Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Veronika Gordeeva"'
Publikováno v:
Veterinary World, Vol 16, Iss 2, Pp 272-280 (2023)
Background and Aim: Histophilus somni is a Gram-negative bacterium belonging to the Pasteurellaceae family that can cause bovine histophilosis. Histophilus may act as a commensal or opportunistic bacterial cattle pathogen. Comparing genomes of the pa
Externí odkaz:
https://doaj.org/article/d13a818797064357900ffe02645ac645
Autor:
Olga Prasolova, Ekaterina Krylova, Alexandra Bogomazova, Irina Soltynskaya, Oleg Sklyarov, Veronika Gordeeva, Irina Timofeeva, Anton Motorygin, Alexander Panin
Publikováno v:
Frontiers in Veterinary Science, Vol 10 (2023)
Over the past 10 years, immunization of cattle in Russia has been performed using vaccines from Brucella abortus strains 82, 19 and 75/79. To prevent brucellosis in small ruminants, two vaccines have been used, from the Brucella melitensis strain REV
Externí odkaz:
https://doaj.org/article/96c503975d014b6c819fd83222d96688
Autor:
Veronika Gordeeva, Elena Sharova, Konstantin Babalyan, Rinat Sultanov, Vadim M. Govorun, Georgij Arapidi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Whole-exome sequencing is an attractive alternative to microarray analysis because of the low cost and potential ability to detect copy number variations (CNV) of various sizes (from 1–2 exons to several Mb). Previous comparison of the mos
Externí odkaz:
https://doaj.org/article/74053e2546e143b9894809dc6ad427ac
Autor:
Georgij Arapidi, Konstantin Babalyan, Veronika Gordeeva, E. I. Sharova, Vadim M. Govorun, R. Sultanov
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports
Scientific Reports
Whole-exome sequencing is an attractive alternative to microarray analysis because of the low cost and potential ability to detect copy number variations (CNV) of various sizes (from 1–2 exons to several Mb). Previous comparison of the most popular
Publikováno v:
International journal of molecular sciences. 23(4)
Copy number variations (CNVs) are the predominant class of structural genomic variations involved in the processes of evolutionary adaptation, genomic disorders, and disease progression. Compared with single-nucleotide variants, there have been chall