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Microevolution of Pandemic Vibrio parahaemolyticus Assessed by the Number of Repeat Units in Short Sequence Tandem Repeat Regions
(PUBLIC LIBRARY SCIENCE, 2012-01-24)
The emergence of the pandemic strain Vibrio parahaemolyticus O3:K6 in 1996 caused a large increase of diarrhea outbreaks related to seafood consumption in Southeast Asia, and later worldwide. Isolates of this strain ...
Orf virus como plataforma para vacinas vetoriais para suínos e bovinos
(Universidade Federal de Santa MariaBrasilMedicina VeterináriaUFSMPrograma de Pós-Graduação em Medicina VeterináriaCentro de Ciências Rurais, 2018-02-26)
Parapoxvirus ovis (PPVO) or orf virus (ORFV) is the causative agent of contagious ecthyma (or orf), a
mucocutaneous disease that affects mainly sheep and goats. The ORFV belongs to the family
Poxviridae, subfamily ...
Caracterização funcional e envolvimento do operon htrA-XAC3983 na patogenicidade e virulência de Xanthomonas citri subsp. citri
(Universidade Estadual Paulista (Unesp), 2019-07-30)
O cancro cítrico tem como agente causal a bactéria Xanthomonas citri subsp. citri (Xac), que afeta todas as espécies de citros economicamente importantes. O sequenciamento do genoma do isolado 306 desta bactéria (Xac 306) ...
Application of BRED technology to construct recombinant D29 reporter phage expressing EGFP
(Wiley, 2013-06)
Bacteriophage Recombineering of Electroporated DNA (BRED) has been described for construction of gene deletion and point mutations in mycobacteriophages. Using BRED, we inserted a Phsp60-egfp cassette (1143 bp) into the ...
Genetic changes associated with tigecycline resistance in Staphylococcus aureus in vitro-selected mutants belonging to different lineages
(Elsevier Science, 2021-04)
Tigecycline (TGC) resistance remains rare in Staphylococcus aureus worldwide. In this study, 12 TGCresistant S. aureus mutants (TRSAm) were obtained displaying an increase in efflux activity. The isolates belonged to seven ...
RECOMBINATION AS A POSSIBLE MAJOR CAUSE OF GENETIC-HETEROGENEITY IN ANTICARSIA-GEMMATALIS NUCLEAR POLYHEDROSIS-VIRUS WILD POPULATIONS
(Elsevier Science BvAmsterdamHolanda, 1992)
Identification and characterization of novel mutations of the aspartoacylase gene in non-Jewish patients with Canavan disease
(Kluwer Academic Publ, 2002-11-01)
Canavan disease, an inherited leukodystrophy, is caused by mutations in the aspartoacylase (ASPA) gene. It is most common among children of Ashkenazi Jewish descent but has been diagnosed in many diverse ethnic groups. Two ...