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Volumn 2, Issue 5, 2002, Pages 439-444
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Mutated genes in juvenile and variant late infantile neuronal ceroid lipofuscinoses encode lysosomal proteins
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Author keywords
[No Author keywords available]
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Indexed keywords
CLN3 PROTEIN;
CLN5 PROTEIN;
GENE PRODUCT;
LYSOSOME ENZYME;
PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;
UNCLASSIFIED DRUG;
ADENOSINE TRIPHOSPHATASE;
CHAPERONE;
CLN3 PROTEIN, HUMAN;
CLN5 PROTEIN, HUMAN;
FUNGAL PROTEIN;
MEMBRANE PROTEIN;
PROTEIN;
ALLELE;
CELL SPECIFICITY;
CONTROLLED STUDY;
DEGENERATIVE DISEASE;
ELECTROENCEPHALOGRAM;
ENZYME SUBUNIT;
FINLAND;
GENE DELETION;
GENE EXPRESSION;
GENE IDENTIFICATION;
GENE MUTATION;
GENETIC CODE;
HISTOPATHOLOGY;
HOMEOSTASIS;
HUMAN;
IN VITRO STUDY;
KNOCKOUT MOUSE;
LIFESPAN;
LYSOSOME;
MOLECULAR CLONING;
NERVE CELL;
NEURONAL CEROID LIPOFUSCINOSIS;
NONHUMAN;
ONSET AGE;
PH;
PHENOTYPE;
PROTEIN FUNCTION;
PROTEIN LOCALIZATION;
REVIEW;
SEQUENCE HOMOLOGY;
SYNAPTOSOME;
YEAST;
ANIMAL;
DISEASE MODEL;
ENZYMOLOGY;
GENETICS;
METABOLISM;
MITOCHONDRION;
MOUSE;
MUTATION;
PATHOLOGY;
TISSUE DISTRIBUTION;
ADENOSINETRIPHOSPHATASE;
ALLELES;
ANIMAL;
DISEASE MODELS, ANIMAL;
FUNGAL PROTEINS;
GENE DELETION;
HUMAN;
HYDROGEN-ION CONCENTRATION;
LYSOSOMES;
MEMBRANE PROTEINS;
MICE;
MITOCHONDRIA;
MUTATION;
NEURONAL CEROID-LIPOFUSCINOSIS;
PROTEINS;
SUPPORT, NON-U.S. GOV'T;
TISSUE DISTRIBUTION;
ADENOSINE TRIPHOSPHATASES;
ANIMALS;
HUMANS;
MEMBRANE GLYCOPROTEINS;
MOLECULAR CHAPERONES;
NEURONAL CEROID-LIPOFUSCINOSES;
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EID: 0035990974
PISSN: 15665240
EISSN: None
Source Type: Journal
DOI: 10.2174/1566524023362311 Document Type: Review |
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Times cited : (25)
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References (35)
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