1 1 proteins expressed in Xenopus oocytes with
phylogenic analyses of the ALMT family.
2 Phylogenic analyses revealed that oyster Jumonji cluster
3 Phylogenic analyses suggest that CBF5-CBF4 resulted from
4 mbers of informative sites for comprehensive
phylogenic analysis and greater refinement of viral link
5 gent families divided into subfamilies using
phylogenic analysis and knowledge of GPCR function.
6 Phylogenic analysis indicates that the PHPs are generall
7 Phylogenic analysis indicates that Torso is found outsid
8 Based on a
phylogenic analysis of human CD109 with other human homo
9 ent types of receptor motifs that align with
phylogenic analysis of these motifs in the FMN and Cbl r
10 Phylogenic analysis revealed A. pullorum is most closely
11 Haplotype networks and
phylogenic analysis revealed evolution of Sub1B and Sub1
12 Clustering and
phylogenic analysis reveals the potential to use these d
13 A
phylogenic analysis showed that L. aurata trypsin (LAT)
14 Phylogenic analysis showed that LeARG1 and -2, like all
15 Phylogenic analysis shows that more than half of the S.
16 Structural and
phylogenic analysis shows that while the MTPs are struct
17 Phylogenic analysis suggests that it has evolved indepen
18 Here we report
phylogenic analysis using whole genomic sequences from s
19 TORS [ARRs]) form three subfamilies based on
phylogenic analysis, with subfamily 1 having seven membe
20 nate immune lectin receptors, disrupting the
phylogenic basis of this glycomic recognition mechanism.
21 human ISG repertoires and made a genomic and
phylogenic characterization of the main gene families.
22 The InvD1L
phylogenic clade was found only in invertebrates, sugges
23 ocalized (AHL) genes, which evolved into two
phylogenic clades.
24 mited set of annotated 16S rRNA sequences or
phylogenic clustering of sequences based on arbitrary si
25 ciation is non-trivial as both can result in
phylogenic congruence.
26 This
phylogenic conservation and association with a key adhes
27 the mechanism of hedgehog signaling and the
phylogenic conservation of hedgehog function in vertebra
28 Phylogenic data show that the NH2-terminal region has ev
29 The
phylogenic dissection of MTP and apolipoprotein B functi
30 of l-mer features of whole genomes to infer
phylogenic distances.
31 To investigate the
phylogenic distribution of elicitor activity, we tested
32 We then selected nine
phylogenic diverse cutinases for recombinant production
33 Here we present
phylogenic evidence for reversal of an obligate mutualis
34 amples were sequenced and placed in a global
phylogenic framework of hundreds of BQCV strains.
35 allowed the construction of a new and robust
phylogenic genealogy of BCG strains.
36 Phylogenic investigations showed that TvPirin homologs a
37 ontained transcripts of oleosin of a novel M
phylogenic lineage.
38 d with stabilizing oleosins of at least five
phylogenic lineages and perform different functions.
39 ddition, by correlation of chemical data and
phylogenic microarray data, we identified several bacter
40 ities during the 50-day incubations by using
phylogenic microarrays and 454 pyrosequencing to identif
41 p sequence variants, those more central in a
phylogenic network than ID 1 or 55 elicited anti-fHbp an
42 rotoctista) is discussed with respect to the
phylogenic or taxonomic relationships of organisms.
43 s suggest that no clear relationship between
phylogenic organization and catalytic specificities is e
44 ino-acid attributes, predicted structure and
phylogenic patterns; and uses a combination of Inductive
45 Genotypes were analyzed for
phylogenic relatedness and genotypic composition among t
46 groESL sequencing results delineated the
phylogenic relationships among Neorickettsia spp.
47 ce on the evolution of each serovar, and the
phylogenic relationships between the serovars are of gre
48 Analysis of sequence identity profiles and
phylogenic relationships grouped chromosome blocks into
49 We report here the genomic organization and
phylogenic relationships of CD109, a member of the the a
50 By clearly resolving
phylogenic relationships, we uncovered mutated LCP1 and
51 TRAP3-18 activity are consistent with recent
phylogenic sequence analyses suggesting GTRAP3-18 and JM
52 ion within epidemiological, geographical and
phylogenic settings.
53 at intron regions contain a similar level of
phylogenic signal as do coding regions.
54 Phylogenic species trees were constructed for each indiv
55 Structural and
phylogenic studies suggest that the enzymes evolved from
56 known fossil calibration points in molecular
phylogenic studies.
57 y; the hidden states refer to the unobserved
phylogenic topology underlying the relatedness at a geno
58 Phylogenic tree analysis showed that the heavy chains of
59 The
phylogenic tree constructed of 56 ALDH sequences of huma
60 Structure-based sequence analysis and
phylogenic tree construction reveal determinants of subs
61 A
phylogenic tree including 36 Y. pestis strains highlight
62 osomal RFLPs were analyzed, a ribotype-based
phylogenic tree was constructed, and case-control and co
63 in and among species and mapping them onto a
phylogenic tree.
64 otein that occupies a distinct branch in the
phylogenic tree.
65 by analyzing subcompositions defined on the
phylogenic tree.
66 From these data,
phylogenic trees have been constructed that define popul
67 pan several kingdoms, sequence alignment and
phylogenic trees strongly suggest an evolutionary link a
68 Protein
phylogenic trees were constructed using both the maximum
69 hese results suggest that HAI may complement
phylogenic variant assignment, providing additional insi
70 FHbp is classified in three
phylogenic variant groups that have limited antigenic cr
71 ell for SEB and TSST-1, two widely different
phylogenic variants, suggests that the DRalpha1-linker-T