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Volumn 8, Issue 1, 2001, Pages 100-102
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Niemann-Pick Disease versus acid sphingomyelinase deficiency [1]
a a a a b c d a |
Author keywords
[No Author keywords available]
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Indexed keywords
CERAMIDE;
SPHINGOMYELIN;
SPHINGOMYELIN PHOSPHODIESTERASE;
ADULTHOOD;
ANIMAL CELL;
ANIMAL MODEL;
APOPTOSIS;
B LYMPHOCYTE;
CELL TRANSFORMATION;
CLINICAL FEATURE;
CONTROLLED STUDY;
DEGENERATIVE DISEASE;
DISEASE CLASSIFICATION;
DISEASE SEVERITY;
ENZYME ACTIVITY;
EPSTEIN BARR VIRUS;
FEMALE;
HYDROLYSIS;
INFANCY;
LETTER;
LIPID METABOLISM;
LIVER CELL;
MEMBRANE DAMAGE;
MOUSE;
NIEMANN PICK DISEASE;
NONHUMAN;
OVARY DEVELOPMENT;
PHENOTYPE;
POINT MUTATION;
PRIORITY JOURNAL;
SECOND MESSENGER;
SIGNAL TRANSDUCTION;
SPLEEN CELL;
T LYMPHOCYTE;
TREMOR;
ANIMALS;
APOPTOSIS;
CAVEOLIN 1;
CAVEOLINS;
CELLS, CULTURED;
CERAMIDES;
FIBROBLASTS;
HUMANS;
LIVER;
MICE;
MICE, KNOCKOUT;
NIEMANN-PICK DISEASES;
PHENOTYPE;
RADIATION TOLERANCE;
SIGNAL TRANSDUCTION;
SPHINGOMYELIN PHOSPHODIESTERASE;
SPLEEN;
ANIMALIA;
HUMAN HERPESVIRUS 4;
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EID: 0035137630
PISSN: 13509047
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.cdd.4400775 Document Type: Letter |
Times cited : (26)
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References (29)
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