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)