ライフサイエンスコーパス: DNA sequence analyses

1 to be centromeric DNA by genetic mapping and DNA sequence analyses.

2 ation in FhbA among isolates was analyzed by DNA sequence analyses.

3 tase polymerase chain reaction, cloning, and DNA sequence analyses.

4 een identified solely on the basis of recent DNA sequence analyses.

5 optera based on non-neural morphological and DNA sequence analyses.

6 rthropods in morphological and mitochondrial DNA sequence analyses.

7 ne and suggest that applying simple rules of DNA sequence analyses across species may be difficult.

8 DNA sequence analyses also supported previous studies in

9 -strand conformation polymorphism (SSCP) and DNA sequence analyses and PCR-based deletion analyses fo

10 Comparative DNA sequence analyses are an essential tool in the funct

11 Using PCR and DNA sequence analyses, atcS and atcR were demonstrated t

12 olytene chromosome in situ hybridization and DNA sequence analyses confirmed that Hermes elements wer

13 DNA sequence analyses established that this Cy insertion

14 single-strand conformation polymorphism and DNA sequencing analyses for mutations in all known LQT g

15 Physical mapping and DNA sequence analyses have established that six of these

16 resistant tobacco cells on selective medium, DNA sequence analyses identified base conversions in the

17 Marker sorting and DNA sequence analyses identified sets of monophyletic ma

18 Physiological data and DNA sequence analyses indicate that the benzoate pathway

19 Waxy DNA sequence analyses indicate that the splice donor mut

20 Amongst these Rbmx-like genes, DNA sequence analyses indicate that two other mouse auto

21 ethylation-specific PCR and sodium bisulfite DNA sequencing analyses indicate that the HMW-MAA promot

22 PCR and DNA sequence analyses indicated the following.

23 DNA sequencing analyses indicated that these encoded pro

24 Using Western blot, real-time PCR, and DNA sequencing analyses it was shown that restriction an

25 ed in 15 probands with apical hypertrophy by DNA sequence analyses of 9 sarcomere protein genes and 3

26 type-specific HPV infections persisted, and DNA sequence analyses of a subset revealed that all were

27 Hybridization and DNA sequence analyses of cloned kinetochore DNA fragment

28 ratories have begun to undertake comparative DNA sequence analyses of orthologous chromosome segments

29 The evidence comes from DNA sequence analyses of regions within or very near the

30 ility testing, molecular fingerprinting, and DNA sequence analyses of resistant MAC isolates.

31 DNA sequence analyses of the breakpoint junctions in 47

32 PCR and DNA sequence analyses of the citrate synthase (gltA) gen

33 DNA sequence analyses of the region affected by the smal

34 yhole limpet, an observation common to other DNA sequence analyses of these taxa.

35 DNA sequencing analyses of 10 subcloned cDNA fragments,

36 Surprisingly, DNA sequence analyses on mutant clones revealed the pres

37 Restriction mapping and DNA sequencing analyses provide evidence that mutants ca

38 DNA sequence analyses revealed 4 UL4-based genotypes, 2

39 Deletion and DNA sequence analyses revealed an open reading frame hom

40 DNA sequence analyses revealed HPRT gene mutations in ea

41 DNA sequence analyses revealed that acc is composed of e

42 Restriction enzyme digestion and DNA sequence analyses revealed that an exon, exon 8A, en

43 DNA sequence analyses revealed that B. garinii and B. af

44 DNA sequence analyses revealed that replication of TC/AG

45 DNA sequence analyses revealed that the stalled products

46 DNA sequence analyses showed interpatient specific mutat

47 Extensive DNA sequence analyses showed no changes from the baselin

48 Results from DNA sequence analyses showed that a 39-kb composite tran

49 Previous DNA sequence analyses showed that CTnDOT att sites conta

50 fluorescence in situ hybridization, PCR, and DNA sequence analyses showed that the distal inv(6) brea

51 Southern blot hybridization and DNA sequence analyses showed that the nic1 AChR alpha-su

52 In support of these findings, DNA sequencing analyses showed that the mutational spect

53 PCR and DNA sequence analyses suggest that the number of tandem

54 nal ulcer disease), rapid urease testing and DNA sequence analyses suggested the presence of H. cinae

55 umors, by using methylation-specific PCR and DNA sequence analyses to analyze the methylation status

56 We performed DNA sequence analyses to detect bacterial species in 945

57 single-strand conformation polymorphism and DNA sequence analyses to identify mutations in MEF2A in

58 Polymerase chain reaction and DNA sequence analyses were done on archival tissue speci

59 ated with molecular dynamics simulations and DNA sequence analyses were found to be correlated, indic

60 uthern hybridization, PCR amplification, and DNA sequence analyses were performed on the toxin A (tcd

61 ingle-nucleotide polymorphism and subsequent DNA sequence analyses were performed on the vlsE gene an

62 Heteroduplex and DNA sequence analyses were then performed to identify th