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Results 1 - 10 of 347 for lysosomal
  1. Lysosomal acid lipase deficiency is an inherited condition characterized by problems with the breakdown and use of fats and cholesterol in the body (lipid metabolism). ...
  2. ... gene provides instructions for producing an enzyme called lysosomal acid lipase. This enzyme is found in cell ... and recycle materials the cell no longer needs. Lysosomal acid lipase breaks down fats (lipids) such as ...
  3. ... gene provides instructions for making a protein called lysosomal integral membrane protein-2 (LIMP-2). As its ... glucocerebroside. The LIMP-2 protein remains in the lysosomal membrane after transporting beta-glucocerebrosidase and is important ...
  4. ... molecules to build up inside lysosomes are called lysosomal storage disorders. Mutations that eliminate NEU1 enzyme activity ... acetylneuraminyl hydrolase exo-alpha-sialidase FLJ93471 G9 sialidase lysosomal sialidase N-acetyl-alpha-neuraminidase 1 NANH NEU ...
  5. ... T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein a T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3 T-cell, immune regulator 1, ...
  6. ... Elsevier; 2020:chap 104. Krasnewich DM, Sidransky E. Lysosomal storage diseases. In: Goldman L, Schafer AI, eds. ...
  7. ... MPS I do not make an enzyme called lysosomal alpha-L-iduronidase. This enzyme helps break down ...
  8. ... instructions for making a protein known as the lysosomal trafficking regulator. Researchers believe that this protein plays ... and recycle worn-out cell components. Although the lysosomal trafficking regulator protein is involved in the normal ...
  9. ... deficiency Alpha-mannosidase deficiency Deficiency of alpha-mannosidase Lysosomal alpha B mannosidosis Lysosomal alpha-D-mannosidase deficiency Mannosidosis Genetic Testing Registry: ...
  10. ... the condition. Beta-D-mannosidosis Beta-mannosidase deficiency Lysosomal beta A mannosidosis Lysosomal beta-mannosidase deficiency Genetic Testing Registry: Beta-D- ...
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