Tissue culture studies in the lipid storage disorders (Q65000756)

3 July 2019

title

Tissue culture studies in the lipid storage disorders (English)

1 reference

https://api.crossref.org/works/10.1016/0009-3084(70)90022-8

23 May 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5476324

23 May 2023

1 reference

https://api.crossref.org/works/10.1016/0009-3084(70)90022-8

23 May 2023

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https://api.crossref.org/works/10.1016/0009-3084(70)90022-8

23 May 2023

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https://api.crossref.org/works/10.1016/0009-3084(70)90022-8

23 May 2023

author name string

H. R. Sloan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5476324

23 May 2023

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=5476324

23 May 2023

publication date

1 October 1970

1 reference

3 July 2019

full work available at URL

https://api.elsevier.com/content/article/PII:0009308470900228?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/0009-3084(70)90022-8

https://api.elsevier.com/content/article/PII:0009308470900228?httpAccept=text/plain

23 May 2023

1 reference

https://api.crossref.org/works/10.1016/0009-3084(70)90022-8

Chemistry and Physics of Lipids

23 May 2023

published in

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3 July 2019

volume

5

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3 July 2019

issue

1

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3 July 2019

page(s)

250-260

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3 July 2019

Properties of galactosemic cells in culture

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The cerebral defect in Tay-Sachs disease and Niemann-Pick disease

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Diagnosis of gaucher's disease and niemann-pick disease with small samples of venous blood

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Gaucher's Disease: A Genetic Disease Detected in Skin Fibroblast Cultures

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Deficiency of sphingomyelin-cleaving enzyme activity in tissue cultures derived from patients with Niemann-Pick disease

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β-Galactosidase in Tissue Culture Derived from Human Skin and Bone Marrow: Enzyme defect in GM1 Gangliosidosis

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ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM

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Gml-ganglioside accumulation and β-galactosidase deficiency in a case of Gml-gangliosidosis (Landing disease)

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Metachromatic Leukodystrophy: Diagnosis with Samples of Venous Blood

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EVIDENCE FOR THE GENETIC BLOCK IN METACHROMATIC LEUCODYSTROPHY (ML).

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Metachromatic leukodystrophy (sulfatide lipidoses) cultured in vitro.

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A simple method for the isolation and purification of total lipides from animal tissues

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Fetal Complications of Amniocentesis

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Diagnosis of the adrenogenital syndrome before birth

23 May 2023

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Intrauterine diagnosis and management of genetic defects

23 May 2023

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Biochemical diagnosis of an X-linked disease in utero.

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Intrauterine diagnosis of the hurler and hunter syndromes

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23 May 2023

Identifiers

1 reference

3 July 2019

1 reference

3 July 2019