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Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals (European Journal of Human Genetics, (2024), 32, 8, (928-937), 10.1038/s41431-024-01610-1)Layo-Carris, Dana E ; Lubin, Emily E ; Sangree, Annabel K ; Clark, Kelly J ; Durham, Emily L ; Gonzalez, Elizabeth M ; Smith, Sarina ; Angireddy, Rajesh ; Wang, Xiao Min ; Weiss, Erin ; Toutain, Annick ; Mendoza-Londono, Roberto ; Dupuis, Lucie ; Damseh, Nadirah ; Velasco, Danita ; Valenzuela, Irene ; Codina-Solà, Marta ; Ziats, Catherine ; Have, Jaclyn ; Clarkson, Katie ; Steel, Dora ; Kurian, Manju ; Barwick, Katy ; Carrasco, Diana ; Dagli, Aditi I ; Nowaczyk, M. J.M ; Hančárová, Miroslava ; Bendová, Šárka ; Prchalova, Darina ; Sedláček, Zdeněk ; Baxová, Alica ; Nowak, Catherine Bearce ; Douglas, Jessica ; Chung, Wendy K ; Longo, Nicola ; Platzer, Konrad ; Klöckner, Chiara ; Averdunk, Luisa ; Wieczorek, Dagmar ; Krey, Ilona ; Zweier, Christiane ; Reis, Andre ; Balci, Tugce ; Simon, Marleen ; Kroes, Hester Y ; Wiesener, Antje ; Vasileiou, Georgia ; Marinakis, Nikolaos M ; Veltra, Danai ; Sofocleous, Christalena ; Kosma, Konstantina ; Synodinos, Joanne Traeger ; Voudris, Konstantinos A ; Vuillaume, Marie Laure ; Gueguen, Paul ; Derive, Nicolas ; Colin, Estelle ; Battault, Clarisse ; Au, Billie ; Delatycki, Martin ; Wallis, Mathew ; Gallacher, Lyndon ; Majdoub, Fatma ; Smal, Noor ; Weckhuysen, Sarah ; Schoonjans, An Sofie ; Kooy, R. Frank ; Meuwissen, Marije ; Cocanougher, Benjamin T ; Taylor, Kathryn ; Pizoli, Carolyn E ; McDonald, Marie T ; James, Philip ; Roeder, Elizabeth R ; Littlejohn, Rebecca ; Borja, Nicholas A ; Thorson, Willa ; King, Kristine ; Stoeva, Radka ; Suerink, Manon ; Nibbeling, Esther ; Baskin, Stephanie ; Guyader, Gwenaël L.E ; Kaplan, Julie ; Muss, Candace ; Carere, Deanna Alexis ; Bhoj, Elizabeth J.K ; Bryant, Laura M2024Texto completo disponível |
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Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria(European Journal of Human Genetics, (2021), 29, 8, (1186-1197), 10.1038/s41431-021-00858-1)Savige, Judy ; Storey, Helen ; Watson, Elizabeth ; Hertz, Jens Michael ; Deltas, Constantinos ; Renieri, Alessandra ; Mari, Francesca ; Hilbert, Pascale ; Plevova, Pavlina ; Byers, Peter ; Cerkauskaite, Agne ; Gregory, Martin ; Cerkauskiene, Rimante ; Ljubanovic, Danica Galesic ; Becherucci, Francesca ; Errichiello, Carmela ; Massella, Laura ; Aiello, Valeria ; Lennon, Rachel ; Hopkinson, Louise ; Koziell, Ania ; Lungu, Adrian ; Rothe, Hansjorg Martin ; Hoefele, Julia ; Zacchia, Miriam ; Martic, Tamara Nikuseva ; Gupta, Asheeta ; van Eerde, Albertien ; Gear, Susie ; Landini, Samuela ; Palazzo, Viviana ; al-Rabadi, Laith ; Claes, Kathleen ; Corveleyn, Anniek ; Van Hoof, Evelien ; van Geel, Micheel ; Williams, Maggie ; Ashton, Emma ; Belge, Hendica ; Ars, Elisabeth ; Bierzynska, Agnieszka ; Gangemi, Concetta ; Lipska-Ziętkiewicz, Beata S2024Texto completo disponível |
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Spotlight on overlooked lignin monomers: HydroxycinnamaldehydesOliveira, Dyoni M ; Cao, DechangOxford University Press (OUP) 2024Texto completo disponível |
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Yet another acetate in the wall – RWA-C regulates wood xylan acetylation in poplarOliveira, Dyoni MOxford University Press (OUP) 2024Texto completo disponível |
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Hérédité et cancerDOCAMPO MARTINEZ, Elisa ; MARTIN, Marie ; GANGOLF, Marjorie ; HARVENGT, Julie ; BULK, Saskia ; SEGERS, Karin ; LEROI, Natacha ; LETE, Céline ; PALMARICCIOTTI, Valérie ; Freire Chadrina, Maria ; LAMBERT, Frédéric ; Bours, VincentUniversité de Liège. Revue Médicale de Liège 2021Texto completo disponível |
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Correction: Stereotactic ablative radiotherapy or best supportive care in patients with localized pancreatic cancer not receiving chemotherapy and surgery (PANCOSAR): a nationwide multicenter randomized controlled trial according to a TwiCs design (BMC Cancer, (2022), 22, 1, (1363), 10.1186/s12885-022-10419-4)for the Dutch Pancreatic Cancer Group2023Texto completo disponível |
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Cycling with brakes: ABA-INSENSITIVE4 controls cell cycle arrest in the root meristemDubois, MariekeOxford University Press (OUP) 2023Texto completo disponível |
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Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole bloodLevy, Michael A ; Beck, David B ; Metcalfe, Kay ; Douzgou, Sofia ; Sithambaram, Sivagamy ; Cottrell, Trudie ; Ansar, Muhammad ; Kerkhof, Jennifer ; Mignot, Cyril ; Nougues, Marie-Christine ; Keren, Boris ; Moore, Hannah W ; Oegema, Renske ; Giltay, Jacques C ; Simon, Marleen ; van Jaarsveld, Richard H ; Bos, Jessica ; van Haelst, Mieke ; Motazacker, M Mahdi ; Boon, Elles M J ; Santen, Gijs W E ; Ruivenkamp, Claudia A L ; Alders, Marielle ; Luperchio, Teresa Romeo ; Boukas, Leandros ; Ramsey, Keri ; Narayanan, Vinodh ; Schaefer, G Bradley ; Bonasio, Roberto ; Doheny, Kimberly F ; Stevenson, Roger E ; Banka, Siddharth ; Sadikovic, Bekim ; Fahrner, Jill A2021Texto completo disponível |
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Correction to 'DNA polymerase gamma mutations that impair holoenzyme stability cause catalytic subunit depletion'Silva-Pinheiro, Pedro ; Pardo-Hernández, Carlos ; Reyes, Aurelio ; Tilokani, Lisa ; Mishra, Anup ; Cerutti, Raffaele ; Li, Shuaifeng ; Rozsivalova, Dieu-Hien ; Valenzuela, Sebastian ; Dogan, Sukru A ; Peter, Bradley ; Fernández-Silva, Patricio ; Trifunovic, Aleksandra ; Prudent, Julien ; Minczuk, Michal ; Bindoff, Laurence ; Macao, Bertil ; Zeviani, Massimo ; Falkenberg, Maria ; Viscomi, CarloOxford University Press (OUP) 2021Texto completo disponível |
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Clinical and genetic characteristics of children with acute lymphoblastic leukemia and Li–Fraumeni syndromeWinter, Greta ; Kirschner-Schwabe, Renate ; Groeneveld-Krentz, Stefanie ; Escherich, Gabriele ; Möricke, Anja ; von Stackelberg, Arend ; Stanulla, Martin ; Bailey, Simon ; Richter, Lisa ; Steinemann, Doris ; Ripperger, Tim ; Escudero, Adela ; Farah, Roula ; Lohi, Olli ; Wadt, Karin ; Jongmans, Marjolijn ; van Engelen, Nienke ; Eckert, Cornelia ; Kratz, Christian Peter2021Texto completo disponível |