Pages that link to "Q42623011"
The following pages link to Alternative splicing in the fragile X gene FMR1. (Q42623011):
Displaying 50 items.
- A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein (Q22010778) (← links)
- Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome (Q24310518) (← links)
- FXR1, an autosomal homolog of the fragile X mental retardation gene (Q24321996) (← links)
- mRNA 3'end processing: A tale of the tail reaches the clinic (Q24601240) (← links)
- Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them (Q24648900) (← links)
- Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast (Q24795709) (← links)
- Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies (Q28115047) (← links)
- FMRP targets distinct mRNA sequence elements to regulate protein expression (Q28117931) (← links)
- The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer (Q28118840) (← links)
- Translational regulation of the human achaete-scute homologue-1 by fragile X mental retardation protein (Q28119013) (← links)
- The fragile X gene and its function (Q28201533) (← links)
- Characterization and localization of the FMR-1 gene product associated with fragile X syndrome (Q28270283) (← links)
- Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein (Q28273516) (← links)
- FMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brain (Q28487767) (← links)
- Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets (Q28583305) (← links)
- Molecular and cellular genetics of fragile X syndrome (Q33537385) (← links)
- Biology of the fragile X mental retardation protein, an RNA-binding protein (Q33765369) (← links)
- Short- and long-term memory are modulated by multiple isoforms of the fragile X mental retardation protein (Q33891889) (← links)
- FMR1 gene and fragile X syndrome (Q34141674) (← links)
- Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective (Q34226308) (← links)
- The Fragile X mental retardation protein (Q34446600) (← links)
- Pharmacological reactivation of inactive genes: the fragile X experience (Q34446607) (← links)
- A presynaptic role for FMRP during protein synthesis-dependent long-term plasticity in Aplysia. (Q34505148) (← links)
- Alternative poly(A) site selection in complex transcription units: means to an end? (Q34630891) (← links)
- The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge (Q35170163) (← links)
- Dissecting the expression relationships between RNA-binding proteins and their cognate targets in eukaryotic post-transcriptional regulatory networks (Q36012895) (← links)
- De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity (Q36333998) (← links)
- Reciprocal changes in DNA methylation and hydroxymethylation and a broad repressive epigenetic switch characterize FMR1 transcriptional silencing in fragile X syndrome (Q36549606) (← links)
- Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs (Q37295048) (← links)
- The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation (Q38317052) (← links)
- The fragile X syndrome: implications of molecular genetics for the clinical syndrome (Q40754963) (← links)
- Autism: the point of view from fragile X studies (Q40835732) (← links)
- A nuclear role for the Fragile X mental retardation protein (Q41077534) (← links)
- Fragile X syndrome in humans and mice (Q41167683) (← links)
- Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome (Q41315849) (← links)
- Base stacking and even/odd behavior of hairpin loops in DNA triplet repeat slippage and expansion with DNA polymerase (Q41740863) (← links)
- Animal model for fragile X syndrome (Q41751628) (← links)
- Recombinant bacterial expression and purification of human fragile X mental retardation protein isoform 1. (Q41773333) (← links)
- Prenatal Diagnosis of Fragile X: Can a Full Mutation Allele in the FMR1 Gene Contract to a Normal Size? (Q45329800) (← links)
- Splice form-dependent regulation of axonal arbor complexity by FMRP. (Q47934635) (← links)
- cDNA Libraries from Single Human Preimplantation Embryos (Q48040915) (← links)
- Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat (Q48255852) (← links)
- Analysis of the Fragile X mental retardation protein isoforms 1, 2 and 3 interactions with the G-quadruplex forming semaphorin 3F mRNA. (Q50777684) (← links)
- Fmr1 knockout mouse has a distinctive strain-specific learning impairment (Q51075210) (← links)
- Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation (Q51973695) (← links)
- Association between idiopathic premature ovarian failure and fragile X premutation (Q51978995) (← links)
- Assessment of FMR1 expression by reverse transcriptase-polymerase chain reaction of KH domains. (Q51996297) (← links)
- Neurodevelopmental effects of the FMR-1 full mutation in humans. (Q52019051) (← links)
- KH domains within the FMR1 sequence suggest that fragile X syndrome stems from a defect in RNA metabolism (Q52034009) (← links)
- Fragile X syndrome: From protein function to therapy. (Q54782597) (← links)