نتایج جستجو برای: SETX gene

تعداد نتایج: 1141403  

Ehsan Moghanloo Fatemeh Minoochehr Maghsoud Seifi Saeid Morovvati Shahram Teimourian, Ziba Morovvati

Hereditary ataxias (HA) are a group of inherited neurological disorders caused by changes in genes. At least 115 different mutations in the senataxin (SETX) gene causing ataxia have been identified. There are no reports of any SETX gene mutation among the Iranian population. Here we report on two cases with homozygous and heterozygous mutations in which one patient was affected by HA with oculo...

2013
Lorenzo Nanetti Simona Cavalieri Viviana Pensato Alessandra Erbetta Davide Pareyson Marta Panzeri Giovanna Zorzi Carlo Antozzi Isabella Moroni Cinzia Gellera Alfredo Brusco Caterina Mariotti

OBJECTIVES/BACKGROUND Ataxia with oculomotor apraxia defines a group of genetically distinct recessive ataxias including ataxia-telangectasia (A-T, ATM gene), ataxia with oculomotor apraxia type 1 (AOA1, APTX gene) and type 2 (AOA2, SETX gene). Although, a few unique clinical features differentiate each of these forms, the patients also share common clinical signs, such as the presence of cereb...

2014
Wei Wang Zhi Wei

Advances in next-generation sequencing technology have made it possible to comprehensively interrogate the entire spectrum of genomic variations including rare variants. They may help capture the remaining genetic heritability which has not been fully explained by previous genome-wide association studies. Here we performed a gene-based genome-wide scan to identify hypertension susceptibility lo...

Journal: :Human molecular genetics 2014
Brent L Fogel Ellen Cho Amanda Wahnich Fuying Gao Olivier J Becherel Xizhe Wang Francesca Fike Leslie Chen Chiara Criscuolo Giuseppe De Michele Alessandro Filla Abigail Collins Angelika F Hahn Richard A Gatti Genevieve Konopka Susan Perlman Martin F Lavin Daniel H Geschwind Giovanni Coppola

Senataxin, encoded by the SETX gene, contributes to multiple aspects of gene expression, including transcription and RNA processing. Mutations in SETX cause the recessive disorder ataxia with oculomotor apraxia type 2 (AOA2) and a dominant juvenile form of amyotrophic lateral sclerosis (ALS4). To assess the functional role of senataxin in disease, we examined differential gene expression in AOA...

2013
Martin F. Lavin Abrey J. Yeo Olivier J. Becherel

Ataxia oculomotor apraxia type 2 (AOA2) is a rare autosomal recessive disorder characterized by cerebellar atrophy, peripheral neuropathy, loss of Purkinje cells and elevated α-fetoprotein. AOA2 is caused by mutations in the SETX gene that codes for the high molecular weight protein senataxin. Mutations in this gene also cause dominant neurodegenerative disorders. Similar to that observed for o...

Journal: :Rare Diseases 2014

2014
Patricia Richard James L Manley

Senataxin (SETX) is a putative RNA:DNA helicase that is mutated in two distinct juvenile neurological disorders, AOA2 and ALS4. SETX is involved in the response to oxidative stress and is suggested to resolve R loops formed at transcription termination sites or at sites of collisions between the transcription and replication machineries. R loops are hybrids between RNA and DNA that are believed...

2016
Cong Lu Yi-Cen Zheng Yi Dong Hong-Fu Li

BACKGROUND Autosomal recessive cerebellar ataxias (ARCA) are a group of neurodegenerative disorders characterized by early onset of gait impairment, disturbed limb coordination, dysarthria, and eye movement abnormalities, most likely due to the degeneration of cerebellum, brainstem, and spinal cord. Despite of the rarity, ARCA are both clinically and genetically heterogeneous. To date, more tha...

Journal: :Nature Structural & Molecular Biology 2015

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