Adult fragile X syndrome: Clinico-neuropathologic findings

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Items 101–200 of 359

1. Auditory Processing in Fragile X Syndrome
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2. Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders
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3. Deregulated mTOR-mediated translation in intellectual disability.
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4. Alterations in CA1 hippocampal synapses in a mouse model of fragile X syndrome
   Safdar Jawaid, Grahame J. Kidd, Jing Wang, Carrie Swetlik, Ranjan Dutta, Bruce D. Trapp · 2017 · Glia
5. Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structure
   Cheryl L. Gatto, Kendal S. Broadie · 2008 · Development
6. Wnt Signaling in the Central Nervous System: New Insights in Health and Disease
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7. Altered structural and functional synaptic plasticity with motor skill learning in a mouse model of fragile x syndrome.
   Padmashri, Ragunathan, Reiner, Benjamin C., Suresh, Anand, Spartz, Elizabeth, Dunaevsky, Anna · 2013 · The Journal of Neuroscience
8. Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development
   Andreea S. Pop, Baltazar Gomez‐Mancilla, Giovanni Neri, Rob Willemsen, Fabrizio Gasparini · 2013 · Psychopharmacology
9. Long-lasting effects of minocycline on behavior in young but not adult Fragile X mice.
   Dansie, L.E., Phommahaxay, K., Okusanya, A.G., Uwadia, J., Huang, M., Rotschafer, S.E., Razak, K.A., Ethell, D.W., Ethell, I.M. · 2013 · Neuroscience
10. Modelling brain diseases in mice: the challenges of design and analysis
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11. Therapeutic Potential of Metabotropic Glutamate Receptor Modulators
    Nanna Hovelsø, Florence Sotty, Liliana P. Montezinho, Paulo S. Pinheiro, Kjartan Frisch Herrik, Arne Mørk · 2012 · Current Neuropharmacology
12. Regulation of dendritic spine stability
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13. Rescue of dendritic spine phenotype in Fmr1 KO mice with the mGluR5 antagonist AFQ056/Mavoglurant
    Pop, Andreea S., Levenga, Josien, de Esch, Celine E. F., Buijsen, Ronald A. M., Nieuwenhuizen, Ingeborg M., Li, Tracy, Isaacs, Aaron, Gasparini, Fabrizio, Oostra, Ben A., Willemsen, Rob · 2014 · Psychopharmacology
14. Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice
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15. Plasticity of dendritic spines: Molecular function and dysfunction in neurodevelopmental disorders
    Jun Nishiyama · 2019 · Psychiatry and Clinical Neurosciences
16. Increased rates of cerebral glucose metabolism in a mouse model of fragile X mental retardation
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17. Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene.
    Spencer, Corinne M., Graham, Deanna F., Yuva-Paylor, Lisa A., Nelson, David L., Paylor, Richard · 2008 · Behavioral Neuroscience
18. Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome
    Greco, Claudia M, Navarro, Celestine S, Hunsaker, Michael R, Maezawa, Izumi, Shuler, John F, Tassone, Flora, Delany, Mary, Au, Jacky W, Berman, Robert F, Jin, Lee-Way et al. · 2011 · Molecular Autism
19. BDNF and TrkB in neuronal differentiation of Fmr1-knockout mouse
    Verna Louhivuori, Annalisa Vicario, Marko Uutela, Tomi Rantamäki, Lauri M. Louhivuori, Eero Ċastrén, Enrico Tongiorgi, Karl E.O. Åkerman, Maija L. Castrén · 2010 · Neurobiology of Disease
20. Fragile X Syndrome: From Molecular Aspect to Clinical Treatment
    Dragana D. Protic, Ramkumar Aishworiya, María Jimena Salcedo‐Arellano, Si Jie Tang, Jelena Milisavljevic, Filip Mitrovic, Randi Jenssen Hagerman, Dejan B. Budimirovic · 2022 · International Journal of Molecular Sciences
21. Dynamics and pathology of dendritic spines
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22. Neuroanatomy in fragile X females: the posterior fossa.
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23. Understanding fragile X syndrome: insights from animal models
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24. Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase
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25. Kallmann syndrome gene (KAL-X) is not mutated in schizophrenia
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26. Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolism
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27. Developmental studies in fragile X syndrome
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28. Matrix metalloproteinase-9 involvement in the structural plasticity of dendritic spines
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29. Profilin, a multi‐modal regulator of neuronal plasticity
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30. Hippocampal deficits in neurodevelopmental disorders
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31. miR-132 Regulates Dendritic Spine Structure by Direct Targeting of Matrix Metalloproteinase 9 mRNA
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32. Hippocampal dysfunction and cognitive impairment in Fragile-X Syndrome
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33. Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome
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34. Differential translation and fragile X syndrome
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35. Fragile X mental retardation protein regulates new neuron differentiation in the adult olfactory bulb
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36. Effect of the Deficits of Fragile X Mental Retardation Protein on Cognitive Status of Fragile X Males and Females Assessed by Robust Pedigree Analysis
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37. Fragile X syndrome
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38. Biology of the fragile X mental retardation protein, an RNA-binding protein
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39. Early continuous inhibition of group 1 mGlu signaling partially rescues dendritic spine abnormalities in the Fmr1 knockout mouse model for fragile X syndrome
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40. Modulation of actin dynamics by Rac1 to target cognitive function
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41. The discovery of dendritic spines by Cajal in 1888 and its relevance in the present neuroscience
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42. Activity-dependent modulation of neural circuit synaptic connectivity
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43. Preliminary communication: Neuroanatomical variations of the posterior fossa in men with the fragile X (Martin‐Bell) syndrome
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44. Psychopathology in fragile X syndrome.
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45. Fragile X syndrome: Associated neurological abnormalities and developmental disabilities
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46. Early life stress inhibits expression of a novel innate immune pathway in the developing hippocampus
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47. Mapping nonverbal IQ in young boys with fragile X syndrome
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48. Is mental retardation a defect of synapse structure and function?
    Magdalena Chechlacz, Joseph G. Gleeson · 2003 · Pediatric Neurology
49. Cellular distribution of the fragile X mental retardation protein in the mouse brain
    Diego A. R. Zorio, Christine M. Jackson, Yong Liu, Edwin W. Rubel, Yuan Wang · 2016 · The Journal of Comparative Neurology
50. Matrix Metalloproteinases and Minocycline: Therapeutic Avenues for Fragile X Syndrome
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51. Which Comes First in Fragile X Syndrome, Dendritic Spine Dysgenesis or Defects in Circuit Plasticity?
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52. Understanding intellectual disability and autism spectrum disorders from common mouse models: synapses to behaviour
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53. Casting a net on dendritic spines: The extracellular matrix and its receptors
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54. Stimulated Emission Depletion (STED) Microscopy Reveals Nanoscale Defects in the Developmental Trajectory of Dendritic Spine Morphogenesis in a Mouse Model of Fragile X Syndrome
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55. Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome
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56. Epilepsy and fragile X syndrome: A follow‐up study
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57. What’s hAPPening at synapses? The role of amyloid β-protein precursor and β-amyloid in neurological disorders
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58. Altered mossy fiber distributions in adult Fmr1 (FVB) knockout mice
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59. Sensory stimulation increases cortical expression of the fragile X mental retardation protein in vivo
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60. Environmental enrichment induces neuroplastic changes in middle age female BalbC mice and increases the hippocampal levels of BDNF, p-Akt and p-MAPK1/2
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61. Normal Neurogenesis but Abnormal Gene Expression in Human Fragile X Cortical Progenitor Cells
    Anita Bhattacharyya, Erin McMillan, Kyle Wallace, Thomas C. Tubon, Elizabeth E. Capowski, Clive Niels Svendsen · 2008 · Stem Cells and Development
62. Input transformation by dendritic spines of pyramidal neurons
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63. The Role of Rac GTPase in Dendritic Spine Morphogenesis and Memory
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64. Decreased cohesin in the brain leads to defective synapse development and anxiety-related behavior
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65. Physiological consequences of morphologically detectable synaptic plasticity: potential uses for examining recovery following damage
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66. Pathological and neuropathological findings in two males with fragile‐X syndrome
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67. Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO mice
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68. Whisker stimulation-dependent translation of FMRP in the barrel cortex requires activation of type I metabotropic glutamate receptors
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69. Activity-dependent regulation of dendritic growth and maintenance by glycogen synthase kinase 3β
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70. DIAGNOSIS OF THE FRAGILE X SYNDROME (MARTIN‐BELL SYNDROME). CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT Xq28
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71. White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging
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72. Longitudinal changes in cognitive and adaptive behavior in fragile X females: a prospective multicenter analysis.
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73. Fragile X syndrome: From targets to treatments
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74. Mechanisms, models, and mental retardation
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75. Reduced Cortical Folding in Mental Retardation
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76. Molecular and Cellular Aspects of Mental Retardation in the Fragile X Syndrome: From Gene Mutation/s to Spine Dysmorphogenesis
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77. Functional brain activation during cognition is related to FMR1 gene expression
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78. Common Defects of Spine Dynamics and Circuit Function in Neurodevelopmental Disorders: A Systematic Review of Findings From in Vivo Optical Imaging of Mouse Models
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79. BDNF Regulates the Expression of Fragile X Mental Retardation Protein mRNA in the Hippocampus
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80. A converging‐methods approach to fragile X syndrome
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81. Fragile X mental retardation protein regulates trans-synaptic signaling inDrosophila
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82. Intense and specialized dendritic localization of the fragile X mental retardation protein in binaural brainstem neurons: a comparative study in the alligator, chicken, gerbil, and human
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83. Accelerators, Brakes, and Gears of Actin Dynamics in Dendritic Spines
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84. Finding novel distinctions between the sAPPα-mediated anabolic biochemical pathways in Autism Spectrum Disorder and Fragile X Syndrome plasma and brain tissue
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85. The Prenatal Diagnosis of the Fragile X Syndrome
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86. Altered Connectivity and Synapse Maturation of the Hippocampal Mossy Fiber Pathway in a Mouse Model of the Fragile X Syndrome
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87. Abnormal neuronal morphology and neurochemistry in the auditory brainstem of Fmr1 knockout rats.
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88. A normal genetic variation modulates synaptic MMP-9 protein levels and the severity of schizophrenia symptoms.
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89. Post-translational modifications of the Fragile X Mental Retardation Protein in neuronal function and dysfunction
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90. Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: A new perspective
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91. Heads‐up: New roles for the fragile X mental retardation protein in neural stem and progenitor cells
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92. Acamprosate in a mouse model of fragile X syndrome: modulation of spontaneous cortical activity, ERK1/2 activation, locomotor behavior, and anxiety
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93. Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene
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94. How did the human brain evolve? a proposal based on new evidence from in vivo brain imaging during attention and ideation
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95. Review of targeted treatments in fragile X syndrome
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96. Olfactory bulb mitral cell dendritic pruning abnormalities in a mouse model of the Fragile-X mental retardation syndrome: Further support for FMRP's involvement in dendritic development
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97. The Fragile X Mental Retardation Protein in Circadian Rhythmicity and Memory Consolidation
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98. Imbalance of synaptic actin dynamics as a key to fragile X syndrome?
    Kristin Michaelsen‐Preusse, Jonas Feuge, Martin Körte · 2018 · The Journal of Physiology
99. Cognitive and behavioral correlates of caudate subregion shape variation in fragile X syndrome
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100. Experience and sleep-dependent synaptic plasticity: from structure to activity
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