ライフサイエンスコーパス: resistant gene

1 sitive (wild-type) allele is dominant to the resistant gene.

2 aining why YPC1 was cloned as a fumonisin B1-resistant gene.

3 a phosphoglycerate kinase-promoted neomycin-resistant gene.

4 (FMT) would reduce the number of antibiotic-resistant genes.

5 or mobile genetic elements carrying multiple resistant genes.

6 ll lines, expressing three to four multidrug-resistant genes.

7 well-suited to further study of duplication-resistant genes.

8 cloned in plasmids with different antibiotic resistant genes.

9 ls and their overlap with oncogenic and drug-resistant genes.

10 sm of the IL-17A-Act1/CEBPB axis on these CS-resistant genes.

11 polymorphisms in the P falciparum multidrug resistant gene 1 (pfmdr1) and the in-vitro and in-vivo r

12 Here we used the multidrug-resistant gene 2 knockout (Mdr2(-/-)) mouse model to elu

13 We classify resistant genes according to their sensitivity to 11 chr

14 t common penicillinase, ESBL, and carbapenem resistant genes across isolates, respectively.

15 Therefore, resistant genes and pathogens may only gain a survival a

16 identities, identify potential antimicrobial resistant genes and virulence factors, and identify gene

17 majority of known malaria antigens and drug-resistant genes are highly polymorphic and under various

18 pproaches to contrast the fate of antibiotic-resistant genes (ARG) in anaerobic, aerobic, and AAS bio

19 whether monitoring wastewater for antibiotic-resistant genes (ARGs) and/or bacteria resistant to anti

20 Antibiotic resistant genes (ARGs) are considered as a new pollutant

21 otic-resistant bacteria (ARB) and antibiotic-resistant genes (ARGs) in human gut microbiota have sign

22 ibute toward the dissemination of antibiotic resistant genes (ARGs) is poorly understood.

23 halosporin families), and several antibiotic-resistant genes (ARGs) throughout a full distribution sy

24 abundance and mobile potential of antibiotic resistant genes (ARGs), prior to determining the correla

25 tion effluent, each carrying 9-11 antibiotic-resistant genes (ARGs).

26 with an internal deletion and the hygromycin-resistant gene as selection marker.

27 ew 9-plex assay to detect mobilized colistin resistant genes as clinically relevant targets for antim

28 ied to four of the most prominent carbapenem-resistant genes: bla(OXA-48), bla(NDM), bla(VIM), and bl

29 eting plasmid containing a loxP-flanked drug-resistant gene cassette to assist selection of rare targ

30 tI1 mediates the recombination of antibiotic-resistant gene cassettes between different integrons in

31 thologous groups of proteins, and antibiotic-resistant gene categories.

32 raction and identified putative up regulated resistant genes Coffee rust disease, caused by the fungu

33 Together, these Dicer-resistant genes constitute an mRNA expression signature

34 enomes for taxonomic composition, antibiotic-resistant gene content, and characterised the Escherichi

35 l municipal sewage, predominantly carbapenem-resistant genes (e.g., bla(NDM), bla(VIM)).

36 trast to wild-type mice, CaMKIIdelta phospho-resistant gene-edited mice showed a mortality rate of on

37 viously, overamplification of the glyphosate-resistant gene encoding 5-enolpyruvylshikimate-3-phospha

38 Dominant effects of resistant genes expressed in antigen-presenting cells of

39 y the highest rate of RD (77%) and multidrug resistant gene expression (ABCG2, MDR1).

40 The wheat HB4 event harboring a drought-resistant gene from sunflowers, received regulatory appr

41 present with other ARGs including carbapenem-resistant genes in 6 metagenome-assembled genomes (MAGs)

42 Our effort to identify novel drug-resistant genes in cyclophosphamide-resistant EMT6 mouse

43 ing tools are excellent at detecting BGCs or resistant genes in general, but provide little help in p

44 ting the selection of rare and/or carbapenem-resistant genes in Hospital A.

45 observed widespread enrichment of antibiotic-resistant genes in the gut, with a median 15% (95% CI 10

46 to investigate the existence of duplication-resistant genes in the sequenced genomes of 20 flowering

47 ce of genetic material, including antibiotic-resistant genes, in aquatic environments.

48 ke protein (RLP) locus, including Foc race 1-resistant genes, is absent in the Gros Michel Ze subgeno

49 The approach for identification of candidate resistant genes led to identification of 352 differentia

50 ontinues to acquire virulence and antibiotic-resistant genes located on mobile genetic elements such

51 Two colistin-resistant genes, mcr-1.1 and mcr-3.5, a carbapenemase ge

52 We found that, compared with methylation-resistant genes, methylation-prone genes have a lower fr

53 well as the activation of many other stress-resistant genes, mitochondrial respiratory chain genes,

54 Antibiotic-, disinfectant-, and heavy-metal-resistant genes on the same plasmid underscore the poten

55 ) promote long-range transport of antibiotic resistant genes or (2) serve to gain insights into the t

56 dexamethasone) or siRNA targeting multi-drug resistant gene (p-glycoprotein) in late-stage metastatic

57 the genes for human NOSII and the puromycin-resistant gene (pac).

58 This increase included antibiotic-resistant genes previously classified as threats to publ

59 Thus, we identified and cross-validated ERT-resistant gene product modules that, when leveraged with

60 y activity against P-gp 170, a multiple drug resistant gene product.

61 are mammalian counterparts of plant disease-resistant gene products that may function as cytosolic r

62 rs Apaf-1/Ced-4 and a class of plant disease-resistant gene products.

63 ple where hgcA and the antiseptic/antibiotic resistant gene (qacG) were colocated on the same contig,

64 By contrast, a ;fusion-resistant' gene, Raldh3 (also known as Aldh1a3), that en

65 e cDNA of the bcl-2, bcl-xL, or the neomycin-resistant genes, respectively.

66 ile genetic elements; coding for heavy metal resistant genes, response regulators or transcription fa

67 is influenced by the presence of a diabetes-resistant gene(s) closely linked to the IFN-gammaR loci

68 the antibiotic resistance phenotypes and/or resistant genes, singly or in combination, was documente

69 against synthetic wheats carrying the major resistant gene Stb16q have been identified.

70 oform of mice and rats is relatively ouabain resistant, gene-targeting strategies were used to produc

71 cide, especially in tandem with an herbicide-resistant gene that kills all nonhybrids, facilitating t

72 bidopsis has been used as a source for virus-resistant genes that derive from alterations in essentia

73 the need to mitigate the spread of these co-resistant genes to safeguard public health.

74 As a case study, we multiplexed 3 carbapenem-resistant genes to show the impact of this approach on g

75 Restoration of duplication-resistant genes to singleton status could be important t

76 ample were used to detect nine antimicrobial-resistant genes using qPCR and 16S rRNA sequencing.

77 ronic transcription of Venus and a puromycin-resistant gene via the foot-and-mouth disease virus self

78 We found that when a gentamicin-resistant gene was present in resistant enterococci from

79 ct the conversion of mutations in antibiotic-resistant genes, we demonstrate gene repair of point and

80 Fluoroquinolone antibiotic-resistant genes were aquired by 97 (54%) of 181 travelle

81 icated that OxyR1-activated oxidative stress-resistant genes were highly expressed in oxyR2 mutants e

82 ence factor genes and 41 distinct antibiotic resistant genes were identified.

83 We have found a group of "duplication-resistant" genes, which have undergone convergent restor