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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1984-3-30
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pubmed:abstractText |
Lysosomal and plasma membrane sialidase activities in lymphocytes were studied in four patients with sialidosis with partial beta-galactosidase deficiency, four obligate heterozygotes, and three siblings of a patient. Lysosomal sialidase activity in homozygotes was absent, and that in heterozygotes was significantly decreased to 70% of control level. The results indicate that carriers can be detected by the assay of lysosomal sialidase activity of lymphocytes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0364-5134
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
15
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
181-3
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:6703657-Adult,
pubmed-meshheading:6703657-Cell Membrane,
pubmed-meshheading:6703657-Heterozygote Detection,
pubmed-meshheading:6703657-Humans,
pubmed-meshheading:6703657-Lactose Intolerance,
pubmed-meshheading:6703657-Lymphocytes,
pubmed-meshheading:6703657-Lysosomes,
pubmed-meshheading:6703657-Male,
pubmed-meshheading:6703657-Middle Aged,
pubmed-meshheading:6703657-Neuraminidase
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pubmed:year |
1984
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pubmed:articleTitle |
Carrier detection of sialidosis with partial beta-galactosidase deficiency by the assay of lysosomal sialidase in lymphocytes.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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