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1 rescued by the CbRh1 homologue from the worm Caenorhabditis briggsae.
2  srz genes in C. elegans and 28 srz genes in Caenorhabditis briggsae.
3 regulatory sequences are highly conserved in Caenorhabditis briggsae.
4 d near-perfect order in the related nematode Caenorhabditis briggsae.
5 habditis elegans and the partial sequence of Caenorhabditis briggsae.
6 nsposon is active in C. elegans isolates and Caenorhabditis briggsae.
7 we sequenced uaf-1 from the related nematode Caenorhabditis briggsae.
8 c offspring in the self-fertilizing nematode Caenorhabditis briggsae.
9  one-cell stage embryo of its close relative Caenorhabditis briggsae.
10  TRA-1-binding sites in the related nematode Caenorhabditis briggsae, 19 of which are conserved betwe
11 availability of the whole genome sequence of Caenorhabditis briggsae, a closely related nematode to C
12 dition, we have cloned a XOL-1 ortholog from Caenorhabditis briggsae, a related nematode that diverge
13                       Comparative studies of Caenorhabditis briggsae and C. elegans have provided ins
14                                              Caenorhabditis briggsae and C. elegans have similar demo
15 ies of self-fertilizing rhabditid nematodes, Caenorhabditis briggsae and C. elegans, which the eviden
16  analysis of important signaling pathways in Caenorhabditis briggsae and Caenorhabditis elegans revea
17  small let-7 RNAs in Caenorhabditis elegans, Caenorhabditis briggsae and Drosophila melanogaster geno
18 rgenic regions of Caenorhabditis elegans and Caenorhabditis briggsae and found a mosaic pattern with
19 prising 86 of the 88 genes) are conserved in Caenorhabditis briggsae, and 22 families are conserved i
20 umber of Tc3-like transposons in C. elegans, Caenorhabditis briggsae, and Drosophila melanogaster, wh
21 ral cells in both Caenorhabditis elegans and Caenorhabditis briggsae, but acts in the excretory duct
22 ww.ensembl.org as ESTgenes for the mosquito, Caenorhabditis briggsae, C. elegans, zebrafish, human, m
23  species in the nematode family Rhabditidae (Caenorhabditis briggsae, Caenorhabditis elegans, and Osc
24 resence and absence of C. elegans operons in Caenorhabditis briggsae, Caenorhabditis remanei, and Cae
25                 Using Caenorhabditis elegans-Caenorhabditis briggsae comparison, CompareProspector fo
26  in the environmental RNAi defective species Caenorhabditis briggsae, confers environmental RNAi.
27  fitness in the same strains: two strains of Caenorhabditis briggsae decline in body size about twice
28 rkhead genes in the closely related nematode Caenorhabditis briggsae does not appear to correspond co
29 es of homologous genes between C.elegans and Caenorhabditis briggsae for 26 GC-AG introns, the C at t
30 nes are also clustered in the C. elegans and Caenorhabditis briggsae genomes.
31    WABA was used to align 8 million bases of Caenorhabditis briggsae genomic DNA against the entire 9
32 show that in the convergently hermaphroditic Caenorhabditis briggsae, GLD-1 acts to promote oogenesis
33 tive analyses of the closely related species Caenorhabditis briggsae have been integrated into WormBa
34 omology search of EST data banks retrieved a Caenorhabditis briggsae homolog of BRI, indicating that
35 We have identified, cloned and sequenced the Caenorhabditis briggsae homologue of the C. elegans gene
36                                          The Caenorhabditis briggsae homologue of the Caenorhabditis
37 ndently in C. elegans and its close relative Caenorhabditis briggsae; (ii) there is a large degree of
38  of orthologous HS genes from C. elegans and Caenorhabditis briggsae indicated that the identified DN
39 e genomic sequence from the related nematode Caenorhabditis briggsae indicates that it also has a lar
40  size and shape, which were also observed in Caenorhabditis briggsae, indicating evolutionary conserv
41                                 The nematode Caenorhabditis briggsae is a model for comparative devel
42 nized Serratia species, termed South African Caenorhabditis briggsae isolate (SCBI), is both a mutual
43  (SCBI), is both a mutualist of the nematode Caenorhabditis briggsae KT0001 and a pathogen of lepidop
44 ulatory region of Caenorhabditis elegans and Caenorhabditis briggsae mab-9, a T-box gene known to be
45 parative sequence analysis of C. elegans and Caenorhabditis briggsae mec-4 genes was used to initiate
46                      We first identified the Caenorhabditis briggsae orthologue of itr-1, Cbitr-1.
47  of the nematodes Caenorhabditis elegans and Caenorhabditis briggsae provide an excellent opportunity
48                                              Caenorhabditis briggsae provides a natural comparison sp
49 ing the nematodes Caenorhabditis elegans and Caenorhabditis briggsae, respectively, were recently ide
50 ty cultures of a different nematode species, Caenorhabditis briggsae, resulting in part from deletion
51 ies, and comparisons with a few orthologs in Caenorhabditis briggsae, reveal ongoing processes of gen
52 lso present results from the WGS assembly of Caenorhabditis briggsae sequenced to about 11x coverage.
53 onal genomic analysis between C. elegans and Caenorhabditis briggsae to characterize the CSR-1 pathwa
54  cloned and compared in the related organism Caenorhabditis briggsae to identify evolutionarily conse
55             We demonstrate that the nematode Caenorhabditis briggsae tra-2 gene and the human oncogen
56                                           In Caenorhabditis briggsae, we also find an MX-dependent in
57  1.1-kb element to homologous sequences from Caenorhabditis briggsae, we identified evolutionarily co
58 cterize the selenoproteomes of C.elegans and Caenorhabditis briggsae with three independent algorithm
59 g an independent introgression fragment from Caenorhabditis briggsae X Chromosome in an otherwise Cae

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