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1 one-cell stage embryo of its close relative Caenorhabditis briggsae.
2 rescued by the CbRh1 homologue from the worm Caenorhabditis briggsae.
3 srz genes in C. elegans and 28 srz genes in Caenorhabditis briggsae.
4 regulatory sequences are highly conserved in Caenorhabditis briggsae.
5 d near-perfect order in the related nematode Caenorhabditis briggsae.
6 habditis elegans and the partial sequence of Caenorhabditis briggsae.
7 we sequenced uaf-1 from the related nematode Caenorhabditis briggsae.
8 c offspring in the self-fertilizing nematode Caenorhabditis briggsae.
9 nsposon is active in C. elegans isolates and 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
16 ies of self-fertilizing rhabditid nematodes, Caenorhabditis briggsae and C. elegans, which the eviden
17 analysis of important signaling pathways in Caenorhabditis briggsae and Caenorhabditis elegans revea
18 small let-7 RNAs in Caenorhabditis elegans, Caenorhabditis briggsae and Drosophila melanogaster geno
19 rgenic regions of Caenorhabditis elegans and Caenorhabditis briggsae and found a mosaic pattern with
20 prising 86 of the 88 genes) are conserved in Caenorhabditis briggsae, and 22 families are conserved i
21 umber of Tc3-like transposons in C. elegans, Caenorhabditis briggsae, and Drosophila melanogaster, wh
22 ral cells in both Caenorhabditis elegans and Caenorhabditis briggsae, but acts in the excretory duct
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 between the closely related nematode species Caenorhabditis briggsae (Cbr) and Caenorhabditis elegans
28 fitness in the same strains: two strains of Caenorhabditis briggsae decline in body size about twice
29 rkhead genes in the closely related nematode Caenorhabditis briggsae does not appear to correspond co
30 es of homologous genes between C.elegans and Caenorhabditis briggsae for 26 GC-AG introns, the C at t
32 WABA was used to align 8 million bases of Caenorhabditis briggsae genomic DNA against the entire 9
33 show that in the convergently hermaphroditic Caenorhabditis briggsae, GLD-1 acts to promote oogenesis
34 tive analyses of the closely related species Caenorhabditis briggsae have been integrated into WormBa
35 ode Caenorhabditis elegans and its relative, Caenorhabditis briggsae Here, we report on a collection
36 omology search of EST data banks retrieved a Caenorhabditis briggsae homolog of BRI, indicating that
37 We have identified, cloned and sequenced the Caenorhabditis briggsae homologue of the C. elegans gene
39 ndently in C. elegans and its close relative Caenorhabditis briggsae; (ii) there is a large degree of
40 of orthologous HS genes from C. elegans and Caenorhabditis briggsae indicated that the identified DN
41 e genomic sequence from the related nematode Caenorhabditis briggsae indicates that it also has a lar
42 size and shape, which were also observed in Caenorhabditis briggsae, indicating evolutionary conserv
44 nized Serratia species, termed South African Caenorhabditis briggsae isolate (SCBI), is both a mutual
45 (SCBI), is both a mutualist of the nematode Caenorhabditis briggsae KT0001 and a pathogen of lepidop
46 ulatory region of Caenorhabditis elegans and Caenorhabditis briggsae mab-9, a T-box gene known to be
47 parative sequence analysis of C. elegans and Caenorhabditis briggsae mec-4 genes was used to initiate
50 of the nematodes Caenorhabditis elegans and Caenorhabditis briggsae provide an excellent opportunity
52 ing the nematodes Caenorhabditis elegans and Caenorhabditis briggsae, respectively, were recently ide
53 ty cultures of a different nematode species, Caenorhabditis briggsae, resulting in part from deletion
54 ies, and comparisons with a few orthologs in Caenorhabditis briggsae, reveal ongoing processes of gen
55 ht C. elegans (Orsay virus) and its relative Caenorhabditis briggsae (Santeuil virus, Le Blanc virus,
56 lso present results from the WGS assembly of Caenorhabditis briggsae sequenced to about 11x coverage.
57 onal genomic analysis between C. elegans and Caenorhabditis briggsae to characterize the CSR-1 pathwa
58 cloned and compared in the related organism Caenorhabditis briggsae to identify evolutionarily conse
61 o restore mss function to the androdioecious Caenorhabditis briggsae, we examined how mating system a
63 1.1-kb element to homologous sequences from Caenorhabditis briggsae, we identified evolutionarily co
64 and Santeuil, which both specifically infect Caenorhabditis briggsae, were also found to form fibrous
65 investigate this issue by using the nematode Caenorhabditis briggsae, which reproduces as a hermaphro
66 cterize the selenoproteomes of C.elegans and Caenorhabditis briggsae with three independent algorithm
67 g an independent introgression fragment from Caenorhabditis briggsae X Chromosome in an otherwise Cae