Literature DB >> 11945522

The hydrolysis of Tay-Sachs ganglioside (TSG) by human N-acetyl-beta-D-hexosaminidase A.

K Sandhoff1.   

Abstract

Entities:  

Year:  1970        PMID： 11945522     DOI： 10.1016/0014-5793(70)80564-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN： 0014-5793            Impact factor:   4.124


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  18 in total

Review 1.  Basic findings and current developments in sphingolipidoses.

Authors:  H Pilz; R Heipertz; D Seidel
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

2.  Purification and chemical characterization of human hexosaminidases A and B.

Authors:  J E Lee; A Yoshida
Journal:  Biochem J       Date:  1976-12-01       Impact factor: 3.857

3.  Hexosaminidase assays.

Authors:  Michaela Wendeler; Konrad Sandhoff
Journal:  Glycoconj J       Date:  2009-11       Impact factor: 2.916

Review 4.  Glycosphingolipid hydrolases: properties and molecular genetics.

Authors:  M Wan Ho; A G Norden; J A Alhadeff; J S O'Brien
Journal:  Mol Cell Biochem       Date:  1977-10-07       Impact factor: 3.396

5.  Gangliosidosis with total hexosaminidase deficiency: clinical, biochemical and ultrastructural studies and comparison with conventional cases of Tay-Sachs disease.

Authors:  G Fontaine; A Résibois; M Tondeur; G Jonniaux; J P Farriaux; W Voet; E Maillard; H Loeb
Journal:  Acta Neuropathol       Date:  1973-01-30       Impact factor: 17.088

6.  [Preliminary results in the prenatal diagnosis of Tay-Sachs disease by isoelectric focusing of hexosaminidase A (author's transl)].

Authors:  K Harzer
Journal:  Klin Wochenschr       Date:  1974-02-01

7.  Absence of -N-acetyl-D-hexosaminidase A activity in a healthy woman.

Authors:  J Vidgoff; N R Buist; J S O'Brien
Journal:  Am J Hum Genet       Date:  1973-07       Impact factor: 11.025

8.  Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.

Authors:  R Navon; B Padeh; A Adam
Journal:  Am J Hum Genet       Date:  1973-05       Impact factor: 11.025

9.  [Enzymatic studies on the blood of carriers of a Tay-Sachs disease variant (variant O)].

Authors:  K Harzer; K Sandhoff; H Schall; F Kollmann
Journal:  Klin Wochenschr       Date:  1971-11-01

10.  [Juvenile GM2 gangliosidosis with altered substrate specificity of hexosaminidase A (author's transl)].

Authors:  J Zerfowski; K Sandhoff
Journal:  Acta Neuropathol       Date:  1974-03-26       Impact factor: 17.088
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