ライフサイエンスコーパス: Caenorhabditis elegans protein

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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 report that CED-8, a Caenorhabditis elegans protein implicated in controlling

12 I has strong sequence similarity to EAT-4, a Caenorhabditis elegans protein implicated in glutamaterg

13 Caenorhabditis elegans protein kinase A (PKAI(CE)) is te

14 Caenorhabditis elegans protein kinase C adapter proteins

15 Here, we show that the Caenorhabditis elegans protein LAF-1, a DDX3 RNA helicas

16 These include the Caenorhabditis elegans protein LAF-1, which forms P gran

17 domain and shares sequence homology with the Caenorhabditis elegans protein, Mig-10, involved in embr

18 PSAP) shares a significant similarity with a Caenorhabditis elegans protein of unknown function.

19 ein product bears homology to CELF37C12.2, a Caenorhabditis elegans protein of unknown function.

20 ed subfamily of four proteins, including two Caenorhabditis elegans proteins of as yet unknown functi

21 xxWxxx GYF), also found in several yeast and Caenorhabditis elegans proteins of unknown function.

22 es 64% sequence identity with a hypothetical Caenorhabditis elegans protein, presumably the p66 homol

23 n-protein and protein-RNA interactions among Caenorhabditis elegans proteins required for NMD.

24 ith the Escherichia coli and the presumptive Caenorhabditis elegans proteins, respectively, and conta

25 Two mammalian homologs of the Caenorhabditis elegans protein Ric-8 were identified in

26 The Src-homology-3 (SH3) domain of the Caenorhabditis elegans protein Sem-5 binds proline-rich

27 n and is a functional homologue of SEL-12, a Caenorhabditis elegans protein that facilitates signalli

28 (Rcm) is highly similar to that of UNC-5, a Caenorhabditis elegans protein that is essential for dor

29 unction as transcriptional activators, and a Caenorhabditis elegans protein that is thought to functi

30 We have identified a complex of interacting Caenorhabditis elegans proteins that are involved in the

31 Kindlin-1 is a human homolog of the Caenorhabditis elegans protein UNC-112, a membrane-assoc

32 regions (SUN (Sad1 and UNC) domain) with the Caenorhabditis elegans protein UNC-84 whose mutation dis

33 a biological role for HSBP1, the homologous Caenorhabditis elegans protein was overexpressed in body

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