Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jean-Baptiste Rivière"'
Autor:
Karl Grenier, MD, PhD, Jean-Baptiste Rivière, PhD, Bouchra Ouled Amar Bencheikh, PhD, Andrea Liliam Gomez Corredor, PhD, Benjamin Christopher Shieh, MD, Hangjun Wang, MD, Pierre Olivier Fiset, MD, PhD, Sophie Camilleri-Broët, MD, PhD
Publikováno v:
JTO Clinical and Research Reports, Vol 4, Iss 7, Pp 100530- (2023)
Introduction: Translocations of the ROS1 gene were found to drive tumorigenesis in 1% to 2% of lung adenocarcinoma. In clinical practice, ROS1 rearrangements are often screened by immunohistochemistry (IHC) before confirmation with either fluorescenc
Externí odkaz:
https://doaj.org/article/9f9cb44d4e1641f0a394aabbb3688464
Autor:
Chunmei Li, Victor L Jensen, Kwangjin Park, Julie Kennedy, Francesc R Garcia-Gonzalo, Marta Romani, Roberta De Mori, Ange-Line Bruel, Dominique Gaillard, Bérénice Doray, Estelle Lopez, Jean-Baptiste Rivière, Laurence Faivre, Christel Thauvin-Robinet, Jeremy F Reiter, Oliver E Blacque, Enza Maria Valente, Michel R Leroux
Publikováno v:
PLoS Biology, Vol 14, Iss 3, p e1002416 (2016)
Cilia have a unique diffusion barrier ("gate") within their proximal region, termed transition zone (TZ), that compartmentalises signalling proteins within the organelle. The TZ is known to harbour two functional modules/complexes (Meckel syndrome [M
Externí odkaz:
https://doaj.org/article/8218a5f05b2d4ec7ac530fd44daeffc4
Autor:
Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, Eric Rider, Polina Bukshpun, Mari Wakahiro, Susan L Christian, Jean-Baptiste Rivière, Christopher T Sullivan, Jyotsna Sudi, Michael J Herriges, Alexander R Paciorkowski, A James Barkovich, Joseph T Glessner, Kathleen J Millen, Hakon Hakonarson, William B Dobyns, Elliott H Sherr
Publikováno v:
PLoS Genetics, Vol 9, Iss 10, p e1003823 (2013)
Agenesis of the corpus callosum (ACC), cerebellar hypoplasia (CBLH), and polymicrogyria (PMG) are severe congenital brain malformations with largely undiscovered causes. We conducted a large-scale chromosomal copy number variation (CNV) discovery eff
Externí odkaz:
https://doaj.org/article/38bc6373d53e49c3b54ea00de1a412d8
Autor:
Cynthia V Bourassa, Jean-Baptiste Rivière, Patrick A Dion, Geneviève Bernard, Sabrina Diab, Michel Panisset, Sylvain Chouinard, Nicolas Dupré, Hélène Fournier, John Raelson, Majid Belouchi, Guy A Rouleau
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e16254 (2011)
Essential tremor (ET) is a complex genetic disorder for which no causative gene has been found. Recently, a genome-wide association study reported that two variants in the LINGO1 locus were associated to this disease. The aim of the present study was
Externí odkaz:
https://doaj.org/article/4bc29343cc0b4aab9350dd534097d709
Autor:
David Rosenblatt, Caitlin Zacharias, Kyana Arbabian, David Watkins, Jean-Baptiste Riviere, Brian Gilfix, Krithika Ragupathi
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100888- (2024)
Externí odkaz:
https://doaj.org/article/a668f32f39c943608db62751fb1ebf83
Autor:
Nicole Ezer, Hangjun Wang, Andrea Gomez Corredor, Pierre Olivier Fiset, Ayesha Baig, Léon C. van Kempen, George Chong, Marianne S.M. Issac, Richard Fraser, Alan Spatz, Jean-Baptiste Riviere, Philippe Broët, Jonathan Spicer, Sophie Camilleri-Broët, MD, PhD
Publikováno v:
Cancer Treatment and Research Communications, Vol 29, Iss , Pp 100484- (2021)
MicroAbstract: Integration of Next Generation Sequencing (NGS) information for use in distinguishing between Multiple Primary Lung Cancer and intrapulmonary metastasis was evaluated. We used a probabilistic model, comprehensive histologic assessment
Externí odkaz:
https://doaj.org/article/dc04ed82ecd74740b72116c2e0a8e691
Autor:
Jean‐Baptiste Rivière, Dominique J. Verlaan, Masoud Shekarabi, Ronald G. Lafrenière, Mélanie Bénard, Vazken M. Der Kaloustian, Zuhayr Shbaklo, Guy A. Rouleau
Publikováno v:
Annals of Neurology; Oct2004, Vol. 56 Issue 4, p572-575, 4p