| P2093 | author name string | David Stiles | |
| | Karen Usdin | |
| | Vaishali Handa | |
| | Daman Kumari | |
| | George Poy | |
| | Margaret Cam | |
| | Deena Goldwater | |
| P2860 | cites work | Fragile X genotype characterized by an unstable region of DNA. | Q43980470 |
| | Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n | Q44229778 |
| | Decreased cAMP response element-mediated transcription: an early event in exon 1 and full-length cell models of Huntington's disease that contributes to polyglutamine pathogenesis | Q44662096 |
| | Neuronal dysfunction in a polyglutamine disease model occurs in the absence of ubiquitin-proteasome system impairment and inversely correlates with the degree of nuclear inclusion formation | Q45295822 |
| | Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons. | Q45296540 |
| | Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | Q46124789 |
| | CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein. | Q46960848 |
| | RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | Q47071910 |
| | Fragile X premutations in familial premature ovarian failure | Q57943475 |
| | Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles | Q24610645 |
| | Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method | Q25938999 |
| | Summaries of Affymetrix GeneChip probe level data | Q27860888 |
| | A fragile balance: FMR1 expression levels | Q28204712 |
| | The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome | Q28507736 |
| | Studies of FRAXA and FRAXE in women with premature ovarian failure | Q33681082 |
| | Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome. | Q34146206 |
| | Premature ovarian failure in the fragile X syndrome | Q34306135 |
| | Nonapoptotic neurodegeneration in a transgenic mouse model of Huntington's disease | Q35176635 |
| | Transcription defects induced by repeat expansion: fragile X syndrome, FRAXE mental retardation, progressive myoclonus epilepsy type 1, and Friedreich ataxia | Q35550055 |
| | The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer | Q37369000 |
| | Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice | Q38335797 |
| | Parkin facilitates the elimination of expanded polyglutamine proteins and leads to preservation of proteasome function. | Q40658225 |
| | Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families | Q43728556 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 2702-2708 | |
| P577 | publication date | 2005-04-18 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | Long CGG-repeat tracts are toxic to human cells: implications for carriers of Fragile X premutation alleles | |
| P478 | volume | 579 | |