| Q89748818 | A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis |
| Q30475341 | Antioxidants improve early survival of cardiomyoblasts after transplantation to the myocardium |
| Q28740984 | Association of FMR1 genotypes with in vitro fertilization (IVF) outcomes based on ethnicity/race |
| Q34416088 | BRCA1/2 mutations appear embryo-lethal unless rescued by low (CGG n<26) FMR1 sub-genotypes: explanation for the "BRCA paradox"? |
| Q39866921 | CGG Repeat-Associated Non-AUG Translation Utilizes a Cap-Dependent Scanning Mechanism of Initiation to Produce Toxic Proteins |
| Q42068973 | CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome |
| Q37021134 | CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome. |
| Q34955465 | CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS |
| Q33649307 | CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size. |
| Q48730129 | Can the FMR1 (fragile X) gene serve as predictor of response to ovarian stimulation? |
| Q51855004 | Can the FMR1 gene predict early ovarian aging? |
| Q36016185 | Comparison of ovarian FMR1 genotypes and sub-genotypes in oocyte donors and infertile women |
| Q30668605 | Computational investigation of RNA CUG repeats responsible for myotonic dystrophy 1 |
| Q27667903 | Crystal structures of CGG RNA repeats with implications for fragile X-associated tremor ataxia syndrome |
| Q58705431 | Curvilinear Association Between Language Disfluency and CGG Repeat Size Across the Normal, Intermediate, and Premutation Range |
| Q35317411 | Decreased fragile X mental retardation protein expression underlies amygdala dysfunction in carriers of the fragile X premutation. |
| Q28386414 | Defining ovarian reserve to better understand ovarian aging |
| Q55262442 | Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience. |
| Q34983517 | Distribution of AGG interruption patterns within nine world populations. |
| Q35697473 | Elevated FMR1 mRNA in premutation carriers is due to increased transcription. |
| Q28729961 | Evolutionary genomics of human intellectual disability |
| Q30886335 | Exploring possible DNA structures in real-time polymerase kinetics using Pacific Biosciences sequencer data |
| Q34074523 | Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans |
| Q33381599 | Expression patterns of protein kinases correlate with gene architecture and evolutionary rates |
| Q51902846 | FMR1 alleles in Parkinson's disease: relation to cognitive decline and hallucinations, a longitudinal study. |
| Q56369931 | FMR1 expression in human granulosa cells increases with exon 1 CGG repeat length depending on ovarian reserve |
| Q47748992 | FMR1 genotype interacts with parenting stress to shape health and functional abilities in older age. |
| Q51927334 | FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure. |
| Q37216636 | FMR1: a gene with three faces |
| Q24801535 | Facile FMR1 mRNA structure regulation by interruptions in CGG repeats |
| Q34521866 | Fragile X mental retardation protein expression in Alzheimer's disease |
| Q33775485 | Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome. |
| Q34106386 | How the FMR1 gene became relevant to female fertility and reproductive medicine |
| Q64927158 | Human Models Are Needed for Studying Human Neurodevelopmental Disorders. |
| Q33376873 | Identifying intrinsic and extrinsic determinants that regulate internal initiation of translation mediated by the FMR1 5' leader |
| Q34612704 | Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning |
| Q33786496 | Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age. |
| Q50278166 | Investigating the relationship between FMR1 allele length and cognitive ability in children: a subtle effect of the normal allele range on the normal ability range? |
| Q51926110 | Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms. |
| Q33808904 | Long tract of untranslated CAG repeats is deleterious in transgenic mice |
| Q34153985 | Low-normal FMR1 CGG repeat length: phenotypic associations |
| Q39659851 | NF-Y, AP2, Nrf1 and Sp1 regulate the fragile X-related gene 2 (FXR2). |
| Q38802827 | RAN translation-What makes it run? |
| Q36189626 | Regulation of human PTCH1b expression by different 5' untranslated region cis-regulatory elements |
| Q48713025 | Relevance of triple CGG repeats in the FMR1 gene to ovarian reserve |
| Q49905433 | Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome. |
| Q36491908 | SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndrome |
| Q24596776 | Sequencing the unsequenceable: expanded CGG-repeat alleles of the fragile X gene |
| Q38437658 | Small Molecule Recognition and Tools to Study Modulation of r(CGG)(exp) in Fragile X-Associated Tremor Ataxia Syndrome |
| Q36088922 | Small regulatory RNAs in mammals |
| Q40103612 | Structural diversity of triplet repeat RNAs |
| Q58777280 | Targeted Reactivation of Transcription in Fragile X Syndrome Embryonic Stem Cells |
| Q28295969 | The FMR1 Gene as Regulator of Ovarian Recruitment and Ovarian Reserve |
| Q35061671 | The FMR1 gene and fragile X-associated tremor/ataxia syndrome |
| Q64106801 | The FMRpolyGlycine Protein Mediates Aggregate Formation and Toxicity Independent of the CGG mRNA Hairpin in a Cellular Model for FXTAS |
| Q37204533 | The biological effects of simple tandem repeats: lessons from the repeat expansion diseases |
| Q24533443 | The fragile-X premutation: a maturing perspective |
| Q28731275 | The impact in older women of ovarian FMR1 genotypes and sub-genotypes on ovarian reserve |
| Q38901729 | The impact of FMR1 gene mutations on human reproduction and development: a systematic review |
| Q36875089 | The role of genetic and autoimmune factors in premature ovarian failure. |
| Q36082875 | The tetraplex (CGG)n destabilizing proteins hnRNP A2 and CBF-A enhance the in vivo translation of fragile X premutation mRNA. |
| Q37004710 | Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats. |
| Q37421101 | Translation of the FMR1 mRNA is not influenced by AGG interruptions |
| Q36749500 | Trisomic pregnancy and intermediate CGG repeat length at the FMR1 locus |
| Q26996649 | Unstable mutations in the FMR1 gene and the phenotypes |