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Showing results for antonio taxon
Your search for Antonio Tazon retrieved no results
The rise of taxon-specific epitope predictors.
Campelo F, Lobo FP. Campelo F, et al. Brief Bioinform. 2024 Jan 22;25(2):bbae092. doi: 10.1093/bib/bbae092. Brief Bioinform. 2024. PMID: 38493292 Free PMC article.
While this approach may be reasonable if one aims to develop one-size-fits-all models, it may be counterproductive if the proteins for which the model is expected to generalize are known to come from a specific subset of phylogenetically related pathogens. There is mounting evide …
While this approach may be reasonable if one aims to develop one-size-fits-all models, it may be counterproductive if the proteins for which …
Implementation of Objective PASC-Derived Taxon Demarcation Criteria for Official Classification of Filoviruses.
Bào Y, Amarasinghe GK, Basler CF, Bavari S, Bukreyev A, Chandran K, Dolnik O, Dye JM, Ebihara H, Formenty P, Hewson R, Kobinger GP, Leroy EM, Mühlberger E, Netesov SV, Patterson JL, Paweska JT, Smither SJ, Takada A, Towner JS, Volchkov VE, Wahl-Jensen V, Kuhn JH. Bào Y, et al. Viruses. 2017 May 11;9(5):106. doi: 10.3390/v9050106. Viruses. 2017. PMID: 28492506 Free PMC article.
Until now, genus and species demarcation were based on arbitrarily chosen filovirus genome sequence divergence values (50% for genera, 30% for species) and arbitrarily chosen phenotypic virus or virion characteristics. Here we report filovirus genome sequence-based taxon d …
Until now, genus and species demarcation were based on arbitrarily chosen filovirus genome sequence divergence values (50% for genera, 30% f …
A conceptual framework for nomenclatural stability and validity of medically important fungi: a proposed global consensus guideline for fungal name changes supported by ABP, ASM, CLSI, ECMM, ESCMID-EFISG, EUCAST-AFST, FDLC, IDSA, ISHAM, MMSA, and MSGERC.
de Hoog S, Walsh TJ, Ahmed SA, Alastruey-Izquierdo A, Alexander BD, Arendrup MC, Babady E, Bai F-Y, Balada-Llasat J-M, Borman A, Chowdhary A, Clark A, Colgrove RC, Cornely OA, Dingle TC, Dufresne PJ, Fuller J, Gangneux J-P, Gibas C, Glasgow H, Gräser Y, Guillot J, Groll AH, Haase G, Hanson K, Harrington A, Hawksworth DL, Hayden RT, Hoenigl M, Hubka V, Johnson K, Kus JV, Li R, Meis JF, Lackner M, Lanternier F, Leal SM Jr, Lee F, Lockhart SR, Luethy P, Martin I, Kwon-Chung KJ, Meyer W, Nguyen MH, Ostrosky-Zeichner L, Palavecino E, Pancholi P, Pappas PG, Procop GW, Redhead SA, Rhoads DD, Riedel S, Stevens B, Sullivan KO, Vergidis P, Roilides E, Seyedmousavi A, Tao L, Vicente VA, Vitale RG, Wang Q-M, Wengenack NL, Westblade L, Wiederhold N, White L, Wojewoda CM, Zhang SX. de Hoog S, et al. J Clin Microbiol. 2023 Nov 21;61(11):e0087323. doi: 10.1128/jcm.00873-23. Epub 2023 Oct 26. J Clin Microbiol. 2023. PMID: 37882528 Free PMC article.
We urge taxonomists to provide diagnostic markers of taxonomic novelties. Given the instability of phylogenetic trees due to variable taxon sampling, we advocate to maintain genera at the largest possible size. ...
We urge taxonomists to provide diagnostic markers of taxonomic novelties. Given the instability of phylogenetic trees due to variable tax
Phylogenetic relationships of the Boana pulchella Group (Anura: Hylidae).
Faivovich J, D P Pinheiro P, Lyra ML, Pereyra MO, Baldo D, Muñoz A, Reichle S, Brandão RA, Giaretta AA, C Thomé MT, Chaparro JC, Baêta D, Libardi Widholzer R, Baldo J, Lehr E, Wheeler WC, C A Garcia P, Haddad CFB. Faivovich J, et al. Mol Phylogenet Evol. 2021 Feb;155:106981. doi: 10.1016/j.ympev.2020.106981. Epub 2020 Oct 13. Mol Phylogenet Evol. 2021. PMID: 33059068
The phylogenetic analyses recover the monophyly of the B. pulchella Group with lower support than previous studies, as a result of the inclusion of the B. claresignata Group, which is recovered as its sister taxon. Within the B. pulchella Group, the inclusion of almost all …
The phylogenetic analyses recover the monophyly of the B. pulchella Group with lower support than previous studies, as a result of the inclu …
Phylogenomic analysis of the Neotropical fish subfamily Characinae using ultraconserved elements (Teleostei: Characidae).
Souza CS, Melo BF, Mattox GMT, Oliveira C. Souza CS, et al. Mol Phylogenet Evol. 2022 Jun;171:107462. doi: 10.1016/j.ympev.2022.107462. Epub 2022 Mar 28. Mol Phylogenet Evol. 2022. PMID: 35358689
Given their diversity, taxonomic importance, and the lack of a taxon-dense phylogeny, we sought to buttress the systematic understanding of Characinae collecting DNA sequence data from ultraconserved elements (UCEs) of the genome from 98 specimens covering 57 species (61%) …
Given their diversity, taxonomic importance, and the lack of a taxon-dense phylogeny, we sought to buttress the systematic understand …
Campylobacter vulpis sp. nov. isolated from wild red foxes.
Parisi A, Chiara M, Caffara M, Mion D, Miller WG, Caruso M, Manzari C, Florio D, Capozzi L, D'Erchia AM, Manzulli V, Zanoni RG. Parisi A, et al. Syst Appl Microbiol. 2021 May;44(3):126204. doi: 10.1016/j.syapm.2021.126204. Epub 2021 Apr 2. Syst Appl Microbiol. 2021. PMID: 33895623
Average nucleotide identity, average amino acid identity and in silico DNA-DNA hybridization analyses confirmed that the isolates represent a novel taxon for which the name Campylobacter vulpis sp. nov. is proposed, with isolate 251/13(T) (=CCUG 70587(T) = LMG 30110(T)) as …
Average nucleotide identity, average amino acid identity and in silico DNA-DNA hybridization analyses confirmed that the isolates represent …
Sulcisporasupratumida sp. nov. (Phaeosphaeriaceae, Pleosporales) on Anthoxanthumodoratum from Italy.
Senanayake IC, Jeewon R, Camporesi E, Hyde KD, Zeng YJ, Tian SL, Xie N. Senanayake IC, et al. MycoKeys. 2018 Aug 7;(38):35-46. doi: 10.3897/mycokeys.38.27729. eCollection 2018. MycoKeys. 2018. PMID: 30123029 Free PMC article.
Sulcispora is typified by S.pleurospora. We collected a sulcispora-like taxon on leaves of Anthoxanthumodoratum L. in Italy and obtained single ascospore isolates. ...
Sulcispora is typified by S.pleurospora. We collected a sulcispora-like taxon on leaves of Anthoxanthumodoratum L. in Italy and obtai …
Checking the checkered taxonomy of Plötz's checkered skippers (Hesperiidae: Pyrgini).
Zhang J, Cong Q, Burns JM, Grishin NV. Zhang J, et al. Taxon Rep Int Lepid Surv. 2022;10:5. doi: 10.5281/zenodo.6510282. Epub 2022 May 1. Taxon Rep Int Lepid Surv. 2022. PMID: 35530660 Free PMC article.
Lectotypes are designated for the following 5 taxa: Pyrgus (Scelothrix [sic]) bellatrix Plotz, 1884 (type locality Argentina: Buenos Aires), Pyrgus (Pyrgus) willi Plotz, 1884 (type locality in Brazil: Minas Gerais), Pyrgus (Pyrgus) albescens Plotz, 1884 (type locality in Mexico), …
Lectotypes are designated for the following 5 taxa: Pyrgus (Scelothrix [sic]) bellatrix Plotz, 1884 (type locality Argentina: Buenos Aires), …
Microbiomes of Blood-Feeding Triatomines in the Context of Their Predatory Relatives and the Environment.
Tarabai H, Floriano AM, Zima J Jr, Filová N, Brown JJ, Roachell W, Smith RL, Beatty NL, Vogel KJ, Nováková E. Tarabai H, et al. Microbiol Spectr. 2023 Aug 17;11(4):e0168123. doi: 10.1128/spectrum.01681-23. Epub 2023 Jun 8. Microbiol Spectr. 2023. PMID: 37289079 Free PMC article.
As in triatomines, microbiome dissimilarities among species correlate with dominance of a single bacterial taxon. These include Rickettsia, Lactobacillus, "Candidatus Midichloria," and Zymobacter, which are often accompanied by known symbiotic genera, i.e., Wolbachia, "Can …
As in triatomines, microbiome dissimilarities among species correlate with dominance of a single bacterial taxon. These include Ricke …
73 results