Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lucas T. Husquin"'
Autor:
Lucas T. Husquin, Maxime Rotival, Maud Fagny, Hélène Quach, Nora Zidane, Lisa M. McEwen, Julia L. MacIsaac, Michael S. Kobor, Hugues Aschard, Etienne Patin, Lluis Quintana-Murci
Publikováno v:
Genome Biology, Vol 19, Iss 1, Pp 1-17 (2018)
Abstract Background DNA methylation is influenced by both environmental and genetic factors and is increasingly thought to affect variation in complex traits and diseases. Yet, the extent of ancestry-related differences in DNA methylation, their gene
Externí odkaz:
https://doaj.org/article/743757f00ca14b97969e29f1ebd85894
Autor:
Laurent Abel, Laurie H. Glimcher, Lluis Quintana-Murci, Nico Marr, Fatima Al Ali, Jean Marc Doisne, David Langlais, Jacinta Bustamante, Marc Weisshaar, Jing Han, Jamila El Baghdadi, Frédéric Batteux, Manon Roynard, Yichao Shen, Mathieu Bourgey, Flore Rozenberg, Federica Sallusto, Peng Zhang, David Jarrossay, Carmen Oleaga-Quintas, Jean-Laurent Casanova, Daniela Latorre, Gaspard Kerner, Mahbuba Rahman, Houda Elarabi, Federico Mele, Yoann Seeleuthner, James P. Di Santo, Stuart G. Tangye, Michael S. Kobor, Janet Markle, Dusan Bogunovic, Stéphanie Boisson-Dupuis, Julia L. Maclsaac, Lucas T. Husquin, Lisa Worley, Conor Gruber, Cindy S. Ma, Jérémie Rosain, Taushif Khan, Thomas L. Carroll, Mohamed Jeljeli, Abderrahmane Errami, Anne Puel, Qiang Pan-Hammarström, Philippe Gros, Ibithal Benhsaien, Aziz Bousfiha, Fatima Ailal, Carys A. Croft, Rui Yang, Masato Ogishi
Publikováno v:
Cell
Cell, 2020, 183 (7), pp.1826-1847.e31. ⟨10.1016/j.cell.2020.10.046⟩
Cell, Elsevier, 2020, 183 (7), pp.1826-1847.e31. ⟨10.1016/j.cell.2020.10.046⟩
Cell, 2020, 183 (7), pp.1826-1847.e31. ⟨10.1016/j.cell.2020.10.046⟩
Cell, Elsevier, 2020, 183 (7), pp.1826-1847.e31. ⟨10.1016/j.cell.2020.10.046⟩
International audience; Inborn errors of human interferon gamma (IFN-γ) immunity underlie mycobacterial disease. We report a patient with mycobacterial disease due to inherited deficiency of the transcription factor T-bet. The patient has extremely
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad4b0b417659433e7af8596ff7bd993
https://hal-pasteur.archives-ouvertes.fr/pasteur-03260339
https://hal-pasteur.archives-ouvertes.fr/pasteur-03260339
Autor:
Qiang Pan-Hammarström, Mathieu Bourgey, Conor Gruber, Fatima Al Ali, Lluis Quintana-Murci, Federico Mele, James P. Di Santo, Jean-Marc Doisne, Carmen Oleaga-Quintas, Flore Rozenberg, Carys A. Croft, Taushif Khan, Aziz Bousfiha, Daniela Latorre, Fatima Ailal, Houda Elarabi, Cindy S. Ma, Yoann Seeleuthner, Jing Han, Lucas T. Husquin, Stéphanie Boisson-Dupuis, David Jarrossay, Thomas L. Carroll, Janet Markle, Jean-Laurent Casanova, Anne Puel, Peng Zhang, David Langlais, Mohamed Jeljeli, Dusan Bogunovic, Jérémie Rosain, Laurent Abel, Gaspard Kerner, Lisa Worley, Laurie H. Glimcher, Michael S. Kobor, Nico Marr, Rui Yang, Frédéric Batteux, Julia L. Maclsaac, Yichao Shen, Stuart G. Tangye, Jacinta Bustamante, Marc Weisshaar, Federica Sallusto, Mahbuba Rahman, Manon Roynard, Philippe Gros, Ibithal Benhsaien, Jamila El Baghdadi
SummaryInborn errors of human IFN-γ immunity underlie mycobacterial disease. We report a patient with mycobacterial disease due to an inherited deficiency of the transcription factor T-bet. This deficiency abolishes the expression of T-bet target ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08c1642ef19977309a239fcf2364cefd
https://doi.org/10.1101/2020.08.31.274589
https://doi.org/10.1101/2020.08.31.274589
Autor:
Steve Horvath, Lucas T. Husquin, David T.S. Lin, Christopher F. Rider, Michael S. Kobor, Lluis Quintana-Murci, Alexander M. Morin, Christopher Carlsten, Katia E Ramadori, Julia L. MacIsaac, Lisa M. McEwen, Meaghan J. Jones, Rachel D. Edgar
Publikováno v:
Clinical Epigenetics
Clinical Epigenetics, 2018, 10 (1), pp.123. ⟨10.1186/s13148-018-0556-2⟩
Clinical Epigenetics, BioMed Central, 2018, 10 (1), pp.123. ⟨10.1186/s13148-018-0556-2⟩
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-9 (2018)
Clinical Epigenetics, 2018, 10 (1), pp.123. ⟨10.1186/s13148-018-0556-2⟩
Clinical Epigenetics, BioMed Central, 2018, 10 (1), pp.123. ⟨10.1186/s13148-018-0556-2⟩
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-9 (2018)
Background: The capacity of technologies measuring DNA methylation (DNAm) is rapidly evolving, as are the options for applicable bioinformatics methods. The most commonly used DNAm microarray, the Illumina Infinium HumanMethylation450 (450K array), h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4e1a1113b672091a0842886be4b609e
https://hal-pasteur.archives-ouvertes.fr/pasteur-02550471/document
https://hal-pasteur.archives-ouvertes.fr/pasteur-02550471/document
Autor:
Lisa M McEwen, Meaghan J Jones, David Tse Shen Lin, Rachel D Edgar, Lucas T Husquin, Julia L MacIsaac, Katia E Ramadori, Alexander M Morin, Christopher F Rider, Chris Carlsten, Lluís Quintana-Murci, Steve Horvath, Michael S Kobor
Publikováno v:
Clinical Epigenetics, Vol 10, Iss 1, Pp 1-9 (2018)
Abstract Background The capacity of technologies measuring DNA methylation (DNAm) is rapidly evolving, as are the options for applicable bioinformatics methods. The most commonly used DNAm microarray, the Illumina Infinium HumanMethylation450 (450K a
Externí odkaz:
https://doaj.org/article/c7c9511d89d7403dbd78d2c6ae04b322