نتایج جستجو برای: glucocerebrosidase

تعداد نتایج: 825  

Journal: :The Yale Journal of Biology and Medicine 1982
Margretta R. Seashore

A number of investigators have attempted to treat Gaucher disease with exogenous glucocerebrosidase. Although at times encouraging biochemical changes and suggestive alterations in organomegaly have been reported, overall, the results of enzyme replacement therapy must be judged to be a failure. In order to understand this lack of success with a promising treatment modality, four aspects of enz...

2013
Yoram Tekoah Salit Tzaban Tali Kizhner Mariana Hainrichson Anna Gantman Myriam Golembo David Aviezer Yoseph Shaaltiel

The glycosylation of recombinant β-glucocerebrosidase, and in particular the exposure of mannose residues, has been shown to be a key factor in the success of ERT (enzyme replacement therapy) for the treatment of GD (Gaucher disease). Macrophages, the target cells in GD, internalize β-glucocerebrosidase through MRs (mannose receptors). Three enzymes are commercially available for the treatment ...

2017
Shi-Yu Yang Michelle Beavan Kai-Yin Chau Jan-Willem Taanman Anthony H.V. Schapira

Numerically the most important risk factor for the development of Parkinson's disease (PD) is the presence of mutations in the glucocerebrosidase GBA1 gene. In vitro and in vivo studies show that GBA1 mutations reduce glucocerebrosidase (GCase) activity and are associated with increased α-synuclein levels, reflecting similar changes seen in idiopathic PD brain. We have developed a neural crest ...

Journal: :The Journal of clinical investigation 1990
J Sorge E Gross C West E Beutler

Gaucher disease is due to mutations involving the glucocerebrosidase gene. A closely homologous pseudogene is located approximately 16 kD downstream from the functional gene. Sequence analysis of clones from cDNA libraries made from skin fibroblast cultures showed several independent clones with the sequence of an aberrantly processed pseudogene message. Examination of cellular RNA from lymphob...

2004
Fernanda Timm Seabra Souza Alexandre Silva de Mello Kristiane Michelin Janice Carneiro Coelho

The effect of four antibiotics (amikacin, clindamycin, cephalothin and vancomycin) was investigated considering that bacterial infection in fibroblasts cultures is a very frequent event. The investigation included the effect of the antibiotics on fibroblast growth and on the activity of the enzyme glucocerebrosidase. The antibiotics were added to the fibroblast cultures and cell growth was eval...

Journal: :Movement disorders : official journal of the Movement Disorder Society 2005
Lorraine N Clark Angelique Nicolai Shehla Afridi Juliette Harris Helen Mejia-Santana Lisa Strug Lucien J Cote Elan D Louis Howard Andrews Cheryl Waters Blair Ford Steven Frucht Stanley Fahn Richard Mayeux Ruth Ottman K Marder

Mutations in the beta-glucocerebrosidase gene cause Gaucher's disease, one of the most common lysosomal lipid storage diseases in the Ashkenazi Jewish population. The occurrence of parkinsonism in patients with Type 1 Gaucher's disease has been noted previously. In this pilot study, we evaluated a possible association between Parkinson's disease (PD) and the beta-glucocerebrosidase gene N370S a...

2011
Samantha Kimball Francis Choy Agnes Zay Dominick Amato

Gaucher disease (GD) is characterized by reduced activity of glucocerebrosidase leading to complications in the reticuloendothelial system. N396T, a rarer mutation of the glucocerebrosidase gene, has been encountered in Portuguese populations and has generally been associated with milder phenotypes. This report presents brief histories of two Portuguese sisters, both with homozygous N396T mutat...

Journal: :Journal of medical genetics 1998
A Chabás L Gort M Montfort F Castelló M C Domínguez D Grinberg L Vilageliu

Gaucher disease results, in most patients, from mutations in the gene encoding glucocerebrosidase. Mutation D409H is the third most frequent in Spanish patients, accounting for 5.7% of all mutated alleles. This allele is associated mainly with the neurological forms of the disease. Recently, homozygosity for the D409H mutation has been associated with a particular phenotype, including specific ...

Journal: :Seizure 2011
João Chaves Idalina Beirão Andrea Balreira Paulo Gaspar Daniel Caiola M. Clara Sá-Miranda José L. Lima

Action myoclonus-renal failure syndrome (AMRF) is considered a rare form of progressive myoclonus epilepsy (PME) associated with renal failure. A mutation on the gene encoding the lysosomal integral membrane protein type 2-LIMP-2 (SCARB2), the receptor responsible for targeting glucocerebrosidase to the lysosomes, was recently described, allowing a better understanding of its etiopathogenesis. ...

Journal: :Stem cell reports 2016
Hugo J R Fernandes Elizabeth M Hartfield Helen C Christian Evangelia Emmanoulidou Ying Zheng Heather Booth Helle Bogetofte Charmaine Lang Brent J Ryan S Pablo Sardi Jennifer Badger Jane Vowles Samuel Evetts George K Tofaris Kostas Vekrellis Kevin Talbot Michele T Hu William James Sally A Cowley Richard Wade-Martins

Heterozygous mutations in the glucocerebrosidase gene (GBA) represent the strongest common genetic risk factor for Parkinson's disease (PD), the second most common neurodegenerative disorder. However, the molecular mechanisms underlying this association are still poorly understood. Here, we have analyzed ten independent induced pluripotent stem cell (iPSC) lines from three controls and three un...

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