نتایج جستجو برای: glucocerebrosidase

تعداد نتایج: 825  

Journal: :Journal of Parkinson's Disease 2017

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Wei Zheng Janak Padia Daniel J Urban Ajit Jadhav Ozlem Goker-Alpan Anton Simeonov Ehud Goldin Douglas Auld Mary E LaMarca James Inglese Christopher P Austin Ellen Sidransky

Gaucher disease is an autosomal recessive lysosomal storage disorder caused by mutations in the glucocerebrosidase gene. Missense mutations result in reduced enzyme activity that may be due to misfolding, raising the possibility of small-molecule chaperone correction of the defect. Screening large compound libraries by quantitative high-throughput screening (qHTS) provides comprehensive informa...

Journal: :Molecular and chemical neuropathology 1995
R Willemsen V Tybulewicz E Sidransky W K Eliason B M Martin M E LaMarca A J Reuser M Tremblay H Westphal R C Mulligan

Gaucher mice, created by targeted disruption of the glucocerebrosidase gene, are totally deficient in glucocerebrosidase and have a rapidly deteriorating clinical course analogous to the most severely affected type 2 human patients. An ultrastructural study of tissues from these mice revealed glucocerebroside accumulation in bone marrow, liver, spleen, and brain. This glycolipid had a character...

Journal: :Human molecular genetics 2008
Andrea Balreira Paulo Gaspar Daniel Caiola João Chaves Idalina Beirão José Lopes Lima Jorge Eduardo Azevedo Maria Clara Sá Miranda

The main clinical features of two siblings from a consanguineous marriage were progressive myoclonic epilepsy without intellectual impairment and a nephrotic syndrome with a strong accumulation of C1q in capillary loops and mesangium of kidney. The biochemical analysis of one of the patients revealed a normal beta-glucocerebrosidase activity in leukocytes, but a severe enzymatic deficiency in c...

2016
Elma Aflaki Nima Moaven Daniel K. Borger Grisel Lopez Wendy Westbroek Jae Jin Chae Juan Marugan Samarjit Patnaik Emerson Maniwang Ashley N. Gonzalez Ellen Sidransky

Gaucher disease, the inherited deficiency of lysosomal glucocerebrosidase, is characterized by the presence of glucosylcer-amide macrophages, the accumulation of glucosylceramide in lysosomes and the secretion of inflammatory cytokines. However, the connection between this lysosomal storage and inflammation is not clear. Studying macrophages derived from peripheral monocytes from patients with ...

2016
Aya Narita Kentarou Shirai Shinji Itamura Atsue Matsuda Akiko Ishihara Kumi Matsushita Chisako Fukuda Norika Kubota Rumiko Takayama Hideo Shigematsu Anri Hayashi Tomohiro Kumada Kotaro Yuge Yoriko Watanabe Saori Kosugi Hiroshi Nishida Yukiko Kimura Yusuke Endo Katsumi Higaki Eiji Nanba Yoko Nishimura Akiko Tamasaki Masami Togawa Yoshiaki Saito Yoshihiro Maegaki Kousaku Ohno Yoshiyuki Suzuki

OBJECTIVE Gaucher disease (GD) is a lysosomal storage disease characterized by a deficiency of glucocerebrosidase. Although enzyme-replacement and substrate-reduction therapies are available, their efficacies in treating the neurological manifestations of GD are negligible. Pharmacological chaperone therapy is hypothesized to offer a new strategy for treating the neurological manifestations of ...

2011
Radosław Kwapiszewski Maciej Skolimowski Karina Ziółkowska Elżbieta Jędrych Michał Chudy Artur Dybko Zbigniew Brzózka

An integrated microfluidic system that coupled lysis of two cell lines: L929 fibroblasts and A549 epithelial cells, with fluorescence-based enzyme assay was developed to determine β-glucocerebrosidase activity. The microdevice fabricated in poly(dimethylsiloxane) consists of three main parts: a chemical cell lysis zone based on the sheath flow geometry, a micromeander and an optical fibers dete...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید