نتایج جستجو برای: npc2

تعداد نتایج: 199  

Journal: :The Journal of clinical investigation 2014
Danielle te Vruchte Anneliese O Speak Kerri L Wallom Nada Al Eisa David A Smith Christian J Hendriksz Louise Simmons Robin H Lachmann Alison Cousins Ralf Hartung Eugen Mengel Heiko Runz Michael Beck Yasmina Amraoui Jackie Imrie Elizabeth Jacklin Kate Riddick Nicole M Yanjanin Christopher A Wassif Arndt Rolfs Florian Rimmele Naomi Wright Clare Taylor Uma Ramaswami Timothy M Cox Caroline Hastings Xuntian Jiang Rohini Sidhu Daniel S Ory Begona Arias Mylvaganam Jeyakumar Daniel J Sillence James E Wraith Forbes D Porter Mario Cortina-Borja Frances M Platt

Lysosomal storage disorders (LSDs) occur at a frequency of 1 in every 5,000 live births and are a common cause of pediatric neurodegenerative disease. The relatively small number of patients with LSDs and lack of validated biomarkers are substantial challenges for clinical trial design. Here, we evaluated the use of a commercially available fluorescent probe, Lysotracker, that can be used to me...

Journal: :BMC Pharmacology 2009
Audun O Vik-Mo Johan Fernø Silje Skrede Vidar M Steen

BACKGROUND Disturbances in lipid homeostasis and myelination have been proposed in the pathophysiology of schizophrenia and bipolar disorder. We have previously shown that several antipsychotic and antidepressant drugs increase lipid biosynthesis through activation of the Sterol Regulatory Element-Binding Protein (SREBP) transcription factors, which control the expression of numerous genes invo...

2010
Sandra L. Schmid Marilyn G. Farquhar

A symposium was held at the University of California, San Diego, to honor the contributions of Nobel Laureate, George Palade, to cell biology. The speakers included Günter Blobel, on the structure and function of nuclear pore complexes; Peter Walter, on the unfolded protein response in health and disease; Randy Schekman, on human disease-linked mutations in the COPII machinery; Scott Emr, on th...

Journal: :Journal of neuropathology and experimental neurology 2013
Jessica H Bagel Tracey U Sikora Maria Prociuk Jill P Pesayco Andrew P Mizisin G Diane Shelton Charles H Vite

Niemann-Pick disease type C (NPC disease) is an incurable, neurodegenerative, autosomal recessive disease caused by mutations in either the NPC1 or the NPC2 gene. These mutations affect the intracellular trafficking of lipids and cholesterol, resulting in the intralysosomal accumulation of unesterified cholesterol and glycosphingolipids. These abnormalities are associated with clinical ataxia a...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2011
Nina H Pipalia Casey C Cosner Amy Huang Anamitra Chatterjee Pauline Bourbon Nathan Farley Paul Helquist Olaf Wiest Frederick R Maxfield

Niemann-Pick type C (NPC) disease is predominantly caused by mutations in the NPC1 protein that affect intracellular cholesterol trafficking and cause accumulation of unesterified cholesterol and other lipids in lysosomal storage organelles. We report the use of a series of small molecule histone deacetylase (HDAC) inhibitors in tissue culture models of NPC human fibroblasts. Some HDAC inhibito...

2015
Hanna Alobaidy

Niemann-Pick disease (NP-C) is a lysosomal storage disease in which impaired intracellular lipid transport leads to accumulation of cholesterol and glycosphingolipids in various neurovisceral tissues. It is an autosomal recessive disorder, caused by mutations in the NPC1 or NPC2 genes. The clinical spectrum is grouped by the age of onset and onset of neurological manifestation: pre/perinatal; e...

2017
Maria Dolores Ledesma

In this case series, we demonstrate that Ursodeoxycholic acid (UDCA) improves liver dysfunction in Niemann-Pick type C (NPC) and may restore a suppressed cytochrome p450 system. NPC disease is a progressive neurodegenerative lysosomal storage disease caused by mutations in either the or genes. Liver disease is a common feature presenting either NPC1 NPC2 acutely as cholestatic jaundice in t...

2009
James E Wraith Jackie Imrie

Niemann-Pick disease type C (NP-C) is an autosomal recessive disorder characterized by progressive neurological deterioration leading to premature death. The disease is caused by mutations in one of two genes, NPC1 or NPC2, leading to impaired intracellular lipid transport and build-up of lipids in various tissues, particularly the brain. Miglustat (Zavesca(R)), a reversible inhibitor of glycos...

2015
Cristina Frías-López Francisca C. Almeida Sara Guirao-Rico Joel Vizueta Alejandro Sánchez-Gracia Miquel A. Arnedo Julio Rozas Kimberly Bishop-Lilly

The funnel-web spider Macrothele calpeiana is a charismatic Mygalomorph with a great interest in basic, applied and translational research. Nevertheless, current scarcity of genomic and transcriptomic data of this species clearly limits the research in this non-model organism. To overcome this limitation, we launched the first tissue-specific enriched RNA-seq analysis in this species using a su...

2017
S Bajaj M Muranjan S Karande D Prabhat

Pulmonary manifestations are seldom recognized as symptoms of storage disorders. The report describes the diagnostic journey in a 30-month-old male infant, born of a third-degree consanguineous marriage referred to our institute as severe persistent asthma. History revealed that the child had progressively worsening breathlessness and persistent dry cough not associated with fever but accompani...

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