نتایج جستجو برای: npc2

تعداد نتایج: 199  

2013
Peter Bauer David J. Balding Hans H. Klünemann David E. J. Linden Daniel S. Ory Mercè Pineda Josef Priller Frederic Sedel Audrey Muller Harbajan Chadha-Boreham Richard W. D. Welford Daniel S. Strasser Marc C. Patterson

Niemann-Pick disease type C (NP-C) is a rare, autosomal-recessive, progressive neurological disease caused by mutations in either the NPC1 gene (in 95% of cases) or the NPC2 gene. This observational, multicentre genetic screening study evaluated the frequency and phenotypes of NP-C in consecutive adult patients with neurological and psychiatric symptoms. Diagnostic testing for NP-C involved NPC...

Journal: :Cell Metabolism 2009

2014
Stefania Zampieri Ezio Bianchi Carlo Cantile Roberta Saleri Bruno Bembi Andrea Dardis

Niemann-Pick C disease (NPC) is an autosomal recessive lysosomal storage disorder characterized by accumulation of unesterified cholesterol and other lipids within the lysosomes due to mutation in NPC1 or NPC2 genes. A feline model of NPC carrying a mutation in NPC1 gene has been previously described. We have identified two kittens affected by NPC disease due to a mutation in NPC2 gene. They ma...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Lina Abi-Mosleh Rodney E Infante Arun Radhakrishnan Joseph L Goldstein Michael S Brown

A handoff model has been proposed to explain the egress from lysosomes of cholesterol derived from receptor-mediated endocytosis of LDL. Cholesterol is first bound by soluble Niemann-Pick C2 (NPC2) protein, which hands off the cholesterol to the N-terminal domain of membrane-bound NPC1. Cells lacking NPC1 or NPC2 accumulate LDL-derived cholesterol in lysosomes and fail to deliver LDL cholestero...

2018
Jiao Zhu Mengbuo Guo Liping Ban Li-Mei Song Yang Liu Paolo Pelosi Guirong Wang

Niemann-Pick proteins type C2 (NPC2) are carriers of cholesterol in vertebrates, with a single member in each species. The high sequence conservation between mammals and across vertebrates is related to their common function. In contrast, NPC2 proteins in arthropods have undergone extensive duplication and differentiation, probably under environmental pressure, and are likely to have different ...

Journal: :Human molecular genetics 2003
Titta S Blom Matts D Linder Karen Snow Helena Pihko Michael W Hess Eija Jokitalo Ville Veckman Ann-Christine Syvänen Elina Ikonen

Niemann-Pick type C (NPC) disease is a fatal recessively inherited lysosomal cholesterol-sphingolipidosis. Mutations in the NPC1 gene cause approximately 95% of the cases, the rest being caused by NPC2 mutations. Here the molecular basis of a severe infantile form of the disease was dissected. The level of NPC1 protein in the patient fibroblasts was similar to that in control cells. However, th...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Yuko Ishida Wataru Tsuchiya Takeshi Fujii Zui Fujimoto Mitsuhiro Miyazawa Jun Ishibashi Shigeru Matsuyama Yukio Ishikawa Toshimasa Yamazaki

Ants are eusocial insects that are found in most regions of the world. Within its caste, worker ants are responsible for various tasks that are required for colony maintenance. In their chemical communication, α-helical carrier proteins, odorant-binding proteins, and chemosensory proteins, which accumulate in the sensillum lymph in the antennae, play essential roles in transferring hydrophobic ...

2015
Tamihiro Kamata Hong Jin Susan Giblett Bipin Patel Falguni Patel Charles Foster Catrin Pritchard

The tumour microenvironment is known to play an integral role in facilitating cancer progression at advanced stages, but its function in some pre-cancerous lesions remains elusive. We have used the (V600) (E)BRAF-driven mouse lung model that develop premalignant lesions to understand stroma-tumour interactions during pre-cancerous development. In this model, we have found that immature macropha...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Nobutaka Ohgami Dennis C Ko Matthew Thomas Matthew P Scott Catherine C Y Chang Ta-Yuan Chang

Niemann-Pick type C (NPC) 1 protein plays important roles in moving cholesterol and other lipids out of late endosomes by means of vesicular trafficking, but it is not known whether NPC1 directly interacts with cholesterol. We performed photoaffinity labeling of intact cells expressing fluorescent protein (FP)-tagged NPC1 by using [(3)H]7,7-azocholestanol ([(3)H]AC). After immunoprecipitation, ...

2003
Marie T Vanier

Niemann-Pick disease type C (NPC) is an autosomal recessive neurovisceral lipid storage with a wide spectrum of clinical phenotypes. At the cellular level, the disorder is characterized by accumulation of unesterified cholesterol and glycolipids in the lysosomal/late endosomal system. Approximatively 95% of patients have mutations in the NPC1 gene (mapped at 18q11) which encodes a large membran...

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