ライフサイエンスコーパス: parallel evolution

1 gent evolution and of the common scenario of parallel evolution.

2 may have been rediscovered multiple times by parallel evolution.

3 int component, reveals a spectacular case of parallel evolution.

4 brates and thus present a remarkable case of parallel evolution.

5 the South African species are the result of parallel evolution.

6 s of their adaptive solutions-will show more parallel evolution.

7 e, evidently has enhanced the probability of parallel evolution.

8 We find parallel evolution across three scales: within individua

9 Here we show rapid parallel evolution across two closely related but geogra

10 ebrates using statistical methods that model parallel evolution, although the extent to which sequenc

11 in an evolving population, (3) low rates of parallel evolution and convergent evolution between spec

12 ng with phages exhibited a greater degree of parallel evolution and faster selective sweeps than popu

13 t this amphibious lifestyle is an example of parallel evolution and has arisen from strictly terrestr

14 y in two or more strains, a process known as parallel evolution, and a substantial fraction of the pa

15 genes and mutations, the molecular basis of parallel evolution, and the evolutionary forces driving

16 ons in independent lineages, which is termed parallel evolution; and the evolution in independent lin

17 d to extract deeper signal from the noise of parallel evolution, areal readaptation, and contact.

18 This study indicates that analyzing parallel evolution at the genetic level could help to an

19 four requirements for establishing adaptive parallel evolution at the protein sequence level and use

20 onstructions indicated multiple instances of parallel evolution, at least one definitive case of conv

21 order characters appear susceptible to some parallel evolution because of mechanistic constraints, t

22 proteins without salivary function, implying parallel evolution by conservation of ancestral characte

23 ication can be acquired and expanded through parallel evolution, enabling tumors to adapt while maint

24 Parallel evolution experiments enable the recognition of

25 However, in the parallel evolution experiments in the presence of rifamp

26 pgi, delta ppc, delta pta, and delta tpi) in parallel evolution experiments of each mutant.

27 This was done using four parallel evolution experiments that employed low or grad

28 be an unusually high level of convergent and parallel evolution (homoplasy).

29 same nucleus experience both independent and parallel evolution, (ii) differential lineage-specific s

30 t that these data provide a clear example of parallel evolution in a complex neuromechanical system,

31 es including the quantitative measurement of parallel evolution in independent lineages and the ident

32 ships among metastases, the scale of ongoing parallel evolution in metastatic and primary sites, and

33 This provides evidence of parallel evolution in mitochondrial gene order for anima

34 Such parallel evolution indicates that natural selection has

35 If parallel evolution is perfect, then the implication is t

36 Parallel evolution is the acquisition of identical adapt

37 closely related lineages (frequently termed "parallel" evolution) is often assumed to result from cha

38 re is not conserved, suggesting independent, parallel evolution leading to the same catalytic functio

39 ples from the Old World) can be explained by parallel evolution of a human-like Sia expression patter

40 l innovations may have set the stage for the parallel evolution of ballistic predatory strikes.

41 om large gene families strongly implies that parallel evolution of both structural genes and trans-fa

42 Our study shows that parallel evolution of CAM is present among subfamilies o

43 ient core chondrogenic network underlies the parallel evolution of cartilage tissues in Ecdysozoa, Lo

44 Parallel evolution of CCR5-null alleles in humans and so

45 ion can provide a molecular basis for rapid, parallel evolution of dramatic phenotypic change in natu

46 ith intratumor heterogeneity and resulted in parallel evolution of driver somatic copy-number alterat

47 This could be attributed to parallel evolution of drug resistance mutations resultin

48 Here, we review the parallel evolution of fluorescence microscopy methods an

49 Phylogenetic analysis suggests parallel evolution of gigantism in Triassic sauropterygi

50 that this taxon may instead be an example of parallel evolution of human-like traits among apes aroun

51 evelop an automated assay for monitoring the parallel evolution of hundreds of Escherichia coli popul

52 We hypothesize parallel evolution of inhibitor cystine knot toxins from

53 Thus parallel evolution of low-plated sticklebacks has occurr

54 We specifically detect parallel evolution of multiple SETD2 mutations within di

55 Here we show that the parallel evolution of petal lobe anthocyanin (PLA) pigme

56 opens up broad avenues of research into the parallel evolution of stereoscopic computations and poss

57 onary change in natural populations and that parallel evolution of stickleback low-plated phenotypes

58 te such complexity, evidence is emerging for parallel evolution of subclones, mediated through distin

59 The parallel evolution of the "same" inversion may be promot

60 onvergent evolutionary origins and massively parallel evolution of the entire transcriptomes in symbi

61 ding epidemiology of substance use demands a parallel evolution of the HIV specialist-beyond HIV to d

62 The ancient duplication of ER and the parallel evolution of the two ER isoforms suggest that,

63 Subclones displayed parallel evolution of treatment resistance in some cases

64 erichia coli thereby provide examples of the parallel evolution of two regulatory nascent chains that

65 We compared the parallel evolution of wild-type and engineered noncompet

66 Extensive within-strain parallel evolution, often involving identical nucleotide

67 independently derived, due to convergence or parallel evolution, or less likely, that they experience

68 ence of comparable evolutionary constraints (parallel evolution) rather than of functional orthology.

69 inct terminal signaling mechanism, and their parallel evolution suggested that they inhabited an equi

70 tions of the previous experiment showed less parallel evolution than the small populations of this ex

71 BDM incompatibilities commonly arise during parallel evolution, they might be virtually inevitable,

72 The surprisingly large contribution of parallel evolution to the development of the domain comb

73 Parallel evolution was also identified in non-coding reg

74 Parallel evolution was rampant, both across replicates o

75 s-if a single adaptive solution exists, then parallel evolution will be observed among highly diverge

76 etic theory predicts that the probability of parallel evolution will decline with an increase in the

77 Although parallel evolution within independent primate species is