Increased GABA receptor binding in dominantly-inherited cerebellar ataxias

[1]  R. Olsen,et al.  γ‐Aminobutyric acid receptors in normal human brain and Huntington disease , 1982, Neurology.

[2]  J. Palacios,et al.  High affinity GABA receptors — Autoradiographic localization , 1981, Brain Research.

[3]  O. Snead,et al.  Olivopontocerebellar atrophy in children: A report of seven cases in two families , 1981, Annals of neurology.

[4]  S. Kish,et al.  Neurotransmitter amino acids in dominantly inherited cerebellar disorders , 1981, Neurology.

[5]  R. Olsen,et al.  gamma-Aminobutyric acid receptor binding in mammalian brain. Heterogeneity of binding sites. , 1981, Molecular pharmacology.

[6]  S. Snyder,et al.  Neurotransmitter receptor localizations: Brain lesion induced alterations in benzodiazepine, GABA, β-adrenergic and histamine H1-receptor binding , 1980, Brain Research.

[7]  R. Olsen,et al.  GABA and picrotoxinin receptors in clonal nerve cells , 1980, Nature.

[8]  F. V. Defeudis,et al.  Na+‐Independent Binding of [3H]GABA and [3H]Muscimol to Subcellular Particles of Neural Primary Cultures and Whole Brain , 1980, Journal of neurochemistry.

[9]  A. Guidotti,et al.  GABA receptors in clonal cell lines: a model for study of benzodiazepine action at molecular level. , 1979, Science.

[10]  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.

[11]  K. Mikoshiba,et al.  Localization of gamma‐aminobutyric acid receptor binding in the mammalian cerebellum high levels in granule layer and depletion in agranular cerebella of mutant mice , 1978, Journal of neurochemistry.

[12]  R. Currier,et al.  Aspartate‐taurine imbalance in dominantly inherited olivopontocerebellar atrophy , 1977, Neurology.

[13]  Story C. Landis,et al.  Olivopontocerebellar degeneration. Clinical and ultrastructural abnormalities. , 1974, Archives of neurology.

[14]  Shirley Hansen,et al.  Huntington's Chorea , 1973 .

[15]  R. Currier,et al.  Spinocerebellar ataxia , 1972, Neurology.

[16]  B. Konigsmark,et al.  THE OLIVOPONTOCEREBELLAR ATROPHIES: A REVIEW , 1970, Medicine.

[17]  K. Krnjević,et al.  Iontophoretic studies of neurones in the mammalian cerebral cortex , 1963, The Journal of physiology.

[18]  Oliver H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[19]  J. Schut.  HEREDITARY ATAXIA: Clinical Study Through Six Generations , 1950 .

[20]  C. R. Prasad,et al.  Lack of Na+ ‐independent binding of [3H]GABA or [3H]Muscimol to subcellular particles of C6 glioma cells , 1982 .

[21]  T. Perry,et al.  A versatile lithium buffer elution system for single column automatic amino acid chromatography. , 1968, Journal of chromatography.