Pages that link to "Q38317052"

The following pages link to The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation (Q38317052):

Displaying 50 items.

• A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein (Q22010778) (← links)
• The human 20-kDa 5'-(CGG)(n)-3'-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter (Q22253241) (← links)
• A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P (Q24291408) (← links)
• On the aggregation properties of FMRP--a link with the FXTAS syndrome? (Q24298281) (← links)
• The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction (Q24300712) (← links)
• The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2 (Q24303859) (← 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)
• Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain (Q24324461) (← links)
• A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern (Q24567552) (← links)
• Fragile x syndrome (Q24633000) (← 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)
• A pilot open label, single dose trial of fenobam in adults with fragile X syndrome. (Q24654933) (← links)
• Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits (Q24657867) (← links)
• Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation (Q24657890) (← links)
• Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast (Q24795709) (← links)
• RNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA Pathway (Q26747489) (← links)
• Mouse Genetic Models of Human Brain Disorders (Q26752246) (← links)
• Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP (Q26773167) (← links)
• Development and plasticity of the Drosophila larval neuromuscular junction (Q26820443) (← links)
• Fragile X spectrum disorders (Q26824376) (← links)
• Emerging pharmacologic treatment options for fragile X syndrome (Q26829152) (← links)
• Unstable mutations in the FMR1 gene and the phenotypes (Q26996649) (← links)
• The pathophysiology of fragile X (and what it teaches us about synapses) (Q27010675) (← links)
• The unstable repeats--three evolving faces of neurological disease (Q27025923) (← links)
• Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules (Q27308310) (← links)
• Structural Studies of the Tandem Tudor Domains of Fragile X Mental Retardation Related Proteins FXR1 and FXR2 (Q27665857) (← links)
• Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome (Q27732663) (← links)
• The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (Q27743918) (← links)
• Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP) (Q28079967) (← links)
• G-quadruplexes: Emerging roles in neurodegenerative diseases and the non-coding transcriptome (Q28084249) (← links)
• Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies (Q28115047) (← links)
• FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association (Q28115097) (← links)
• Fragile X mental retardation protein stimulates ribonucleoprotein assembly of influenza A virus (Q28115134) (← links)
• Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs (Q28115922) (← links)
• In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein (Q28116617) (← links)
• MOV10 and FMRP regulate AGO2 association with microRNA recognition elements (Q28117661) (← links)
• Translational regulation of the human achaete-scute homologue-1 by fragile X mental retardation protein (Q28119013) (← links)
• Fragile X mental retardation protein FMRP binds mRNAs in the nucleus (Q28119156) (← links)
• Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations (Q28141005) (← links)
• New insights into fragile X syndrome: from molecules to neurobehaviors (Q28182730) (← links)
• The fragile X gene and its function (Q28201533) (← links)
• Identification of mRNA/protein (mRNP) complexes containing Puralpha, mStaufen, fragile X protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor (Q28216333) (← links)
• Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes (Q28249379) (← links)
• RNA and microRNAs in fragile X mental retardation (Q28290772) (← links)
• Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2 (Q28292748) (← links)
• Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes (Q28303541) (← links)
• The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif (Q28348391) (← links)
• The Epac1 signaling pathway regulates Cl- secretion via modulation of apical KCNN4c channels in diarrhea (Q28385670) (← links)
• FMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brain (Q28487767) (← links)