ライフサイエンスコーパス: intragenic recombination

1 y the H1H2 haplotype, a result attributed to intragenic recombination.

2 were derived by horizontal DNA transfer and intragenic recombination.

3 ry of horizontal gene transfer and extensive intragenic recombination.

4 or were ancient SLS genes that had undergone intragenic recombination.

5 leles for this gene that are the products of intragenic recombination.

6 n linkage-disequilibrium mapping and somatic intragenic recombination.

7 the complete genes by a series of segmental intragenic recombinations.

8 obtained direct evidence for a high rate of intragenic recombination across this 58 kb region.

9 Nevertheless, it appears that intragenic recombination alone is insufficient to accoun

10 We find extensive intragenic recombination among all haplotypes except the

11 resented for introgressive hybridization and intragenic recombination among lineages of the F. gramin

12 Next, we examined intragenic recombination among the core genes and found

13 mydia psittaci were analyzed for evidence of intragenic recombination and for linkage equilibrium.

14 phic central repeat region arises by mitotic intragenic recombination, and (ii) the population struct

15 alleles of distant taxa showed a history of intragenic recombination, and high intrinsic levels of r

16 al evidence that there has been a history of intragenic recombination at ompA including one instance

17 tic data and with the original hypothesis of intragenic recombination based on PGM1 isozyme analysis.

18 Intragenic recombination between sapA7 and sapAp8, media

19 ea mays) NLR protein Rp1-D21 derives from an intragenic recombination between two NLRs, Rp1-D and Rp1

20 ted drastically reduced rates of spontaneous intragenic recombination but were proficient for spontan

21 on previous ones by explicitly incorporating intragenic recombination, by utilizing orthologous seque

22 These findings suggest that intragenic recombination contributed to the generation o

23 We are interested in how intragenic recombination contributes to the evolution of

24 rp1 diversity is promoted by a high rate of intragenic recombination coupled with a tendency for gen

25 onderance of allelic mosaicism suggests that intragenic recombination, coupled with selection imposed

26 However, significant associations between intragenic recombination events and variation in gene ex

27 ons affect the frequency and distribution of intragenic recombination events at bz, creating hotspots

28 Three mutations and four intragenic recombination events between the three mutati

29 This kept the overall number of intragenic recombination events nearly invariable in a g

30 However, intragenic recombination events not associated with flan

31 The results indicate that most intragenic recombination events occur at one of the muta

32 and intraspecies horizontal DNA transfer and intragenic recombination events.

33 Recombinants isolated from most meiotic intragenic recombination experiments in maize, but not i

34 Intragenic recombination explores a unique subset of seq

35 erived for their variance in the presence of intragenic recombination for a panmictic population of f

36 In half the cases in which such somatic intragenic recombination had occurred, reduction to homo

37 The results suggest that intragenic recombination has occurred in the evolutionar

38 ree windows were discordant, indicating that intragenic recombination has occurred within this locus.

39 to assess the relative roles of mutation vs. intragenic recombination in contributing to observed pol

40 ere observed, suggesting potential roles for intragenic recombination in plant phenotypic diversity.

41 Moreover, there is evidence for intragenic recombination in the history of the haplotype

42 Here we investigate intragenic recombination in Wolbachia bacteria, consider

43 Intragenic recombination is a relatively rare, but evolu

44 Intragenic recombination is active in these introns, as

45 rains is generated principally by mutations, intragenic recombination is higher within genes situated

46 ination in the history of MHC genes, because intragenic recombination may efficiently regenerate alle

47 expected by random chance alone, and neither intragenic recombination nor increased mutability can ex

48 c synonymous nucleotide sites indicated that intragenic recombination of horizontally exchanged DNA h

49 Here, we show that high frequency intragenic recombination, on the order of 30%, occurs in

50 Intragenic recombination or mutation involving the opa g

51 s to construct haplotypes which suggest that intragenic recombination played a major role in the gene

52 Intragenic recombination rapidly creates protein sequenc

53 xplain the difference between intergenic and intragenic recombination rates at wx.

54 The unusually high rate of intragenic recombination seen in bz may be related to th

55 Our samples show evidence of intragenic recombination, so the scarcity of recombinati

56 The processes of intragenic recombination that generate the repeats occur

57 Allelic intragenic recombination was associated with 2% crossing

58 allowed us to compare indirect estimates of intragenic recombination with the meiotic data from fami

59 Although none of these methods detected intragenic recombination within omcB, differences in div