Utilitzem cookies
Aquest lloc web utilitza cookies per a oferir-vos la informació més rellevant. Si vosté continua navegant, accepta aquestes cookies.
Aquest lloc web utilitza cookies per a oferir-vos la informació més rellevant. Si vosté continua navegant, accepta aquestes cookies.
Ho sabíeu?
Podeu fer doble clic en una paraula per a buscar-la a TermGallery.
Podeu fer doble clic en una paraula per a buscar-la a TermGallery.
Significats de lysosomal storage en anglès
Encara no tenim significats per a "lysosomal storage".
Ús de lysosomal storage en anglès
1
Mice lacking ClC-7 show altered lysosomal function that leads to severe lysosomal storage.
2
Abundant lysosomal storage was present in many sites by 14 dpn.
3
We systematically review the emerging genetic links between lysosomal storage disorders and PD.
4
Non-immune hydrops fetalis is the most severe presenting feature of lysosomal storage disorders.
5
In the brain, hippocampal and neocortical neurons and meningeal cells showed lysosomal storage.
6
Enzyme replacement therapy (ERT) effectively reverses storage in several lysosomal storage diseases.
7
Gaucher disease is the most common lysosomal storage disorder due to glucosylceramidase enzyme deficiency.
8
These results may have important implications for ERT for lysosomal storage diseases with CNS involvement.
9
Objective: Fabry disease is a rare X-linked inherited lysosomal storage disorder affecting multiple organ systems.
10
Introduction: Gaucher disease (GD) is the most common lysosomal storage disorder.
11
Genetic mutations that cause specific enzyme deficiencies account for more than 40 lysosomal storage disorders.
12
Gaucher disease (GD) represents the most common lysosomal storage defect.
13
Cardiovascular manifestations of lysosomal storage disease (LSD) are a significant health problem for affected patients.
14
A deficiency in human AC activity leads to the lysosomal storage disorder, Farber disease (FD).
15
Gaucher disease is the most common lysosomal storage disorder caused by deficiency of the lysosomal enzyme glucocerebrosidase.
16
The mucopolysaccharidoses are a group of lysosomal storage disorders caused by defects in the degradation of glycosaminoglycans.
Aquesta col·locació està formada per:
Lysosomal storage a través del temps
Lysosomal storage per variant geogràfica
Estats Units d'Amèrica
Comú