Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration

R. N. Rosenberg, C. Banner

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Immunochemical analyses (Western blots) of cerebellar homogenates for glutamate dehydrogenase (GDH) from patients with spinocerebellar degeneration and control subjects were conducted. Four patients with autosomal dominant Joseph disease type of spinocerebellar degeneration, one patient with autosomal olivopontocerebellar degeneration and four control subjects were studied. GDH was of the same molecular weight and amount in all patients and control subjects. These data together with normal GDH activity from these same homogenates published previously support the view that GDH is not involved in the pathogenesis of these types of dominantly inherited spinocerebellar degeneration.

Original languageEnglish (US)
Pages (from-to)666-668
Number of pages3
JournalJournal of Neurology Neurosurgery and Psychiatry
Volume52
Issue number5
StatePublished - 1989

Fingerprint

Spinocerebellar Degenerations
Glutamate Dehydrogenase
Proteins
Olivopontocerebellar Atrophies
Machado-Joseph Disease
Molecular Weight
Western Blotting

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Neuroscience(all)
  • Neuropsychology and Physiological Psychology

Cite this

Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration. / Rosenberg, R. N.; Banner, C.

In: Journal of Neurology Neurosurgery and Psychiatry, Vol. 52, No. 5, 1989, p. 666-668.

Research output: Contribution to journalArticle

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