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1   This position is conserved in a homologous Caenorhabditis elegans protein.
2 ar to previously identified mouse, human and Caenorhabditis elegans proteins.
3 e mammalian proteins FADD and Apaf-1 and the Caenorhabditis elegans protein CED-4.
4                        Here we show that the Caenorhabditis elegans protein CLR-1 (CLeaR) is a recept
5                             We find that the Caenorhabditis elegans protein DAF-16 binds the IGFBP-1
6 stances between Saccharomyces cerevisiae and Caenorhabditis elegans proteins did not reveal any diffe
7                       Here, we show that the Caenorhabditis elegans protein DPY-28 controls two such
8 melanogaster proteins Ash2 and Trithorax and Caenorhabditis elegans protein DPY-30, which are implica
9 ricopeptide repeat protein homologous to the Caenorhabditis elegans protein DYF1 that was highly expr
10 , -2, and -3 are mammalian homologs LIN-7, a Caenorhabditis elegans protein essential for vulval deve
11                       Here we identified the Caenorhabditis elegans protein huntingtin-interacting pr
12                 Here we report that CED-8, a Caenorhabditis elegans protein implicated in controlling
13 I has strong sequence similarity to EAT-4, a Caenorhabditis elegans protein implicated in glutamaterg
14                                              Caenorhabditis elegans protein kinase A (PKAI(CE)) is te
15                                              Caenorhabditis elegans protein kinase C adapter proteins
16                       Here, we show that the Caenorhabditis elegans protein LAF-1, a DDX3 RNA helicas
17                            These include the Caenorhabditis elegans protein LAF-1, which forms P gran
18 domain and shares sequence homology with the Caenorhabditis elegans protein, Mig-10, involved in embr
19 active zone (AZ). We previously identified a Caenorhabditis elegans protein named Clarinet (CLA-1) ba
20 this pipeline with a study of five conserved Caenorhabditis elegans proteins-NEKL-2, NEKL-3, MLT-2, M
21 PSAP) shares a significant similarity with a Caenorhabditis elegans protein of unknown function.
22 ein product bears homology to CELF37C12.2, a Caenorhabditis elegans protein of unknown function.
23 ed subfamily of four proteins, including two Caenorhabditis elegans proteins of as yet unknown functi
24 xxWxxx GYF), also found in several yeast and Caenorhabditis elegans proteins of unknown function.
25 es 64% sequence identity with a hypothetical Caenorhabditis elegans protein, presumably the p66 homol
26 re, we report the identification of PLP-1, a Caenorhabditis elegans protein related to the human sing
27 n-protein and protein-RNA interactions among Caenorhabditis elegans proteins required for NMD.
28 ith the Escherichia coli and the presumptive Caenorhabditis elegans proteins, respectively, and conta
29                Two mammalian homologs of the Caenorhabditis elegans protein Ric-8 were identified in
30       The Src-homology-3 (SH3) domain of the Caenorhabditis elegans protein Sem-5 binds proline-rich
31 n and is a functional homologue of SEL-12, a Caenorhabditis elegans protein that facilitates signalli
32  (Rcm) is highly similar to that of UNC-5, a Caenorhabditis elegans protein that is essential for dor
33 unction as transcriptional activators, and a Caenorhabditis elegans protein that is thought to functi
34  We have identified a complex of interacting Caenorhabditis elegans proteins that are involved in the
35          Kindlin-1 is a human homolog of the Caenorhabditis elegans protein UNC-112, a membrane-assoc
36 regions (SUN (Sad1 and UNC) domain) with the Caenorhabditis elegans protein UNC-84 whose mutation dis
37  a biological role for HSBP1, the homologous Caenorhabditis elegans protein was overexpressed in body