ERCC1/XPF protects short telomeres from homologous recombination in Arabidopsis thaliana.

by Jean-Baptiste Vannier, Annie Depeiges, Charles White, Maria Eugenia Gallego
Published 2009-02-01

TRF1 averts chromatin remodelling, recombination and replication dependent-break induced replication at mouse telomeres

by Rosa Maria Porreca, Emilia Herrera-Moyano, Eleni Skourti, Pui Pik Law, Roser Gonzalez Franco, Alex Montoya, Peter Faull, Holger Kramer, Jean-Baptiste Vannier
Published 2020-01-01

Visualising G-quadruplex DNA dynamics in live cells by fluorescence lifetime imaging microscopy

by Peter A. Summers, Benjamin W. Lewis, Jorge Gonzalez-Garcia, Rosa M. Porreca, Aaron H. M. Lim, Paolo Cadinu, Nerea Martin-Pintado, David J. Mann, Joshua B. Edel, Jean Baptiste Vannier, Marina K. Kuimova, Ramon Vilar
Published 2021-01-01

A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.

by Bari J Ballew, Vijai Joseph, Saurav De, Grzegorz Sarek, Jean-Baptiste Vannier, Travis Stracker, Kasmintan A Schrader, Trudy N Small, Richard O'Reilly, Chris Manschreck, Megan M Harlan Fleischut, Liying Zhang, John Sullivan, Kelly Stratton, Meredith Yeager, Kevin Jacobs, Neelam Giri, Blanche P Alter, Joseph Boland, Laurie Burdett, Kenneth Offit, Simon J Boulton, Sharon A Savage, John H J Petrini
Published 2013-08-01

Corrigendum: Clinical and Molecular Heterogeneity of RTEL1 Deficiency

by Carsten Speckmann, Carsten Speckmann, Sushree Sangita Sahoo, Sushree Sangita Sahoo, Sushree Sangita Sahoo, Marta Rizzi, Marta Rizzi, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Nina Kathrin Serwas, Marc Hoemberg, Natalja Damatova, Detlev Schindler, Jean-Baptiste Vannier, Simon J. Boulton, Ulrich Pannicke, Gudrun Göhring, Kathrin Thomay, J. J. Verdu-Amoros, Holger Hauch, Wilhelm Woessmann, Gabriele Escherich, Eckart Laack, Liliana Rindle, Maximilian Seidl, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Christine Jandrasits, Brigitte Strahm, Klaus Schwarz, Stephan R. Ehl, Stephan R. Ehl, Charlotte Niemeyer, Charlotte Niemeyer, Charlotte Niemeyer, Kaan Boztug, Kaan Boztug, Kaan Boztug, Kaan Boztug, Marcin W. Wlodarski, Marcin W. Wlodarski, Marcin W. Wlodarski
Published 2017-10-01

Clinical and Molecular Heterogeneity of RTEL1 Deficiency

by Marcin W. Wlodarski, Marcin W. Wlodarski, Marcin W. Wlodarski, Carsten Speckmann, Carsten Speckmann, Sushree Sangita Sahoo, Sushree Sangita Sahoo, Marta Rizzi, Marta Rizzi, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Nina Kathrin Serwas, Marc Hoemberg, Natalja Damatova, Detlev Schindler, Jean-Baptiste Vannier, Simon J. Boulton, Ulrich Pannicke, Gudrun Göhring, Kathrin Thomay, J. J. Verdu-Amoros, Holger Hauch, Wilhelm Woessmann, Gabriele Escherich, Eckart Laack, Liliana Rindle, Maximilian Seidl, Maximilian Seidl, Anne Rensing-Ehl, Ekkehart Lausch, Christine Jandrasits, Brigitte Strahm, Klaus Schwarz, Stephan R. Ehl, Stephan R. Ehl, Charlotte Niemeyer, Charlotte Niemeyer, Charlotte Niemeyer, Kaan Boztug, Kaan Boztug, Kaan Boztug, Kaan Boztug
Published 2017-05-01