Literature DB >> 1192826

Tay-Sachs and Sandhoff-Jatzkewitz diseases: complementation of hexosaminidase A deficiency by somatic cell hybridization.

M C Rattazzi, J A Brown, R G Davidson, T B Shows.   

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Year:  1975        PMID： 1192826     DOI： 10.1159/000130393

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  4 in total

Review 1.  Biochemistry and genetics of gangliosidoses.

Authors:  K Sandhoff; H Christomanou
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

2.  Genetic complementation in somatic cell hybrids of four variants of infantile GM2 gangliosidosis.

Authors:  S Sonderfeld; S Brendler; K Sandhoff; H Galjaard; A T Hoogeveen
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  The expression of hex A and hex B isozymes of hexosaminidase in parental and experimental human fibroblast cells and their components.

Authors:  M T Bladon
Journal:  Biochem Genet       Date:  1981-10       Impact factor: 1.890

4.  Juvenile Sandhoff Disease: complementation tests with Sandhoff and Tay-Sachs disease using polyethylene glycol-induced cell fusion.

Authors:  S Wood
Journal:  Hum Genet       Date:  1978-04-24       Impact factor: 4.132
  4 in total

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