Mandel JL - Search Results

1

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.

Schaeffer C, Bardoni B, Mandel JL, Ehresmann B, Ehresmann C, Moine H. Schaeffer C, et al. Among authors: mandel jl. EMBO J. 2001 Sep 3;20(17):4803-13. doi: 10.1093/emboj/20.17.4803. EMBO J. 2001. PMID: 11532944 Free PMC article.

2

The chicken dystrophin cDNA: striking conservation of the C-terminal coding and 3' untranslated regions between man and chicken.

Lemaire C, Heilig R, Mandel JL. Lemaire C, et al. Among authors: mandel jl. EMBO J. 1988 Dec 20;7(13):4157-62. doi: 10.1002/j.1460-2075.1988.tb03311.x. EMBO J. 1988. PMID: 3072195 Free PMC article.

3

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation.

Devys D, Lutz Y, Rouyer N, Bellocq JP, Mandel JL. Devys D, et al. Among authors: mandel jl. Nat Genet. 1993 Aug;4(4):335-40. doi: 10.1038/ng0893-335. Nat Genet. 1993. PMID: 8401578

4

Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms.

Sittler A, Devys D, Weber C, Mandel JL. Sittler A, et al. Among authors: mandel jl. Hum Mol Genet. 1996 Jan;5(1):95-102. doi: 10.1093/hmg/5.1.95. Hum Mol Genet. 1996. PMID: 8789445

5

Analysis of domains affecting intracellular localization of the FMRP protein.

Bardoni B, Sittler A, Shen Y, Mandel JL. Bardoni B, et al. Among authors: mandel jl. Neurobiol Dis. 1997;4(5):329-36. doi: 10.1006/nbdi.1997.0142. Neurobiol Dis. 1997. PMID: 9440121

6

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. Hum Mol Genet. 1998 Dec;7(13):2121-8. doi: 10.1093/hmg/7.13.2121. Hum Mol Genet. 1998. PMID: 9817930

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. Among authors: mandel jl. Hum Mol Genet. 1999 Dec;8(13):2557-66. doi: 10.1093/hmg/8.13.2557. Hum Mol Genet. 1999. PMID: 10556305

8

Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12.

Bardoni B, Giglio S, Schenck A, Rocchi M, Mandel JL. Bardoni B, et al. Among authors: mandel jl. Cytogenet Cell Genet. 2000;89(1-2):11-3. doi: 10.1159/000015580. Cytogenet Cell Genet. 2000. PMID: 10894927 No abstract available.

9

FMR1 gene and fragile X syndrome.

Bardoni B, Mandel JL, Fisch GS. Bardoni B, et al. Among authors: mandel jl. 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.

10

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P.

Schenck A, Bardoni B, Moro A, Bagni C, Mandel JL. Schenck A, et al. Among authors: mandel jl. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8844-9. doi: 10.1073/pnas.151231598. Epub 2001 Jul 3. Proc Natl Acad Sci U S A. 2001. PMID: 11438699 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

388 results

Search Page

Filters