ライフサイエンスコーパス: resistant gene

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

2 a phosphoglycerate kinase-promoted neomycin-resistant gene.

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

4 or mobile genetic elements carrying multiple resistant genes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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