[1] Episomal segregation of the adenovirus enhancer sequence by conditional genome rearrangement abrogates late viral gene expression

[2] Transferable beta-lactamase. A new mechanism for in vitro penicillin resistance in Streptococcus faecalis

[3] A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation

[4] The 22,000-kilodalton protein of respiratory syncytial virus is a major target for Kd-restricted cytotoxic T lymphocytes from mice primed by infection

[5] High dose of plasmid IL-15 inhibits immune responses in an influenza non-human primates immunogenicity model

[6] Sterol-dependent repression of low density lipoprotein receptor promoter mediated by 16-base pair sequence adjacent to binding site for transcription factor Sp1

[7] Comparison of extraintestinal pathogenic Escherichia coli strains from human and avian sources reveals a mixed subset representing potential zoonotic pathogens

[8] Isoform 1c of sterol regulatory element binding protein is less active than isoform 1a in livers of transgenic mice and in cultured cells

[9] Different activation domains of Sp1 govern formation of multimers and mediate transcriptional synergism

[10] Extracellular matrix production regulation by TGF-beta in corneal endothelial cells

[11] Mammalian GLD-2 homologs are poly(A) polymerases

[12] Avian-pathogenic Escherichia coli strains are similar to neonatal meningitis E. coli strains and are able to cause meningitis in the rat model of human disease

[13] The rise and fall of Escherichia coli O15 in a London teaching hospital

[14] Nuclear protein that binds sterol regulatory element of low density lipoprotein receptor promoter. I. Identification of the protein and delineation of its target nucleotide sequence

[15] Heterologous expression of a position 2-substituted (1-->3)-beta-D-glucan in Lactococcus lactis

[16] Comparison of Escherichia coli isolates implicated in human urinary tract infection and avian colibacillosis

[17] Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

[18] Role of T-region borders in Agrobacterium host range

[19] Analysis of two pheromone-responsive conjugative multiresistance plasmids carrying the novel mobile optrA locus from Enterococcus faecalis

[20] Epidemic IncX3 plasmids spreading carbapenemase genes in the United Arab Emirates and worldwide

[21] Antibiotic resistance and heavy metal tolerance plasmids: the antimicrobial bulletproof properties of Escherichia fergusonii isolated from poultry

[22] Comparative analysis of KPC-2-encoding chimera plasmids with multi-replicon IncR:IncpA1763-KPC:IncN1 or IncFIIpHN7A8:IncpA1763-KPC: IncN1

[23] Comparative analysis of bla KPC-2- and rmtB-carrying IncFII-family pKPC-LK30/pHN7A8 hybrid plasmids from Klebsiella pneumoniae CG258 strains disseminated among multiple Chinese hospitals

[24] Comparative genomics of five different resistance plasmids coexisting in a clinical multi-drug resistant Citrobacter freundii isolate

[25] Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

[26] Analysis of two pheromone-responsive conjugative multiresistance plasmids carrying the novel mobile optrA locus from Enterococcus faecalis

[27] Epidemic IncX3 plasmids spreading carbapenemase genes in the United Arab Emirates and worldwide

[28] Analysis of two pheromone-responsive conjugative multiresistance plasmids carrying the novel mobile optrA locus from Enterococcus faecalis

[29] Epidemic IncX3 plasmids spreading carbapenemase genes in the United Arab Emirates and worldwide

[30] Antibiotic resistance and heavy metal tolerance plasmids: the antimicrobial bulletproof properties of Escherichia fergusonii isolated from poultry

[31] Comparative analysis of KPC-2-encoding chimera plasmids with multi-replicon IncR:IncpA1763-KPC:IncN1 or IncFIIpHN7A8:IncpA1763-KPC: IncN1

[32] Comparative analysis of bla KPC-2- and rmtB-carrying IncFII-family pKPC-LK30/pHN7A8 hybrid plasmids from Klebsiella pneumoniae CG258 strains disseminated among multiple Chinese hospitals

[33] Comparative genomics of five different resistance plasmids coexisting in a clinical multi-drug resistant Citrobacter freundii isolate

[34] Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

[35] Genetic Characterization of -Bearing Plasmids Harbored by Food-Borne Cephalosporin-Resistant Strains in China.

[36] Procarcinogens - Determination and Evaluation by Yeast-Based Biosensor Transformed with Plasmids Incorporating RAD54 Reporter Construct and Cytochrome P450 Genes.

[37] Author Correction: Split intein-mediated selection of cells containing two plasmids using a single antibiotic (Nature Communications, (2019), 10, 1, 10.1038/s41467-019-12911-1)

[38] Genomic Analysis of Hospital Plumbing Reveals Diverse Reservoir of Bacterial Plasmids Conferring Carbapenem Resistance

[39] Antibiotic resistance plasmids of Staphylococcus aureus and their clinical importance

[40] construction of two mcherry plasmids (pxg-mcherry) for transgenic leishmania: valuable tools for future molecular analysis

[41] carriage of blandm-1 in pseudomonas aeruginosa through multiple inc type plasmids in a tertiary referral hospital of northeast india

[42] overcoming the specific toxicity of large plasmids electrotransfer in primary cells in vitro

[43] carbapenem-resistant klebsiella pneumoniae isolates from egypt containing blandm-1 on incr plasmids and its association with rmtf

[44] Beyond the Core Genome: Tracking Plasmids in Outbreaks of Multidrug-resistant Bacteria

[45] Dutch patients, retail chicken meat and poultry share the same ESBL genes, plasmids and strains

[46] Acquisition of avian pathogenic Escherichia coli plasmids by a commensal E. coli isolate enhances its abilities to kill chicken embryos, grow in human urine, and colonize the murine kidney

[47] Chromosomal integration and location on IncT plasmids of the bla <inf>CTX-M-2</inf> gene in Proteus mirabilis clinical isolates

[48] Identification of mucAB-like homologs on two IncT plasmids, R394 and Rts-1

[49] Conjugation systems of IncT plasmids