(Q34101307)

31 July 2017

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title

Niemann-Pick type C: a disorder of cellular cholesterol trafficking (English)

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31 July 2017

D S Ory

1

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31 July 2017

language of work or name

English

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publication date

1 December 2000

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Biochimica et Biophysica Acta

31 July 2017

published in

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31 July 2017

volume

1529

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31 July 2017

issue

1-3

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31 July 2017

page(s)

331-339

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Niemann-Pick disease: a review of eighteen patients.

31 July 2017

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

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Early-lethal pulmonary form of Niemann-Pick type C disease belonging to a second, rare genetic complementation group

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7 January 2021

Recent advances in elucidating Niemann-Pick C disease

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Linkage of Niemann-Pick Disease Type D to the Same Region of Human Chromosome 18 as Niemann-Pick Disease Type C

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7 January 2021

Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotype

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7 January 2021

Complementation studies in Niemann-Pick disease type C indicate the existence of a second group

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7 January 2021

Linkage of Niemann-Pick disease type C to human chromosome 18

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7 January 2021

Co-cultivation of Niemann-Pick disease type C fibroblasts belonging to complementation groups alpha and beta stimulates LDL-derived cholesterol esterification

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7 January 2021

Alleviation of neuronal ganglioside storage does not improve the clinical course of the Niemann-Pick C disease mouse

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7 January 2021

Embryonic Striatal Neurons from Niemann-Pick Type C Mice Exhibit Defects in Cholesterol Metabolism and Neurotrophin Responsiveness

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7 January 2021

Cholesterol accumulation in tissues of the Niemann-pick type C mouse is determined by the rate of lipoprotein-cholesterol uptake through the coated-pit pathway in each organ

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Lipoprotein metabolism in the macrophage: implications for cholesterol deposition in atherosclerosis

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7 January 2021

Intracellular trafficking of cholesterol monitored with a cyclodextrin

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7 January 2021

Evidence for a cholesterol transport pathway from lysosomes to endoplasmic reticulum that is independent of the plasma membrane

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7 January 2021

A defect in cholesterol esterification in Niemann-Pick disease (type C) patients

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7 January 2021

Cholesterol movement in Niemann-Pick type C cells and in cells treated with amphiphiles

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7 January 2021

Role of Niemann-Pick type C1 protein in intracellular trafficking of low density lipoprotein-derived cholesterol

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7 January 2021

The Niemann-Pick C1 protein resides in a vesicular compartment linked to retrograde transport of multiple lysosomal cargo

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7 January 2021

Cholesterol modulates membrane traffic along the endocytic pathway in sphingolipid-storage diseases

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7 January 2021

Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene

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7 January 2021

Mutations in NPC1 highlight a conserved NPC1-specific cysteine-rich domain

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7 January 2021

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7 January 2021

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7 January 2021

Niemann-Pick C1 protein: obligatory roles for N-terminal domains and lysosomal targeting in cholesterol mobilization

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7 January 2021

Mutations in the leucine zipper motif and sterol-sensing domain inactivate the Niemann-Pick C1 glycoprotein

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7 January 2021

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7 January 2021

The genomic organization and polymorphism analysis of the human Niemann-Pick C1 gene

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7 January 2021

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7 January 2021

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Maternal Pumilio acts together with Nanos in germline development in Drosophila embryos

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7 January 2021

Sterols regulate cycling of SREBP cleavage-activating protein (SCAP) between endoplasmic reticulum and Golgi

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7 January 2021

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7 January 2021

Cholesterol modification of hedgehog signaling proteins in animal development

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7 January 2021

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

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7 January 2021

Mobilization of late-endosomal cholesterol is inhibited by Rab guanine nucleotide dissociation inhibitor

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7 January 2021

Extensive Glycosphingolipid Depletion in the Liver and Lymphoid Organs of Mice Treated withN-Butyldeoxynojirimycin

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7 January 2021

N-butyldeoxygalactonojirimycin: a more selective inhibitor of glycosphingolipid biosynthesis than N-butyldeoxynojirimycin, in vitro and in vivo

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7 January 2021

Glycosphingolipid depletion in fabry disease lymphoblasts with potent inhibitors of glucosylceramide synthase

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7 January 2021

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7 January 2021

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Identifiers

DOI

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release_h3j47qwjvrd2jgxf47w3o3flu4

31 July 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/h3j47qwjvrd2jgxf47w3o3flu4

24 November 2022

mapped directly with Wikidata item

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