Mutant mice as a model for cerebellar ataxia
暂无分享,去创建一个
[1] S. Nishiike,et al. Co-localization of glutamate, choline acetyltransferase and glycine in the mammalian vestibular ganglion and periphery. , 1999, Neuroreport.
[2] B. Liss,et al. The weaver Mouse gain-of-functionPhenotype of Dopaminergic Midbrain Neurons Is Determined by Coactivation of wvGirk2 and K-ATP Channels , 1999, The Journal of Neuroscience.
[3] D. Surmeier,et al. Rescue of Cerebellar Granule Cells from Death in weaver NR1 Double Mutants , 1999, The Journal of Neuroscience.
[4] U. Grüsser-Cornehls,et al. Vermectomy enhances parvalbumin expression and improves motor performance in Weaver mutant mice: an animal model for cerebellar ataxia , 1999, Neuroscience.
[5] T. Maeda,et al. Characterization of G-Protein-Gated K+ Channels Composed of Kir3.2 Subunits in Dopaminergic Neurons of the Substantia Nigra , 1999, The Journal of Neuroscience.
[6] U. Grüsser-Cornehls,et al. Course and targets of the calbindin D‐28k subpopulation of primary vestibular afferents , 1998, The Journal of comparative neurology.
[7] U. Grüsser-Cornehls,et al. Improvement in motor performance of Weaver mutant mice following lesions of the cerebellum , 1998, Behavioural Brain Research.
[8] N. Heintz,et al. The Lurcher Mutation and Ionotropic Glutamate Receptors: Contributions to Programmed Neuronal Death In vivo , 1998, Brain pathology.
[9] H. Zoghbi,et al. Mice Lacking Ataxin-1 Display Learning Deficits and Decreased Hippocampal Paired-Pulse Facilitation , 1998, The Journal of Neuroscience.
[10] U. Misgeld,et al. Pore Mutation in a G-Protein-Gated Inwardly Rectifying K+ Channel Subunit Causes Loss of K+-Dependent Inhibition in weaver Hippocampus , 1998, The Journal of Neuroscience.
[11] Jörg Bäurle,et al. Dependence of parvalbumin expression on Purkinje cell input in the deep cerebellar nuclei , 1998, The Journal of comparative neurology.
[12] G. A. Kevetter,et al. Use of calcium‐binding proteins to map inputs in vestibular nuclei of the gerbil , 1997, The Journal of comparative neurology.
[13] Christian Lüscher,et al. G Protein-Coupled Inwardly Rectifying K+ Channels (GIRKs) Mediate Postsynaptic but Not Presynaptic Transmitter Actions in Hippocampal Neurons , 1997, Neuron.
[14] D. Linden,et al. Neurodegeneration in Lurcher mice caused by mutation in δ2 glutamate receptor gene , 1997, Nature.
[15] C Helmchen,et al. Diverse effects of Purkinje cell loss on deep cerebellar and vestibular nuclei neurons in Purkinje cell degeneration mutant mice: A possible compensatory mechanism , 1997, The Journal of comparative neurology.
[16] O. Grüsser,et al. Co‐localization of glycine and calbindin D‐28k in the vestibular ganglion of the rat , 1997, Neuroreport.
[17] Y Agid,et al. An immunocytochemical study on the distribution of two G-protein-gated inward rectifier potassium channels (GIRK2 and GIRK4) in the adult rat brain , 1997, Neuroscience.
[18] B. Ghetti,et al. In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice. , 1997, Journal of Neuropathology and Experimental Neurology.
[19] U. Grüsser-Cornehls,et al. Differential number of glycine‐ and GABA‐immunopositive neurons and terminals in the deep cerebellar nuclei of normal and Purkinje cell degeneration mutant mice , 1997, The Journal of comparative neurology.
[20] Y. Jan,et al. Heteromultimerization of G-Protein-Gated Inwardly Rectifying K+ Channel Proteins GIRK1 and GIRK2 and Their Altered Expression in weaver Brain , 1996, The Journal of Neuroscience.
[21] Richard Hawkes,et al. Absence Epilepsy in Tottering Mutant Mice Is Associated with Calcium Channel Defects , 1996, Cell.
[22] K. Zilles,et al. Neuronal Hyperexcitability and Reduction of GABAA-Receptor Expression in the Surround of Cerebral Photothrombosis , 1996, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.
[23] W. Stühmer,et al. IRK(1–3) and GIRK(1–4) Inwardly Rectifying K+Channel mRNAs Are Differentially Expressed in the Adult Rat Brain , 1996, The Journal of Neuroscience.
[24] C. Heizmann,et al. α-Parvalbumin reduces depolarizationminduced elevations of cytosolic free calcium in human neuroblastoma cells , 1996 .
[25] Masahiko Watanabe,et al. Developmental changes in expression and distribution of the glutamate receptor channel delta 2 subunit according to the Purkinje cell maturation. , 1996, Brain research. Developmental brain research.
[26] E. Hess,et al. Chromosomal localization of the neurological mouse mutations tottering (tg), Purkinje cell degeneration (pcd), and nervous (nr). , 1996, Brain research. Molecular brain research.
[27] W. Zhang,et al. Amelioration of the behavioral phenotype in genetically ataxic mice through bilateral intracerebellar grafting of fetal Purkinje cells. , 1996, Cell transplantation.
[28] B. Birren,et al. Disruption of the nuclear hormone receptor RORα in staggerer mice , 1996, Nature.
[29] U. Grüsser-Cornehls,et al. Electrophysiology and GABA-immunocytochemistry in the vestibular nuclei of normal (C57BL/6J) and Leaner mutant mice , 1995, Brain Research.
[30] J. Meinzen-Derr,et al. Selective elimination of cerebellar output in the genetically dystonic rat , 1995, Brain Research.
[31] R. Nowakowski,et al. Morphological abnormalities in the hippocampus of the weaver mutant mouse , 1995, Brain Research.
[32] W. Zhang,et al. Graft-induced restoration of function in hereditary cerebellar ataxia , 1995, Neuroreport.
[33] T. Schneider,et al. Molecular biology of calcium channels. , 1995, Kidney international.
[34] David R. Cox,et al. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation , 1995, Nature Genetics.
[35] Youngnam Kang,et al. Impairment of motor coordination, Purkinje cell synapse formation, and cerebellar long-term depression in GluRδ2 mutant mice , 1995, Cell.
[36] K. Ikeda,et al. Molecular cloning of a mouse G-protein-activated K+ channel (mGIRK1) and distinct distributions of three GIRK (GIRK1, 2 and 3) mRNAs in mouse brain. , 1995, Biochemical and biophysical research communications.
[37] N. Dieringer,et al. Size‐related colocalization of glycine and glutamate immunoreactivity in frog and rat vestibular afferents , 1994, The Journal of comparative neurology.
[38] S. Takashima,et al. Vermis lesions in acute cerebellar ataxia: a sequential imaging study , 1994, Brain and Development.
[39] L. Abbott,et al. Purkinje cell loss from alternating sagittal zones in the cerebellum of leaner mutant mice , 1994, Brain Research.
[40] R. Currier,et al. Decreased insulin-like growth factor I-mediated protein tyrosine phosphorylation in human olivopontocerebellar atrophy and lurcher mutant mouse , 1994, Journal of the Neurological Sciences.
[41] T. Mittmann,et al. Lesion-induced transient suppression of inhibitory function in rat neocortex in vitro , 1994, Neuroscience.
[42] N. Leclerc,et al. Effects of nervous mutation on purkinje cell compartments defined by Zebrin II and 9-O-acetylated gangliosides expression , 1994, Neuroscience Research.
[43] U. Grüsser‐Cornehls,et al. Calbindin D-28k in the lateral vestibular nucleus of mutant mice as a tool to reveal Purkinje cell plasticity , 1994, Neuroscience Letters.
[44] R. J. Mullen,et al. Retinal degeneration in the nervous mutant mouse. I. Light microscopic cytopathology and changes in the interphotoreceptor matrix , 1993, The Journal of comparative neurology.
[45] M. LeDoux,et al. Cerebellectomy Eliminates the Motor Syndrome of the Genetically Dystonic Rat , 1993, Experimental Neurology.
[46] Joan F. Lorden,et al. Abnormal cerebellar output in rats with an inherited movement disorder , 1992, Experimental Neurology.
[47] U. Grüsser-Cornehls,et al. Plasticity of GABAergic terminals in Deiters' nucleus of weaver mutant and normal mice: a quantitative light microscopic study , 1992, Brain Research.
[48] R. Currier,et al. Inositol 1,4,5-trisphosphate metabolism in the cerebella of Lurcher mutant mice and patients with olivopontocerebellar atrophy , 1992, Journal of the Neurological Sciences.
[49] P. Conn. Methods in neurosciences , 1991 .
[50] C. Sotelo,et al. The reconstruction of cerebellar circuits , 1991, Trends in Neurosciences.
[51] R. Currier,et al. Inositol 1,4,5-triphosphate receptors and protein kinase C in olivopontocerebellar atrophy , 1991, Brain Research.
[52] U Büttner,et al. Fastigial nucleus activity in the alert monkey during slow eye and head movements. , 1991, Journal of neurophysiology.
[53] J. Hore,et al. Cerebellar dysmetria at the elbow, wrist, and fingers. , 1991, Journal of neurophysiology.
[54] M. Celio,et al. Calbindin D-28k and parvalbumin in the rat nervous system , 1990, Neuroscience.
[55] R. Rosenberg. Autosomal dominant cerebellar phenotypes , 1990, Neurology.
[56] C. Heizmann,et al. Coexistence of parvalbumin and glycine in the rat brainstem , 1990, Brain Research.
[57] G. Brüning,et al. Autoradiographic analysis of benzodiazepine receptors in mutant mice with cerebellar defects. , 1990, Journal of Chemical Neuroanatomy.
[58] Richard J Smeyne,et al. Postnatal development of the wild-type and weaver cerebellum after embryonic administration of propylthiouracil (PTU). , 1990, Brain research. Developmental brain research.
[59] C. Batini. Cerebellar localization and colocalization of GABA and calcium binding protein-D28K. , 1990, Archives italiennes de biologie.
[60] S. Ozawa,et al. Change in calcium permeability caused by quinolinic acid in cultured rat hippocampal neurons , 1989, Neuroscience Letters.
[61] B. Ghetti,et al. The dendritic dopamine projection of the substantia nigra: phenotypic denominator of weaver gene action in hetero- and homozygosity , 1989, Brain Research.
[62] D. Prince,et al. Frequency‐dependent depression of inhibition in guinea‐pig neocortex in vitro by GABAB receptor feed‐back on GABA release. , 1989, The Journal of physiology.
[63] Richard J Smeyne,et al. Development and death of external granular layer cells in the weaver mouse cerebellum: a quantitative study , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[64] Anthony E. Lang,et al. Movement Disorders: A Comprehensive Survey , 1989 .
[65] F. D. Silva,et al. Kindling induced changes in parvalbumin immunoreactivity in rat hippocampus and its relation to long-term decrease in GABA-immunoreactivity , 1989, Brain Research.
[66] C. Gerday,et al. Monoclonal antibodies directed against the calcium binding protein parvalbumin. , 1988, Cell calcium.
[67] N. Delhaye-bouchaud,et al. Stability of inferior olivary neurons in rodents. I. Moderate cell loss in adult Purkinje cell degeneration mutant mouse. , 1988, Brain research.
[68] K. Herrup,et al. Regional differences in cytoarchitecture of the weaver cerebellum suggest a new model for weaver gene action , 1987, Neuroscience.
[69] C. Sotelo,et al. Cerebellar mutations affecting the postnatal survival of Purkinje cells in the mouse disclose a longitudinal pattern of differentially sensitive cells. , 1987, Developmental biology.
[70] C. Sotelo,et al. Non-Purkinje cell GABAergic innervation of the deep cerebellar nuclei: A quantitative immunocytochemical study in C57BL and in Purkinje cell degeneration mutant mice , 1986, Brain Research.
[71] A. Graybiel,et al. Expression of the weaver gene in dopamine-containing neural systems is dose-dependent and affects both striatal and nonstriatal regions , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[72] M. Alexander,et al. Principles of Neural Science , 1981 .
[73] B. Ghetti,et al. NERVE CELL ATROPHY AND LOSS IN THE INFERIOR OLIVARY COMPLEX OF PURKINJE CELL DEGENERATION (ved) MUTANT MICE , 1986 .
[74] J. Hatfield,et al. Mitochondrial dysfunction in spinocerebellar and macular degeneration , 1985 .
[75] I. Whishaw,et al. Dopamine depletion, stimulation or blockade in the rat disrupts spatial navigation and locomotion dependent upon beacon or distal cues , 1985, Behavioural Brain Research.
[76] S. O’Gorman. Degeneration of thalamic neurons in “Purkinje cell degeneration” mutant mice. II. Cytology of neuron loss , 1985, The Journal of comparative neurology.
[77] R. Sidman,et al. Degeneration of thalamic neurons in “Purkinje cell degeneration” mutant mice. I. Distribution of neuron loss , 1985, The Journal of comparative neurology.
[78] G. Blatt,et al. A qualitative and quantitative light microscopic study of the inferior olivary complex of normal, reeler, and weaver mutant mice , 1985, The Journal of comparative neurology.
[79] H. J. Baker,et al. Characterization of the rat mutant dystonic (dt): a new animal model of dystonia musculorum deformans , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[80] J. E. Vaughn,et al. Immunocytochemical localization of glutamic acid decarboxylase in the dorsal lateral vestibular nucleus: Evidence for an intrinsic and extrinsic GABAergic innervation , 1984, Neuroscience Letters.
[81] Masao Ito. The Cerebellum And Neural Control , 1984 .
[82] C. Heizmann,et al. Parvalbumin in non-muscle tissues of the rat. Quantitation and immunohistochemical localization. , 1984, The Journal of biological chemistry.
[83] Adam M. Sillito,et al. The influence of GABAergic inhibitory processes on the receptive field structure of X and Y cells in cat dorsal lateral geniculate nucleus (dLGN) , 1983, Brain Research.
[84] E. Eidelberg,et al. Recovery of locomotor function in cats after localized cerebellar lesions , 1983, Brain Research.
[85] R. J. Mullen,et al. Retinal degeneration in the pcd cerebellar mutant mouse. I. Light microscopic and autoradiographio analysis , 1982, The Journal of comparative neurology.
[86] K. Herrup,et al. Interaction of granule, Purkinje and inferior olivary neurons in lurcher chimeric mice. II. Granule cell death , 1982, Brain Research.
[87] R. J. Mullen,et al. Granule cell as a site of gene action in the weaver mouse cerebellum: evidence from heterozygous mutant chimeras , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[88] K. Herrup,et al. Cerebellar cell degeneration in the leaner mutant mouse , 1982, Neuroscience.
[89] A. Harding. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'. , 1982, Brain : a journal of neurology.
[90] B. Ghetti,et al. Dopamine deficiency in the weaver mutant mouse , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[91] A. Kaszniak,et al. Cerebellar atrophy , 1981, Neurology.
[92] D. Zee,et al. Effects of ablation of flocculus and paraflocculus of eye movements in primate. , 1981, Journal of neurophysiology.
[93] C. Heizmann,et al. Calcium-binding protein parvalbumin as a neuronal marker , 1981, Nature.
[94] A. Harding. Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features. , 1981, Brain : a journal of neurology.
[95] G. Glaser,et al. Cerebellar gangliosides and phospholipids in mutant mice with ataxia and epilepsy: the Tottering/Leaner syndrome , 1981, Brain Research.
[96] J. Dichgans,et al. Delayed and enhanced long latency reflexes as the possible cause of postural tremor in late cerebellar atrophy. , 1981, Brain : a journal of neurology.
[97] V. V. Fanardjian,et al. Spatial organization of the cerebellar corticovestibular projection in the cat , 1980, Neuroscience.
[98] C. Sotelo. Mutant mice and the formation of cerebellar circuitry , 1980, Trends in Neurosciences.
[99] K. Caddy,et al. Structural and quantitative studies on the normal C3H and Lurcher mutant mouse. , 1979, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[100] J. Noebels. Analysis of inherited epilepsy using single locus mutations in mice. , 1979, Federation proceedings.
[101] Karl Herrup,et al. Regional variation and absence of large neurons in the cerebellum of the staggerer mouse , 1979, Brain Research.
[102] R L Sidman,et al. Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering. , 1979, Science.
[103] R. Sidman,et al. Neurochemical and morphological consequences of axon terminal degeneration in cerebellar deep nuclei of mice with inherited purkinje cell degeneration , 1979, Brain Research.
[104] B. Ghetti,et al. STUDIES ON THE PURKINJE CELL DEGENERATION (pcd) MUTANT: PRIMARY PATHOLOGY AND TRANSNEURONAL CHANGES , 1978 .
[105] J. Glowinski,et al. Release of dopamine in both caudate nuclei and both substantia nigrae in response to unilateral stimulation of cerebellar nuclei in the cat , 1978, Brain Research.
[106] N. A. Kotb,et al. Neurological syndromes produced by some toxic metals encountered industrially or environmentally , 1978, Zeitschrift fur Ernahrungswissenschaft.
[107] M. Berry,et al. The Purkinje cell dendritic tree in mutant mouse cerebellum. A quantitative Golgi study of Weaver and Staggerer mice , 1978, Brain Research.
[108] R. J. Mullen. Site of pcd gene action and Purkinje cell mosaicism in cerebella of chimaeric mice , 1977, Nature.
[109] J. Changeux,et al. Anatomical, physiological and biochemical studies of the cerebellum from Reeler mutant mouse. , 1977, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[110] Doris B. Wilson,et al. Cerebellar histogenesis in the lurcher (Lc) mutant mouse , 1977, The Journal of comparative neurology.
[111] V. Chan‐Palay. Cerebellar Dentate Nucleus: Organization, Cytology and Transmitters , 1977 .
[112] A. Streissguth,et al. THE EFFECTS OF MODERATE ALCOHOL CONSUMPTION DURING PREGNANCY ON FETAL GROWTH AND MORPHOGENESIS , 1977, Pediatric Research.
[113] D. Robinson. Adaptive gain control of vestibuloocular reflex by the cerebellum. , 1976, Journal of neurophysiology.
[114] C. H. Yoon. Pleiotropic effect of the staggerer gene , 1976, Brain Research.
[115] J. Menkes. Letter: Toxic polyneuropathy due to methyl n-butyl ketone. , 1976, Archives of neurology.
[116] J. Changeux,et al. Anatomical, physiological and biochemical studies on the cerebellum from mutant mice. III. Protein differences associated with the weaver, staggerer and nervous mutations , 1976, Brain Research.
[117] M. Okamoto,et al. Some aspects of the spinal cord in anencephalus , 1976 .
[118] R. J. Mullen,et al. Two new types of retinal degeneration in cerebellar mutant mice , 1975, Nature.
[119] C. Sotelo. Anatomical, physiological and biochemical studies of the cerebellum from mutant mice. II. Morphological study of cerebellar cortical neurons and circuits in the weaver mouse , 1975, Brain Research.
[120] K. Caddy,et al. Preliminary observations on the cerebellum in the mutant mouse lurcher , 1975, Brain Research.
[121] E P Gardner,et al. Single-unit responses to natural vestibular stimuli and eye movements in deep cerebellar nuclei of the alert rhesus monkey. , 1975, Journal of neurophysiology.
[122] R. Galen,et al. Methyl iodide intoxication. A case report. , 1975, Annals of Internal Medicine.
[123] J. Mendell,et al. Toxic polyneuropathy due to methyl n-butyl ketone. An industrial outbreak. , 1975 .
[124] R. Maurice-Williams,et al. Mechanism of production of gait unsteadiness by tumours in the posterior fossa. , 1975, Journal of neurology, neurosurgery, and psychiatry.
[125] C. Sotelo,et al. Bergmann fibers and granular cell migration in the cerebellum of homozygous weaver mutant mouse. , 1974, Brain research.
[126] J. Desclin. Histological evidence supporting the inferior olive as the major source of cerebellar climbing fibers in the rat. , 1974, Brain research.
[127] R. Isaacson. The Limbic System , 1974, Springer US.
[128] J. Changeux,et al. Transsynaptic degeneration 'en cascade' in the cerebellar cortex of staggerer mutant mice. , 1974, Brain research.
[129] T. Shiida,et al. Visual influence on rabbit horizontal vestibulo-ocular reflex presumably effected via the cerebellar flocculus. , 1974, Brain research.
[130] P. Rakić,et al. Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant mice , 1973, The Journal of comparative neurology.
[131] P. Rakić,et al. Organization of cerebellar cortex secondary to deficit of granule cells in weaver mutant mice , 1973, The Journal of comparative neurology.
[132] W. Precht,et al. Removal of vestibular commissural inhibition by antagonists of GABA and glycine. , 1973, Brain research.
[133] S. Oda. [The observation of rolling mouse Nagoya (rol), a new neurological mutant, and its maintenance (author's transl)]. , 1973, Jikken dobutsu. Experimental animals.
[134] S. Landis. Changes in neuronal mitochondrial shape in brains of nervous mutant mice. , 1973, The Journal of heredity.
[135] A. Streissguth,et al. Pattern of Malformation in Offspring of Chronic Alcoholic Mothers , 1995, Alcohol health and research world.
[136] J. Eccles. The cerebellum as a computer: patterns in space and time. , 1973, The Journal of physiology.
[137] H. M. Dembitzer,et al. CEREBELLAR ALTERATIONS IN THE WEAVER MOUSE , 1973, The Journal of cell biology.
[138] C. Yoon,et al. Abnormal rate of granule cell migration in the cerebellum of "Weaver" mutant mice. , 1972, Developmental biology.
[139] N. Iwahori,et al. Structural organization of the interpositus and the dentate nuclei. , 1971, Brain research.
[140] H. Meier,et al. Three syndromes produced by two mutant genes in the mouse. Clinical, pathological, and ultrastructural bases of tottering, leaner, and heterozygous mice. , 1971, The Journal of heredity.
[141] A. Igata. [Ataxia associated with infections and toxicosis]. , 1971, Nihon rinsho. Japanese journal of clinical medicine.
[142] J. Albus. A Theory of Cerebellar Function , 1971 .
[143] J H Milsum,et al. Characteristics of neural transmission from the semicircular canal to the vestibular nuclei of cats , 1970, The Journal of physiology.
[144] F. Fonnum,et al. Glutamate decarboxylase in inhibitory neurons. A study of the enzyme in Purkinje cell axons and boutons in the cat. , 1970, Brain research.
[145] B. Konigsmark,et al. THE OLIVOPONTOCEREBELLAR ATROPHIES: A REVIEW , 1970, Medicine.
[146] C. H. Yoon. Disturbances in developmental pathways leading to a neurological disorder of genetic origin, "leaner", in mice. , 1969, Developmental biology.
[147] D. Marr. A theory of cerebellar cortex , 1969, The Journal of physiology.
[148] E. Mancall,et al. Alterations of the cerebellar cortex in nutritional encephalopathy , 1965, Neurology.
[149] S. Yamada. Polineuritis caused in the Workers Exposed to n-Hexane , 1964 .
[150] P. Milner,et al. Activity changes following partial hippocampal lesions in rats. , 1963, Journal of comparative and physiological psychology.
[151] W. N. Dember,et al. Alternation and exploration in rats with hippocampal lesions. , 1962, Journal of comparative and physiological psychology.
[152] R. Sidman,et al. Staggerer, a New Mutation in the Mouse Affecting the Cerebellum , 1962, Science.
[153] O. Pompeiano,et al. The fastigiovestibular projection in the cat. An experimental study with silver impregnation methods , 1962, The Journal of comparative neurology.
[154] S. Tóth. THE EFFECT OF THE REMOVAL OF THE NUCLEUS DENTATUS ON THE PARKINSONIAN SYNDROME , 1961 .
[155] R. Adams,et al. A Restricted Form of Cerebellar Cortical Degeneration Occurring in Alcoholic Patients , 1959 .
[156] R. Dejong,et al. THE NEUROLOGIC EXAMINATION , 1959 .
[157] R. Dow,et al. The Physiology and Pathology of the Cerebellum , 1958 .
[158] O. Pompeiano,et al. Spino‐vestibular fibers in the cat. An experimental study , 1957, The Journal of comparative neurology.
[159] R. E. Correll. The effect of bilateral hippocampal stimulation on the acquisition and extinction of an instrumental response. , 1957, Journal of comparative and physiological psychology.
[160] B. Katz,et al. A study of the ‘desensitization’ produced by acetylcholine at the motor end‐plate , 1957, The Journal of physiology.
[161] P. Maclean. Chemical and electrical stimulation of hippocampus in unrestrained animals. I. Methods and electroencephalographic findings. , 1957, A.M.A. archives of neurology and psychiatry.
[162] G. Jervis. Concordant primary atrophy of the cerebellar granules in monozygotic twins. , 1954, Acta geneticae medicae et gemellologiae.
[163] A. Brodal,et al. Neurological Anatomy in Relation to Clinical Medicine , 1950 .
[164] R. Norman. PRIMARY DEGENERATION OF THE GRANULAR LAYER OF THE CEREBELLUM: AN UNUSUAL FORM OF FAMILIAL CEREBELLAR ATROPHY OCCURRING IN EARLY LIFE , 1940 .
[165] G. Holmes. THE CEREBELLUM OF MAN , 1939 .
[166] Robert S. Dow,et al. The fiber connections of the posterior parts of the cerebellum in the rat and cat , 1936 .
[167] R. de Nó. The central projection of the nerve endings of the internal ear , 1933 .
[168] G. Holmes. THE SYMPTOMS OF ACUTE CEREBELLAR INJURIES DUE TO GUNSHOT INJURIES , 1917 .
[169] H. Müller,et al. Scar modulation in subacute and chronic CNS lesions: Effects on axonal regeneration. , 1999, Restorative neurology and neuroscience.
[170] G. Orban,et al. Reorganization in the visual cortex after retinal and cortical damage. , 1999, Restorative neurology and neuroscience.
[171] J. Dichgans,et al. The genetic basis of hereditary ataxia. , 1997, Progress in brain research.
[172] Wei-Hua Lee,et al. Grafted cerebellar cells in a mouse model of hereditary ataxia express IGF–I system genes and partially restore behavioral function , 1996, Nature Medicine.
[173] F. Krug,et al. Enlargement of GAD-immunopositive terminals in the lateral vestibular nucleus (LVN) of weaver mutant mice. , 1995, Histology and histopathology.
[174] T. Knöpfel,et al. Activity induced elevations of intracellular calcium concentration in neurons of the deep cerebellar nuclei. , 1994, Journal of neurophysiology.
[175] R. Currier,et al. The phosphoinositide second messenger system in human OPCA and the mouse model. , 1993, Advances in neurology.
[176] Harding Ae. Clinical features and classification of inherited ataxias. , 1993, Advances in neurology.
[177] H. Diener,et al. Pathophysiology of cerebellar ataxia , 1992, Movement disorders : official journal of the Movement Disorder Society.
[178] L. Triarhou. Weaver Gene Expression in Central Nervous System , 1992 .
[179] R. Tsien,et al. Molecular diversity of voltage-dependent Ca2+ channels. , 1991, Trends in pharmacological sciences.
[180] M. Ito. A new physiological concept on cerebellum. , 1990, Revue neurologique.
[181] M. Ito,et al. Long-term depression. , 1989, Annual review of neuroscience.
[182] L. Bolis,et al. Calcium and Calcium Binding Proteins , 1988, Proceedings in Life Sciences.
[183] H. Flohr. Post-Lesion Neural Plasticity , 1988, Springer Berlin Heidelberg.
[184] C. Heizmann. Parvalbumin in Non-Muscle Cells , 1988 .
[185] U. Grüsser-Cornehls,et al. Compensatory Mechanisms at the Level of the Vestibular Nuclei Following Post-Natal Degeneration of Specific Cerebellar Cell Classes and Ablation of the Cerebellum in Mutant Mice , 1988 .
[186] H C Pape,et al. Excitatory and differential disinhibitory actions of acetylcholine in the lateral geniculate nucleus of the cat. , 1986, The Journal of physiology.
[187] B. G. Grover,et al. Cerebellar afferents in normal and Weaver mutant mice. , 1986, Brain, Behavior and Evolution.
[188] G. Paxinos. The Rat nervous system , 1985 .
[189] P. Zilla,et al. Ectopic parvalbumin-positive cells in the cerebellum of the adult mutant mouse 'nervous'. , 1985, Acta anatomica.
[190] G. Goodall,et al. Permanency of gait improvement induced by vestibular stimulation in the mutant mouse staggerer. , 1985, Journal of neurogenetics.
[191] A. Harding. The hereditary ataxias and related disorders , 1984 .
[192] Margaret C. Green,et al. Genetic variants and strains of the laboratory mouse , 1981 .
[193] J. Bloedel,et al. Disorders of the cerebellum , 1981 .
[194] J. Glowinski,et al. Control of the activity of the two dopaminergic systems by cortical, cerebellar and sensory afferents in the cat. , 1979, Applied neurophysiology.
[195] R. J. Mullen,et al. The development and degeneration of Purkinje cells in pcd mutant mice , 1978, The Journal of comparative neurology.
[196] P. Rakić,et al. Mechanisms of cortical development: a view from mutations in mice. , 1978, Annual review of neuroscience.
[197] M. Udo,et al. Cerebellar control of locomotion investigated in cats: discharges from Deiters' neurones, EMG and limb movements during local cooling of the cerebellar cortex. , 1976, Progress in brain research.
[198] O. Burešová,et al. Techniques and Basic Experiments for the Study of Brain and Behavior , 1976 .
[199] K. Nakane. Postnatal development of brain in mice with congenital ataxia, rolling (rol) and tottering (tg). Abstr. , 1976 .
[200] R. J. Mullen,et al. Purkinje cell degeneration, a new neurological mutation in the mouse. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[201] C. Sotelo. Dendritic abnormalities of Purkinje cells in the cerebellum of neurologic mutant mice (weaver and staggerer). , 1975, Advances in neurology.
[202] P. Rakić,et al. Weaver mutant mouse cerebellum: defective neuronal migration secondary to abnormality of Bergmann glia. , 1973, Proceedings of the National Academy of Sciences of the United States of America.
[203] R. Llinás,et al. Neuronal circuit reorganization in mammalian agranular cerebellar cortex. , 1973, Journal of neurobiology.
[204] F. D. Carlson. Physiological and Biochemical Aspects of Nervous Integration , 1968 .
[205] N. Zervas,et al. Cerebellar dentatectomy in primates and humans. , 1967, Transactions of the American Neurological Association.
[206] S. Yamada. AN OCCURRENCE OF POLYNEURITIS BY N-HEXANE IN THE POLYETHYLENE LAMINATING PLANTS , 1964 .
[207] Ramón y Cajal,et al. Histologie du système nerveux de l'homme & des vertébrés , 1909 .
[208] G. Holmes. A FORM OF FAMILIAL DEGENERATION OF THE CEREBELLUM , 1908 .