Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1. - Wikidata - wikimedia - TriplyDB

Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1.

Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1.

http://www.wikidata.org/entity/Q36122424

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Collaborative development of 2-hydroxypropyl-β-cyclodextrin for the treatment of Niemann-Pick type C1 disease Genomic expression analyses reveal lysosomal, innate immunity proteins, as disease correlates in murine models of a lysosomal storage disorder Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism Investigations Pre-symptomatic activation of antioxidant responses and alterations in glucose and pyruvate metabolism in Niemann-Pick Type C1-deficient murine brain Defective Cytochrome P450-Catalysed Drug Metabolism in Niemann-Pick Type C Disease Gpnmb Is a Potential Marker for the Visceral Pathology in Niemann-Pick Type C Disease Mitochondrial Gene Expression Profiles and Metabolic Pathways in the Amygdala Associated with Exaggerated Fear in an Animal Model of PTSD.Analytical Characterization of Methyl-β-Cyclodextrin for Pharmacological Activity to Reduce Lysosomal Cholesterol Accumulation in Niemann-Pick Disease Type C1 Cells.Niemann-Pick C disease and mobilization of lysosomal cholesterol by cyclodextrin Altered transition metal homeostasis in Niemann-Pick disease, type C1.Cholesterol homeostatic responses provide biomarkers for monitoring treatment for the neurodegenerative disease Niemann-Pick C1 (NPC1)Alterations in gene expression in mutant amyloid precursor protein transgenic mice lacking Niemann-Pick type C1 protein Comprehensive analysis of gene expression profiles of the beet armyworm Spodoptera exigua larvae challenged with Bacillus thuringiensis Vip3Aa toxin.Identification of a biomarker in cerebrospinal fluid for neuronopathic forms of Gaucher disease.Quantitative Proteomics of Human Fibroblasts with I1061T Mutation in Niemann-Pick C1 (NPC1) Protein Provides Insights into the Disease Pathogenesis.Corpus callosum diffusion tensor imaging and volume measures are associated with disease severity in pediatric Niemann-Pick disease type C1.Complement is dispensable for neurodegeneration in Niemann-Pick disease type C.Necroptosis in Niemann-Pick disease, type C1: a potential therapeutic target.Efficacy of N-acetylcysteine in phenotypic suppression of mouse models of Niemann-Pick disease, type C1.Cerebrospinal Fluid Calbindin D Concentration as a Biomarker of Cerebellar Disease Progression in Niemann-Pick Type C1 Disease.Identification of Niemann-Pick C1 disease biomarkers through sphingolipid profiling Plasma signature of neurological disease in the monogenetic disorder Niemann-Pick Type C.Mitochondrial cholesterol: mechanisms of import and effects on mitochondrial function.NMR analysis reveals significant differences in the plasma metabolic profiles of Niemann Pick C1 patients, heterozygous carriers, and healthy controls.Identification of lysosomal Npc1-binding proteins: Cathepsin D activity is regulated by NPC1.HPGCD outperforms HPBCD as a potential treatment for Niemann-Pick disease type C during disease modeling with iPS cells.Increased Regenerative Capacity of the Olfactory Epithelium in Niemann-Pick Disease Type C1.Role of Diffusion Tensor Imaging in Prognostication and Treatment Monitoring in Niemann-Pick Disease Type C1.Normalization of Hepatic Homeostasis in the Npc1nmf164 Mouse Model of Niemann-Pick Type C Disease Treated with the Histone Deacetylase Inhibitor Vorinostat.Geranylgeranyl pyrophosphate is crucial for neuronal survival but has no special role in Purkinje cell degeneration in Niemann Pick type C1 disease.The extending spectrum of NPC1-related human disorders: from Niemann-Pick C1 Disease to obesity.Complement drives glucosylceramide accumulation and tissue inflammation in Gaucher disease.The susceptibility of cochlear outer hair cells to cyclodextrin is not related to their electromotile activity

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Microarray expression analysis and identification of serum biomarkers for Niemann-Pick disease, type C1.

http://www.wikidata.org/entity/Q36122424

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2012 nî lūn-bûn

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Human Molecular Genetics

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Microarray expression analysis ...... Niemann-Pick disease, type C1.

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Bhavesh Borate

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Celine V M Cluzeau

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Daniel S Ory

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Forbes D Porter

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Michelle K Dail

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Nicole Yanjanin

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Rao Fu

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Steven U Walkley

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P2860

Chronic cyclodextrin treatment of murine Niemann-Pick C disease ameliorates neuronal cholesterol and glycosphingolipid storage and disease progression

Identification of HE1 as the second gene of Niemann-Pick C disease

Defective endocytic trafficking of NPC1 and NPC2 underlying infantile Niemann-Pick type C disease

NPC2 facilitates bidirectional transfer of cholesterol between NPC1 and lipid bilayers, a step in cholesterol egress from lysosomes

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis

The Nova Scotia (type D) form of Niemann-Pick disease is caused by a G3097-->T transversion in NPC1.

Structure of a cholesterol-binding protein deficient in Niemann-Pick type C2 disease

The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements

2-hydroxypropyl-beta-cyclodextrin raises hearing threshold in normal cats and in cats with Niemann-Pick type C disease

Cellular and molecular mechanisms of fibrosis

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3632-3646

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10.1093/HMG/DDS193

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21

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William J Pavan

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225042200

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22619379

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3406758

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