| scholarly article | Q13442814 |
| P2093 | author name string | Y Zhang | |
| G Dreyfuss | |||
| M C Siomi | |||
| R L Nussbaum | |||
| S Srinivasan | |||
| A Dutra | |||
| J P O'Connor | |||
| P2860 | cites work | 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 |
| FMR1 protein: conserved RNP family domains and selective RNA binding | Q24311412 | ||
| FXR1, an autosomal homolog of the fragile X mental retardation gene | Q24321996 | ||
| Genomic sequencing | Q24594942 | ||
| Characterization and primary structure of the poly(C)-binding heterogeneous nuclear ribonucleoprotein complex K protein | Q24630724 | ||
| The scanning model for translation: an update | Q24679648 | ||
| Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction | Q25938986 | ||
| A novel genetic system to detect protein-protein interactions | Q27860915 | ||
| Conserved structures and diversity of functions of RNA-binding proteins | Q27861066 | ||
| The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein | Q28117885 | ||
| Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox | Q28235115 | ||
| Monoclonal antibody characterization of the C proteins of heterogeneous nuclear ribonucleoprotein complexes in vertebrate cells | Q28263029 | ||
| The pre-mRNA binding K protein contains a novel evolutionarily conserved motif | Q28267734 | ||
| Characterization and localization of the FMR-1 gene product associated with fragile X syndrome | Q28270283 | ||
| Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome | Q28273791 | ||
| Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization | Q29616823 | ||
| The mRNA poly(A)-binding protein: localization, abundance, and RNA-binding specificity. | Q34322199 | ||
| A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome | Q35195709 | ||
| Transcriptional regulation by dimerization: two sides to an incestuous relationship | Q37909289 | ||
| The role of specific protein-RNA and protein-protein interactions in positive and negative control of pre-mRNA splicing by Transformer 2. | Q38310868 | ||
| The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation | Q38317052 | ||
| A yeast protein HX has homologies with the histone H2AF expressed in chicken embryo | Q40419727 | ||
| Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis | Q41133769 | ||
| Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome | Q41178713 | ||
| The U2B'' RNP motif as a site of protein-protein interaction. | Q41230779 | ||
| A point mutation in the FMR-1 gene associated with fragile X mental retardation | Q41579799 | ||
| Absence of expression of the FMR-1 gene in fragile X syndrome | Q41669091 | ||
| Fragile X genotype characterized by an unstable region of DNA. | Q43980470 | ||
| Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome | Q44959699 | ||
| Labeling of the centromeric region on human chromosome 8 by in situ hybridization | Q46100332 | ||
| Fragile X syndrome without CCG amplification has an FMR1 deletion | Q52042510 | ||
| Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island | Q57951231 | ||
| Immunological methods for purification and characterization of heterogeneous nuclear ribonucleoprotein particles | Q68424588 | ||
| P433 | issue | 21 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | FMRP translational regulator 1 | Q905435 |
| protein heterodimerization activity | Q14762999 | ||
| FMR1 autosomal homolog 2 | Q21109364 | ||
| FMR1 autosomal homolog 1 | Q21112435 | ||
| P304 | page(s) | 5358-66 | |
| P577 | publication date | 1995-11-01 | |
| P1433 | published in | The EMBO Journal | Q1278554 |
| P1476 | title | The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2 | |
| P478 | volume | 14 |
| Q34155406 | A feed-forward mechanism involving Drosophila fragile X mental retardation protein triggers a replication stress-induced DNA damage response |
| Q24291408 | 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 |
| Q35581584 | A metabolomic and systems biology perspective on the brain of the fragile X syndrome mouse model |
| Q30484632 | A mouse model of the human Fragile X syndrome I304N mutation |
| Q34778991 | A non-canonical start codon in the Drosophila fragile X gene yields two functional isoforms |
| Q35483780 | A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function. |
| Q34649828 | A novel role for the RNA-binding protein FXR1P in myoblasts cell-cycle progression by modulating p21/Cdkn1a/Cip1/Waf1 mRNA stability |
| Q41077534 | A nuclear role for the Fragile X mental retardation protein |
| Q34505148 | A presynaptic role for FMRP during protein synthesis-dependent long-term plasticity in Aplysia. |
| Q37143251 | A study of the ultrastructure of fragile-X-related proteins |
| Q52589784 | Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies. |
| Q36410140 | Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes |
| Q37577454 | Activity-dependent modulation of neural circuit synaptic connectivity |
| Q37190453 | Altered hippocampal synaptic plasticity in the FMR1 gene family knockout mouse models |
| Q35661585 | Amygdala regulation of fear and emotionality in fragile X syndrome |
| Q90479569 | Analysis of the Cancer Genome Atlas Data Reveals Novel Putative ncRNAs Targets in Hepatocellular Carcinoma |
| Q90010722 | Axonal localization of the fragile X family of RNA binding proteins is conserved across mammals |
| Q35081841 | Bcl-2-associated transcription factor 1 interacts with fragile X-related protein 1. |
| Q37082928 | CMP‑N‑acetylneuraminic acid synthetase interacts with fragile X related protein 1. |
| Q34590406 | Candidate RNA-binding proteins regulating extrasomatic mRNA targeting and translation in mammalian neurons |
| Q34443306 | Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties |
| Q47783701 | Cell type-dependent axonal localization of translational regulators and mRNA in mouse peripheral olfactory neurons |
| Q54462803 | Characterization of DUF724 gene family in Arabidopsis thaliana. |
| Q33605779 | Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein |
| Q21266637 | Characterization of the mouse Dazap1 gene encoding an RNA-binding protein that interacts with infertility factors DAZ and DAZL |
| Q36265538 | Chromosomal fragility and human genetic disorders |
| Q34289151 | Circadian rhythm-dependent alterations of gene expression in Drosophila brain lacking fragile X mental retardation protein |
| Q61814920 | Comparative Behavioral Phenotypes of KO, Het, and KO/ Het Mice |
| Q35844954 | Comparison of Equivalence between Two Commercially Available S499-Phosphorylated FMRP Antibodies in Mice |
| Q35990787 | Conservation of the RNA Transport Machineries and Their Coupling to Translation Control across Eukaryotes |
| Q41619835 | Deficient Sleep in Mouse Models of Fragile X Syndrome |
| Q42651961 | Dendritic Homeostasis Disruption in a Novel Frontotemporal Dementia Mouse Model Expressing Cytoplasmic Fused in Sarcoma |
| Q28079967 | Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP) |
| Q37295048 | Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs |
| Q92755413 | EGFP insertional mutagenesis reveals multiple FXR2P fibrillar states with differing ribosome association in neurons |
| Q39720686 | Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression |
| Q64071638 | Expression and Characterization of Human Fragile X Mental Retardation Protein Isoforms and Interacting Proteins in Human Cells |
| Q28756274 | Expression of fragile X mental retardation protein within the vocal control system of developing and adult male zebra finches |
| Q46403963 | Expression of three zebrafish orthologs of human FMR1-related genes and their phylogenetic relationships. |
| Q64930832 | FMRP - G-quadruplex mRNA - miR-125a interactions: Implications for miR-125a mediated translation regulation of PSD-95 mRNA. |
| Q33578330 | FMRP S499 is phosphorylated independent of mTORC1-S6K1 activity |
| Q51817294 | FMRP regulates the transition from radial glial cells to intermediate progenitor cells during neocortical development. |
| Q36246867 | FXR1P but not FMRP regulates the levels of mammalian brain-specific microRNA-9 and microRNA-124 |
| Q48110353 | FXR2P Exerts a Positive Translational Control and Is Required for the Activity-Dependent Increase of PSD95 Expression. |
| Q47836386 | Fragile X granules are a family of axonal ribonucleoprotein particles with circuit-dependent protein composition and mRNA cargos |
| Q30475446 | Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P |
| Q34318418 | Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected]. |
| Q33605244 | Fragile X mental retardation protein regulates translation by binding directly to the ribosome |
| Q28086823 | Fragile X mental retardation protein: A paradigm for translational control by RNA-binding proteins |
| Q28303541 | Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes |
| Q34002202 | Fragile X protein family member FXR1P is regulated by microRNAs |
| Q48306723 | Fragile X related protein 1 (FXR1P) regulates proliferation of adult neural stem cells. |
| Q28505448 | Fragile X related protein 1 clusters with ribosomes and messenger RNAs at a subset of dendritic spines in the mouse hippocampus |
| Q28507308 | Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure |
| Q34185158 | Fragile X syndrome. Molecular and clinical insights and treatment issues |
| Q38162720 | Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development |
| Q37900184 | Fragile X-associated disorders: a clinical overview. |
| Q36744675 | Fragile X-related proteins regulate mammalian circadian behavioral rhythms |
| Q38940268 | Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci. |
| Q42249362 | Global Analysis of mRNA, Translation, and Protein Localization: Local Translation Is a Key Regulator of Cell Protrusions. |
| Q24645150 | Identification of AUF1 (heterogeneous nuclear ribonucleoprotein D) as a component of the alpha-globin mRNA stability complex |
| Q52613428 | Immunohistochemical Expression of FXR1 in Canine Normal Tissues and Melanomas. |
| Q47382701 | Increased Cardiac Arrhythmogenesis Associated with Gap Junction Remodeling with Upregulation of RNA Binding Protein FXR1. |
| Q34435526 | Increasing our understanding of human cognition through the study of Fragile X Syndrome |
| Q24565016 | Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein family |
| Q24554385 | Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex |
| Q37577761 | Macro role(s) of microRNAs in fragile X syndrome? |
| Q42063025 | Molecular and genetic analysis of the Drosophila model of fragile X syndrome |
| Q24795709 | Muscle specific fragile X related protein 1 isoforms are sequestered in the nucleus of undifferentiated myoblast |
| Q47071293 | Mutational analysis establishes a critical role for the N terminus of fragile X mental retardation protein FMRP. |
| Q39659851 | NF-Y, AP2, Nrf1 and Sp1 regulate the fragile X-related gene 2 (FXR2). |
| Q38222192 | Nervous translation, do you get the message? A review of mRNPs, mRNA-protein interactions and translational control within cells of the nervous system |
| Q35724788 | Noncoding RNAs in mental retardation |
| Q24531856 | Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P |
| Q26747489 | RNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA Pathway |
| Q37399680 | RNA-mediated pathogenesis in fragile X-associated disorders |
| Q61795880 | Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy |
| Q41773333 | Recombinant bacterial expression and purification of human fragile X mental retardation protein isoform 1. |
| Q58790351 | Regulation of Adult Neurogenesis by the Fragile X Family of RNA Binding Proteins |
| Q24644556 | Self-association of the single-KH-domain family members Sam68, GRP33, GLD-1, and Qk1: role of the KH domain |
| Q33891889 | Short- and long-term memory are modulated by multiple isoforms of the fragile X mental retardation protein |
| Q24648900 | 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 |
| Q47934635 | Splice form-dependent regulation of axonal arbor complexity by FMRP. |
| Q27665857 | Structural Studies of the Tandem Tudor Domains of Fragile X Mental Retardation Related Proteins FXR1 and FXR2 |
| Q35729925 | Substitution of critical isoleucines in the KH domains of Drosophila fragile X protein results in partial loss-of-function phenotypes. |
| Q38693916 | Synaptic vesicle dynamic changes in a model of fragile X. |
| Q24791894 | Targeting fragile X. |
| Q37332148 | Temporal requirements of the fragile x mental retardation protein in modulating circadian clock circuit synaptic architecture |
| Q42591469 | The FRAXE Syndrome: is it time for routine screening? |
| Q57307468 | The Fragile X Protein and Genome Function |
| Q35234080 | The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice |
| Q37367404 | The KH domain protein encoded by quaking functions as a dimer and is essential for notochord development in Xenopus embryos |
| Q28258198 | The RNA binding protein FXR1 is a new driver in the 3q26-29 amplicon and predicts poor prognosis in human cancers |
| Q33938446 | The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis |
| Q28348391 | The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif |
| Q37359934 | The fragile X mental retardation protein in circadian rhythmicity and memory consolidation |
| Q28588486 | The fragile X mental retardation protein inhibits translation via interacting with mRNA |
| Q73484548 | The fragile X syndrome |
| Q35170163 | The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge |
| Q37238015 | The microRNA pathway and fragile X mental retardation protein |
| Q27308310 | Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules |
| Q90597084 | Widespread RNA editing dysregulation in brains from autistic individuals |
| Q64260753 | as a Model to Study the Multiple Phenotypes, Related to Genome Stability of the Fragile-X Syndrome |
| Q33755357 | dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster |
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