نتایج جستجو برای: npc1

تعداد نتایج: 544  

Journal: :International journal of sciences 2023

Male patients with NPC1 heterozygous mutation (Npc1+/-) are prone to obesity and diabetes, yet the mechanism remains unclear. In this study, male Npc1+/- mice (C57BL/6C-Npc1) were used evaluate effects of combined 60% high-fat diet (HFD) on glucolipid metabolism, cholesterol accumulation, islet dysfunction β-cell dedifferentiation. Compared HFD-Npc1+/+ or fed low-fat (LFD), body weight HFD-Npc1...

2015
Zuzana Krčková Jitka Brouzdová Michal Daněk Daniela Kocourková Dominique Rainteau Eric Ruelland Olga Valentová Přemysl Pejchar Jan Martinec

The Arabidopsis non-specific phospholipase C (NPC) protein family is encoded by the genes NPC1 - NPC6. It has been shown that NPC4 and NPC5 possess phospholipase C activity; NPC3 has lysophosphatidic acid phosphatase activity. NPC3, 4 and 5 play roles in the responses to hormones and abiotic stresses. NPC1, 2 and 6 has not been studied functionally yet. We found that Arabidopsis NPC1 expressed ...

Journal: :American Journal of Pathology 2021

Abstract Niemann-Pick type C disease (NP-C) is a lysosomal storage disorder characterized by cholesterol accumulation caused loss-of-function mutations in the Npc1 gene. NP-C primarily affects brain, causing neuronal damage and affecting motor coordination. In addition, considerable liver malfunction common. Recently, we demonstrated that depletion of annexin A6 (ANXA6), which most abundant inv...

Journal: :Human molecular genetics 2012
Robert A Maue Robert W Burgess Bing Wang Christine M Wooley Kevin L Seburn Marie T Vanier Maximillian A Rogers Catherine C Chang Ta-Yuan Chang Brent T Harris David J Graber Carlos A A Penatti Donna M Porter Benjamin S Szwergold Leslie P Henderson John W Totenhagen Theodore P Trouard Ivan A Borbon Robert P Erickson

We have identified a point mutation in Npc1 that creates a novel mouse model (Npc1(nmf164)) of Niemann-Pick type C1 (NPC) disease: a single nucleotide change (A to G at cDNA bp 3163) that results in an aspartate to glycine change at position 1005 (D1005G). This change is in the cysteine-rich luminal loop of the NPC1 protein and is highly similar to commonly occurring human mutations. Genetic an...

2012
Anuja Krishnan Emily Happy Miller Andrew S. Herbert Melinda Ng Esther Ndungo Sean P. Whelan John M. Dye Kartik Chandran

We recently demonstrated that Niemann-Pick C1 (NPC1), a ubiquitous 13-pass cellular membrane protein involved in lysosomal cholesterol transport, is a critical entry receptor for filoviruses. Here we show that Niemann-Pick C1-like1 (NPC1L1), an NPC1 paralog and hepatitis C virus entry factor, lacks filovirus receptor activity. We exploited the structural similarity between NPC1 and NPC1L1 to co...

Journal: :Human molecular genetics 2017
Randy J Chandler Ian M Williams Alana L Gibson Cristin D Davidson Arturo A Incao Brandon T Hubbard Forbes D Porter William J Pavan Charles P Venditti

Niemann-Pick disease, type C1 (NPC1) is a heritable lysosomal storage disease characterized by a progressive neurological degeneration that causes disability and premature death. A murine model of NPC1 disease (Npc1-/-) displays a rapidly progressing form of NPC1 disease which is characterized by weight loss, ataxia, increased cholesterol storage, loss of cerebellar Purkinje neurons and early l...

Journal: :Molecular biology of the cell 2001
D C Ko M D Gordon J Y Jin M P Scott

People homozygous for mutations in the Niemann-Pick type C1 (NPC1) gene have physiological defects, including excess accumulation of intracellular cholesterol and other lipids, that lead to drastic neural and liver degeneration. The NPC1 multipass transmembrane protein is resident in late endosomes and lysosomes, but its functions are unknown. We find that organelles containing functional NPC1-...

Journal: :Journal of cell science 2006
Yuki Ohsaki Yuko Sugimoto Michitaka Suzuki Hiroshi Hosokawa Tamotsu Yoshimori Joanna P Davies Yiannis A Ioannou Marie T Vanier Kousaku Ohno Haruaki Ninomiya

Niemann-Pick disease type C (NPC) is an inherited lipid storage disorder caused by mutations in NPC1 or NPC2. NPC1 is a polytopic glycoprotein that contains a sterol-sensing domain, whereas NPC2 is a soluble protein that contains an MD-2-like lipid-recognition domain. In the current study, we addressed the hypothesis that ubiquitylation of NPC1 might be regulated by cholesterol. We found that d...

2014
Yuta Tanaka Yoichi Ishitsuka Yusei Yamada Yuki Kondo Toru Takeo Naomi Nakagata Taishi Higashi Keiichi Motoyama Hidetoshi Arima Muneaki Matsuo Katsumi Higaki Kousaku Ohno Tetsumi Irie

Hydroxypropyl-β-cyclodextrin (HPBCD) is an attractive drug candidate against Niemann-Pick Type C (NPC) disease. However, the safety of HPBCD treatment for NPC patients remains to be elucidated. In this study, we examined the acute toxicity of HPBCD in Npc1-deficient mice. When treated with HPBCD (20,000 mg/kg, subcutaneously), over half of the wild-type (Npc1+/+) or Npc1+/- mice died by 72 h af...

Journal: :Biochimica et biophysica acta 2011
Kyle B Peake Robert B Campenot Dennis E Vance Jean E Vance

Niemann-Pick Type C (NPC) disease is an autosomal recessive disorder that results in accumulation of cholesterol and other lipids in late endosomes/lysosomes and leads to progressive neurodegeneration and premature death. The mechanism by which lipid accumulation causes neurodegeneration remains unclear. Inappropriate activation of microglia, the resident immune cells of the central nervous sys...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید