Necroptosis in Niemann–Pick disease, type C1: a potential therapeutic target-Reference-Cited by-同舟云学术

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Necroptosis in Niemann–Pick disease, type C1: a potential therapeutic target

Published:2016-03 Issue:3 Volume:7 Page:e2147-e2147
ISSN:2041-4889
Container-title:Cell Death & Disease
language:en
Short-container-title:Cell Death Dis

Author:

Cougnoux A,Cluzeau C,Mitra S,Li R,Williams I,Burkert K,Xu X,Wassif C A,Zheng W,Porter F D

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology,Cellular and Molecular Neuroscience,Immunology

Link

http://www.nature.com/articles/cddis201616.pdf

Reference51 articles.

1. Vanier MT . Niemann-Pick disease type C. Orphanet J Rare Dis 2010; 5: 16.

2. Wassif CA, Cross JL, Iben J, Sanchez-Pulido L, Cougnoux A, Platt FM et al. High incidence of unrecognized visceral/neurological late-onset Niemann-Pick disease, type C1, predicted by analysis of massively parallel sequencing data sets. Genet Med 2015; 18: 41–48.

3. Walkley SU, Suzuki K . Consequences of NPC1 and NPC2 loss of function in mammalian neurons. Biochim Biophys Acta 2004; 1685: 48–62.

4. Lloyd-Evans E, Morgan AJ, He X, Smith DA, Elliot-Smith E, Sillence DJ et al. Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium. Nat Med 2008; 14: 1247–1255.

5. Patterson MC, Vecchio D, Prady H, Abel L, Wraith JE . Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study. Lancet Neurol 2007; 6: 765–772.

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