نتایج جستجو برای: s ataxia frda

تعداد نتایج: 727598  

Journal: :Archives of neurology 2002
I Silveira C Miranda L Guimarães M-C Moreira I Alonso P Mendonça A Ferro J Pinto-Basto J Coelho F Ferreirinha J Poirier E Parreira J Vale C Januário C Barbot A Tuna J Barros R Koide S Tsuji S E Holmes R L Margolis L Jardim M Pandolfo P Coutinho J Sequeiros

BACKGROUND Ten neurodegenerative disorders characterized by spinocerebellar ataxia (SCA) are known to be caused by trinucleotide repeat (TNR) expansions. However, in some instances the molecular diagnosis is considered indeterminate because of the overlap between normal and affected allele ranges. In addition, the mechanism that generates expanded alleles is not completely understood. OBJECTI...

Journal: :Human molecular genetics 2009
Alessandro Campanella Elisabetta Rovelli Paolo Santambrogio Anna Cozzi Franco Taroni Sonia Levi

Mitochondrial ferritin (FtMt) is a nuclear-encoded iron-sequestering protein that specifically localizes in mitochondria. In mice it is highly expressed in cells characterized by high-energy consumption, while is undetectable in iron storage tissues like liver and spleen. FtMt expression in mammalian cells was shown to cause a shift of iron from cytosol to mitochondria, and in yeast it rescued ...

Journal: :Genomics 2015
S Pérez-Luz A Gimenez-Cassina I Fernández-Frías R Wade-Martins J Díaz-Nido

Friedreich's ataxia (FRDA) is the most common form of hereditary ataxia caused by recessive mutations in the FXN gene. Recent results have indicated the presence of different frataxin isoforms due to alternative gene expression mechanisms. Our previous studies demonstrated the advantages of using high-capacity herpes simplex virus type 1 (HSV-1) amplicon vectors containing the entire FXN genomi...

2013
Pierre Chapdelaine Zoé Coulombe Amina Chikh Catherine Gérard Jacques P Tremblay

TALEs targeting a promoter sequence and fused with a transcription activation domain (TAD) may be used to specifically induce the expression of a gene as a potential treatment for haploinsufficiency. This potential therapeutic approach was applied to increase the expression of frataxin in fibroblasts of Friedreich ataxia (FRDA) patients. FRDA fibroblast cells were nucleofected with a pCR3.1 exp...

2016
Rosella Abeti Ebru Uzun Indhushri Renganathan Tadashi Honda Mark A. Pook Paola Giunti

Friedreich’s ataxia (FRDA) is an autosomal recessive disorder, caused by reduced levels of the protein frataxin. This protein is located in the mitochondria, where it functions in the biogenesis of iron-sulphur clusters (ISCs), which are important for the function of the mitochondrial respiratory chain complexes. Moreover, disruption in iron biogenesis may lead to oxidative stress. Oxidative st...

Journal: :Molecular therapy : the journal of the American Society of Gene Therapy 2007
Filip Lim Gloria M Palomo Christina Mauritz Alfredo Giménez-Cassina Belen Illana Francisco Wandosell Javier Díaz-Nido

There is currently no effective treatment for Friedreich's ataxia (FA), the most common of the hereditary ataxias. The disease is caused by mutations in FRDA that drastically reduce expression levels of the mitochondrial protein frataxin. In FA animal models, a key difficulty is obtaining the precise levels of frataxin expression in the appropriate tissues to provoke pathology without early let...

2015
Elisabetta Soragni C. James Chou James R. Rusche Joel M. Gottesfeld

The genetic defect in Friedreich's ataxia (FRDA) is the hyperexpansion of a GAA•TTC triplet in the first intron of the FXN gene, encoding the essential mitochondrial protein frataxin. Histone post-translational modifications near the expanded repeats are consistent with heterochromatin formation and consequent FXN gene silencing. Using a newly developed human neuronal cell model, derived from p...

Journal: :Brain : a journal of neurology 2009
Filippo Fortuna Piero Barboni Rocco Liguori Maria Lucia Valentino Giacomo Savini Cinzia Gellera Caterina Mariotti Giovanni Rizzo Caterina Tonon David Manners Raffaele Lodi Alfredo A Sadun Valerio Carelli

Optic neuropathy is common in mitochondrial disorders, but poorly characterized in Friedreich's ataxia (FRDA), a recessive condition caused by lack of the mitochondrial protein frataxin. We investigated 26 molecularly confirmed FRDA patients by studying both anterior and posterior sections of the visual pathway using a new, integrated approach. This included visual field testing and optical coh...

Journal: :Human molecular genetics 2007
Yuxi Shan Eleonora Napoli Gino Cortopassi

The neurodegenerative disorder Friedreich's ataxia (FRDA) is caused by mutations in frataxin, a mitochondrial protein whose function remains controversial. Using co-immunoprecipitation and mass spectrometry we identified multiple interactors of mitochondrial frataxin in mammalian cells. One interactor was mortalin/GRP75, a homolog of the yeast ssq1 chaperone that integrates iron-sulfur clusters...

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