نتایج جستجو برای: ژن fxn

تعداد نتایج: 16212  

Journal: :Frontiers in Molecular Neuroscience 2015

2011
Francesco Saccà Giorgia Puorro Antonella Antenora Angela Marsili Alessandra Denaro Raffaele Piro Pierpaolo Sorrentino Chiara Pane Alessandra Tessa Vincenzo Brescia Morra Sergio Cocozza Giuseppe De Michele Filippo M. Santorelli Alessandro Filla

BACKGROUND Friedreich's ataxia (FRDA) is the most common hereditary ataxia among caucasians. The molecular defect in FRDA is the trinucleotide GAA expansion in the first intron of the FXN gene, which encodes frataxin. No studies have yet reported frataxin protein and mRNA levels in a large cohort of FRDA patients, carriers and controls. METHODOLOGY/PRINCIPAL FINDINGS We enrolled 24 patients w...

Journal: :iranian journal of child neurology 0
mohammad mehdi heidari* 1. department of biology, school of sciences, yazd university, yazd, iran mehri khatami 1. department of biology, school of sciences, yazd university, yazd, iran jafar pourakrami 2. department of biology, faculty of sciences, science and research branch of the islamic azad university, tehran, iran.

how to cite this article: heidari mm , khatami m, pourakrami j. novel point mutations in frataxin gene in iranian patients with friedreich’s ataxia. iran j child neurol. 2014 winter; 8(1):32-36.   objective friedreich’s ataxia is the most common form of hereditary ataxia with autosomal recessive pattern. more than 96% of patients are homozygous for gaa repeat extension on both alleles in the fi...

2016
Andria V. Rodrigues V. RODRIGUES ANDRIA V. RODRIGUES Pamela Riggs-Gelasco

................................................................................................................ 146 AUTOBIOGRAPHICAL STATEMENT ......................................................................... 148

2012
Ernesto A. Roman Santiago E. Faraj Mariana Gallo Andres G. Salvay Diego U. Ferreiro Javier Santos

Frataxin (FXN) is an α/β protein that plays an essential role in iron homeostasis. Apparently, the function of human FXN (hFXN) depends on the cooperative formation of crucial interactions between helix α1, helix α2, and the C-terminal region (CTR) of the protein. In this work we quantitatively explore these relationships using a purified recombinant fragment hFXN90-195. This variant shows the ...

Behnam Kamalidehghan, Elham Khalili, Massoud Houshmand, Mohammad Hossein Salehi, Omid Aryani,

Background: Friedreich ataxia (FRDA) is an autosomal recessive disorder caused by guanine-adenine-adenine (GAA) triplet expansions in the FXN gene. Its product, frataxin, which severely reduces in FRDA patients, leads to oxidative damage in mitochondria. The purpose of this study was to evaluate the triple nucleotide repeated expansions in Iranian FRDA patients and to elucidate distinguishable ...

Journal: :iranian biomedical journal 0
محمد حسین صالحی mohammad hossein salehi مسعود هوشمند massoud houshmand امید آریانی omid aryani بهنام کمالی دهقان behnam kamalidehghan الهام خلیلی elham khalili

background: friedreich ataxia (frda) is an autosomal recessive disorder caused by guanine-adenine-adenine (gaa) triplet expansions in the fxn gene. its product, frataxin, which severely reduces in frda patients, leads to oxidative damage in mitochondria. the purpose of this study was to evaluate the triple nucleotide repeated expansions in iranian frda patients and to elucidate distinguishable ...

Journal: :The Journal of biological chemistry 2011
Daman Kumari Rea Erika Biacsi Karen Usdin

Expansion of a GAA · TTC repeat in the first intron of the frataxin (FXN) gene causes an mRNA deficit that results in Friedreich ataxia (FRDA). The region flanking the repeat on FRDA alleles is associated with more extensive DNA methylation than is seen on normal alleles and histone modifications typical of repressed genes. However, whether these changes are responsible for the mRNA deficit is ...

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