Literature DB >> 7242684

[Chance and discovery in research on the cause of infantile amaurotic idiocy].

H Jatzkewitz.   

Abstract

Infantile amaurotic idiocy-the classical type known as "Tay-Sachs disease" -is the consequence of the accumulation of a ganglioside and a closely related derivation in the human brain. The accumulation of both substances is due to a genetically induced deficiency of their common catabolic enzyme system. K. Sandhoff discovered three enzymic variants of the disease, which, taken together, did not reveal any apparent causal relationship between enzymic defect and substrate accumulation. The role of chance and discovery in finding the three variants as well as in the elucidation of their causes is described.

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Year:  1981        PMID: 7242684     DOI: 10.1007/bf01047328

Source DB:  PubMed          Journal:  Naturwissenschaften        ISSN: 0028-1042


  12 in total

1.  Variation of beta-N-acetylhexosaminidase-pattern in Tay-Sachs disease.

Authors:  K Sandhoff
Journal:  FEBS Lett       Date:  1969-08       Impact factor: 4.124

2.  Low molecular weight proteins in secondary lysosomes as activators of different sphingolipid hydrolases.

Authors:  W Mraz; G Fischer; H Jatzkewitz
Journal:  FEBS Lett       Date:  1976-08-01       Impact factor: 4.124

3.  EVIDENCE FOR THE GENETIC BLOCK IN METACHROMATIC LEUCODYSTROPHY (ML).

Authors:  E MEHL; H JATZKEWITZ
Journal:  Biochem Biophys Res Commun       Date:  1965-05-03       Impact factor: 3.575

4.  On a biochemically special form of infantile amaturotic idiocy.

Authors:  H JATZKEWITZ; K SANDHOFF
Journal:  Biochim Biophys Acta       Date:  1963-06-18

5.  The activator of cerebroside sulphatase. Purification from human liver and identification as a protein.

Authors:  G Fischer; H Jatzkewitz
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1975-05

6.  Purification, biochemical and immunological characterisation of hexosaminidase A from variant AB of infantile GM2 gangliosidosis.

Authors:  E Conzelmann; K Sandhoff; H Nehrkorn; B Geiger; R Arnon
Journal:  Eur J Biochem       Date:  1978-03

7.  Enzyme alterations and lipid storage in three variants of Tay-Sachs disease.

Authors:  K Sandhoff; K Harzer; W Wässle; H Jatzkewitz
Journal:  J Neurochem       Date:  1971-12       Impact factor: 5.372

8.  Deficient hexosaminidase activity in an exceptional case of Tay-Sachs disease with additional storage of kidney globoside in visceral organs.

Authors:  K Sandhoff; U Andreae; H Jatzkewitz
Journal:  Pathol Eur       Date:  1968

9.  [A cerebrosidesulfatase from swine kidney].

Authors:  E Mehl; H Jatzkewitz
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1964

10.  AB variant of infantile GM2 gangliosidosis: deficiency of a factor necessary for stimulation of hexosaminidase A-catalyzed degradation of ganglioside GM2 and glycolipid GA2.

Authors:  E Conzelmann; K Sandhoff
Journal:  Proc Natl Acad Sci U S A       Date:  1978-08       Impact factor: 11.205

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  1 in total

1.  [Glycolipids of the cell surface--biochemistry of their decomposition].

Authors:  K Sandhoff; T Kolter
Journal:  Naturwissenschaften       Date:  1995-09
  1 in total

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