Showing 1 - 14 results of 14 for search 'Alexandre F.R. Stewart', tempo de consulta: 0.07s
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Activation of tyrosine phosphatases in the progression of Alzheimer's disease por Alexandre F. R. Stewart, Hsiao-Huei Chen
Publicado 2020-01-01
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Savior Siblings Might Rescue Fetal Lethality But Not Adult Lymphoma in Irf2bp2-Null Mice por Ragnar O. Vilmundarson, Ragnar O. Vilmundarson, Ragnar O. Vilmundarson, Niloufar Heydarikhorneh, Niloufar Heydarikhorneh, Niloufar Heydarikhorneh, An Duong, An Duong, An Duong, Tiffany Ho, Tiffany Ho, Tiffany Ho, Kianoosh Keyhanian, Kianoosh Keyhanian, Kianoosh Keyhanian, Kianoosh Keyhanian, Fariborz Soheili, Fariborz Soheili, Fariborz Soheili, Hsiao-Huei Chen, Hsiao-Huei Chen, Hsiao-Huei Chen, Hsiao-Huei Chen, Hsiao-Huei Chen, Alexandre F. R. Stewart, Alexandre F. R. Stewart, Alexandre F. R. Stewart
Publicado 2022-07-01
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Identification of a phosphorylation-dependent nuclear localization motif in interferon regulatory factor 2 binding protein 2. por Allen C T Teng, Naif A M Al-Montashiri, Brian L M Cheng, Philip Lou, Pinar Ozmizrak, Hsiao-Huei Chen, Alexandre F R Stewart
Publicado 2011-01-01
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Loss of IRF2BP2 in Microglia Increases Inflammation and Functional Deficits after Focal Ischemic Brain Injury por Shelly A. Cruz, Shelly A. Cruz, Shelly A. Cruz, Aswin Hari, Aswin Hari, Aswin Hari, Zhaohong Qin, Zhaohong Qin, Pascal Couture, Pascal Couture, Pascal Couture, Hua Huang, Hua Huang, Hua Huang, Diane C. Lagace, Diane C. Lagace, Diane C. Lagace, Alexandre F. R. Stewart, Alexandre F. R. Stewart, Hsiao-Huei Chen, Hsiao-Huei Chen, Hsiao-Huei Chen, Hsiao-Huei Chen, Hsiao-Huei Chen
Publicado 2017-07-01
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Correction: Rare Copy Number Variants Contribute to Congenital Left-Sided Heart Disease. por Marc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath Christopher Lionel, Guylaine D'Amours, Emmanuelle Lemyre, Rebecca Cullum, Jean-Luc Bigras, Maryse Thibeault, Philippe Chetaille, Alexandre Montpetit, Paul Khairy, Bert Overduin, Sabine Klaassen, Pamela Hoodless, Philip Awadalla, Julie Hussin, Youssef Idaghdour, Mona Nemer, Alexandre F. R. Stewart, Cornelius Boerkoel, Stephen W. Scherer, Andrea Richter, Marie-Pierre Dubé, Gregor Andelfinger
Publicado 2013-03-01
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Rare copy number variants contribute to congenital left-sided heart disease. por Marc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath Christopher Lionel, Guylaine D'Amours, Emmanuelle Lemyre, Rebecca Cullum, Jean-Luc Bigras, Maryse Thibeault, Philippe Chetaille, Alexandre Montpetit, Paul Khairy, Bert Overduin, Sabine Klaassen, Pamela Hoodless, Philip Awadalla, Julie Hussin, Youssef Idaghdour, Mona Nemer, Alexandre F R Stewart, Cornelius Boerkoel, Stephen W Scherer, Andrea Richter, Marie-Pierre Dubé, Gregor Andelfinger
Publicado 2012-09-01
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Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease. por Ville-Petteri Mäkinen, Mete Civelek, Qingying Meng, Bin Zhang, Jun Zhu, Candace Levian, Tianxiao Huan, Ayellet V Segrè, Sujoy Ghosh, Juan Vivar, Majid Nikpay, Alexandre F R Stewart, Christopher P Nelson, Christina Willenborg, Jeanette Erdmann, Stefan Blakenberg, Christopher J O'Donnell, Winfried März, Reijo Laaksonen, Stephen E Epstein, Sekar Kathiresan, Svati H Shah, Stanley L Hazen, Muredach P Reilly, Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium, Aldons J Lusis, Nilesh J Samani, Heribert Schunkert, Thomas Quertermous, Ruth McPherson, Xia Yang, Themistocles L Assimes
Publicado 2014-07-01
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Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. por Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne S Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers Ef Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill A Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz
Publicado 2021-07-01
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Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. por Enrique Audain, Anna Wilsdon, Jeroen Breckpot, Jose M G Izarzugaza, Tomas W Fitzgerald, Anne-Karin Kahlert, Alejandro Sifrim, Florian Wünnemann, Yasset Perez-Riverol, Hashim Abdul-Khaliq, Mads Bak, Anne S Bassett, D Woodrow Benson, Felix Berger, Ingo Daehnert, Koenraad Devriendt, Sven Dittrich, Piers Ef Daubeney, Vidu Garg, Karl Hackmann, Kirstin Hoff, Philipp Hofmann, Gregor Dombrowsky, Thomas Pickardt, Ulrike Bauer, Bernard D Keavney, Sabine Klaassen, Hans-Heiner Kramer, Christian R Marshall, Dianna M Milewicz, Scott Lemaire, Joseph S Coselli, Michael E Mitchell, Aoy Tomita-Mitchell, Siddharth K Prakash, Karl Stamm, Alexandre F R Stewart, Candice K Silversides, Reiner Siebert, Brigitte Stiller, Jill A Rosenfeld, Inga Vater, Alex V Postma, Almuth Caliebe, J David Brook, Gregor Andelfinger, Matthew E Hurles, Bernard Thienpont, Lars Allan Larsen, Marc-Phillip Hitz
Publicado 2021-09-01
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