Resultats de la cerca - Pierre Lepage

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  1. 1
    Isolation from human cerebrospinal fluid of a new insulin‐like growth factor‐binding protein with a selective affinity for IGF‐II

    Isolation from human cerebrospinal fluid of a new insulin‐like growth factor‐binding protein with a selective affinity for IGF‐II per Monireh Roghani, Paul Hossenlopp, Pierre Lepage, Alain Balland, M Binoux

    Publicat 1989
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  2. 2
    Genetic profiles of ten Dirofilaria immitis isolates susceptible or resistant to macrocyclic lactone heartworm preventives

    Genetic profiles of ten Dirofilaria immitis isolates susceptible or resistant to macrocyclic lactone heartworm preventives per Catherine Bourguinat, Kathy Keller, Jianguo Xia, Pierre Lepage, Tom L. McTier, Debra J. Woods, Roger K. Prichard

    Publicat 2017
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  3. 3
    Common Polymorphisms in the Promoter of the Visfatin Gene (<i>PBEF1</i>) Influence Plasma Insulin Levels in a French-Canadian Population

    Common Polymorphisms in the Promoter of the Visfatin Gene (<i>PBEF1</i>) Influence Plasma Insulin Levels in a French-Canadian Population per Swneke D. Bailey, J. Concepción Loredo‐Osti, Pierre Lepage, Janet Faith, Joelle Fontaine, Katia Desbiens, Thomas J. Hudson, Claude Bouchard, Daniel Gaudet, Louis Pérusse, Marie‐Claude Vohl, James C. Engert

    Publicat 2006
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  4. 4
    Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the <i>TYK2</i> gene

    Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the <i>TYK2</i> gene per David A. Dyment, M. Zameel Cader, Michael J. Chao, Matthew R. Lincoln, Katie Morrison, Giulio Disanto, Julia M. Morahan, Gabriele C. DeLuca, A. Dessa Sadovnick, Pierre Lepage, Alexandre Montpetit, George C. Ebers, Sreeram V. Ramagopalan

    Publicat 2012
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  5. 5
    5′ Flanking Variants of Resistin Are Associated With Obesity

    5′ Flanking Variants of Resistin Are Associated With Obesity per James C. Engert, Marie‐Claude Vohl, Scott M. Williams, Pierre Lepage, Jorge Loredo‐Osti, Janet Faith, Carole Doré, Yannick Renaud, Noël P. Burtt, Amélie Villeneuve, Joel N. Hirschhorn, David Altshuler, Leif Groop, Jean‐Pierre Després, Daniel Gaudet, Thomas J. Hudson

    Publicat 2002
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  6. 6
    K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas

    K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas per Dong-Anh Khuong-Quang, Pawel Buczkowicz, Patricia Rakopoulos, Xiao-Yang Liu, Adam M. Fontebasso, Éric Bouffet, Ute Bartels, Steffen Albrecht, Jeremy Schwartzentruber, Louis Létourneau, Mathieu Bourgey, Guillaume Bourque, Alexandre Montpetit, Geneviève Bourret, Pierre Lepage, Adam Fleming, Peter Lichter, Marcel Kool, Andreas von Deimling, Dominik Sturm, Andrey Korshunov, Damien Faury, David Jones, Jacek Majewski, Stefan M. Pfister, Nada Jabado, Cynthia Hawkins

    Publicat 2012
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  7. 7
    Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas

    Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas per Adam M. Fontebasso, Jeremy Schwartzentruber, Dong-Anh Khuong-Quang, Xiao-Yang Liu, Dominik Sturm, Andrey Korshunov, David Jones, Hendrik Witt, Marcel Kool, Steffen Albrecht, Adam Fleming, Djihad Hadjadj, Stephan Busche, Pierre Lepage, Alexandre Montpetit, Alfredo Staffa, Noha Gerges, Magdalena Zakrzewska, Krzysztof Zakrzewski, Paweł P. Liberski, Péter Hauser, Miklós Garami, Álmos Klekner, László Bognár, Gelareh Zadeh, Damien Faury, Stefan M. Pfister, Nada Jabado, Jacek Majewski

    Publicat 2013
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  8. 8
    Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)

    Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome) per Martin Hřebı́ček, Lenka Mrázová, Volkan Seyrantepe, Stéphanie Durand, Nicole M. Roslin, Lenka Nosková, Hana Hartmannová, Robert Ivánek, Alena Čížková, Helena Poupětová, Jakub Sikora, Jana Uřinovská, Viktor Stránecký, J Zeman, Pierre Lepage, David Roquis, Andrei Verner, Jérôme Ausseil, Clare Beesley, Irène Maire, Ben J. H. M. Poorthuis, Jiddeke van de Kamp, Otto P. van Diggelen, Ron A. Wevers, Thomas J. Hudson, Takuya Fujiwara, Jacek Majewski, Kenneth Morgan, Stanislav Kmoch, Alexey V. Pshezhetsky

    Publicat 2006
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  9. 9
    Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations

    Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations per Leanne de Kock, Nelly Sabbaghian, François Plourde, Archana Srivastava, Evan Weber, Dorothée Bouron‐Dal Soglio, Nancy Hamel, Joon Hyuk Choi, Sung‐Hye Park, Cheri Deal, Megan M. Kelsey, Megan K. Dishop, Adam J. Esbenshade, John F. Kuttesch, Thomas S. Jacques, Arie Perry, Heinz E. Leichter, Philippe Maeder, Marie‐Anne Bründler, Justin Warner, James Neal, Margaret Zacharin, Márta Korbonits, Trevor Cole, Heidi Traunecker, Thomas W. McLean, Fabio Rotondo, Pierre Lepage, Steffen Albrecht, Éva Horváth, Kálmán Kovács, John R. Priest, William D. Foulkes

    Publicat 2014
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  10. 10
    Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19

    Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 per Gundula Povysil, Guillaume Butler‐Laporte, Ning Shang, Chen Wang, Atlas Khan, Manal Alaamery, Tomoko Nakanishi, Sirui Zhou, Vincenzo Forgetta, Robert Eveleigh, Mathieu Bourgey, Naveed Aziz, Steven J.M. Jones, Bartha Maria Knoppers, Stephen W. Scherer, Lisa J. Strug, Pierre Lepage, Jiannis Ragoussis, Guillaume Bourque, Jahad Alghamdi, Nora Aljawini, Nour Albes, Hani Al-Afghani, Bader Alghamdi, Mansour Almutairi, Ebrahim Mahmoud, Leen Abu‐Safieh, Hadeel El Bardisy, Fawz S. Al Harthi, Abdulraheem Alshareef, Bandar A. Suliman, Saleh A. Alqahtani, Abdulaziz Almalik, May Alrashed, Salam Massadeh, Vincent Mooser, Mark Lathrop, Fawzy Mohamed, Yaseen M. Arabi, Hamdi Mbarek, Chadi Saad, Wadha Al‐Muftah, Junghyun Jung, Serghei Mangul, Radja Badji, Asma Al Thani, Said I. Ismail, Ali G. Gharavi, Malak Abedalthagafi, J. Brent Richards, David B. Goldstein, Krzysztof Kiryluk

    Publicat 2021
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  11. 11
    Variation in genomic landscape of clear cell renal cell carcinoma across Europe

    Variation in genomic landscape of clear cell renal cell carcinoma across Europe per Ghislaine Scélo, Yasser Riazalhosseini, Liliana Greger, Louis Létourneau, Mar González-Porta, Magdalena B. Wozniak, Mathieu Bourgey, Patricia Harnden, Lars Egevad, Sharon M. Jackson, Mehran Karimzadeh, Madeleine Arseneault, Pierre Lepage, Alexandre How‐Kit, Antoine Daunay, Victor Renault, Hélène Blanché, Emmanuel Tubacher, Jeremy Sehmoun, Juris Vīksna, Edgars Celms, Mārtiņš Opmanis, Andris Zarins, Naveen Vasudev, Morag Seywright, Behnoush Abedi‐Ardekani, Christine Carreira, Peter J. Selby, Jon Cartledge, Graham Byrnes, Jiří Zavadil, Jing Su, Ivana Holcátová, A. Brisuda, Давид Заридзе, Anush Moukeria, Lenka Foretová, Marie Navrátilová, Dana Mateș, Viorel Jinga, Artem V. Artemov, Artem Nedoluzhko, Alexander M. Mazur, Sergey Rastorguev, Eugenia Boulygina, Simon Heath, Marta Gut, Marie‐Thérèse Bihoreau, Doris Lechner, Mario Foglio, Marta Gut, K. G. Skryabin, Egor Prokhortchouk, Anne Cambon‐Thomsen, Johan Rung, Guillaume Bourque, Paul Brennan, Jörg Tost, Rosamonde E. Banks, Alvis Brāzma, G.M. Lathrop

    Publicat 2014
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  12. 12
    A first update on mapping the human genetic architecture of COVID-19

    A first update on mapping the human genetic architecture of COVID-19 per Gita A. Pathak, Juha Karjalainen, Christine Stevens, Benjamin M. Neale, Mark J. Daly, Andrea Ganna, Shea J. Andrews, Masahiro Kanai, Mattia Cordioli, Renato Polimanti, Nadia V. Harerimana, Matti Pirinen, Rachel G. Liao, Karolina Chwiałkowska, Amy Trankiem, Mary K. Balaconis, Huy Nguyen, Matthew Solomonson, Kumar Veerapen, Brooke N. Wolford, Genevieve Roberts, Daniel J. Park, Catherine A. Ball, Marie V. Coignet, Shannon McCurdy, Spencer C. Knight, Raghavendran Partha, Brooke Rhead, Miao Zhang, Nathan Berkowitz, Michael Gaddis, Keith Noto, Luong Ruiz, Miloš Pavlović, Eurie L. Hong, Kristin A. Rand, Ahna R. Girshick, Harendra Guturu, Asher Haug Baltzell, Mari Niemi, Souad Rahmouni, Julien Guntz, Y Beguin, Mattia Cordioli, Sara Pigazzini, Lindokuhle Nkambule, Michel Georges, Michel Moutschen, Benoît Misset, Gilles Darcis, Julien Guiot, Samira Azarzar, Stéphanie Gofflot, Sabine Claassen, Olivier Malaise, Pascale Huynen, Christelle Meuris, Marie Thys, Jessica Jacques, Philippe Léonard, Frédéric Frippiat, Jean‐Baptiste Giot, Anne-Sophie Sauvage, Christian Von Frenckell, Yasmine Belhaj, Bernard Lambermont, Tomoko Nakanishi, David Morrison, Vincent Mooser, J. Brent Richards, Guillaume Butler‐Laporte, Vincenzo Forgetta, Rui Li, Biswarup Ghosh, Lætitia Laurent, Alexandre Bélisle, Danielle Henry, Tala Abdullah, Olumide Adeleye, Noor Mamlouk, Nofar Kimchi, Zaman Afrasiabi, Nardin Rezk, Branka Vulesevic, Meriem Bouab, Charlotte Guzman, Louis Petitjean, Chris Tselios, Xiaoqing Xue, Jonathan Afilalo, Marc Afilalo, Maureen Oliveira, Bluma Brenner, Nathalie Brassard, Madéleine Durand, Erwin Schurr, Pierre Lepage, Jiannis Ragoussis, Daniel Auld, Michaël Chassé

    Publicat 2022
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