Neu4, a novel human lysosomal lumen sialidase, confers normal phenotype to sialidosis and galactosialidosis cells

Journal of Biological Chemistry

Volumn 279, Issue 35, 2004, Pages 37021-37029

  Seyrantepe, Volkan ^a   Landry, Karine ^a   Trudel, Stéphanie ^a   Hassan, Jacob A ^b   Morales, Carlos R ^b   Pshezhetsky, Alexey V ^a  

^a UNIVERSITY OF MONTREAL   (Canada)

^b MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; GENES; MUTAGENESIS; PATIENT MONITORING; POLYSACCHARIDES; TISSUE;

ENZYMATIC ACTIVITY; LYSOSOMES;

ENZYMES;

COMPLEMENTARY DNA; LYSOSOME ENZYME; PHOSPHORUS 32; POLYADENYLATED RNA; SIALIDASE;

AMINO ACID SEQUENCE; ANIMAL CELL; ARTICLE; CATALYSIS; CELL FRACTIONATION; CHROMOSOME 2; CONFOCAL MICROSCOPY; DEGENERATIVE DISEASE; ELECTRON MICROSCOPY; ENZYME ACTIVITY; ENZYME DEFICIENCY; GENE; GENE EXPRESSION; GENE MUTATION; GENETIC DISORDER; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE MICROSCOPY; ISOTOPE LABELING; LYSOSOME; NEU1 GENE; NEU2 GENE; NEU3 GENE; NEU4 GENE; NEUROLOGIC DISEASE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PLASMID; PRIORITY JOURNAL; SIALIDOSIS; SKIN FIBROBLAST;

ANIMALIA; MAMMALIA;

EID: 4344608107     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.M404531200     Document Type: Article

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