δ-Tocopherol Reduces Lipid Accumulation in Niemann-Pick Type C1 and Wolman Cholesterol Storage Disorders*
暂无分享,去创建一个
U. Baxa | W. Pavan | Noel Southall | C. Austin | Jingbo Xiao | Wei Zheng | J. Marugan | M. Swaroop | A. Remaley | D. Ory | Wei Sun | J. McKew | S. Walkley | Miao Xu | F. Porter | C. Davidson | Ke Liu | Rohini Sidhu | Sally Firnkes
[1] W. Pavan,et al. Plasma and Tissue Concentrations of α-Tocopherol and δ-Tocopherol Following High Dose Dietary Supplementation in Mice , 2012, Nutrients.
[2] W. Nyhan,et al. Wolman disease/cholesteryl ester storage disease , 2011 .
[3] S. Pfeffer,et al. Niemann–Pick type C 1 function requires lumenal domain residues that mediate cholesterol-dependent NPC2 binding , 2011, Proceedings of the National Academy of Sciences.
[4] A. Ballabio,et al. Transcriptional Activation of Lysosomal Exocytosis Promotes Cellular Clearance , 2011, Developmental cell.
[5] B. Davidson,et al. Clarifying lysosomal storage diseases , 2011, Trends in Neurosciences.
[6] N. Yoshida,et al. Starvation and rapamycin differentially regulate host cell lysosome exocytosis and invasion by Trypanosoma cruzi metacyclic forms , 2011, Cellular microbiology.
[7] K. Sandhoff,et al. Lysosomal lipid storage diseases. , 2011, Cold Spring Harbor perspectives in biology.
[8] M. Pineda,et al. New agents and approaches to treatment in Niemann-Pick type C disease. , 2011, Current pharmaceutical biotechnology.
[9] Ruili Huang,et al. The NCGC Pharmaceutical Collection: A Comprehensive Resource of Clinically Approved Drugs Enabling Repurposing and Chemical Genomics , 2011, Science Translational Medicine.
[10] Paul Helquist,et al. Histone deacetylase inhibitor treatment dramatically reduces cholesterol accumulation in Niemann-Pick type C1 mutant human fibroblasts , 2011, Proceedings of the National Academy of Sciences.
[11] Y. Ioannou,et al. Cyclodextrin Induces Calcium-Dependent Lysosomal Exocytosis , 2010, PloS one.
[12] M. Vanier. Niemann-Pick disease type C , 2010, Orphanet journal of rare diseases.
[13] J. Katsaras,et al. The location and behavior of alpha-tocopherol in membranes. , 2010, Molecular nutrition & food research.
[14] R. Brigelius-Flohé,et al. alpha-Tocopherol enhances degranulation in RBL-2H3 mast cells. , 2010, Molecular nutrition & food research.
[15] C. Cross,et al. Dietary alpha-tocopherol and neuromuscular health: search for optimal dose and molecular mechanisms continues! , 2010, Molecular nutrition & food research.
[16] F. Maxfield,et al. Chemical screen to reduce sterol accumulation in Niemann-Pick C disease cells identifies novel lysosomal acid lipase inhibitors. , 2009, Biochimica et biophysica acta.
[17] D. Ory,et al. Chronic Cyclodextrin Treatment of Murine Niemann-Pick C Disease Ameliorates Neuronal Cholesterol and Glycosphingolipid Storage and Disease Progression , 2009, PloS one.
[18] Joseph L. Goldstein,et al. Structure of N-Terminal Domain of NPC1 Reveals Distinct Subdomains for Binding and Transfer of Cholesterol , 2009, Cell.
[19] J. Pais de Barros,et al. 7-Ketocholesterol Incorporation into Sphingolipid/Cholesterol-enriched (Lipid Raft) Domains Is Impaired by Vitamin E , 2009, The Journal of Biological Chemistry.
[20] J. Repa,et al. Reversal of defective lysosomal transport in NPC disease ameliorates liver dysfunction and neurodegeneration in the npc1−/− mouse , 2009, Proceedings of the National Academy of Sciences.
[21] D. Sviridov,et al. Asymmetry in the Lipid Affinity of Bihelical Amphipathic Peptides , 2008, Journal of Biological Chemistry.
[22] A. Galione,et al. Niemann-Pick disease type C1 is a sphingosine storage disease that causes deregulation of lysosomal calcium , 2008, Nature Medicine.
[23] C. Patterson,et al. Plasma tocopherols and risk of cognitive impairment in an elderly Italian cohort. , 2008, The American journal of clinical nutrition.
[24] Elina Ikonen,et al. Cellular cholesterol trafficking and compartmentalization , 2008, Nature Reviews Molecular Cell Biology.
[25] O. Qureshi,et al. Regulation of P2X4 receptors by lysosomal targeting, glycan protection and exocytosis , 2007, Journal of Cell Science.
[26] R. Parker,et al. Influence of major structural features of tocopherols and tocotrienols on their ω-oxidation by tocopherol-ω-hydroxylase Published, JLR Papers in Press, February 6, 2007. , 2007, Journal of Lipid Research.
[27] R. Arantes,et al. A Role for Synaptotagmin VII-Regulated Exocytosis of Lysosomes in Neurite Outgrowth from Primary Sympathetic Neurons , 2006, The Journal of Neuroscience.
[28] C. Sen,et al. Tocotrienols: Vitamin E beyond tocopherols. , 2006, Life sciences.
[29] E. Eggermont. Recent advances in vitamin E metabolism and deficiency , 2006, European Journal of Pediatrics.
[30] H. Büssow,et al. Exocytosis of storage material in a lysosomal disorder. , 2005, Biochemical and biophysical research communications.
[31] Xianlin Han,et al. Toward fingerprinting cellular lipidomes directly from biological samples by two-dimensional electrospray ionization mass spectrometry. , 2004, Analytical biochemistry.
[32] J. Breslow,et al. Intracellular Cholesterol Transport , 2004, Arteriosclerosis, thrombosis, and vascular biology.
[33] D. Ory. The niemann-pick disease genes; regulators of cellular cholesterol homeostasis. , 2004, Trends in cardiovascular medicine.
[34] L. Appel,et al. Supplementation of Diets with α-Tocopherol Reduces Serum Concentrations of γ- and δ-Tocopherol in Humans , 2003 .
[35] P. Yancey,et al. Importance of different pathways of cellular cholesterol efflux. , 2003, Arteriosclerosis, thrombosis, and vascular biology.
[36] R. Parker,et al. Cytochrome P450 omega-hydroxylase pathway of tocopherol catabolism. Novel mechanism of regulation of vitamin E status. , 2002, The Journal of biological chemistry.
[37] E. Caler,et al. Plasma Membrane Repair Is Mediated by Ca2+-Regulated Exocytosis of Lysosomes , 2001, Cell.
[38] D. Rader,et al. Phenotypic correction of lipid storage and growth arrest in wolman disease fibroblasts by gene transfer of lysosomal acid lipase. , 2001, Human gene therapy.
[39] M. Wolman. Wolman Disease and Its Treatment , 1995, Clinical pediatrics.
[40] T. Koeda,et al. Type C Niemann-Pick disease Detection and quantification of cholesterol-accumulating cells in bone marrow , 1993, Brain and Development.
[41] J. Alroy,et al. Ultrastructural findings in skin from patients with Niemann-Pick disease, type C. , 1990, Pediatric neurology.
[42] S. Patel,et al. Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblasts. , 1986, The Journal of biological chemistry.
[43] Lysosomal Storage Diseases , 1986, The Lancet.
[44] A. Norman,et al. Studies on the biological properties of polyene antibiotics. Evidence for the direct interaction of filipin with cholesterol. , 1972, The Journal of biological chemistry.
[45] W. J. Dyer,et al. A rapid method of total lipid extraction and purification. , 1959, Canadian journal of biochemistry and physiology.
[46] K. Nagashima,et al. Biological tissue and cell culture specimen preparation for TEM nanoparticle characterization. , 2011, Methods in molecular biology.
[47] C. Cellai,et al. Altered cholesterol ester cycle in skin fibroblasts from patients with Alzheimer's disease. , 2009, Journal of Alzheimer's disease : JAD.
[48] M. Patterson,et al. PART 16 : LYSOSOMAL DISORDERS Chapter 145 : Niemann-Pick Disease Type C : A Lipid Trafficking Disorder , 2007 .
[49] S. Morley,et al. The α‐Tocopherol Transfer Protein , 2007 .
[50] R. Gillies,et al. Tamoxifen and vitamin E treatments delay symptoms in the mouse model of Niemann-Pick C. , 2004, Journal of applied genetics.