Acid sphingomyelinase-deficient mice mimic the neurovisceral form of human lysosomal storage disease (Niemann-Pick disease)

This publication has 13 references indexed in Scilit:

• Phospholipid signaling
  Cell, 1995
• Functional dichotomy of neutral and acidic sphingomyelinases in tumor necrosis factor signaling
  Cell, 1994
• Programmed Cell Death Induced by Ceramide
  Science, 1993
• Molecular Cloning of the Acid Sphingomyelinase of the Mouse and the Organization and Complete Nucleotide Sequence of the Gene
  Biological Chemistry Hoppe-Seyler, 1992
• Type C Niemann-Pick Disease: Biochemical Aspects and Phenotypic Heterogeneity
  Developmental Neuroscience, 1991
• Biochemical Basis of Late-Onset Neurolipidoses
  Developmental Neuroscience, 1991
• Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1→p15.4
  Genomics, 1991
• Niemann-Pick Disease in a Poodle Dog
  Veterinary Pathology, 1979
• A Simple Chemical Method for Labelling Phosphatidylcholine and Sphingomyelin in the Choline Moiety
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1971
• Über die Natur der Phosphatide und anderer Lipoide des Gehirns und der Leber bei der Niemann-Pickschen Krankheit. [12. Mitteilung über Phosphatide.]
  Hoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1935