Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hélène Dreau"'
Autor:
Anna Schuh, Hélène Dreau, Andreas Heger, David Sims, Fritz Offner, Bruno Verhasselt, Jan Philippé, André Efira, Virginie De Wilde, Marie Maerevoet, Radu Firescu, Philippe Mineur, Nathalie Meuleman, Peter Hillmen, David Bruce, Adele Timbs, Adam Burns, Pauline Robbe, Marek Mraz, Ruth Clifford, Karlien Pieters, Emerence Crompot, Thomas Smith, Basile Stamatopoulos
Supplementary Data Table S1: general characterisctic of the different cohorts of patients Supplementary Data Table S2: characterisctic of Population A Supplementary Data Table S3: characterisctic of Population B Supplementary Data Table S4: character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e8b6261612d72e47a04ba5cab498fb5
https://doi.org/10.1158/1078-0432.22474745
https://doi.org/10.1158/1078-0432.22474745
Autor:
Anna Schuh, Hélène Dreau, Andreas Heger, David Sims, Fritz Offner, Bruno Verhasselt, Jan Philippé, André Efira, Virginie De Wilde, Marie Maerevoet, Radu Firescu, Philippe Mineur, Nathalie Meuleman, Peter Hillmen, David Bruce, Adele Timbs, Adam Burns, Pauline Robbe, Marek Mraz, Ruth Clifford, Karlien Pieters, Emerence Crompot, Thomas Smith, Basile Stamatopoulos
Purpose: Unmutated (UM) immunoglobulin heavy chain variable region (IgHV) status or IgHV3-21 gene usage is associated with poor prognosis in chronic lymphocytic leukemia (CLL) patients. Interestingly, IgHV3-21 is often co-expressed with light chain I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57cdf1c245710e45d783276bd3991dd4
https://doi.org/10.1158/1078-0432.c.6528896.v1
https://doi.org/10.1158/1078-0432.c.6528896.v1
Autor:
Anna Schuh, Hélène Dreau, Andreas Heger, David Sims, Fritz Offner, Bruno Verhasselt, Jan Philippé, André Efira, Virginie De Wilde, Marie Maerevoet, Radu Firescu, Philippe Mineur, Nathalie Meuleman, Peter Hillmen, David Bruce, Adele Timbs, Adam Burns, Pauline Robbe, Marek Mraz, Ruth Clifford, Karlien Pieters, Emerence Crompot, Thomas Smith, Basile Stamatopoulos
Supplementary Data Figure S1. Determination of IgLV3-21 positivity by real-time PCR. Supplementary Data Figure S2: CLL-OS analysis including only CLL-related deaths. Supplementary Data Figure S3. Validation of the poor prognosis associated with IgLV3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c290abb945e53d972d785077c5b18f34
https://doi.org/10.1158/1078-0432.22474742
https://doi.org/10.1158/1078-0432.22474742
Autor:
Alistair T. Pagnamenta, Carme Camps, Edoardo Giacopuzzi, John M. Taylor, Mona Hashim, Eduardo Calpena, Pamela J. Kaisaki, Akiko Hashimoto, Jing Yu, Edward Sanders, Ron Schwessinger, Jim R. Hughes, Gerton Lunter, Helene Dreau, Matteo Ferla, Lukas Lange, Yesim Kesim, Vassilis Ragoussis, Dimitrios V. Vavoulis, Holger Allroggen, Olaf Ansorge, Christian Babbs, Siddharth Banka, Benito Baños-Piñero, David Beeson, Tal Ben-Ami, David L. Bennett, Celeste Bento, Edward Blair, Charlotte Brasch-Andersen, Katherine R. Bull, Holger Cario, Deirdre Cilliers, Valerio Conti, E. Graham Davies, Fatima Dhalla, Beatriz Diez Dacal, Yin Dong, James E. Dunford, Renzo Guerrini, Adrian L. Harris, Jane Hartley, Georg Hollander, Kassim Javaid, Maureen Kane, Deirdre Kelly, Dominic Kelly, Samantha J. L. Knight, Alexandra Y. Kreins, Erika M. Kvikstad, Craig B. Langman, Tracy Lester, Kate E. Lines, Simon R. Lord, Xin Lu, Sahar Mansour, Adnan Manzur, Reza Maroofian, Brian Marsden, Joanne Mason, Simon J. McGowan, Davide Mei, Hana Mlcochova, Yoshiko Murakami, Andrea H. Németh, Steven Okoli, Elizabeth Ormondroyd, Lilian Bomme Ousager, Jacqueline Palace, Smita Y. Patel, Melissa M. Pentony, Chris Pugh, Aboulfazl Rad, Archana Ramesh, Simone G. Riva, Irene Roberts, Noémi Roy, Outi Salminen, Kyleen D. Schilling, Caroline Scott, Arjune Sen, Conrad Smith, Mark Stevenson, Rajesh V. Thakker, Stephen R. F. Twigg, Holm H. Uhlig, Richard van Wijk, Barbara Vona, Steven Wall, Jing Wang, Hugh Watkins, Jaroslav Zak, Anna H. Schuh, Usha Kini, Andrew O. M. Wilkie, Niko Popitsch, Jenny C. Taylor
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-25 (2023)
Abstract Background Whole genome sequencing is increasingly being used for the diagnosis of patients with rare diseases. However, the diagnostic yields of many studies, particularly those conducted in a healthcare setting, are often disappointingly l
Externí odkaz:
https://doaj.org/article/c9f00f4d0c70402d8c69f3f7e4981fbc
Autor:
Oliver C. Lomas, Sarah Gooding, Maite Cabes, Helene Dreau, Edward Wilson, Paolo Polzella, Genomics England Research Consortium, Karthik Ramasamy, Angela D. Hamblin
Publikováno v:
eJHaem, Vol 2, Iss 4, Pp 809-812 (2021)
Abstract Multiple myeloma is characterized by chromosomal abnormalities and genetic variation, which may inform prognosis and guide treatment. This pilot study sought to examine the feasibility of incorporating Whole Genome Sequencing (WGS) alongside
Externí odkaz:
https://doaj.org/article/0907cfd5cbae46de90683fdc9405e99f
Autor:
Ryan M. Baxley, Wendy Leung, Megan M. Schmit, Jacob Peter Matson, Lulu Yin, Marissa K. Oram, Liangjun Wang, John Taylor, Jack Hedberg, Colette B. Rogers, Adam J. Harvey, Debashree Basu, Jenny C. Taylor, Alistair T. Pagnamenta, Helene Dreau, Jude Craft, Elizabeth Ormondroyd, Hugh Watkins, Eric A. Hendrickson, Emily M. Mace, Jordan S. Orange, Hideki Aihara, Grant S. Stewart, Edward Blair, Jeanette Gowen Cook, Anja-Katrin Bielinsky
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-19 (2021)
Minichromosome maintenance protein 10 (MCM10) is critical for eukaryotic DNA replication. Here, by modelling MCM10 variants in human cell lines, the authors reveal a mechanism of MCM10-associated disease, finding that loss of MCM10 function constrain
Externí odkaz:
https://doaj.org/article/fcda6dd35e9949f888622bfe0a813011
Autor:
Hannah E. Roberts, Maria Lopopolo, Alistair T. Pagnamenta, Eshita Sharma, Duncan Parkes, Lorne Lonie, Colin Freeman, Samantha J. L. Knight, Gerton Lunter, Helene Dreau, Helen Lockstone, Jenny C. Taylor, Anna Schuh, Rory Bowden, David Buck
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
Abstract Recent advances in throughput and accuracy mean that the Oxford Nanopore Technologies PromethION platform is a now a viable solution for genome sequencing. Much of the validation of bioinformatic tools for this long-read data has focussed on
Externí odkaz:
https://doaj.org/article/e945e04ccd3245778164376c6ae22f52