Resultats de la cerca - Stéphane Dubois
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The CYP2B2 Phenobarbital Response Unit Contains an Accessory Factor Element and a Putative Glucocorticoid Response Element Essential for Conferring Maximal Phenobarbital Responsive... per Catherine M. Stoltz, Marie-Hélène Vachon, Eric Trottier, Stéphane Dubois, Yanick Paquet, Alan Anderson
Publicat 1998Artigo -
2
Exome sequencing identifies mutations in the gene<i>TTC7A</i>in French-Canadian cases with hereditary multiple intestinal atresia per Mark E. Samuels, Jacek Majewski, Najmeh Alirezaie, Isabel Fernández, Ferrán Casals, Natalie Patey, Hélène Decaluwe, Isabelle Gosselin, Élie Haddad, Alan Hodgkinson, Youssef Idaghdour, Valérie Marchand, Jacques L. Michaud, Marc‐André Rodrigue, Sylvie Desjardins, Stéphane Dubois, Françoise Le Deist, Philip Awadalla, Vincent Raymond, Bruno Maranda
Publicat 2013Artigo -
3
Mutations of the Forkhead/Winged-Helix Gene, FKHL7, in Patients with Axenfeld-Rieger Anomaly per Alan J. Mears, Tim Jordan, Farideh Mirzayans, Stéphane Dubois, Tsutomu Kume, Michael Parlee, Robert Ritch, Ben F. Koop, Wen-Lin Kuo, Colin C. Collins, Jody Marshall, Douglas B. Gould, W G Pearce, Peter Carlsson, Sven Enerbäck, Jean Morissette, Shomi S. Bhattacharya, Brigid L.M. Hogan, Vincent Raymond, Michael A. Walter
Publicat 1998Artigo -
4
Exome sequencing identifies breast cancer susceptibility genes and defines the contribution of coding variants to breast cancer risk per Naomi Wilcox, Martine Dumont, Anna González‐Neira, Sara Carvalho, Charles Joly Beauparlant, Marco Crotti, Craig Luccarini, Penny Soucy, Stéphane Dubois, Rocío Núñez‐Torres, Guillermo Pita, Eugene J. Gardner, Joe Dennis, M. Rosario Alonso, Núria Álvarez, Caroline Baynes, Annie Claude Collin-Deschesnes, Sylvie Desjardins, Heiko Becher, Sabine Behrens, Manjeet K. Bolla, Jose E. Castelao, Jenny Chang-Claude, Sten Cornelissen, Thilo Dörk, Christoph Engel, Manuela Gago‐Dominguez, Pascal Guénel, Andreas Hadjisavvas, Eric Hahnen, Mikael Hartman, Belén Herráez, Benita Kiat Tee Tan, Veronique Kiak Mien Tan, Su-Ming Tan, Geok Hoon Lim, Ern Yu Tan, Peh Joo Ho, Alexis Jiaying Khng, Audrey Jung, Renske Keeman, Marion Kiechle, Jingmei Li, Maria A. Loizidou, Michael Lush, Kyriaki Michailidou, Mihalis I. Panayiotidis, Xueling Sim, Soo‐Hwang Teo, Jonathan P. Tyrer, Lizet E. van der Kolk, Cecilia Wahlström, Qin Wang, John R. B. Perry, Javier Benítez, Marjanka K. Schmidt, Rita K. Schmutzler, Paul D.P. Pharoah, Arnaud Droit, Alison M. Dunning, Anders Kvist, Peter Devilee, Douglas F. Easton, Jacques Simard
Publicat 2023Revisão -
5
Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes per Laura Fachal, Hugues Aschard, Jonathan Beesley, Daniel R. Barnes, Jamie Allen, Siddhartha Kar, Karen A. Pooley, Joe Dennis, Kyriaki Michailidou, Constance Turman, Penny Soucy, Audrey Lemaçon, Michael Lush, Jonathan P. Tyrer, Maya Ghoussaini, Mahdi Moradi Marjaneh, Xia Jiang, Simona Agata, Kristiina Aittomäki, M. Rosario Alonso, Irene L. Andrulis, Hoda Anton‐Culver, Natalia Antonenkova, Aðalgeir Arason, Volker Arndt, Kristan J. Aronson, Banu K. Arun, Bernd Auber, Paul L. Auer, Jacopo Azzollini, Judith Balmañà, Rósa B. Barkardóttir, Daniel Barrowdale, Alicia Beeghly‐Fadiel, Javier Benı́tez, Marina Bermisheva, Katarzyna Białkowska, Amie Blanco, Carl Blomqvist, William J. Blot, Natalia Bogdanova, Stig E. Bojesen, Manjeet K. Bolla, Bernardo Bonanni, Åke Borg, Kristin Bosse, Hiltrud Brauch, Hermann Brenner, Ignacio Briceño, Ian W. Brock, Angela Brooks‐Wilson, Thomas Brüning, Barbara Burwinkel, Saundra S. Buys, Qiuyin Cai, Trinidad Caldés, Maria A. Caligo, Nicola J. Camp, Ian Campbell, Federico Canzian, Jason S. Carroll, Brian D. Carter, Jose E. Castelao, Jocelyne Chiquette, Hans Christiansen, Wendy K. Chung, Kathleen Claes, Christine L. Clarke, Margriet Collée, Sten Cornelissen, Fergus J. Couch, Angela Cox, Simon S. Cross, Cezary Cybulski, Kamila Czene, Mary B. Daly, Miguel de la Hoya, Peter Devilee, Orland Dı́ez, Yuan Chun Ding, Gillian S. Dite, Susan M. Domchek, Thilo Dörk, Isabel dos–Santos–Silva, Arnaud Droit, Stéphane Dubois, Martine Dumont, M. Durán, Lorraine Durcan, Miriam Dwek, Diana Eccles, Christoph Engel, Mikael Eriksson, D. Gareth Evans, Peter A. Fasching, Olivia Fletcher, Giuseppe Floris, Henrik Flyger, Lenka Foretová, William D. Foulkes
Publicat 2020Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Breast cancer
Cancer
Exome
Exome sequencing
Missense mutation
Mutation
Transcription factor
Allele
Aniridia
Biochemistry
CDKN2A
CHEK2
Cell biology
Compound heterozygosity
Computational biology
Cytochrome
Enhancer
Enzyme
Estrogen receptor
Exon
Expression quantitative trait loci
Forkhead Transcription Factors
Genetic association
Genetic linkage
Genome-wide association study
Genotype
Germline mutation