(Q70459037)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single "Gaucher gene" (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference

R A Gravel

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

A Leung

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

publication date

1 January 1983

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

volume

65

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11 October 2019

issue

2

1 reference

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11 October 2019

page(s)

112-116

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https://scigraph.springernature.com/pub.10.1007/bf00286645

11 October 2019

exact match

0 references

cites work

Isolation and Characterization of Glucocerebrosidase from Human Placental Tissue

1 reference

12 December 2020

Assignment of the gene for acid beta-glucosidase to human chromosome 1

1 reference

12 December 2020

Analysis of genetic complementation by whole-cell microtechniques in fibroblast heterokaryons

1 reference

12 December 2020

Properties of beta-glucosidase in cultured skin fibroblasts from controls and patients with Gaucher disease

1 reference

12 December 2020

Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharides

1 reference

12 December 2020

Isolation of heat-stable glucocerebrosidase activators from the spleens of three variants of Gaucher's disease

1 reference

12 December 2020

Quantitative assays of enzyme activity in single cells: early prenatal diagnosis of genetic disorders

1 reference

12 December 2020

Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts

1 reference

12 December 2020

Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Chronic Gaucher's disease: heat-resistance of leukocyte glucocerebrosidase in relation to some clinical parameters

1 reference

12 December 2020

Enzyme replacement therapy in Gaucher's disease: large-scale purification of glucocerebrosidase suitable for human administration

1 reference

12 December 2020

Kinetic analysis of genetic complementation in heterokaryons of propionyl CoA carboxylase-deficient human fibroblasts

1 reference

12 December 2020

Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant

1 reference

12 December 2020

Enzymic diagnosis in 27 cases with Gaucher's disease

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00286645

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418635%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference