Torthaí cuardaigh - Pietro Fratta

Beachtaigh na torthaí
  1. 1
    Cytoplasmic functions of TDP-43 and FUS and their role in ALS

    Cytoplasmic functions of TDP-43 and FUS and their role in ALS de réir Nicol Birsa, Matthew P. Bentham, Pietro Fratta

    Foilsithe / Cruthaithe 2019
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  2. 2
    The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

    The Overlapping Genetics of Amyotrophic Lateral Sclerosis and Frontotemporal Dementia de réir Yevgeniya Abramzon, Pietro Fratta, Bryan J. Traynor, Ruth Chia

    Foilsithe / Cruthaithe 2020
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  3. 3
    Is SOD1 loss of function involved in amyotrophic lateral sclerosis?

    Is SOD1 loss of function involved in amyotrophic lateral sclerosis? de réir Rachele A. Saccon, Rosie Bunton-Stasyshyn, Elizabeth Fisher, Pietro Fratta

    Foilsithe / Cruthaithe 2013
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  4. 4
    Quantitative analysis of cryptic splicing associated with TDP-43 depletion

    Quantitative analysis of cryptic splicing associated with TDP-43 depletion de réir Jack Humphrey, Warren Emmett, Pietro Fratta, Adrian M. Isaacs, Vincent Plagnol

    Foilsithe / Cruthaithe 2017
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  5. 5
    The role of hnRNPs in frontotemporal dementia and amyotrophic lateral sclerosis

    The role of hnRNPs in frontotemporal dementia and amyotrophic lateral sclerosis de réir Alexander Bampton, Lauren M. Gittings, Pietro Fratta, Tammaryn Lashley, Ariana Gatt

    Foilsithe / Cruthaithe 2020
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  6. 6
    Disease mechanism, biomarker and therapeutics for spinal and bulbar muscular atrophy (SBMA)

    Disease mechanism, biomarker and therapeutics for spinal and bulbar muscular atrophy (SBMA) de réir Atsushi Hashizume, Kenneth H. Fischbeck, Maria Pennuto, Pietro Fratta, Masahisa Katsuno

    Foilsithe / Cruthaithe 2020
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  7. 7
    The era of cryptic exons: implications for ALS-FTD

    The era of cryptic exons: implications for ALS-FTD de réir Puja R. Mehta, Anna‐Leigh Brown, Michael E. Ward, Pietro Fratta

    Foilsithe / Cruthaithe 2023
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  8. 8
    Beyond motor neurons: expanding the clinical spectrum in Kennedy’s disease

    Beyond motor neurons: expanding the clinical spectrum in Kennedy’s disease de réir Raquel Manzano, Gianni Sorarù, Christopher Grunseich, Pietro Fratta, Emanuela Zuccaro, Maria Pennuto, Carlo Rinaldi

    Foilsithe / Cruthaithe 2018
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  9. 9
    Transcriptomic analysis of frontotemporal lobar degeneration with TDP-43 pathology reveals cellular alterations across multiple brain regions

    Transcriptomic analysis of frontotemporal lobar degeneration with TDP-43 pathology reveals cellular alterations across multiple brain regions de réir Rahat Hasan, Jack Humphrey, Conceição Bettencourt, Jia Newcombe, Tammaryn Lashley, Pietro Fratta, Towfique Raj

    Foilsithe / Cruthaithe 2021
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  10. 10
    C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci

    C9orf72 frontotemporal lobar degeneration is characterised by frequent neuronal sense and antisense RNA foci de réir Sarah Mizielinska, Tammaryn Lashley, Frances E. Norona, Emma L. Clayton, Charlotte Ridler, Pietro Fratta, Adrian M. Isaacs

    Foilsithe / Cruthaithe 2013
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  11. 11
    Proteasome Inhibition and Aggresome Formation in Sporadic Inclusion-Body Myositis and in Amyloid-β Precursor Protein-Overexpressing Cultured Human Muscle Fibers

    Proteasome Inhibition and Aggresome Formation in Sporadic Inclusion-Body Myositis and in Amyloid-β Precursor Protein-Overexpressing Cultured Human Muscle Fibers de réir Pietro Fratta, W. King Engel, Janis McFerrin, Kelvin J.A. Davies, Sharon W. Lin, Valerie Askanas

    Foilsithe / Cruthaithe 2005
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  12. 12
    C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes

    C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes de réir Pietro Fratta, Sarah Mizielinska, Andrew J. Nicoll, Mire Zloh, Elizabeth Fisher, Gary N. Parkinson, Adrian M. Isaacs

    Foilsithe / Cruthaithe 2012
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  13. 13
    Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes

    Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes de réir James N. Sleigh, Andrew P. Tosolini, David F. Gordon, Anny Devoy, Pietro Fratta, Elizabeth Fisher, Kevin Talbot, Giampietro Schiavo

    Foilsithe / Cruthaithe 2020
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  14. 14
    Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degeneration

    Nuclear import impairment causes cytoplasmic trans-activation response DNA-binding protein accumulation and is associated with frontotemporal lobar degeneration de réir Agnes L. Nishimura, Vera Župunski, Claire Troakes, Claudia Kathe, Pietro Fratta, Michael Howell, Jean‐Marc Gallo, Tibor Hortobágyi, Christopher E. Shaw, Boris Rogelj

    Foilsithe / Cruthaithe 2010
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  15. 15
    Correlation of clinical and molecular features in spinal bulbar muscular atrophy

    Correlation of clinical and molecular features in spinal bulbar muscular atrophy de réir Pietro Fratta, Niranjanan Nirmalananthan, Luc Masset, Iwona Skorupinska, Toby Collins, Andrea Cortese, Sally Pemble, Andrea Malaspina, Elizabeth Fisher, Linda Greensmith, Michael G. Hanna

    Foilsithe / Cruthaithe 2014
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  16. 16
    Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosis

    Circulating miR-181 is a prognostic biomarker for amyotrophic lateral sclerosis de réir Iddo Magen, Nancy‐Sarah Yacovzada, Eran Yanowski, Anna Coenen-Stass, Julian Großkreutz, Ching‐Hua Lu, Linda Greensmith, Andrea Malaspina, Pietro Fratta, Eran Hornstein

    Foilsithe / Cruthaithe 2021
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  17. 17
    Opinion: more mouse models and more translation needed for ALS

    Opinion: more mouse models and more translation needed for ALS de réir Elizabeth Fisher, Linda Greensmith, Andrea Malaspina, Pietro Fratta, Michael G. Hanna, Giampietro Schiavo, Adrian M. Isaacs, Richard W. Orrell, Thomas J. Cunningham, Abraham Acevedo‐Arozena

    Foilsithe / Cruthaithe 2023
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  18. 18
    Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy

    Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy de réir Andrea Cortese, Vincent Plagnol, Stefen Brady, Roberto Simone, Tammaryn Lashley, Abraham Acevedo‐Arozena, Rohan de Silva, Linda Greensmith, Janice L. Holton, Michael G. Hanna, Elizabeth Fisher, Pietro Fratta

    Foilsithe / Cruthaithe 2014
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  19. 19
    HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing

    HnRNP K mislocalisation is a novel protein pathology of frontotemporal lobar degeneration and ageing and leads to cryptic splicing de réir Alexander Bampton, Ariana Gatt, Jack Humphrey, Sara Cappelli, Dipanjan Bhattacharya, S Foti, Anna‐Leigh Brown, Yasmine T. Asi, Yi Hua Low, Marco Foiani, Towfique Raj, Emanuele Buratti, Pietro Fratta, Tammaryn Lashley

    Foilsithe / Cruthaithe 2021
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  20. 20
    Seeded aggregation of TDP-43 induces its loss of function and reveals early pathological signatures

    Seeded aggregation of TDP-43 induces its loss of function and reveals early pathological signatures de réir Carlo Scialò, Weijia Zhong, Somanath Jagannath, Oscar G. Wilkins, Davide Caredio, Marián Hruška-Plocháň, Flavio Lurati, Martina Peter, Elena De Cecco, Luigi Celauro, Adriano Aguzzi, Giuseppe Legname, Pietro Fratta, Magdalini Polymenidou

    Foilsithe / Cruthaithe 2025
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