نتایج جستجو برای: npc2

تعداد نتایج: 199  

Journal: :Clinical lipidology 2012
Benny Liu

Niemann-Pick type C (NPC) disease is an autosomal recessive neurovisceral lipid and storage disorder characterized by abnormal sequestration of unesterified cholesterol within the late endosomal/lysosomal compartment of all cells in the body. This disease primarily affects children and is characterized by hepatic and pulmonary dysfunction, neurodegeneration and death at an early age. Currently,...

Journal: :Cell 2016
Xin Gong Hongwu Qian Xinhui Zhou Jianping Wu Tao Wan Pingping Cao Weiyun Huang Xin Zhao Xudong Wang Peiyi Wang Yi Shi George F. Gao Qiang Zhou Nieng Yan

Niemann-Pick disease type C (NPC) is associated with mutations in NPC1 and NPC2, whose gene products are key players in the endosomal/lysosomal egress of low-density lipoprotein-derived cholesterol. NPC1 is also the intracellular receptor for Ebola virus (EBOV). Here, we present a 4.4 Å structure of full-length human NPC1 and a low-resolution reconstruction of NPC1 in complex with the cleaved g...

Journal: :Human molecular genetics 2012
Matthew J Elrick Ting Yu Chan Chung Andrew P Lieberman

Niemann-Pick type C disease (NPC) is a childhood onset neurodegenerative disorder arising from lipid-trafficking defects caused by mutations in the NPC1 or NPC2 gene. Marked accumulation of autophagosomes is a prominent feature of NPC cells, yet a detailed understanding of the disease-associated alterations in autophagy and their role in pathogenesis has been lacking. Prior studies have shown t...

2016
Su-Yun Lee Hyung Jin Lee Seong Hwan Kim Young Jin Jeong Hee Kyung Jin Jae-Sung Bae Sang-Myung Cheon Jae Woo Kim

Niemann-Pick disease, type C (NP-C), is caused by NPC1 or NPC2 gene mutations. Progressive neurological, psychiatric, and visceral symptoms are characteristic. Here, we present cases of a brother (Case 1) and sister (Case 2) in their mid-20s with gait disturbance and psychosis. For the Case 1, neurological examination revealed dystonia, ataxia, vertical supranuclear-gaze palsy (VSGP), and globa...

Journal: :Journal of Investigative Dermatology 2022

The skin provides a barrier function mediated by combination of cornified epithelial cells, cell-cell adhesions and epidermal lipids. is compromised in old age which exemplified features such as improper lipid metabolism flattened dermal-epidermal junction. Laminin 332 basement membrane glycoprotein was shown to be decreased aged skin. We have previously demonstrated that the loss laminin leads...

Journal: :Molecular and Cellular Neuroscience 2014
Isabelle Buard Frank W. Pfrieger

Niemann-Pick type C disease is a rare and ultimately fatal lysosomal storage disorder with variable neurologic symptoms. The disease-causing mutations concern NPC1 or NPC2, whose dysfunction entails accumulation of cholesterol in the endosomal-lysosomal system and the selective death of specific neurons, namely cerebellar Purkinje cells. Here, we investigated whether neurodegeneration is preced...

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