نتایج جستجو برای: pick type c1 npc1

تعداد نتایج: 1363808  

2015
Anne-Katrin Giese Hermann Mascher Ulrike Grittner Sabrina Eichler Guido Kramp Jan Lukas Danielle te Vruchte Nada Al Eisa Mario Cortina-Borja Forbes D Porter Frances M Platt Arndt Rolfs

BACKGROUND Lysosomal storage disorders (LSDs), are a heterogeneous group of rare disorders caused by defects in genes encoding for proteins involved in the lysosomal degradation of macromolecules. They occur at a frequency of about 1 in 5,000 live births, though recent neonatal screening suggests a higher incidence. New treatment options for LSDs demand a rapid, early diagnosis of LSDs if maxim...

Journal: :Blood 2014
Anneliese O Speak Danielle Te Vruchte Lianne C Davis Anthony J Morgan David A Smith Nicole M Yanjanin Louise Simmons Ralf Hartung Heiko Runz Eugen Mengel Michael Beck Jackie Imrie Elizabeth Jacklin James E Wraith Christian Hendriksz Robin Lachmann Celine Cognet Rohini Sidhu Hideji Fujiwara Daniel S Ory Antony Galione Forbes D Porter Eric Vivier Frances M Platt

Niemann-Pick type C (NPC) is a neurodegenerative lysosomal storage disorder caused by defects in the lysosomal proteins NPC1 or NPC2. NPC cells are characterized by reduced lysosomal calcium levels and impaired sphingosine transport from lysosomes. Natural killer (NK) cells kill virally infected/transformed cells via degranulation of lysosome-related organelles. Their trafficking from lymphoid ...

2012
Sarah N.R. Pressey David A. Smith Andrew M.S. Wong Frances M. Platt Jonathan D. Cooper

Niemann-Pick disease type C (NPC) is an inherited lysosomal storage disease characterised by accumulation of cholesterol and glycosphingolipids. NPC patients suffer a progressive neurodegenerative phenotype presenting with motor dysfunction, mental retardation and cognitive decline. To examine the onset and progression of neuropathological insults in NPC we have systematically examined the CNS ...

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, ...

Journal: :The Biochemical journal 2005
Fannie W Chen Ronald E Gordon Yiannis A Ioannou

NPC (Niemann-Pick type C) disease is a rare lipidosis characterized by the accumulation of LDL (low-density lipoprotein)-derived non-esterified cholesterol in the E/L (endosomal/lysosomal) system. The gene products that are responsible for the two NPC complementation groups are distinct and dissimilar, yet their cellular and disease phenotypes are virtually indistinguishable. To investigate the...

Journal: :Journal of lipid research 2004
Patrick C Reid Naomi Sakashita Shigeki Sugii Yoshiko Ohno-Iwashita Yukiko Shimada William F Hickey Ta-Yuan Chang

Niemann-Pick type C (NPC) is a neurodegenerative disorder characterized by progressive accumulation of cholesterol, gangliosides, and other lipids in the central nervous system and visceral organs. In the NPC1 mouse model, neurodegeneration and neuronal cell loss occur before postnatal day 21. Whether neuronal cholesterol accumulation occurs in vivo before the first signs of neuronal cell loss ...

2017
Sandra Torres Nuria Matías Anna Baulies Susana Nuñez Cristina Alarcon-Vila Laura Martinez Natalia Nuño Anna Fernandez Joan Caballeria Thierry Levade Alba Gonzalez-Franquesa Pablo Garcia-Rovés Elisa Balboa Silvana Zanlungo Gemma Fabrías Josefina Casas Carlos Enrich Carmen Garcia-Ruiz José C. Fernández-Checa

Niemann Pick type C (NPC) disease is a progressive lysosomal storage disorder caused by mutations in genes encoding NPC1/NPC2 proteins, characterized by neurological defects, hepatosplenomegaly and premature death. While the primary biochemical feature of NPC disease is the intracellular accumulation of cholesterol and gangliosides, predominantly in endolysosomes, mitochondrial cholesterol accu...

2013
Michael Zech Georg Nübling Florian Castrop Angela Jochim Eva C. Schulte Brit Mollenhauer Peter Lichtner Annette Peters Christian Gieger Thorsten Marquardt Marie T. Vanier Philippe Latour Hans Klünemann Claudia Trenkwalder Janine Diehl-Schmid Robert Perneczky Thomas Meitinger Konrad Oexle Bernhard Haslinger Stefan Lorenzl Juliane Winkelmann

Niemann-Pick type C (NPC) disease is a rare autosomal-recessively inherited lysosomal storage disorder caused by mutations in NPC1 (95%) or NPC2. Given the highly variable phenotype, diagnosis is challenging and particularly late-onset forms with predominantly neuropsychiatric presentations are likely underdiagnosed. Pathophysiologically, genetic alterations compromising the endosomal/lysosomal...

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...

2011
Ximing Du Jaspal Kumar Charles Ferguson Timothy A. Schulz Yan Shan Ong Wanjin Hong William A. Prinz Robert G. Parton Andrew J. Brown Hongyuan Yang

Oxysterol-binding protein (OSBP) and its related proteins (ORPs) constitute a large and evolutionarily conserved family of lipid-binding proteins that target organelle membranes to mediate sterol signaling and/or transport. Here we characterize ORP5, a tail-anchored ORP protein that localizes to the endoplasmic reticulum. Knocking down ORP5 causes cholesterol accumulation in late endosomes and ...

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