Bardoni B - Search Results

1

Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo.

Mientjes EJ, Willemsen R, Kirkpatrick LL, Nieuwenhuizen IM, Hoogeveen-Westerveld M, Verweij M, Reis S, Bardoni B, Hoogeveen AT, Oostra BA, Nelson DL. Mientjes EJ, et al. Among authors: bardoni b. Hum Mol Genet. 2004 Jul 1;13(13):1291-302. doi: 10.1093/hmg/ddh150. Epub 2004 May 5. Hum Mol Genet. 2004. PMID: 15128702

2

The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapse.

Zongaro S, Hukema R, D'Antoni S, Davidovic L, Barbry P, Catania MV, Willemsen R, Mari B, Bardoni B. Zongaro S, et al. Among authors: bardoni b. Hum Mol Genet. 2013 May 15;22(10):1971-82. doi: 10.1093/hmg/ddt044. Epub 2013 Feb 5. Hum Mol Genet. 2013. PMID: 23390134

3

Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis.

Khandjian EW, Bardoni B, Corbin F, Sittler A, Giroux S, Heitz D, Tremblay S, Pinset C, Montarras D, Rousseau F, Mandel J. Khandjian EW, et al. Among authors: bardoni b. Hum Mol Genet. 1998 Dec;7(13):2121-8. doi: 10.1093/hmg/7.13.2121. Hum Mol Genet. 1998. PMID: 9817930

4

Reduction of Fmr1 mRNA Levels Rescues Pathological Features in Cortical Neurons in a Model of FXTAS.

Drozd M, Delhaye S, Maurin T, Castagnola S, Grossi M, Brau F, Jarjat M, Willemsen R, Capovilla M, Hukema RK, Lalli E, Bardoni B. Drozd M, et al. Among authors: bardoni b. Mol Ther Nucleic Acids. 2019 Dec 6;18:546-553. doi: 10.1016/j.omtn.2019.09.018. Epub 2019 Sep 26. Mol Ther Nucleic Acids. 2019. PMID: 31671347 Free PMC article.

5

NUFIP1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomes.

Bardoni B, Willemsen R, Weiler IJ, Schenck A, Severijnen LA, Hindelang C, Lalli E, Mandel JL. Bardoni B, et al. Exp Cell Res. 2003 Sep 10;289(1):95-107. doi: 10.1016/s0014-4827(03)00222-2. Exp Cell Res. 2003. PMID: 12941608

6

FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.

Castets M, Schaeffer C, Bechara E, Schenck A, Khandjian EW, Luche S, Moine H, Rabilloud T, Mandel JL, Bardoni B. Castets M, et al. Among authors: bardoni b. Hum Mol Genet. 2005 Mar 15;14(6):835-44. doi: 10.1093/hmg/ddi077. Epub 2005 Feb 9. Hum Mol Genet. 2005. PMID: 15703194

7

A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein.

Bardoni B, Schenck A, Mandel JL. Bardoni B, et al. Hum Mol Genet. 1999 Dec;8(13):2557-66. doi: 10.1093/hmg/8.13.2557. Hum Mol Genet. 1999. PMID: 10556305

8

FMR1 gene and fragile X syndrome.

Bardoni B, Mandel JL, Fisch GS. Bardoni B, et al. Am J Med Genet. 2000 Summer;97(2):153-63. doi: 10.1002/1096-8628(200022)97:2<153::aid-ajmg7>3.0.co;2-m. Am J Med Genet. 2000. PMID: 11180223 Review.

9

The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.

Davidovic L, Bechara E, Gravel M, Jaglin XH, Tremblay S, Sik A, Bardoni B, Khandjian EW. Davidovic L, et al. Among authors: bardoni b. Hum Mol Genet. 2006 May 1;15(9):1525-38. doi: 10.1093/hmg/ddl074. Epub 2006 Mar 28. Hum Mol Genet. 2006. PMID: 16571602

10

Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients.

Davidovic L, Sacconi S, Bechara EG, Delplace S, Allegra M, Desnuelle C, Bardoni B. Davidovic L, et al. Among authors: bardoni b. J Med Genet. 2008 Oct;45(10):679-85. doi: 10.1136/jmg.2008.060541. Epub 2008 Jul 15. J Med Genet. 2008. PMID: 18628314

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