Literature DB >> 416963

Complementation studies with enucleated fibroblasts from different variants of beta-galactosidase deficiency.

H A de Wit-Verbeek, A Hoogeveen, H Galjaard.   

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Year:  1978        PMID： 416963     DOI： 10.1016/0014-4827(78)90104-0

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN： 0014-4827            Impact factor:   3.905


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  6 in total

Review 1.  Biochemistry and genetics of gangliosidoses.

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

2.  The genetic defect in the various types of human beta-galactosidase deficiency.

Authors:  H L Hoeksema; J De Wit; A Westerveld
Journal:  Hum Genet       Date:  1980-02       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.  Assignment of structural beta-galactosidase loci to human chromosomes 3 and 22.

Authors:  J de Wit; H L Hoeksema; D Bootsma; A Westerveld
Journal:  Hum Genet       Date:  1979-10-02       Impact factor: 4.132

5.  Human lysosomal genes: arylsulfatase A and beta-galactosidase.

Authors:  G A Bruns; B J Mintz; A C Leary; V M Regina; P S Gerald
Journal:  Biochem Genet       Date:  1979-12       Impact factor: 1.890

6.  Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblasts.

Authors:  A d'Azzo; D J Halley; A Hoogeveen; H Galjaard
Journal:  Am J Hum Genet       Date:  1980-07       Impact factor: 11.025
  6 in total

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