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Significados de lysosomal storage em inglês

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Uso de lysosomal storage em inglês
1
Mice lacking ClC-7 show altered lysosomal function that leads to severe lysosomal storage.
Pubmed
2
Abundant lysosomal storage was present in many sites by 14 dpn.
Pubmed
3
We systematically review the emerging genetic links between lysosomal storage disorders and PD.
Pubmed
4
Non-immune hydrops fetalis is the most severe presenting feature of lysosomal storage disorders.
Pubmed
5
In the brain, hippocampal and neocortical neurons and meningeal cells showed lysosomal storage.
Pubmed
6
Enzyme replacement therapy (ERT) effectively reverses storage in several lysosomal storage diseases.
Pubmed
7
Gaucher disease is the most common lysosomal storage disorder due to glucosylceramidase enzyme deficiency.
Pubmed
8
These results may have important implications for ERT for lysosomal storage diseases with CNS involvement.
Pubmed
9
Objective: Fabry disease is a rare X-linked inherited lysosomal storage disorder affecting multiple organ systems.
Pubmed
10
Introduction: Gaucher disease (GD) is the most common lysosomal storage disorder.
Pubmed
11
Genetic mutations that cause specific enzyme deficiencies account for more than 40 lysosomal storage disorders.
Pubmed
12
Gaucher disease (GD) represents the most common lysosomal storage defect.
Pubmed
13
Cardiovascular manifestations of lysosomal storage disease (LSD) are a significant health problem for affected patients.
Pubmed
14
A deficiency in human AC activity leads to the lysosomal storage disorder, Farber disease (FD).
Pubmed
15
Gaucher disease is the most common lysosomal storage disorder caused by deficiency of the lysosomal enzyme glucocerebrosidase.
Pubmed
16
The mucopolysaccharidoses are a group of lysosomal storage disorders caused by defects in the degradation of glycosaminoglycans.
Pubmed
Esta colocação é formada por:
Lysosomal storage ao longo do tempo
Lysosomal storage nas variantes da língua
Estados Unidos da América
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