb.2019.01982

الإتاحة: https://doi.org/20.500.12494/15172Test
https://doi.org/10.3389/fmicb.2019.01982Test
https://hdl.handle.net/20.500.12494/15172Test

المؤلفون: Ruiz-Saenz, Julian, Martinez-Gutierrez, Marlen

المصدر: Abdullah N., Kelly J. T., Graham S. C., Birch J., Goncalves-Carneiro D., Mitchell T., et al. . (2018). Structure-guided identification of a nonhuman morbillivirus with zoonotic potential. J. Virol. 92:e01248–18. 10.1128/JVI.01248-18 ; Baker J. A., Sheffy B. E., Robson D. S., Gilmartin J. (1966). Response to measles virus by puppies with maternally transferred distemper antibodies. Cornell Vet. 56:588. [PubMed] [Google Scholar] Behura S. K., Severson D. W. (2013). Codon usage bias: causative factors, quantification methods and genome-wide patterns: with emphasis on insect genomes. Biol. Rev. 88, 49–61. 10.1111/j.1469-185X.2012.00242.x ; Bieringer M., Han J. W., Kendl S., Khosravi M., Plattet ....

مصطلحات موضوعية: distemper, evolution, measle, morbillivirus, Zoonotic disease

وصف الملف: application/pdf

العلاقة: Front Microbiol.; https://www.frontiersin.org/articles/10.3389/fmicb.2019.01982/fullTest; http://hdl.handle.net/20.500.12494/15172Test; Quintero-Gil D, Rendon-Marin S, Martinez-Gutierrez M, Ruiz-Saenz J. Origin of canine distemper virus: consolidating evidence to understand potential zoonoses. Front Microbiol. 2019 Aug 28;10:1982. doi:10.3389/fmicb.2019.01982

الإتاحة: https://doi.org/20.500.12494/15172Test
https://doi.org/10.3389/fmicb.2019.01982Test
https://doi.org/10.1128/JVI.01248-18Test
https://doi.org/10.1111/j.1469-185X.2012.00242.xTest
https://doi.org/10.1371/journal.pone.0057488Test
https://doi.org/10.1038/248344a0Test
https://doi.org/10.30802/AALAS-JAALAS-18-000091Test
https://doi.org/10.1080/21645515.2017.1403677Test
https://doi.org/10.3390/v7020699Test
https://doi.org/10.1128/JVI.03676-13Test

المؤلفون: Ruiz Saenz, Julian, Martinez Gutierrez, Marlen, Arcila Quiceno, Victor, Trejos Suarez, Juanita

المصدر: 1. Nguyen TV, Le Van P, Le Huy C, Weintraub A. Diarrhea caused by rotavirus in children less than 5 years of age in Hanoi, Vietnam. J Clin Microbiol. 2004;42:5745-50. ; 2. Mokomane M, Kasvosve I, Melo E, Pernica JM, Goldfarb DM. The global problem of childhood diarrhoeal diseases: emerging strategies in prevention and management. Ther Adv Infect Dis. 2018;5:29-43. ; 3. GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Infect Dis. 2017;17:909-48. ; 4. Crawford SE, Ramani ....

مصطلحات موضوعية: Acute diarrhoea, Colombia, Molecular characterization, Post-vaccination, Rotavirus

وصف الملف: application/pdf

العلاقة: Rev Inst Med Trop Sao Paulo; https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/31269110Test/; http://hdl.handle.net/20.500.12494/15181Test; Martinez-Gutierrez M, Arcila-Quiceno V, Trejos-Suarez J, Ruiz-Saenz J. (2019) Prevalence and molecular typing of rotavirus in children with acute diarrhoea in Northeastern Colombia. Rev Inst Med Trop Sao Paulo. 2019 Jul 1;61:e34. doi:10.1590/S1678-9946201961034.

الإتاحة: https://doi.org/20.500.12494/15181Test
https://doi.org/10.1590/S1678-9946201961034Test
https://hdl.handle.net/20.500.12494/15181Test

المؤلفون: Martínez Gutiérrez, Marlen, Ruiz Saenz, Julian

مصطلحات موضوعية: Canine distemper virus, Hemagglutinin gene, Genotype, Genome evolution

وصف الملف: application/pdf

العلاقة: Front Microbiol.; https://www.frontiersin.org/articles/10.3389/fmicb.2019.01982/fullTest; http://hdl.handle.net/20.500.12494/15090Test; Quintero-Gil D, Rendon-Marin S, Martinez-Gutierrez M, Ruiz-Saenz J. Origin of canine distemper virus: consolidating evidence to understand potential zoonoses. Front Microbiol. 2019 Aug 28;10:1982.

الإتاحة: https://doi.org/20.500.12494/15090Test
https://doi.org/10.3389/fmicb.2019.01982Test
https://hdl.handle.net/20.500.12494/15090Test

المؤلفون: Martínez Gutiérrez, Marlén, Trujillo-Correa, Andrea Isabel, Quintero-Gil, Diana Carolina, Diaz-Castillo, Fredyc, Quiñones, Winston, Robledo, Sara M

مصطلحات موضوعية: Antiviral, Catechin, Bioprospecting, Dengue virus, Gallic acid, Psidium guajava, Quercetin

وصف الملف: application/pdf

العلاقة: https://bmccomplementalternmed.biomedcentral.com/articles/10.1186/s12906-019-2695-1Test; BMC Complement Altern Med.; 1. Guzman MG, Harris E. Dengue. Lancet. 2015;385(9966):453–65.; 2. Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, Drake JM, Brownstein JS, Hoen AG, Sankoh O. The global distribution and burden of dengue. Nature. 2013;496(7446):504–7.; 3. OPS. Programa Regional de Dengue de la OPS. In: vol. Actualizado a la SE 43 del 2013: Organización Panamericana de la Salud; 2013.; 4. Salles TS, da Encarnação S-GT, de Alvarenga ESL, Guimarães-Ribeiro V, MDF d M, de Castro-Salles PF, dos Santos CR, do Amaral Melo AC, Soares MR, Ferreira DF. History, epidemiology and diagnostics of dengue in the American and Brazilian contexts: a review. Parasit Vectors. 2018;11(1):264.; 5. Organization WH, Research SPf, Diseases TiT, Diseases WHODoCoNT, Epidemic WHO, Alert P. Dengue: guidelines for diagnosis, treatment, prevention and control. Geneva: World Health Organization; 2009.; 6. Simmons CP, Farrar JJ, van Vinh CN, Wills B. Dengue. N Engl J Med. 2012;366(15):1423–32.; 7. Halstead SB. Pathogenesis of dengue: challenges to molecular biology. Science. 1988;239(4839):476–81.; 8. Vaughn DW, Green S, Kalayanarooj S, Innis BL, Nimmannitya S, Suntayakorn S, Endy TP, Raengsakulrach B, Rothman AL, Ennis FA. Dengue viremia titer, antibody response pattern, and virus serotype correlate with disease severity. J Infect Dis. 2000;181(1):2–9.; 9. Chambers TJ, Hahn CS, Galler R, Rice CM. Flavivirus genome organization, expression, and replication. Ann Rev Microbiol. 1990;44(1):649–88.; 11. Bartenschlager R, Miller S. Molecular aspects of dengue virus replication; 2008.; 12. Rodenhuis-Zybert IA, Wilschut J, Smit JM. Dengue virus life cycle: viral and host factors modulating infectivity. Cell Mol Life Sci. 2010;67(16):2773–86.; 13. Lin Y-L, Lei H-Y, Lin Y-S, Yeh T-M, Chen S-H, Liu H-S. Heparin inhibits dengue-2 virus infection of five human liver cell lines. Antivir Res. 2002;56(1):93–6.; 14. Takhampunya R, Ubol S, Houng H-S, Cameron CE, Padmanabhan R. Inhibition of dengue virus replication by mycophenolic acid and ribavirin. J Gen Virol. 2006;87(7):1947–52.; 15. Whitby K, Pierson TC, Geiss B, Lane K, Engle M, Zhou Y, Doms RW, Diamond MS. Castanospermine, a potent inhibitor of dengue virus infection in vitro and in vivo. J Virol. 2005;79(14):8698–706.; 16. Martínez-Gutierrez M, Castellanos JE, Gallego-Gómez JC. Statins reduce dengue virus production via decreased virion assembly. Intervirology. 2011;54(4):202–16.; 17. Low JG, Ooi EE, Vasudevan SG. Current Status of Dengue Therapeutics Research and Development. J Infect Dis. 2017;215(suppl_2):S96–S102.; 18. Kaptein SJ, Neyts J. Towards antiviral therapies for treating dengue virus infections. Curr Opin Pharmacol. 2016;30:1–7.; 19. Lai J-H, Lin Y-L, Hsieh S-L. Pharmacological intervention for dengue virus infection. Biochem Pharmacol. 2017;129:14–25.; 20. Farrar J, Focks D, Gubler D, Barrera R, Guzman M, Simmons C, Kalayanarooj S, Lum L, McCall P, Lloyd L. Towards a global dengue research agenda. Tropical Med Int Health. 2007;12(6):695–9.; https://hdl.handle.net/20.500.12494/15306Test; Trujillo-Correa AI, Quintero-Gil DC, Diaz-Castillo F, Quiñones W, Robledo SM, Martinez-Gutierrez M. In vitro and in silico anti-dengue activity of compounds obtained from Psidium guajava through bioprospecting. BMC Complement Altern Med. 2019 Nov 6;19(1):298.

الإتاحة: https://doi.org/20.500.12494/15306Test
https://doi.org/10.1186/s12906-019-2695-1Test
https://hdl.handle.net/20.500.12494/15306Test

المؤلفون: Ruiz Saenz, Julian, Martínez Gutiérrez, Marlén, Arcila Quiceno, Victor, Trejos Suarez, Juanita

مصطلحات موضوعية: Acute diarrhoea, Colombia, Molecular characterization, Post-vaccination, Rotavirus

وصف الملف: application/pdf

العلاقة: https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/31269110Test/; Rev Inst Med Trop Sao Paulo; 1. Nguyen TV, Le Van P, Le Huy C, Weintraub A. Diarrhea caused by rotavirus in children less than 5 years of age in Hanoi, Vietnam. J Clin Microbiol. 2004;42:5745-50.; 2. Mokomane M, Kasvosve I, Melo E, Pernica JM, Goldfarb DM. The global problem of childhood diarrhoeal diseases: emerging strategies in prevention and management. Ther Adv Infect Dis. 2018;5:29-43.; 3. GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Infect Dis. 2017;17:909-48.; 4. Crawford SE, Ramani S, Tate JE, Parashar UD, Svensson L, Hagbom M, et al. Rotavirus infection. Nat Rev Dis Primers. 2017;3:17083.; 5. Parashar UD, Gibson CJ, Bresse J, Glass RI. Rotavirus and severe childhood diarrhea. Emerg Infect Dis. 2006;12:304-6.; 6. World Health Organization. Meeting of the immunization Strategic Advisory Group of Experts, April 2009: conclusions and recommendations. Wkly Epidemiol Rec. 2009;84:220-36.; 7. Tate JE, Burton AH, Boschi-Pinto C, Parashar UD, World Health Organization-Coordinated Global Rotavirus Surveillance Network. Global, regional, and national estimates of rotavirus mortality in children; 8. Troeger C, Khalil IA, Rao PC, Cao S, Blacker BF, Ahmed T, et al. Rotavirus vaccination and the global burden of rotavirus diarrhea among children younger than 5 years. JAMA Pediatr. 2018;172:958-65.; 9. Bucardo F, Nordgren J. Impact of vaccination on the molecular epidemiology and evolution of group A rotaviruses in Latin America and factors affecting vaccine efficacy. Infect Genet Evol. 2015;34:106-13.; 11. Cáceres DC, Peláez D, Sierra N, Estrada E, Sánchez L. La carga de la enfermedad por rotavirus en niños menores de cinco años, Colombia, 2004. Rev Panam Salud Publica. 2006;20:9-21.; 12. Uribe Yepes MA, Rodríguez Villamizar LA, Gómez González YA, Olaya Gamboa LE, Rodríguez Santamaría SM. Aislamientos de patógenos comunes asociados con enfermedad diarreica aguda en menores de cinco años, Bucaramanga, Colombia. MedUNAB. 2009;12:72-9.; 13. World Health Organization. Manual of rotavirus detection and characterization methods. Geneva: WHO; 2009.; 14. Gouvea V, Glass RI, Woods P, Taniguchi K, Clark HF, Forrester B, et al. Polymerase chain reaction amplification and typing of rotavirus nucleic acid from stool specimens. J Clin Microbiol. 1990;28:276-82.; https://hdl.handle.net/20.500.12494/15181Test; Martinez-Gutierrez M, Arcila-Quiceno V, Trejos-Suarez J, Ruiz-Saenz J. (2019) Prevalence and molecular typing of rotavirus in children with acute diarrhoea in Northeastern Colombia. Rev Inst Med Trop Sao Paulo. 2019 Jul 1;61:e34. doi:10.1590/S1678-9946201961034.

الإتاحة: https://doi.org/20.500.12494/15181Test
https://doi.org/10.1590/S1678-9946201961034Test
https://hdl.handle.net/20.500.12494/15181Test

المؤلفون: Martinez Gutierrez, Marlen, Trujillo-Correa, Andrea Isabel, Quintero-Gil, Diana Carolina, Diaz-Castillo, Fredyc, Quiñones, Winston, Robledo, Sara M

المصدر: 1. Guzman MG, Harris E. Dengue. Lancet. 2015;385(9966):453–65. ; 2. Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, Drake JM, Brownstein JS, Hoen AG, Sankoh O. The global distribution and burden of dengue. Nature. 2013;496(7446):504–7. ; 3. OPS. Programa Regional de Dengue de la OPS. In: vol. Actualizado a la SE 43 del 2013: Organización Panamericana de la Salud; 2013. ; 4. Salles TS, da Encarnação S-GT, de Alvarenga ESL, Guimarães-Ribeiro V, MDF d M, de Castro-Salles PF, dos Santos CR, do Amaral Melo AC, Soares MR, Ferreira DF. History, epidemiology and diagnostics of dengue ....

مصطلحات موضوعية: Antiviral, Catechin, Bioprospecting, Dengue virus, Gallic acid, Psidium guajava, Quercetin

وصف الملف: application/pdf

العلاقة: BMC Complement Altern Med.; https://bmccomplementalternmed.biomedcentral.com/articles/10.1186/s12906-019-2695-1Test; http://hdl.handle.net/20.500.12494/15306Test; Trujillo-Correa AI, Quintero-Gil DC, Diaz-Castillo F, Quiñones W, Robledo SM, Martinez-Gutierrez M. In vitro and in silico anti-dengue activity of compounds obtained from Psidium guajava through bioprospecting. BMC Complement Altern Med. 2019 Nov 6;19(1):298.

الإتاحة: https://doi.org/20.500.12494/15306Test
https://doi.org/10.1186/s12906-019-2695-1Test
https://hdl.handle.net/20.500.12494/15306Test