ライフサイエンスコーパス: genetic evolution

1 our model invokes realistic trends of HIV-1 genetic evolution.

2 important similarities in their patterns of genetic evolution.

3 ls can be used to study metastasis and tumor genetic evolution.

4 d among populations, which I call collateral genetic evolution.

5 ering their immune resistance as a result of genetic evolution.

6 pports and supplements the standard model of genetic evolution.

7 els with, as well as clear differences from, genetic evolution.

8 ssibly Alzheimer's disease, but also due its genetic evolution and complex alternative splicing featu

9 utagenic in mammals, perhaps contributing to genetic evolution and disease.

10 Our findings highlight ongoing genetic evolution and high diversity of circulating RSV-

11 ion tumor-sequencing approach highlights the genetic evolution and non-UVB mutational signatures asso

12 orts on the application of WGS to understand genetic evolution and reconstruct transmission pathways

13 preeminent model system to understand phage genetics, evolution and ecology in obligate intracellula

14 Antigenic evolution was more punctuated than genetic evolution, and genetic change sometimes had a di

15 population size and range have affected our genetic evolution, and recent modeling efforts have reaf

16 rry important implications for complex trait genetics, evolution, and medicine.

17 ary viral sequence diversity and rapid viral genetic evolution are hallmarks of hepatitis C virus (HC

18 ironment we find (1) a high rate of parallel genetic evolution at orthologous nucleotide and amino ac

19 al organisms often show evidence of parallel genetic evolution, but the causes are unclear.

20 nd simultaneously characterize antigenic and genetic evolution by modeling the diffusion of antigenic

21 Furthermore, cultural and genetic evolution can interact with one another and infl

22 finding indicates that cultural change, like genetic evolution, can follow theoretically derived patt

23 tion of genetic variants, different rates of genetic evolution could be found under different selecti

24 tween parasite-stress and cultural outcomes: genetic evolution, developmental plasticity, neurocognit

25 ochastic factors and purifying selection for genetic evolution differs over, at least, three broad in

26 istory of extinct species and to investigate genetic evolution directly.

27 pplications are also predicted in population genetics, evolution, earth sciences, and economics.

28 on of proteomics to the fields of behavioral genetics, evolution, ecology and population dynamics, an

29 The genetic evolution from a benign neurofibroma to a malign

30 can we identify the 'smoking guns' of human genetic evolution from neutral ticks of the molecular ev

31 recent progress in defining the patterns of genetic evolution giving rise to relapse in follicular l

32 Our results suggest that the continuous genetic evolution has not led to significant antigenic d

33 Empirically observed neutral genetic evolution in extremely large clonal populations

34 To investigate genetic evolution in high-grade serous (HGS) ovarian can

35 Sequential analysis in del(5q)-MDS revealed genetic evolution in MDS-SCs and MDS-progenitors prior t

36 Genetic evolution is constrained by gene function, the s

37 al influenza is generally S-shaped while the genetic evolution is half-circle shaped.

38 Our findings show that parallel genetic evolution is strongly biased by constraints and

39 of cultural evolution, inspired by models of genetic evolution, lend support to the former and do not

40 nomic and phylogenetic analyses suggest that genetic evolution may have led to the enhanced virulence

41 n of recent shared ancestry is important for genetics, evolution, medicine, conservation biology, and

42 The genetic evolution of a large population undergoing mutag

43 Thus, genetic evolution of arsS may influence progression to h

44 Although human tumours are shaped by the genetic evolution of cancer cells, evidence also suggest

45 evolving cultural traits, together with the genetic evolution of commensals and parasites that have

46 Here we trace the genetic evolution of EBOV in the current outbreak that h

47 f cell-associated viral DNA and mRNA and the genetic evolution of HIV-1 in seven acutely infected pat

48 The genetic evolution of human immunodeficiency virus type 1

49 een humans and mice and has an impact on the genetic evolution of human sex chromosomes.

50 -existing EGFR(T790M)-positive clones or via genetic evolution of initially EGFR(T790M)-negative drug

51 ccount of mirror neurons should not preclude genetic evolution of its underlying mechanisms.

52 populations reunite, even in the absence of genetic evolution of mate preference.

53 selection as a viable strategy for mimicking genetic evolution of materials as it occurs in nature.

54 A better understanding of the genetic evolution of metastatic disease has the potentia

55 these model systems, our study examines the genetic evolution of metastatic phenotypes.

56 tributed to the extraordinarily rapid recent genetic evolution of our species.

57 A quantitative analysis of the timing of the genetic evolution of pancreatic cancer was performed, in

58 histocompatibility complex can influence the genetic evolution of pathogenic retroviruses in vivo.

59 findings show that LINE-1 contributes to the genetic evolution of PDAC and suggest that somatic inser

60 Genetic evolution of pneumococcal clones from Taiwan(19F

61 Genetic evolution of secondary AML is a dynamic process

62 We conclude that parallel genetic evolution of separate metastatic sites with diff

63 e epigenetic silencing mechanism impacts the genetic evolution of sex chromosomes and contributed to

64 itical role of persistent replication in the genetic evolution of SIV.

65 curious parallel noted by Darwin between the genetic evolution of species and the cultural evolution

66 invention that could not have influenced the genetic evolution of the cortex.

67 Therefore, the genetic evolution of the M gene in H9N2 virus increases

68 Genetic evolution of the simian immunodeficiency virus (

69 pect to the extent of persistent viremia and genetic evolution of the V1 region of envelope.

70 cancer patients in order to reconstruct the genetic evolution of these viruses.

71 These results suggest that genetic evolution of this common colonic commensal has r

72 We have investigated the genetic evolution of three functionally distinct regions

73 ther tools to study genetic similarities and genetic evolution of viral quasispecies.

74 ired to definitively determine the effect of genetic evolution on the inferred hierarchies.

75 correlation between viral setpoint and HIV-1 genetic evolution over time is important in the understa

76 n in the brain progressed with a nonspecific genetic evolution, recurrent migration events, and an ex

77 arkable correspondence between antigenic and genetic evolution, significant differences were observed

78 Genetic evolution that occurs during cancer progression

79 l be needed to completely characterize human genetic evolution, these uniparentally inherited loci ar

80 ks cultural evolution to group selection and genetic evolution to individual selection, this associat

81 ate rates of CD4 T cell loss correlated with genetic evolution within three of four subjects.