Examples of 'lysosomal storage' in a sentence
Meaning of "lysosomal storage"
Lysosomal storage: A group of inherited metabolic disorders characterized by an abnormal build-up of various substances within cells due to enzyme deficiencies in the lysosomes
How to use "lysosomal storage" in a sentence
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lysosomal storage
Gene therapy for lysosomal storage diseases.
Lysosomal storage disease enzymes.
Examples of such are the lysosomal storage diseases.
Nearly all lysosomal storage disorders are autosomal recessive.
It is a recessively inherited lysosomal storage disorder.
All of the lysosomal storage diseases are hereditary.
It is part of a family of diseases called lysosomal storage disorders.
Clarifying lysosomal storage diseases.
This invention is related to the area of lysosomal storage diseases.
Lysosomal storage disorders.
The result is a lysosomal storage disorder.
Lysosomal storage defects in sphingolipid metabolism or sphingolipidoses are also important in humans.
Pompe disease is one of several lysosomal storage disorders.
It is a lysosomal storage disorder.
Intraventricular enzyme delivery for lysosomal storage diseases.
See also
It is a lysosomal storage disease which is commonly listed in the family of leukodystrophies.
Galactosialidosis is a lysosomal storage disease.
Lysosomal storage disorders typically occur in early life because of a genetic error.
It is a type of lysosomal storage disorder.
One disclosure relates to a method of treating a subject with a lysosomal storage disorder.
It belongs to a lysosomal storage disorders.
Fabry disease is one of a group of conditions known as lysosomal storage diseases.
Hundreds of patients with lysosomal storage disorders have been treated by transplantation for many years.
Pharmaceutical compositions and uses directed to lysosomal storage disorders.
These lysosomal storage discascs include Gaucher disease.
Methods and compositions for the treatment of lysosomal storage diseases.
These lysosomal storage diseases include Gaucher disease.
Enzyme replacement therapy has been used for other lysosomal storage diseases.
AGU is a rare lysosomal storage disorder with autosomal recessive inheritance.
A similar principle is now used for the treatment of other lysosomal storage diseases.
NPC is a lysosomal storage disorder in which cholesterol accumulates in the brain.
If the individual has symptoms clinically associated with a certain lysosomal storage disease.
The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme.
All the cells in the body can be affected by lysosomal storage diseases or glycogenosis.
Lysosomal storage and impaired autophagy lead to inflammasome activation in Gaucher macrophages.
Examples of therapeutic agents include the enzymes that are deficient in lysosomal storage diseases.
FD is considered a lysosomal storage disease.
Enzyme replacement therapy is particularly effective when treating certain lysosomal storage diseases.
Deficiency in GCR activity results in a lysosomal storage disease referred to as Gaucher disease.
The present disclosure is in one embodiment related to a method for treating lysosomal storage disorders.
The latter diseases are called lysosomal storage disorders and include Fabry and Batten diseases.
Also described herein are compositions and methods for the treatment of lysosomal storage diseases.
Methods to treat the lysosomal storage disease can also include methods to treat Gaucher disease.
The present invention is aimed at providing new means for treating the lysosomal storage disorders.
Lysosomal Storage Disorders Many of the inherited protein deficient disorders are enzyme deficiencies.
This is where AD differs from other lysosomal storage diseases.
Lysosomal Storage DiseasesCollaboration.
PPS may also be used alone to treat lysosomal storage disorders.
Lysosomal storage diseases, nervous system.
Lysosomal fusion and SNARE function are impaired by cholesterol accumulation in lysosomal storage disorders.
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Examples of using Storage
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Examples of using Lysosomal
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Synthesis of lysosomal enzymes is controlled by nuclear genes
Ketoprofen has been documented to stabilise lysosomal cell membranes
Synthesis of lysosomal enzymes are controlled by nuclear genes