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2. Oropharyngeal resistome remains stable during COVID-19 therapy, while fecal resistome shifts toward a less diverse resistotype

5. A Novel Mastadenovirus from Nyctalus noctula Which Represents a Distinct Evolutionary Branch of Viruses from Bats in Europe.

6. Alphacoronaviruses from bats captured in European Russia in 2015 and 2021 are closely related to those of Northern Europe.

12. Identification and Genetic Characterization of MERS-Related Coronavirus Isolated from Nathusius’ Pipistrelle (Pipistrellus nathusii) near Zvenigorod (Moscow Region, Russia)

16. Gene Loss, Pseudogenization in Plastomes of Genus Allium (Amaryllidaceae), and Putative Selection for Adaptation to Environmental Conditions

17. Additional file 1 of Case report: change of dominant strain during dual SARS-CoV-2 infection

18. Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population

20. Figure 12 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

22. Figure 9 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

23. Figure 3 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

24. Figure 5 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

25. Figure 2 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

26. Supplementary material 1 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

27. Figure 4 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

28. Figure 7 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

29. Figure 8 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

30. Figure 6 from: Zaika MA, Kilian N, Jones K, Krinitsina AA, Nilova MV, Speranskaya AS, Sukhorukov AP (2020) Scorzonera sensu lato (Asteraceae, Cichorieae) – taxonomic reassessment in the light of new molecular phylogenetic and carpological analyses. PhytoKeys 137: 1-85. https://doi.org/10.3897/phytokeys.137.46544

31. rise and spread of the SARS-CoV-2 AY.122 lineage in Russia.

32. Genetic factors of chronic pancreatitis in Russian population

33. Comparative analysis of Illumina and Ion Torrent high-throughput sequencing platforms for identification of plant components in herbal teas

35. NGS sequencing as an efficient instrument of molecular genetic diagnostics in patients with chronic pancreatitis

37. Evolution of blue-flowered species of genus Linum based on high-throughput sequencing of ribosomal RNA genes

38. Figure 2 from: Krinitsina AA, Belenikin MS, Churikova OA, Kuptsov SV, Antipin MI, Logacheva MD, Speranskaya AS (2017) Systematic position of Dryopteris blanfordii subsp. nigrosquamosa (Ching) Fraser-Jenkins within the genus Dryopteris Adans.. PhytoKeys 90: 89-112. https://doi.org/10.3897/phytokeys.88.14745

39. Figure 1 from: Krinitsina AA, Belenikin MS, Churikova OA, Kuptsov SV, Antipin MI, Logacheva MD, Speranskaya AS (2017) Systematic position of Dryopteris blanfordii subsp. nigrosquamosa (Ching) Fraser-Jenkins within the genus Dryopteris Adans.. PhytoKeys 90: 89-112. https://doi.org/10.3897/phytokeys.88.14745

41. miR319, miR390, and miR393 Are Involved in Aluminum Response in Flax (Linum usitatissimum L.)

42. Erratum to “miR319, miR390, and miR393 Are Involved in Aluminum Response in Flax (Linum usitatissimum L.)”

43. Gene expression profiling of flax (Linum usitatissimum L.) under edaphic stress

44. Identification, Expression Analysis, and Target Prediction of Flax Genotroph MicroRNAs Under Normal and Nutrient Stress Conditions

45. Excess fertilizer responsive miRNAs revealed in Linum usitatissimum L

46. Retrotransposon-Based Molecular Markers for Analysis of Genetic Diversity within the GenusLinum

47. Flax Inorganic Phosphate Deficiency Responsive miRNAs

50. Improved Protocols of ITS1-Based Metabarcoding and Their Application in the Analysis of Plant-Containing Products.

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