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

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Items 401–500 of 536

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2. Novel genetic tools facilitate the study of cortical neuron migration
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3. Roles of Reelin/Disabled1 pathway on functional recovery of hemiplegic mice after neural cell transplantation; Reelin promotes migration toward motor cortex and maturation to motoneurons of neural grafts
   Nagisa Nakata Arimitsu, Kenji Takai, Naruyoshi Fujiwara, Jun Shimizu, Yuji Ueda, Sueshige Wakisaka, Chieko Hirotsu, Masanori A. Murayama, Suzuki Tomoko, Noboru Suzuki · 2019 · Experimental Neurology
4. The Fundamental Theorem of Neutral Evolution: Rates of Substitution and Mutation Should Factor in Premeiotic Clusters
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5. Hormonal and morphological study of the pituitaries in reeler mice
   Matilde Lombardero, Kálmán Kovács, Éva Horváth, Ignacio Salazar · 2007 · International Journal of Experimental Pathology
6. Decreased Expression of Synaptophysin 1 (SYP1 Major Synaptic Vesicle Protein p38) and Contactin 6 (CNTN6/NB3) in the Cerebellar Vermis of reln Haplodeficient Mice
   Claudia Castagna, Adalberto Merighi, Laura Lossi · 2019 · Cellular and Molecular Neurobiology
7. Reelin/Dab1 Signaling in the Developing Cerebral Cortex
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8. The Development of Laboratory Animal Science for the Study of Human Muscular and Nervous Diseases in Japan*
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9. From Spontaneous to Induced Neurological Mutations: A Personal Witness of the Ascent of the Mouse Model
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10. Potentialities for and Present Status of Pharmacological Research in Genetically Controlled Mice
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11. Liver esterase abnormalities in hereditary neurological diseases of mice
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12. Neurological Mutants
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13. Differential contribution of P73+ Cajal-Retzius cells and Reelin to cortical morphogenesis
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14. Repurposing Reelin: The new role of radial glia, Reelin and Notch in motor neuron migration
    Alicia L. Hawthorne · 2014 · Experimental Neurology
15. Normal connectivity of thalamorecipient networks in barrel equivalents of the reeler cortex
    Anouk Meeuwissen, Martin Möck, Jochen F. Staiger, Julien Guy · 2023 · Cerebral Cortex
16. Cerebellar Patterning Defects in Mutant Mice
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17. A novel Reelin construct, R36, recovered behavioural deficits in the heterozygous reeler mouse
    Nicole K. Morrill, Qingyou Li, Aurélie Joly‐Amado, Edwin J. Weeber, Kevin R. Nash · 2023 · European Journal of Neuroscience
18. Failure of prosencephalic unfolding and neuronal migration in acardia
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19. Reelin inhibits migration of sympathetic preganglionic neurons in the spinal cord of the chick
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20. NEW PERSPECTIVES IN PEDIATRIC NEUROMUSCULAR DISORDERS Hotel Intercontinental Sydney, Sydney, Australia, August 28, 1998
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21. A comparison of fatty acid activation in sciatic nerve and Schwann cell rich cultures from normal and trembler mice
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22. Mosaic Expression of the Reeler and Normal Phenotypes in the Cerebral Cortex in Reeler‐Normal Chimeras at a Late Embryonic Stage
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23. Electrodiagnostic Studies in a Murine Model of Demyelinating Charcot-Marie-Tooth Disease
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24. USE OF LINKAGE AND CYTOLOGICAL MARKERS TO IDENTIFY MICE DOUBLY AFFECTED BY "STAGGERER" AND "REELER" CONDITIONS
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25. Genetic Dysmyelination Models: A Key to the Mechanisms and Regulation of Myelination
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26. Charcot-Marie-Tooth Disease: Pathology, Genetics, and Animal Models
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27. Reelin, the HPA Axis, and Chronic Stress: Implications for the Neurobiology of Depression
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28. Genetic or therapeutic disruption of the Reelin/Apoer2 signaling pathway improves inflammatory arthritis outcomes
    Laurent Calvier, Catherine R. Wasser, E. Blair Solow, Sharon K. Wu, Bret M. Evers, David S. Karp, Maria Z. Kounnas, Joachim Herz · 2025 · Proceedings of the National Academy of Sciences
29. Animal Models for Brain Research
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30. Thyroid hormones regulate reelin expression in neuropsychiatric disorders
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31. Models of Charcot-Marie-Tooth Disease
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32. Alteration of sulfatide synthesis in control and trembler mice during wallerian degeneration and remyelination
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33. High-Speed Positional Cloning Based on Restriction Landmark Genome Scanning
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34. Cell‐to‐cell Interactions during Development of the Neocortex, with Special Reference to Neuronal Migration*
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35. New Concepts on the Development of the Dentate Gyrus
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36. Caudally pronounced deficiencies in preplate splitting and migration underly a rostro-caudal progression of cortical lamination defects in the reeler brain
    Nieves Mingo-Moreno, Pavel Truschow, Jochen F. Staiger, Robin Jan Wagener · 2024 · Cerebral Cortex
37. Reelin/Disabled‐1 Signalling Contributes to Functional Recovery on Zebrafish After Spinal Cord Injury
    Rong Li, Sudhanshu Sekhar Sahu · 2025 · International Journal of Developmental Neuroscience
38. Development and Developmental Disorders of the Cerebral Cortex
    Hans J. ten Donkelaar, Lana Vasung, Zoltán Molnár, Eleonora Aronica, Martin M. Y. Lammens, Hans van Bokhoven, Karin Kamphuis-van Ulzen, Akira Hori · 2023 · Springer eBooks
39. Radial Migration in the Developing Cerebral Cortex
    Stephen C. Noctor, Christopher L. Cunningham, Arnold R. Kriegstein · 2013 · Elsevier eBooks
40. Models of Neurotoxicity Provide Unique Insight into Normal Development
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41. Transgenic Models of Inherited Neuropathy
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42. Dynamics, nanomechanics and signal transduction in reelin repeats
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43. Notch and neural development
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44. Animal models of epilepsy
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45. Inherited neuromuscular diseases in the mouse: a review of the literature
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46. EVIDENCE OF PROLACTIN CELL DEFICIENCY IN CONNECTION WITH LOW REPRODUCTIVE EFFICIENCY OF FEMALE `TORPID' MICE
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47. Molecular Biology of the Genes Encoding the Major Myelin Proteins
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48. Genetic and Molecular Approaches to Study Neuronal Migration in the Developing Cerebral Cortex
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49. DNA variants are an unlikely explanation for the changing quality of spermatozoa within the same individual
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50. E3 ubiquitin ligases and cerebral cortex development in health and disease
    Nicolas Lambert, Martin Moïse, Laurent Nguyen · 2022 · Developmental Neurobiology
51. Radial migration in the developing cerebral cortex
    Stephen C. Noctor, Christopher L. Cunningham, Arnold R. Kriegstein · 2020 · Elsevier eBooks
52. Apolipoprotein E in Alzheimer's disease: A review of APOE receptors, signalling pathways and therapeutic opportunities
    J. Saravanan, Vigneshwaran Easwaran, Divakar Selvaraj, Venkatesh Gunasekaran, V. Soumya, M. Thiruselvi, M. Laxmana Prasanth, Siddharth Singh, C. Ellaiyarasu, P. Karthik Rai et al. · 2026 · Molecular and Cellular Neuroscience
53. Chapter 19 Genetic basis of peripheral neuropathies
    Linda J. Valentijn, Frank Baas · 1998 · Progress in brain research
54. Modified N-methyl-d-aspartate receptor subunit expression emerges in reeler Purkinje cells after accomplishment of the adult wild-type expression
    Masahiko Watanabe, Irina Maria Moise, Yoshiro Inoue · 1996 · Neuroscience Research
55. Zinc finger proteins in the peripheral nerve of adult normal and Trembler mice
    Isabelle Labatut‐Cazabat, Bertrand Garbay, Alexandre Faveraux, Souad Hilmi, Claude Vital, Claude Cassagne, Klaus G. Petry · 2001 · Journal of the Peripheral Nervous System
56. Analysis of Gene Networks in Cerebellar Development
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57. Genetic influence of a STAU2 frameshift mutation and RELN regulatory elements on performance in Icelandic horses
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58. Biochemistry of autism: changes in serotonin, reelin and oxytocin
    Elizabeta B. Mukaetova‐Ladinska, Jodie Westwood, Elaine King Perry · 2011 · Cambridge University Press eBooks
59. Relation between schizophrenia and Alzheimer's disease: the reelin signaling pathway
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60. Notch and Neural Development
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61. Animal Models for Brain Research
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62. Chapter 32 The molecular basis of the neuropathies of mouse and human
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63. Sarcoplasmic reticulum vesicles from trembler mice: A comparison with material obtained from normal animals
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64. Elevated benzodiazepine receptor density in forebrain of the mutant mouse “Trembler” (TrJ)
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65. Charcot-Marie-Tooth Disease and Related Inherited Myelin Disorders: Molecular Genetics and Implications for Gene Therapy
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66. The Reeler Gene, Formation of Nerve Cell Patterns, and Brain Evolution
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67. Csmd2 interacts with Dab1 and is Required in Reelin-Mediated Neuronal Maturation
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68. Reelin
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69. Cerebellar nuclei cells produce distinct pathogenic spike signatures in mouse models of ataxia, dystonia, and tremor
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70. Reelin Deficiency Alters the Directional Orientation, Apical Localization and Length of Primary Cilia in Principal Neurons in the Cerebral Cortex
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71. Analysis of Reelin function in the molecular mechanisms underlying Alzheimer’s disease
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72. Genetical Study on the New Mutant “falter” Found in the House Mouse (Preliminary notes on experimental breeding and genetics of small mammals, No.1.)
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75. Genetically Defined Myelin Disorders
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76. Cerebellar Mutants in the Laboratory Mouse
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77. Identification and Optogenetic Perturbation of Subsets of preB�tC Neurons in vivo
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78. Neurological Mutant Mice as Genetic Models for Neuronal Transplantation
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79. Der ovarielle Phänotyp der Reelermaus
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83. Snf2l Regulates Foxg1 Expression to Control Cortical Progenitor Cell Proliferation and Differentiation
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95. The SH2 Domain-Containing Adaptor Protein SHD Reversibly Binds the CRKL-SH2 Domain and Knockdown of shdb Impairs Zebrafish Eye Development
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99. Analysis of Gene Networks in Cerebellar Development
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100. House Mouse
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