المؤلفون: Averdunk, Luisa, Huetzen, Maxim A, Moreno-Andrés, Daniel, Kalb, Reinhard, McKee, Shane, Hsieh, Tzung-Chien, Seibt, Annette, Schouwink, Marten, Lalani, Seema, Faqeih, Eissa Ali, Brunet, Theresa, Boor, Peter, Neveling, Kornelia, Hoischen, Alexander, Hildebrandt, Barbara, Graf, Elisabeth, Lu, Linchao, Jin, Weidong, Schaper, Joerg, Omer, Jamal A, Demaret, Tanguy, Fleischer, Nicole, Schindler, Detlev, Krawitz, Peter, Mayatepek, Ertan, Wieczorek, Dagmar, Wang, Lisa L, Antonin, Wolfram, Jachimowicz, Ron D, von Felbert, Verena, Distelmaier, Felix

المصدر: Genetics in Medicine, 25 (7), 100836 (2023-07)

مصطلحات موضوعية: Aging, DNA damage and repair, Mitotic errors, Rothmund-Thomson syndrome, Senescence, Hydroxyurea, CRIPT protein, human, Adaptor Proteins, Signal Transducing, Humans, Cellular Senescence/genetics, DNA Damage, Hydroxyurea/metabolism, Fibroblasts, Mutation, Adaptor Proteins, Signal Transducing/metabolism, Rothmund-Thomson Syndrome/genetics, Rothmund-Thomson Syndrome/diagnosis, Rothmund-Thomson Syndrome/pathology, Cellular Senescence, Genetics (clinical), Human health sciences, Pediatrics, Sciences de la santé humaine, Pédiatrie

Relation: https://api.elsevier.com/content/article/PII:S1098360023008493?httpAccept=text/xml; urn:issn:1098-3600; urn:issn:1530-0366

URL الوصول: https://orbi.uliege.be/handle/2268/305423