scholarly article | Q13442814 |
P2093 | author name string | Oostra B | |
Galjaard H | |||
Willemsen R | |||
Hoogeveen A | |||
Tamanini F | |||
Bontekoe C | |||
P433 | issue | 1 | |
P304 | page(s) | 27-33 | |
P577 | publication date | 1996-08-01 | |
P1433 | published in | Biochemical and Biophysical Research Communications | Q864228 |
P1476 | title | Association of FMRP with ribosomal precursor particles in the nucleolus | |
P478 | volume | 225 |
Q34561427 | A converging-methods approach to fragile X syndrome |
Q35483780 | A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function. |
Q35844502 | Absence of metabotropic glutamate receptor-mediated plasticity in the neocortex of fragile X mice. |
Q41751628 | Animal model for fragile X syndrome |
Q35553216 | Bioinformatic analysis of the nucleolus |
Q33765369 | Biology of the fragile X mental retardation protein, an RNA-binding protein |
Q47074071 | Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene |
Q28141005 | Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations |
Q93178436 | Disruption of RNA Metabolism in Neurological Diseases and Emerging Therapeutic Interventions |
Q37216636 | FMR1: a gene with three faces |
Q34521866 | Fragile X mental retardation protein expression in Alzheimer's disease |
Q51083891 | Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function. |
Q39918863 | Fragile X syndrome -- from genes to cognition |
Q34446594 | Fragile X syndrome and Friedreich's ataxia: two different paradigms for repeat induced transcript insufficiency |
Q33899309 | Fragile X syndrome at the turn of the century. |
Q34733371 | Fragile X syndrome, the Fragile X related proteins, and animal models |
Q54782597 | Fragile X syndrome: From protein function to therapy. |
Q38162720 | Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development |
Q37122910 | Fragile X syndrome: an aging perspective. |
Q21090208 | Initial genomics of the human nucleolus |
Q24554385 | Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex |
Q28583305 | Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets |
Q38225814 | Nucleoli and stress granules: connecting distant relatives. |
Q40066566 | ORF73 LANA homologs of RRV and MneRV2 contain an extended RGG/RG-rich nuclear and nucleolar localization signal that interacts directly with importin β1 for non-classical nuclear import |
Q24531856 | Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P |
Q58790351 | Regulation of Adult Neurogenesis by the Fragile X Family of RNA Binding Proteins |
Q40909839 | Sp1 and AP2 transcription factors are required for the human fragile mental retardation promoter activity in SK-N-SH neuronal cells |
Q28114773 | Subcellular fractionation and localization studies reveal a direct interaction of the fragile X mental retardation protein (FMRP) with nucleolin |
Q24791894 | Targeting fragile X. |
Q35061671 | The FMR1 gene and fragile X-associated tremor/ataxia syndrome |
Q27014002 | The FMRP regulon: from targets to disease convergence |
Q57166264 | The Nucleolus |
Q28201533 | The fragile X gene and its function |
Q73484548 | The fragile X syndrome |
Q74809876 | The fragile X syndrome |
Q30467175 | The role of fragile X mental retardation protein in major mental disorders |
Q24300712 | The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction |
Q28574173 | Transport of fragile X mental retardation protein via granules in neurites of PC12 cells |
Q37376681 | Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons |
Q35550078 | Understanding fragile X syndrome: insights from animal models |
Q73013123 | X-linked mental retardation |
Search more.