ライフサイエンスコーパス: phyletic

1 nonical biomass relations are insensitive to phyletic affiliation (conifers versus angiosperms) and v

2 mainly taxa of Eurasiatic zoogeographic and phyletic affinities, including the first North American

3 Furthermore, phyletic analyses of fitness differences suggested that,

4 this transition are crucial for defining the phyletic body plan and that the mid-developmental transi

5 Conservation of phyletic body plans may have been due to the retention s

6 nique binding sites and identified the major phyletic branches with the largest expansion in the numb

7 associated with extensive evolution on long phyletic branches.

8 heir further investigation may reveal common phyletic conditions and neural substrates underlying the

9 Our key finding was a pattern of phyletic decline in the three most potent resistance tra

10 nd enzyme class of adenosine deaminase whose phyletic distribution among prokaryotes is broad.

11 Phyletic distribution analysis confirms three clusters o

12 in tetrahydromonapterin synthesis via their phyletic distribution and chromosomal clustering pattern

13 GPCR phyletic distribution closely paralleled that of pNPs, i

14 Ten subfamilies show a universal phyletic distribution compatible with presence in the la

15 The U3 nucleolar RNA has a remarkably wide phyletic distribution extending from the Eukarya to the

16 of identified genes; and (ii) estimating the phyletic distribution of constituent microbial species.

17 groups and allowed the reconstruction of the phyletic distribution of receptor families.

18 l gene transfer contributed to the scattered phyletic distribution of the gene fusions.

19 l GlnRS form a monophyletic group, the broad phyletic distribution of this tRNA synthetase suggests t

20 o distinct families and examination of their phyletic distribution suggests that the evolution of thi

21 Phyletic distributions of eukaryotic signalling domains

22 the nearly perfect complementarity of their phyletic distributions suggest that HerA similarly media

23 ntarctic Ocean at 10-14 mya, and of the main phyletic divergence of the AFGP-bearing notothenioid fam

24 On this basis, 'phyletic dwarfs' are predicted to have a greater relativ

25 l detail have instead introduced substantial phyletic error.

26 s, in total, seem consistent with continuous phyletic evolution of temporal trajectories.

27 involving either replacement or accelerated phyletic evolution.

28 daptive substitutions may not be uncommon in phyletic evolution.

29 that body size evolved directionally toward phyletic giantism an order of magnitude faster in therop

30 to have a greater relative brain size than 'phyletic giants'.

31 the best-documented cases of within-lineage phyletic gradualism and, in doing so, revisit the limita

32 gical change without lineage division (e.g., phyletic gradualism or gradual evolution), which has rai

33 y between MHC class I loci in genera of this phyletic group.

34 analyses also revealed the existence of CspZ phyletic groups that correlate with FH binding and with

35 We found that phyletic hierarchical cluster and linear regression netw

36 ysis revealed that the isolate belonged to a phyletic lineage of environmental V. cholerae isolates a

37 Thus, the phyletic link between reef and nonreef communities may h

38 yperthermophily using a flexible approach to phyletic pattern analysis.

39 either a graphical interface or a text-based Phyletic Pattern Expression grammar.

40 Through a systematic study of the phyletic pattern, we show that this WRKY-GCM1 superfamil

41 sequence profile searches, phylogenetic and phyletic-pattern analysis and structure-prediction.

42 Ortholog groups exhibiting specific phyletic patterns may also be identified, using either a

43 Analysis of the phyletic patterns suggests that at least five distinct H

44 Using the phyletic phenocopy paradigm, we draw attention to many w

45 imes in disjoint parts of the code through a phyletic process of competition between lineages.

46 Information for ortholog groups includes the phyletic profile, the list of member proteins and a mult

47 Phyletic relations among haplotypes are largely reticula

48 To date all attempts to derive a phyletic relationship among restriction endonucleases (E

49 imensional (3D) approach for visualizing the phyletic relationship of living animals is proposed and

50 heir receptors can provide information about phyletic relationships and evolutionary processes.

51 ctional organization, and the probable close phyletic relationships of this "family" of hair cell sen

52 their receptors may be useful in determining phyletic relationships.

53 Phyletic representation was more similar within sites th

54 nd is largely responsible for the remarkable phyletic selectivity of omega-atracotoxin-Hv1a.

55 unction in arthropods or insects after their phyletic separation from the annelids.

56 The phyletic specificity of Ae1a provides crucial informatio

57 on these criteria, the chief one being wide phyletic spread, we offer two 'top 10' lists of highly a

58 Although three FhbB phyletic types have been defined (FhbB1, FhbB2, and FhbB