Literature DB >> 2516179

Niemann-Pick disease type C could result from a genetic deficiency of cholesterol egress from the lysosomes.

W R Den Tandt1, F van Hoof.   

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Year:  1989        PMID： 2516179     DOI： 10.1007/bf01802046

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Type C Niemann-Pick disease. Lysosomal accumulation and defective intracellular mobilization of low density lipoprotein cholesterol.

Authors:  J Sokol; J Blanchette-Mackie; H S Kruth; N K Dwyer; L M Amende; J D Butler; E Robinson; S Patel; R O Brady; M E Comly
Journal:  J Biol Chem       Date:  1988-03-05       Impact factor: 5.157

Review 2.  Role of acylcoenzyme A: cholesterol o-acyltransferase in cholesterol metabolism.

Authors:  A A Spector; S N Mathur; T L Kaduce
Journal:  Prog Lipid Res       Date:  1979       Impact factor: 16.195

3.  Type C Niemann-Pick disease. A parallel loss of regulatory responses in both the uptake and esterification of low density lipoprotein-derived cholesterol in cultured fibroblasts.

Authors:  P G Pentchev; H S Kruth; M E Comly; J D Butler; M T Vanier; D A Wenger; S Patel
Journal:  J Biol Chem       Date:  1986-12-15       Impact factor: 5.157

4.  Type-C Niemann-Pick disease: low density lipoprotein uptake is associated with premature cholesterol accumulation in the Golgi complex and excessive cholesterol storage in lysosomes.

Authors:  E J Blanchette-Mackie; N K Dwyer; L M Amende; H S Kruth; J D Butler; J Sokol; M E Comly; M T Vanier; J T August; R O Brady
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205
  4 in total

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