ライフサイエンスコーパス: restriction enzyme analysis

1 T-->A transversion at nucleotide 1796) using restriction enzyme analysis.

2 00 ethnically matched control individuals by restriction enzyme analysis.

3 potentially functional and were confirmed by restriction enzyme analysis.

4 ase chain reaction products was confirmed by restriction enzyme analysis.

5 tained unique ITS alleles distinguishable by restriction enzyme analysis.

6 nd was excluded from 50 unaffected people by restriction enzyme analysis.

7 ific DNA sequences easily distinguishable by restriction enzyme analysis.

8 e confirmed by reverse strand sequencing and restriction enzyme analysis.

9 e between 1997 and 2003 were genome typed by restriction enzyme analysis.

10 transcription-polymerase chain reaction and restriction enzyme analysis.

11 chain reaction (RT-PCR) in combination with restriction enzyme analysis.

12 determined by type-specific PCR followed by restriction enzyme analysis.

13 d mutations in other cases were confirmed by restriction-enzyme analysis.

14 Restriction enzyme analysis and genomic sequencing ident

15 clones were determined to be unique based on restriction enzyme analysis, and 42 of these were found

16 However, using genomic DNA extraction, restriction enzyme analysis, and gel electrophoresis, we

17 Molecular methods, including karyotyping and restriction enzyme analysis, confirmed that the isolates

18 bination of the heteroduplex tracking assay, restriction enzyme analysis, DNA sequencing, and reverse

19 above method where isoelectric focusing and restriction enzyme analysis failed to identify the natur

20 Restriction enzyme analysis indicated that hlp was conse

21 A extracted using this method lent itself to restriction enzyme analysis, ligation, transformation, a

22 Mycobacterium species were identified by restriction enzyme analysis of a 439-bp segment of the 6

23 Comparison with PCR-restriction enzyme analysis of a 441-bp fragment of the

24 Restriction enzyme analysis of DNA from 94 unrelated pat

25 Restriction enzyme analysis of PCR-amplified 16S rRNA ge

26 , which interrogates DNA methylation via the restriction enzyme analysis of PCR-amplified bisulfite t

27 Restriction enzyme analysis of the 3.8-kbp full-site rea

28 ncluded growth and biochemical analysis, PCR-restriction enzyme analysis of the 439-bp Telenti fragme

29 uid chromatography, and, when necessary, PCR-restriction enzyme analysis of the 65-kDa heat shock pro

30 isolates matched the ATCC type strain by PCR restriction enzyme analysis of the 65-kDa hsp gene seque

31 s, B. burgdorferi isolates were subjected to restriction enzyme analysis of the amplified ospC genes

32 n of PCR amplification of 16S rRNA genes and restriction enzyme analysis of the amplified products.

33 tudy was to identify Capnocytophaga spp. via restriction enzyme analysis of this gene (16S rRNA PCR-r

34 ation of each virus strain was determined by restriction enzyme analysis of total cellular DNA, by PC

35 Rapid genetic screening by restriction enzyme analysis of viral DNA amplified direc

36 nd circulation periods were characterized by restriction enzyme analysis of viral DNA and select gene

37 re submitted to plasmid profile analysis and restriction enzyme analysis of whole cell DNA.

38 n of methylation using methylation-sensitive restriction enzyme analysis or focused on single-copy ge

39 sasii isolates from the United States by PCR restriction enzyme analysis (PRA) of the 441-bp Telenti

40 ve group, of which 48 (70%) had the same PCR restriction enzyme analysis (PRA) profile as the hsp65 g

41 On the basis of their susceptibility and restriction enzyme analysis profiles, our findings indic

42 defined by using small-fragment chromosomal restriction-enzyme analysis, pulsed-field gel electropho

43 tests; (ii). molecular techniques involving restriction enzyme analysis (REA) of portions of the 16S

44 polymerase chain reaction (AP-PCR), HindIII restriction enzyme analysis (REA), and pulsed-field gel

45 ile isolates from 102 patients were typed by restriction enzyme analysis (REA), arbitrarily primed PC

46 host species worldwide were characterized by restriction enzyme analysis (REA).

47 In contrast, FRET and restriction enzyme analysis reveal that only PTMs throug

48 Strain delineation by restriction enzyme analysis revealed 28 different strain

49 Direct sequencing and restriction-enzyme analysis revealed that a heterozygous

50 Restriction enzyme analysis showed various changes in pr

51 Based on restriction enzyme analysis, Southern blots, polymerase

52 Although we previously showed by restriction enzyme analysis that CpG methylation in this

53 We used PCR-based methods and restriction-enzyme analysis to detect polymorphisms.

54 Restriction enzyme analysis used to screen 175 unrelated

55 Restriction-enzyme analysis was used to confirm the muta

56 morphic DNA analysis-based genotyping and by restriction enzyme analysis with enzymes BsmAI and NspBI