نتایج جستجو برای: npc1

تعداد نتایج: 544  

Journal: :Molecular & cellular proteomics : MCP 2015
Navin Rauniyar Kanagaraj Subramanian Mathieu Lavallée-Adam Salvador Martínez-Bartolomé William E Balch John R Yates

Niemann-Pick type C (NPC) disease is a fatal neurodegenerative disorder characterized by the accumulation of unesterified cholesterol in the late endosomal/lysosomal compartments. Mutations in the NPC1 protein are implicated in 95% of patients with NPC disease. The most prevalent mutation is the missense mutation I1061T that occurs in ∼ 15-20% of the disease alleles. In our study, an isobaric l...

Journal: :Infection and immunity 2002
Masahisa Watarai Sou-ichi Makino Makoto Michikawa Katsuhiko Yanagisawa Shigeru Murakami Toshikazu Shirahata

Brucella abortus is a facultative intracellular bacterium capable of surviving inside macrophages. Intracellular replication of B. abortus requires the VirB complex, which is highly similar to conjugative DNA transfer systems. In this study, we show that plasma membrane cholesterol of macrophages is required for the VirB-dependent internalization of B. abortus and also contributes to the establ...

Journal: :Journal of virology 2015
Rebecca M Mingo James A Simmons Charles J Shoemaker Elizabeth A Nelson Kathryn L Schornberg Ryan S D'Souza James E Casanova Judith M White

UNLABELLED Ebola virus (EBOV) causes hemorrhagic fevers with high mortality rates. During cellular entry, the virus is internalized by macropinocytosis and trafficked through endosomes until fusion between the viral and an endosomal membrane is triggered, releasing the RNA genome into the cytoplasm. We found that while macropinocytotic uptake of filamentous EBOV viruslike particles (VLPs) expre...

Journal: :Genome research 1999
J Gu X Y Guan M A Ashlock

Gene isolation methods used during positional cloning rely on physical contigs consisting of bacterial artificial chromosomes, P1, or cosmid clones. However, in most instances, the initial framework for physical mapping consists of contigs of yeast artificial chromosome (YACs), large vectors that are suboptimal substrates for gene isolation. Here we report a strategy to identify gene sequences ...

Journal: :European journal of medicinal chemistry 2021

Novel 2-substituted-6-[(4-substituted-1-piperidyl)methyl]-1H-benzimidazoles were designed and synthesized as Ebola virus inhibitors. The proposed structures of the new prepared benzimidazole-piperidine hybrids confirmed based on their spectral data CHN analyses. target compounds screened in vitro for anti-Ebola activity. Among tested molecules, 26a (EC50=0.93 ?M, SI = 10) 25a (EC50=0.64 20) pot...

Journal: :The Journal of biological chemistry 2003
Andrey Frolov Sarah E Zielinski Jan R Crowley Nicole Dudley-Rucker Jean E Schaffer Daniel S Ory

Mutations in the Niemann-Pick disease genes cause lysosomal cholesterol accumulation and impaired low density lipoprotein (LDL) cholesterol esterification. These findings have been attributed to a block in cholesterol movement from lysosomes to the site of the sterol regulatory machinery. In this study we show that Niemann-Pick type C1 (NPC1) and Niemann-Pick type C2 (NPC2) mutants have increas...

2015
William S. Garver Lesley de la Torre Matthew C. Brennan Li Luo David Jelinek Joseph J. Castillo David Meyre Robert A. Orlando Randall A. Heidenreich William F. Rayburn

A genome-wide association study (GWAS) and subsequent replication studies in diverse ethnic groups indicate that common Niemann-Pick C1 gene (NPC1) polymorphisms are associated with morbid-adult obesity or diabetes independent of body weight. The objectives for this prospective cross-sectional study were to determine allele frequencies for NPC1 polymorphisms (644A>G, 1926C>G, 2572A>G, and 3797G...

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005
Keishi Narita Amit Choudhury Kostantin Dobrenis Deepak K Sharma Eileen L Holicky David L Marks Steven U Walkley Richard E Pagano

Niemann-Pick disease type C (NPC) is a genetic disorder in which patient cells exhibit lysosomal accumulation of cholesterol and sphingolipids (SLs) caused by defects in either NPC1 or NPC2 proteins. We previously demonstrated that NPC1 human skin fibroblasts overexpressing endosomal Rab proteins (Rab7 or Rab9) showed a correction in the storage disease phenotype. In the current study, we used ...

2017
Arun Kumar Tharkeshwar Jesse Trekker Wendy Vermeire Jarne Pauwels Ragna Sannerud David A. Priestman Danielle te Vruchte Katlijn Vints Pieter Baatsen Jean-Paul Decuypere Huiqi Lu Shaun Martin Peter Vangheluwe Johannes V. Swinnen Liesbet Lagae Francis Impens Frances M. Platt Kris Gevaert Wim Annaert

Superparamagnetic iron oxide nanoparticles (SPIONs) have mainly been used as cellular carriers for genes and therapeutic products, while their use in subcellular organelle isolation remains underexploited. We engineered SPIONs targeting distinct subcellular compartments. Dimercaptosuccinic acid-coated SPIONs are internalized and accumulate in late endosomes/lysosomes, while aminolipid-SPIONs re...

2012
Mahua Maulik Bibaswan Ghoshal John Kim Yanlin Wang Jing Yang David Westaway Satyabrata Kar

Niemann-Pick type C (NPC) disease, an autosomal recessive disorder caused primarily by loss-of-function mutations in NPC1 gene, is characterized neuropathologically by intracellular cholesterol accumulation, gliosis and neuronal loss in selected brain regions. Recent studies have shown that NPC disease exhibits intriguing parallels with Alzheimer’s disease (AD), including the presence of tau-po...

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