Feng Y - Search Results

1

The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals.

Eberhart DE, Malter HE, Feng Y, Warren ST. Eberhart DE, et al. Among authors: feng y. Hum Mol Genet. 1996 Aug;5(8):1083-91. doi: 10.1093/hmg/5.8.1083. Hum Mol Genet. 1996. PMID: 8842725

2

The fragile X mental retardation protein inhibits translation via interacting with mRNA.

Li Z, Zhang Y, Ku L, Wilkinson KD, Warren ST, Feng Y. Li Z, et al. Among authors: feng y. Nucleic Acids Res. 2001 Jun 1;29(11):2276-83. doi: 10.1093/nar/29.11.2276. Nucleic Acids Res. 2001. PMID: 11376146 Free PMC article.

3

Translational suppression by trinucleotide repeat expansion at FMR1.

Feng Y, Zhang F, Lokey LK, Chastain JL, Lakkis L, Eberhart D, Warren ST. Feng Y, et al. Science. 1995 May 5;268(5211):731-4. doi: 10.1126/science.7732383. Science. 1995. PMID: 7732383

4

Quantitative comparison of FMR1 gene expression in normal and premutation alleles.

Feng Y, Lakkis L, Devys D, Warren ST. Feng Y, et al. Am J Hum Genet. 1995 Jan;56(1):106-13. Am J Hum Genet. 1995. PMID: 7825564 Free PMC article.

5

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes.

Feng Y, Gutekunst CA, Eberhart DE, Yi H, Warren ST, Hersch SM. Feng Y, et al. J Neurosci. 1997 Mar 1;17(5):1539-47. doi: 10.1523/JNEUROSCI.17-05-01539.1997. J Neurosci. 1997. PMID: 9030614 Free PMC article.

6

Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein.

Brown V, Small K, Lakkis L, Feng Y, Gunter C, Wilkinson KD, Warren ST. Brown V, et al. Among authors: feng y. J Biol Chem. 1998 Jun 19;273(25):15521-7. doi: 10.1074/jbc.273.25.15521. J Biol Chem. 1998. PMID: 9624140 Free article.

7

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association.

Feng Y, Absher D, Eberhart DE, Brown V, Malter HE, Warren ST. Feng Y, et al. Mol Cell. 1997 Dec;1(1):109-18. doi: 10.1016/s1097-2765(00)80012-x. Mol Cell. 1997. PMID: 9659908 Free article.

8

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome.

Brown V, Jin P, Ceman S, Darnell JC, O'Donnell WT, Tenenbaum SA, Jin X, Feng Y, Wilkinson KD, Keene JD, Darnell RB, Warren ST. Brown V, et al. Among authors: feng y. Cell. 2001 Nov 16;107(4):477-87. doi: 10.1016/s0092-8674(01)00568-2. Cell. 2001. PMID: 11719188 Free article.

9

A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene.

Lachiewicz AM, Spiridigliozzi GA, McConkie-Rosell A, Burgess D, Feng Y, Warren ST, Tarleton J. Lachiewicz AM, et al. Among authors: feng y. Am J Med Genet. 1996 Aug 9;64(2):278-82. doi: 10.1002/(SICI)1096-8628(19960809)64:2<278::AID-AJMG9>3.0.CO;2-Q. Am J Med Genet. 1996. PMID: 8844065

10

Destabilization and mislocalization of myelin basic protein mRNAs in quaking dysmyelination lacking the QKI RNA-binding proteins.

Li Z, Zhang Y, Li D, Feng Y. Li Z, et al. Among authors: feng y. J Neurosci. 2000 Jul 1;20(13):4944-53. doi: 10.1523/JNEUROSCI.20-13-04944.2000. J Neurosci. 2000. PMID: 10864952 Free PMC article.

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