Siomi MC - Search Results

1

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.

Zhang Y, O'Connor JP, Siomi MC, Srinivasan S, Dutra A, Nussbaum RL, Dreyfuss G. Zhang Y, et al. Among authors: siomi mc. EMBO J. 1995 Nov 1;14(21):5358-66. doi: 10.1002/j.1460-2075.1995.tb00220.x. EMBO J. 1995. PMID: 7489725 Free PMC article.

2

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein.

Siomi H, Siomi MC, Nussbaum RL, Dreyfuss G. Siomi H, et al. Among authors: siomi mc. Cell. 1993 Jul 30;74(2):291-8. doi: 10.1016/0092-8674(93)90420-u. Cell. 1993. PMID: 7688265

3

hnRNP G: sequence and characterization of a glycosylated RNA-binding protein.

Soulard M, Della Valle V, Siomi MC, Piñol-Roma S, Codogno P, Bauvy C, Bellini M, Lacroix JC, Monod G, Dreyfuss G, et al. Soulard M, et al. Among authors: siomi mc. Nucleic Acids Res. 1993 Sep 11;21(18):4210-7. doi: 10.1093/nar/21.18.4210. Nucleic Acids Res. 1993. PMID: 7692398 Free PMC article.

4

FXR1, an autosomal homolog of the fragile X mental retardation gene.

Siomi MC, Siomi H, Sauer WH, Srinivasan S, Nussbaum RL, Dreyfuss G. Siomi MC, et al. Among authors: siomi h. EMBO J. 1995 Jun 1;14(11):2401-8. doi: 10.1002/j.1460-2075.1995.tb07237.x. EMBO J. 1995. PMID: 7781595 Free PMC article.

5

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome.

Siomi H, Choi M, Siomi MC, Nussbaum RL, Dreyfuss G. Siomi H, et al. Among authors: siomi mc. Cell. 1994 Apr 8;77(1):33-9. doi: 10.1016/0092-8674(94)90232-1. Cell. 1994. PMID: 8156595

6

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them.

Siomi MC, Zhang Y, Siomi H, Dreyfuss G. Siomi MC, et al. Among authors: siomi h. Mol Cell Biol. 1996 Jul;16(7):3825-32. doi: 10.1128/MCB.16.7.3825. Mol Cell Biol. 1996. PMID: 8668200 Free PMC article.

7

A novel receptor-mediated nuclear protein import pathway.

Pollard VW, Michael WM, Nakielny S, Siomi MC, Wang F, Dreyfuss G. Pollard VW, et al. Among authors: siomi mc. Cell. 1996 Sep 20;86(6):985-94. doi: 10.1016/s0092-8674(00)80173-7. Cell. 1996. PMID: 8808633 Free article.

8

Transportin: nuclear transport receptor of a novel nuclear protein import pathway.

Nakielny S, Siomi MC, Siomi H, Michael WM, Pollard V, Dreyfuss G. Nakielny S, et al. Among authors: siomi h, siomi mc. Exp Cell Res. 1996 Dec 15;229(2):261-6. doi: 10.1006/excr.1996.0369. Exp Cell Res. 1996. PMID: 8986607 Free article.

9

Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene.

Liu Q, Siomi H, Siomi MC, Fischer U, Zhang Y, Wan L, Dreyfuss G. Liu Q, et al. Among authors: siomi h, siomi mc. Cold Spring Harb Symp Quant Biol. 1996;61:689-97. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246495 Review. No abstract available.

10

Transportin-mediated nuclear import of heterogeneous nuclear RNP proteins.

Siomi MC, Eder PS, Kataoka N, Wan L, Liu Q, Dreyfuss G. Siomi MC, et al. J Cell Biol. 1997 Sep 22;138(6):1181-92. doi: 10.1083/jcb.138.6.1181. J Cell Biol. 1997. PMID: 9298975 Free PMC article.

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