(Q41405155)

30 September 2017

title

Juvenile Sandhoff Disease: complementation tests with Sandhoff and Tay-Sachs disease using polyethylene glycol-induced cell fusion (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A417993

29 June 2022

Juvenile sandhoff disease: Complementation tests with Sandhoff and Tay-Sachs disease using polyethylene glycol-induced cell fusion (English)

1 reference

26 April 2023

1 reference

1 reference

1 reference

26 April 2023

author name string

S. Wood

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A417993

29 June 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=417993

29 June 2022

publication date

1 April 1978

1 reference

30 September 2017

24 April 1978

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=417993

full work available at URL

29 June 2022

http://link.springer.com/content/pdf/10.1007/BF00284766.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00284766/fulltext.html

26 April 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00284766

26 April 2023

1 reference

26 April 2023

1 reference

30 September 2017

volume

41

1 reference

30 September 2017

issue

3

1 reference

30 September 2017

page(s)

325-329

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00284766

30 September 2017

exact match

0 references

cites work

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic complementation after fusion of Tay-Sachs and Sandhoff cells.

1 reference

12 December 2020

Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis

1 reference

12 December 2020

Hexosaminidase isozyme in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease).

1 reference

12 December 2020

Tay-Sachs and Sandhoff's disease: intergenic complementation after somatic cell hybridization.

1 reference

12 December 2020

Chemical characterization and subunit structure of human N-acetylhexosaminidases A and B

1 reference

12 December 2020

Complementation after fusion of Sandhoff- and Tay-Sachs fibroblasts

1 reference

12 December 2020

Progressive cerebeilar ataxia, spasticity, psychomotor retardation, and hexosaminidase deficiency in a 10-year-old child: Juvenile Sandhoff disease

1 reference

12 December 2020

Juvenile Sandhoff disease: some properties of the residual hexosaminidase in cultured fibroblasts

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Production of mammalian somatic cell hybrids by means of polyethylene glycol treatment

1 reference

12 December 2020

Ganglioside GM2 storage diseases: hexosaminidase deficiencies in cultured fibroblasts

1 reference

12 December 2020

Tay-Sachs Disease: Generalized Absence of a Beta-D- N -Acetylhexosaminidase Component

1 reference

12 December 2020

Characterization of Hex S, the major residual beta hexosaminidase activity in type O Gm2 gangliosidosis (Sandhoff-Jatzkewitz disease)

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00284766

1 reference

Dimensions Publication ID

30 September 2017

1053607439

0 references

1 reference