Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

Cited by (536)

Items 201–300 of 536

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4. TWO PEDIGREES OF ECTRODACTYLY
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5. Transient Brown Adipocyte-Like Cells Derive from Peripheral Nerve Progenitors in Response to Bone Morphogenetic Protein 2
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6. Nonneuronal roles for the reelin signaling pathway
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7. Reeler mutant mouse: maintenance of appropriate and reciprocal connections in the cerebral cortex and thalamus
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8. The Reeler Mouse: A Translational Model of Human Neurological Conditions, or Simply a Good Tool for Better Understanding Neurodevelopment?
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9. Directional Neuronal Migration Is Impaired in Mice Lacking Adenomatous Polyposis Coli 2
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10. A behavioral study of the development of hereditary cerebellar ataxia in the shaker rat mutant
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11. The cytoarchitecture of the dorsal cochlear nucleus in the 3‐month‐ and 26‐month‐old C57BL/6 mouse: A golgi impregnation study
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12. Adapting for endocytosis: roles for endocytic sorting adaptors in directing neural development
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13. Reelin demarcates a subset of pre‐Bötzinger complex neurons in adult rat
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14. How does Reelin signaling regulate the neuronal cytoskeleton during migration?
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15. Antidepressant use during pregnancy and serotonin transporter genotype (SLC6A4) Affect newborn serum reelin levels
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16. The reeler gene: a clue to brain development and evolution
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17. Schwann cell multiplication deficit in nerve roots of newborn dystrophic mice
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18. Stick around: Cell–Cell Adhesion Molecules during Neocortical Development
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19. Feature Article: Evolution of Isocortical Organization. A Tentative Scenario Including Roles of Reelin, p35/cdk5 and the Subplate Zone
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20. Myelin mutants: New models and new observations
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21. Dispersion of the neurons expressing layer specific markers in the reeler brain
    Hideyuki Dekimoto, Toshio Terashima, Yu Katsuyama · 2010 · Development Growth & Differentiation
22. Lipid composition of sciatic nerve from dysmyelinating trembler mouse
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23. Acetylcholinesterase‐positive fibers and cell bodies in the cochlear nuclei of normal and reeler mutant mice
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24. Structural Insights into Reelin Function: Present and Future
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25. Reelin Signaling Inactivates Cofilin to Stabilize the Cytoskeleton of Migrating Cortical Neurons
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26. Topical Review: Neuronal Migration in Cortical Development
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27. Dominant ectrodactyly and possible germinal mosaicism.
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28. Observations on the commissural projection to the dentate gyrus in the reeler mutant mouse
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29. Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor
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30. A reeler mutant mouse with a new, spontaneous mutation in the reelin gene
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31. Missplicing resulting from a short deletion in the reelin gene causes reeler‐like neuronal disorders in the mutant shaking rat Kawasaki
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32. Can Clues from Evolution Unlock the Molecular Development of the Cerebellum?
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33. Role of the unfolded protein response in the development of central nervous system
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34. Ectopic corticospinal tract and corticothalamic tract neurons in the cerebral cortex of yotari and reeler mice
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35. Recommendations for measuring whisker movements and locomotion in mice with sensory, motor and cognitive deficits
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36. Role of Reelin in cell positioning in the cerebellum and the cerebellum-like structure in zebrafish
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37. Shared and specific signatures of locomotor ataxia in mutant mice
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38. Developmental distribution of reelin‐positive cells and their secreted product in the rodent spinal cord
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39. Motor learning of mice lacking cerebellar Purkinje cells
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40. Altered Speeds and Trajectories of Neurons Migrating in the Ventricular and Subventricular Zones of the Reeler Neocortex
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41. Role of p35/Cdk5 in Preplate Splitting in the Developing Cerebral Cortex
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42. In vivo studies of brain development by magnetic resonance techniques
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43. Genetics of ocular NAD+-dependent alcohol dehydrogenase and aldehyde dehydrogenase in the mouse: Evidence for genetic identity with stomach isozymes and localization ofAhd-4 on chromosome 11 near trembler
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44. Birth‐date‐dependent segregation of the mouse cerebral cortical neurons in reaggregation cultures
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45. What cerebellar malformations tell us about cerebellar development
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46. The basic helix‐loop‐helix transcription factor TCF4 impacts brain architecture as well as neuronal morphology and differentiation
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47. Neuromyotonia in mice with hereditary myelinopathies
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48. Development and Developmental Disorders of the Human Cerebellum
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49. Cell and molecular mechanisms that control cortical layer formation in the brain
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50. Loss of Reelin protects mice against arterial thrombosis by impairing integrin activation and thrombus formation under high shear conditions
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51. Glial Cell Markers in the Reeler Mutant Mouse: A Biochemical and Immunohistological Study
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52. New insights into behaviour using mouse ENU mutagenesis
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53. The Mouse Mutation Claw Paw: Forelimb Deformity and Delayed Myelination throughout the Peripheral Nervous System
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54. Autism: a large unmet medical need and a complex research problem
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55. A Forward Genetic Screen in Mice Identifies Mutants with Abnormal Cortical Patterning
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56. Role of the postnatal radial glial scaffold for the development of the dentate gyrus as revealed by reelin signaling mutant mice
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57. Entorhinal cortex lesion does not alter reelin messenger RNA expression in the dentate gyrus of young and adult rats
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58. Trajectory analysis unveils reelin’s role in the directed migration of granule cells in the dentate gyrus
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59. Cajal-retzius cells: Recent advances in identity and function
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60. Aberrant survival of hippocampal Cajal-Retzius cells leads to memory deficits, gamma rhythmopathies and susceptibility to seizures in adult mice
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61. Mapping Pathological Phenotypes in Reelin Mutant Mice
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62. Musculotopic organization in the motor trigeminal nucleus of the reeler mutant mouse
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63. Developmental Expression of the P0 Glycoprotein and Basic Protein mRNAs in Normal and Trembler Mutant Mice
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64. The Pathophysiological Link Between Reelin and Autism: Overview and New Insights
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67. C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus
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68. C‐terminal region‐dependent change of antibody‐binding to the Eighth Reelin repeat reflects the signaling activity of Reelin
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69. Intracortical Network Effects Preserve Thalamocortical Input Efficacy in a Cortex Without Layers
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70. The C terminus of p73 is essential for hippocampal development
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71. Disturbances in developmental pathways leading to a neurological disorder of genetic origin, “leaner,” in mice
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72. Altered distribution of inhibitory synaptic terminals in reeler cerebellum with special reference to malposition of GABAergic neurons
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73. Book Review: Cortical Dysgenesis and Epilepsy
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74. Responsible Genes for Neuronal Migration in the Chromosome 17p13.3: Beyond Pafah1b1(Lis1), Crk and Ywhae(14-3-3ε)
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75. Monoallelic and biallelic mutations inRELNunderlie a graded series of neurodevelopmental disorders
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76. Animal models of human genetic diseases: do they need to be faithful to be useful?
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77. Autism: a target of pharmacotherapies?
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78. An electrophysiological and immunohistochemical study of the hippocampus of the reeler mutant mouse
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79. Thalamic connectivity of the primary motor cortex of normal and reeler mutant mice
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80. The Murine Mutation Trembler-J: Proof of Semidominant Expression by Use of the Linked Vestigial Tail Marker
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81. Immunological Analysis of Cellular Heterogeneity in the Cerebellum
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82. Vacillans, a neurological mutant in the house mouse linked with brown
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83. Zinc finger protein gene complexes on mouse chromosomes 8 and 11
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84. Association Analysis of Two Single-Nucleotide Polymorphisms of the RELN Gene with Autism in the South African Population
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85. Proteolytic cleavage of transmembrane cell adhesion molecule L1 by extracellular matrix molecule Reelin is important for mouse brain development
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86. Proper Layering Is Important for Precisely Timed Activation of Hippocampal Mossy Cells
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87. Cellular and molecular mechanisms of neuronal migration in neocortical development
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88. Reelin, tau phosphorylation and psychiatric complications in patients with hippocampal sclerosis and structural abnormalities in temporal lobe epilepsy
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89. Selective Inactivation of Reelin in Inhibitory Interneurons Leads to Subtle Changes in the Dentate Gyrus But Leaves Cortical Layering and Behavior Unaffected
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90. The disorganized visual cortex in reelin-deficient mice is functional and allows for enhanced plasticity
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92. Compartmentation of the reeler cerebellum: Segregation and overlap of spinocerebellar and secondary vestibulocerebellar fibers and their target cells
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93. Chromosomal Localization of Mouse Hair Keratin Genesa
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94. New Strategies for the Treatment of Neuropsychiatric Disorders Based on Reelin Dysfunction
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95. Reelin and apolipoprotein E receptor 2 in the embryonic and mature brain: effects of an evolutionary change in the apoER2 gene
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99. An In Silico Agent-Based Model Demonstrates Reelin Function in Directing Lamination of Neurons during Cortical Development
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100. Cell death and neurodegeneration in the postnatal development of cerebellar vermis in normal and Reeler mice
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