Inhibition of DNA damage response at telomeres improves the detrimental phenotypes of Hutchinson–Gilford Progeria Syndrome
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Published in Nature communications (18.11.2019)
Published in Nature communications (18.11.2019)
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Somatic mutagenesis in satellite cells associates with human skeletal muscle aging
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Published in Nature communications (23.02.2018)
Published in Nature communications (23.02.2018)
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Somatic mutations in vascular wall function and age-associated disease
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Published in European heart journal (21.10.2023)
Published in European heart journal (21.10.2023)
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Transient expression of an adenine base editor corrects the Hutchinson-Gilford progeria syndrome mutation and improves the skin phenotype in mice
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Published in Nature communications (02.06.2022)
Published in Nature communications (02.06.2022)
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Rare progerin-expressing preadipocytes and adipocytes contribute to tissue depletion over time
Revêchon, Gwladys, Viceconte, Nikenza, McKenna, Tomás, Sola Carvajal, Agustín, Vrtačnik, Peter, Stenvinkel, Peter, Lundgren, Torbjörn, Hultenby, Kjell, Franco, Irene, Eriksson, Maria
Published in Scientific reports (30.06.2017)
Published in Scientific reports (30.06.2017)
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Accumulation of Progerin Affects the Symmetry of Cell Division and Is Associated with Impaired Wnt Signaling and the Mislocalization of Nuclear Envelope Proteins
Sola-Carvajal, Agustín, Revêchon, Gwladys, Helgadottir, Hafdis T., Whisenant, Daniel, Hagblom, Robin, Döhla, Julia, Katajisto, Pekka, Brodin, David, Fagerström-Billai, Fredrik, Viceconte, Nikenza, Eriksson, Maria
Published in Journal of investigative dermatology (01.11.2019)
Published in Journal of investigative dermatology (01.11.2019)
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Targeting RAS‐converting enzyme 1 overcomes senescence and improves progeria‐like phenotypes of ZMPSTE24 deficiency
Yao, Haidong, Chen, Xue, Kashif, Muhammad, Wang, Ting, Ibrahim, Mohamed X., Tüksammel, Elin, Revêchon, Gwladys, Eriksson, Maria, Wiel, Clotilde, Bergo, Martin O.
Published in Aging cell (01.08.2020)
Published in Aging cell (01.08.2020)
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Association of the microRNA-Single Nucleotide Polymorphism rs2910164 in miR146a with sporadic breast cancer susceptibility: A case control study
Upadhyaya, Akanksha, Smith, Robert A., Chacon-Cortes, Diego, Revêchon, Gwladys, Bellis, Claire, Lea, Rod A., Haupt, Larisa M., Chambers, Suzanne K., Youl, Philippa H., Griffiths, Lyn R.
Published in Gene (15.01.2016)
Published in Gene (15.01.2016)
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A small-molecule ICMT inhibitor delays senescence of Hutchinson-Gilford progeria syndrome cells
Chen, Xue, Yao, Haidong, Kashif, Muhammad, Revêchon, Gwladys, Eriksson, Maria, Hu, Jianjiang, Wang, Ting, Liu, Yiran, Tüksammel, Elin, Strömblad, Staffan, Ahearn, Ian M, Philips, Mark R, Wiel, Clotilde, Ibrahim, Mohamed X, Bergo, Martin O
Published in eLife (02.02.2021)
Published in eLife (02.02.2021)
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The Heterochromatin protein 1 is a regulator in RNA splicing precision deficient in ulcerative colitis
Mata-Garrido, Jorge, Xiang, Yao, Chang-Marchand, Yunhua, Reisacher, Caroline, Ageron, Elisabeth, Guerrera, Ida Chiara, Casafont, Iñigo, Bruneau, Aurelia, Cherbuy, Claire, Treton, Xavier, Dumay, Anne, Ogier-Denis, Eric, Batsché, Eric, Costallat, Mickael, Revêchon, Gwladys, Eriksson, Maria, Muchardt, Christian, Arbibe, Laurence
Published in Nature communications (18.11.2022)
Published in Nature communications (18.11.2022)
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The Heterochromatin protein 1 is a master regulator in RNA splicing precision deficient in ulcerative colitis
Jorge Mata -Garrido, Yao Xiang, Chang-Marchand, Yunhua, Reisacher, Caroline, Ageron-Ardila, Elisabeth, Guerrera, Chiara, Casafont, Inigo, Bruneau, Aurelia, Cherbuy, Claire, Treton, Xavier, Dumay, Anne, Ogier-Denis, Eric, Batsche, Eric, Costallat, Mickael, Revechon, Gwladys, Eriksson, Maria, Muchardt, Christian, Arbibe, Laurence
Published in bioRxiv (20.03.2022)
Published in bioRxiv (20.03.2022)
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