Search Results - "Ubiparipovic, Stephanie"

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    Rapid in vitro quantification of TDP-43 and FUS mislocalisation for screening of gene variants implicated in frontotemporal dementia and amyotrophic lateral sclerosis by Oyston, Lisa J., Ubiparipovic, Stephanie, Fitzpatrick, Lauren, Hallupp, Marianne, Boccanfuso, Lauren M., Kwok, John B., Dobson-Stone, Carol

    Published in Scientific reports (21-07-2021)
    “…Identified genetic mutations cause 20% of frontotemporal dementia (FTD) and 5-10% of amyotrophic lateral sclerosis (ALS) cases: however, for the remainder of…”
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    Antibody-mediated delivery of CRISPR-Cas9 ribonucleoproteins in human cells by Ubiparipovic, Stephanie, Christ, Daniel, Rouet, Romain

    Published in Protein engineering, design and selection (17-02-2022)
    “…The CRISPR genome editing technology holds great clinical potential for the treatment of monogenetic disorders such as sickle cell disease. The therapeutic in…”
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    Journal Article
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    Rapid and automated quantification of TDP‐43 and FUS mislocalisation for screening of frontotemporal dementia and amyotrophic lateral sclerosis gene variants by Oyston, Lisa J, Ubiparipovic, Stephanie, Fitzpatrick, Lauren, Hallupp, Marianne, Boccanfuso, Lauren M, Kwok, John B, Dobson‐Stone, Carol

    Published in Alzheimer's & dementia (01-12-2021)
    “…Background Identified genetic mutations account for ∼50% of familial frontotemporal dementia (FTD) and ∼70% of familial amyotrophic lateral sclerosis (ALS)…”
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    Journal Article
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