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Phosphorylation of WAVE1 regulates actin polymerization and dendritic spine morphology.
- Published in:
- Nature, 2006, v. 442, n. 7104, p. 814, doi. 10.1038/nature04976
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- Publication type:
- Article
The Hsp90 chaperone controls the biogenesis of L7Ae RNPs through conserved machinery.
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- Journal of Cell Biology, 2008, v. 180, n. 3, p. 579, doi. 10.1083/jcb.200708110
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- Publication type:
- Article
Phosphodiesterase 2A inhibition corrects the aberrant behavioral traits observed in genetic and environmental preclinical models of Autism Spectrum Disorder.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01885-2
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- Publication type:
- Article
Loss of FMR2 further emphasizes the link between deregulation of immediate early response genes FOS and JUN and intellectual disability.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 15, p. 2984, doi. 10.1093/hmg/ddt155
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- Publication type:
- Article
The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapse.
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- Human Molecular Genetics, 2013, v. 22, n. 10, p. 1971, doi. 10.1093/hmg/ddt044
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- Publication type:
- Article
Functional characterization of the AFF (AF4/FMR2) family of RNA-binding proteins: insights into the molecular pathology of FRAXE intellectual disability.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 10, p. 1873, doi. 10.1093/hmg/ddr069
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- Publication type:
- Article
The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 24, p. 3047, doi. 10.1093/hmg/ddm263
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- Publication type:
- Article
The nuclear MicroSpherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 9, p. 1525, doi. 10.1093/hmg/ddl074
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- Publication type:
- Article
FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 6, p. 835, doi. 10.1093/hmg/ddi077
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- Publication type:
- Article
Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 13, p. 1291, doi. 10.1093/hmg/ddh150
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- Publication type:
- Article
Sumoylation regulates FMRP-mediated dendritic spine elimination and maturation.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03222-y
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- Publication type:
- Article
Rett Syndrome and Fragile X Syndrome: Different Etiology With Common Molecular Dysfunctions.
- Published in:
- Frontiers in Cellular Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fncel.2021.764761
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- Publication type:
- Article
New Insights Into the Role of Ca<sub>v</sub>2 Protein Family in Calcium Flux Deregulation in Fmr1-KO Neurons.
- Published in:
- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00342
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- Publication type:
- Article
Modeling Fragile X Syndrome in Drosophila.
- Published in:
- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00124
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- Publication type:
- Article
Applied RNAi: from fundamental research to therapeutic applications.
- Published in:
- 2014
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- Publication type:
- Book Review
Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 1, p. 63, doi. 10.1038/sj.ejhg.5200394
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- Publication type:
- Article
A Novel Role for the RNA--Binding Protein FXR1P in Myoblasts Cell-Cycle Progression by Modulating p21/ Cdkn1a/Cip1/Waf1 mRNA Stability.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003367
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- Publication type:
- Article
The Search for an Effective Therapy to Treat Fragile X Syndrome: Dream or Reality?
- Published in:
- Frontiers in Synaptic Neuroscience, 2017, p. 1, doi. 10.3389/fnsyn.2017.00015
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- Publication type:
- Article
Dendritic targeting of short and long 3' UTR BDNF mRNA is regulated by BDNF or NT-3 and distinct sets of RNA-binding proteins.
- Published in:
- Frontiers in Molecular Neuroscience, 2015, v. 8, p. 1, doi. 10.3389/fnmol.2015.00062
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- Publication type:
- Article
Editorial: Innovative approaches and therapeutic perspectives for early-onset neurodevelopmental disorders: from bench to bedside.
- Published in:
- Frontiers in Neuroscience, 2024, p. 1, doi. 10.3389/fnins.2024.1370030
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- Publication type:
- Article
Missense mutation of Fmr1 results in impaired AMPAR-mediated plasticity and socio-cognitive deficits in mice.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21820-1
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- Publication type:
- Article
Visual Search of Neuropil-Enriched RNAs from Brain In Situ Hybridization Data through the Image Analysis Pipeline Hippo-ATESC.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074481
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- Publication type:
- Article
Depletion of the Fragile X Mental Retardation Protein in Embryonic Stem Cells Alters the Kinetics of Neurogenesis.
- Published in:
- Stem Cells, 2017, v. 35, n. 2, p. 374, doi. 10.1002/stem.2505
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- Publication type:
- Article
Dax-1 Knockdown in Mouse Embryonic Stem Cells Induces Loss of Pluripotency and Multilineage Differentiation.
- Published in:
- Stem Cells, 2009, v. 27, n. 7, p. 1529, doi. 10.1002/stem.78
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- Publication type:
- Article
A Novel Function for Fragile X Mental Retardation Protein in Translational Activation.
- Published in:
- PLoS Biology, 2009, v. 7, n. 1, p. e1000016, doi. 10.1371/journal.pbio.1000016
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- Publication type:
- Article
A Pilot Study on Early-Onset Schizophrenia Reveals the Implication of Wnt, Cadherin and Cholecystokinin Receptor Signaling in Its Pathophysiology.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.792218
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- Publication type:
- Article
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.
- Published in:
- EMBO Journal, 2001, v. 20, n. 17, p. 4803, doi. 10.1093/emboj/20.17.4803
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- Publication type:
- Article
HITS-CLIP in various brain areas reveals new targets and new modalities of RNA binding by fragile X mental retardation protein.
- Published in:
- Nucleic Acids Research, 2018, v. 46, n. 12, p. 6344, doi. 10.1093/nar/gky267
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- Publication type:
- Article
The FMRP/GRK4 mRNA interaction uncovers a new mode of binding of the Fragile X mental retardation protein in cerebellum.
- Published in:
- Nucleic Acids Research, 2015, v. 43, n. 17, p. 8540, doi. 10.1093/nar/gkv801
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- Publication type:
- Article
Human regulator of telomere elongation helicase 1 (RTEL1) is required for the nuclear and cytoplasmic trafficking of pre-U2 RNA.
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- Nucleic Acids Research, 2015, v. 43, n. 3, p. 1834, doi. 10.1093/nar/gku1402
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- Publication type:
- Article
Two sisters with 45,X karyotype: influence of genomic imprinting on phenotype and cognitive profile.
- Published in:
- 2002
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- Publication type:
- research
Childhood-Onset Schizophrenia: A Systematic Overview of Its Genetic Heterogeneity From Classical Studies to the Genomic Era.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01137
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- Publication type:
- Article
FRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structure.
- Published in:
- Nucleic Acids Research, 2009, v. 37, n. 4, p. 1269, doi. 10.1093/nar/gkn1058
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- Publication type:
- Article
Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure.
- Published in:
- Nucleic Acids Research, 2007, v. 35, n. 1, p. 299
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- Publication type:
- Article
CYFIP2 is highly abundant in CD4.
- Published in:
- European Journal of Immunology, 2004, v. 34, n. 4, p. 1217, doi. 10.1002/eji.200324726
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- Publication type:
- Article
Dicentric chromosome Y associated with Leydig cell agenesis and sex reversal.
- Published in:
- Clinical Genetics, 1995, v. 47, n. 1, p. 38, doi. 10.1111/j.1399-0004.1995.tb03919.x
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- Publication type:
- Article
A novel microduplication in INPP5A segregates with schizophrenia spectrum disorder in the family of a patient with both childhood onset schizophrenia and autism spectrum disorder.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 6, p. 1841, doi. 10.1002/ajmg.a.62155
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- Publication type:
- Article
Astrocyte-Secreted Factors Selectively Alter Neural Stem and Progenitor Cell Proliferation in the Fragile X Mouse.
- Published in:
- Frontiers in Cellular Neuroscience, 2016, p. 1, doi. 10.3389/fncel.2016.00126
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- Publication type:
- Article
Fragile X Syndrome as an interneuronopathy: a lesson for future studies and treatments.
- Published in:
- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1171895
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- Publication type:
- Article
82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 14, p. 1689, doi. 10.1093/hmg/ddg181
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- Publication type:
- Article
A novel RNA-binding nuclear protein that interacts with the frgile X mental retardation (FMR1) protein.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 13, p. 2557, doi. 10.1093/hmg/8.13.2557
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- Publication type:
- Article