Friedreich Ataxia Scientific News
Friedreich Ataxia and close related scientific news. Topics related to rare diseases.
Saturday, January 3, 2015
Grant Alert: Modeling Friedreich Ataxia with Patient iPSC-derived Neurons Medizinische Universitt Innsbruck Austrian Science Fund FWF award
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Grant Alert: Modeling Friedreich Ataxia with Patient iPSC-derived Neurons Medizinische Universitt Innsbruck Austrian Science Fund FWF award ...
The emerging role of 5-hydroxymethylcytosine in neurodegenerative diseases
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The emerging role of 5-hydroxymethylcytosine in neurodegenerative diseases . Al-Mahdawi S, Virmouni SA, Pook MA; Frontiers in neuroscience 8...
Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia.
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Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia. Igoillo-Esteve M, Gurgul-Convey E, Hu A, Romag...
Tuesday, December 30, 2014
Frataxin knockdown in human astrocytes triggers cell death and the release of factors that cause neuronal toxicity
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Frataxin knockdown in human astrocytes triggers cell death and the release of factors that cause neuronal toxicity . Frida Loría, Javier Día...
Monday, December 29, 2014
Selective dendritic susceptibility to bioenergetic and redox perturbations in cortical neurons
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Selective dendritic susceptibility to bioenergetic and redox perturbations in cortical neurons . Philip Hasel, Sean Mckay, Jing Qiu, Giles E...
Transition of Thalassaemia and Friedreich ataxia from fatal to chronic diseases
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Transition of Thalassaemia and Friedreich ataxia from fatal to chronic diseases . Annita Kolnagou, Christina N Kontoghiorghe, and George J K...
Highly specific ubiquitin-competing molecules effectively promote frataxin accumulation and partially rescue the aconitase defect in Friedreich ataxia cells
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Highly specific ubiquitin-competing molecules effectively promote frataxin accumulation and partially rescue the aconitase defect in Friedre...
Sunday, December 28, 2014
Identical mutation associated with distinct clinical phenotypes of Friedreich’s ataxia: case report
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Identical mutation associated with distinct clinical phenotypes of Friedreich’s ataxia: case report . M. Malenica, M. Kukuruzović, S. Bitang...
Monday, December 22, 2014
Grant Alert: Elucidating the molecular basis of gene silencing by an ORC-HP1 interaction and their contribution to human health disorders
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Grant Alert: Elucidating the molecular basis of gene silencing by an ORC-HP1 interaction and their contribution to human health disorders . ...
Saturday, December 20, 2014
Molecular genetic analysis of Trinucleotide Repeat Disorders (TRDs) in Indian population and application of repeat primed PCR
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Molecular genetic analysis of Trinucleotide Repeat Disorders (TRDs) in Indian population and application of repeat primed PCR . Aneek Das Bh...
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