EG Allen, J Juncos, R Letz, M Rusin, D … - British Medical Journal, 2008 - jmg.bmj.com Background: Carriers of the FMR1 premutation allele are at a significantly
increased risk for a late-onset neurodegenerative disorder, fragile X-associated
tremor/ataxia syndrome (FXTAS). This disorder is distinct from fragile X ... Cited by 4 - Related articles - BL Direct - All 4 versions
… , N Dolzhanskaya, B Tournier, J Schütt, J … - Proceedings of the National Academy of Sciences, 2008 - National Acad Sciences In Iacoangeli et al. (1), five independent groups report that results published
by Zalfa et al. (2) are not reproducible. Bagni now suggests (3) that different
reagents, antibodies, or procedures might explain this lack of ... Cited by 3 - Related articles - BL Direct - All 7 versions
CS Kogan, J Turk, RJ Hagerman, KM Cornish - American Journal of Medical Genetics Part C: Seminars … - fragilex.org Cary S. Kogan,1* Jeremy Turk,2 Randi J. Hagerman,3,4 and Kim M. Cornish5,6**
1School of Psychology, University of Ottawa, Ottawa, Canada 2Division of
Clinical Developmental Sciences, St. Georges Hospital Medical School, ... Cited by 4 - Related articles - View as HTML - All 4 versions
C Bagni - Proceedings of the National Academy of Sciences, 2008 - National Acad Sciences To the editor: Iacoangeli et al. (1) set out to reexamine our model that FMRP
and the noncoding RNA BC1 act together to bind to mRNAs (2). Basing conclusions
entirely on an inability to find this specific interaction, the authors ... Cited by 4 - Related articles - All 6 versions
U Narayanan, V Nalavadi, M Nakamoto, G … - Journal of Biological Chemistry, 2008 - ASBMB Fragile X syndrome is a common form of cognitive deficit caused by the
functional absence of FMRP, a dendritic RNA-binding protein that represses
translation of specific messages. Although FMRP is phosphorylated in a ... Cited by 5 - Related articles - All 2 versions
LK Pacey, LC Doering - Glia, 2007 - interscience.wiley.com One of the most common causes of mental retardation in humans, Fragile X
syndrome, results from the absence of FMRP, the protein product of the FMR1
gene. In the nervous system, expression of FMRP has been thought to be ... Cited by 6 - Related articles - BL Direct - All 2 versions
Y Trottier, D Devys, JL Mandel - Current biology: CB, 1993 - ncbi.nlm.nih.gov 1: Curr Biol. 1993 Nov 1;3(11):783-6. An expanding story. Trottier Y, Devys
D, Mandel JL. Laboratoire de Genetique Moleculaire-Centre ... Cited by 8 - Related articles
K Fleming, DK Riser, D Kumari, K Usdin - Cytogenet Genome Res, 2003 - content.karger.com Repeat expansion diseases such as fragile X syndrome (FXS) result from increases
in the size of a specific tandem repeat array. In addition to large expansions,
small changes in repeat number and deletions are frequently seen in FXS ... Cited by 8 - Related articles - BL Direct - All 6 versions
- ►oxfordjournals.org J Rohr, EG Allen, K Charen, J Giles, W He, … - Human Reproduction, 2008 - ESHRE BACKGROUND: Women who carry the fragile X mental retardation (FMR1) premutation
are at risk for fragile X-associated primary ovarian insufficiency. Past studies
have shown that carriers who are still cycling have increased levels FSH ... Cited by 8 - Related articles - BL Direct - All 3 versions
[CITATION] FMR1 premutation allele is stable in mice
