未登录 Strategies to improve access to physical activity opportunities for people with physical disabilities Herbison, Jordan D.; Osborne, Meaghan; Andersen, Jessica; Lepage, Pierre; Page, Veronique; Levasseur, Caroline; Beckers, Melissa; Gainforth, Heather L.; Lamontagne, Marie-Eve; Sweet, Shane N. 分享 收藏
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19 Povysil, Gundula; Butler-Laporte, Guillaume; Shang, Ning; Wang, Chen; Khan, Atlas; Alaamery, Manal; Nakanishi, Tomoko; Zhou, Sirui; Forgetta, Vincenzo; Eveleigh, Robert J. M.; Bourgey, Mathieu; Aziz, Naveed; Jones, Steven J. M.; Knoppers, Bartha; Scherer, Stephen W.; Strug, Lisa J.; Lepage, Pierre; Ragoussis, Jiannis; Bourque, Guillaume; Alghamdi, Jahad; Aljawini, Nora; Albes, Nour; Al-Afghani, Hani M.; Alghamdi, Bader; Almutairi, Mansour S.; Mahmoud, Ebrahim Sabri; Abu-Safieh, Leen; El Bardisy, Hadeel; Harthi, Fawz S. Al; Alshareef, Abdulraheem; Suliman, Bandar Ali; Alqahtani, Saleh A.; Almalik, Abdulaziz; Alrashed, May M.; Massadeh, Salam; Mooser, Vincent; Lathrop, Mark; Fawzy, Mohamed; Arabi, Yaseen M.; Mbarek, Hamdi; Saad, Chadi; Al-Muftah, Wadha; Jung, Junghyun; Mangul, Serghei; Badji, Radja; Al Thani, Asma; Ismail, Said I.; Gharavi, Ali G.; Abedalthagafi, Malak S.; Richards, J. Brent; Goldstein, David B.; Kiryluk, Krzysztof 分享 收藏
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Variation in genomic landscape of clear cell renal cell carcinoma across Europe Scelo, Ghislaine; Riazalhosseini, Yasser; Greger, Liliana; Letourneau, Louis; Gonzalez-Porta, Mar; Wozniak, Magdalena B.; Bourgey, Mathieu; Harnden, Patricia; Egevad, Lars; Jackson, Sharon M.; Karimzadeh, Mehran; Arseneault, Madeleine; Lepage, Pierre; How-Kit, Alexandre; Daunay, Antoine; Renault, Victor; Blanche, Helene; Tubacher, Emmanuel; Sehmoun, Jeremy; Viksna, Juris; Celms, Edgars; Opmanis, Martins; Zarins, Andris; Vasudev, Naveen S.; Seywright, Morag; Abedi-Ardekani, Behnoush; Carreira, Christine; Selby, Peter J.; Cartledge, Jon J.; Byrnes, Graham; Zavadil, Jiri; Su, Jing; Holcatova, Ivana; Brisuda, Antonin; Zaridze, David; Moukeria, Anush; Foretova, Lenka; Navratilova, Marie; Mates, Dana; Jinga, Viorel; Artemov, Artem; Nedoluzhko, Artem; Mazur, Alexander; Rastorguev, Sergey; Boulygina, Eugenia; Heath, Simon; Gut, Marta; Bihoreau, Marie-Therese; Lechner, Doris; Foglio, Mario; Gut, Ivo G.; Skryabin, Konstantin; Prokhortchouk, Egor; Cambon-Thomsen, Anne; Rung, Johan; Bourque, Guillaume; Brennan, Paul; Tost, Joerg; Banks, Rosamonde E.; Brazma, Alvis; Lathrop, G. Mark 分享 收藏
Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations 垂体母细胞瘤: 种系DICER1突变的病理特征 de Kock, Leanne; Sabbaghian, Nelly; Plourde, Francois; Srivastava, Archana; Weber, Evan; Bouron-Dal Soglio, Dorothee; Hamel, Nancy; Choi, Joon Hyuk; Park, Sung-Hye; Deal, Cheri L.; Kelsey, Megan M.; Dishop, Megan K.; Esbenshade, Adam; Kuttesch, John F.; Jacques, Thomas S.; Perry, Arie; Leichter, Heinz; Maeder, Philippe; Brundler, Marie-Anne; Warner, Justin; Neal, James; Zacharin, Margaret; Korbonits, Marta; Cole, Trevor; Traunecker, Heidi; McLean, Thomas W.; Rotondo, Fabio; Lepage, Pierre; Albrecht, Steffen; Horvath, Eva; Kovacs, Kalman; Priest, John R.; Foulkes, William D. 分享 收藏
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas Fontebasso, Adam M.; Schwartzentruber, Jeremy; Dong-Anh Khuong-Quang; Liu, Xiao-Yang; Sturm, Dominik; Korshunov, Andrey; Jones, David T. W.; Witt, Hendrik; Kool, Marcel; Albrecht, Steffen; Fleming, Adam; Hadjadj, Djihad; Busche, Stephan; Lepage, Pierre; Montpetit, Alexandre; Staffa, Alfredo; Gerges, Noha; Zakrzewska, Magdalena; Zakrzewski, Krzystof; Liberski, Pawel P.; Hauser, Peter; Garami, Miklos; Klekner, Almos; Bognar, Laszlo; Zadeh, Gelareh; Faury, Damien; Pfister, Stefan M.; Jabado, Nada; Majewski, Jacek 分享 收藏
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Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene Dyment, David A.; Cader, M. Zameel; Chao, Michael J.; Lincoln, Matthew R.; Morrison, Katie M.; Disanto, Giulio; Morahan, Julia M.; De Luca, Gabriele C.; Sadovnick, A. Dessa; Lepage, Pierre; Montpetit, Alexandre; Ebers, George C.; Ramagopalan, Sreeram V. 分享 收藏
K27M mutation in histone H3.3 defines clinically and biologically distinct subgroups of pediatric diffuse intrinsic pontine gliomas Dong-Anh Khuong-Quang; Buczkowicz, Pawel; Rakopoulos, Patricia; Liu, Xiao-Yang; Fontebasso, Adam M.; Bouffet, Eric; Bartels, Ute; Albrecht, Steffen; Schwartzentruber, Jeremy; Letourneau, Louis; Bourgey, Mathieu; Bourque, Guillaume; Montpetit, Alexandre; Bourret, Genevieve; Lepage, Pierre; Fleming, Adam; Lichter, Peter; Kool, Marcel; von Deimling, Andreas; Sturm, Dominik; Korshunov, Andrey; Faury, Damien; Jones, David T.; Majewski, Jacek; Pfister, Stefan M.; Jabado, Nada; Hawkins, Cynthia 分享 收藏
Periodic 48 h feed withdrawal improves glucose tolerance in growing pigs by enhancing adipogenesis and lipogenesis Mir, Priya S.; He, Mao L.; Travis, Gregory; Entz, Toby; McAllister, Tim; Marchand, Sigrid; Schaefer, Al; Meadus, Jon; Lepage, Pierre; Okine, Erasmus; Dodson, Michael V. 分享 收藏
Rare variants in the CYP27B1 gene are associated with multiple sclerosis Ramagopalan, Sreeram V.; Dyment, David A.; Cader, M. Zameel; Morrison, Katie M.; Disanto, Giulio; Morahan, Julia M.; Berlanga-Taylor, Antonio J.; Handel, Adam; De Luca, Gabriele C.; Sadovnick, A. Dessa; Lepage, Pierre; Montpetit, Alexandre; Ebers, George C. 分享 收藏
Spartacus attending the 2005 AAAI conference Michaud, F.; Cote, C.; Letourneau, D.; Brosseau, Y.; Valin, J. -M.; Beaudry, E.; Raievsky, C.; Ponchon, A.; Moisan, P.; Lepage, P.; Morin, Y.; Gagnon, F.; Giguere, P.; Roux, M. -A.; Caron, S.; Frenette, P.; Kabanza, F. 分享 收藏
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Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome) Hrebicek, Martin; Mrazova, Lenka; Seyrantepe, Volkan; Durand, Stephaine; Roslin, Nicole M.; Noskova, Lenka; Hartmannova, Hana; Ivanek, Robert; Cizkova, Alena; Poupetova, Helena; Sikora, Jakub; Urinovska, Jana; Stranecky, Viktor; Zeman, Jiri; Lepage, Pierre; Roquis, David; Verner, Andrei; Ausseil, Jerome; Beesley, Clare E.; Maire, Irene; Poorthuis, Ben J. H. M.; van de Kamp, Jiddeke; van Diggelen, Otto P.; Wevers, Ron A.; Hudson, Thomas J.; Fujiwara, T. Mary; Majewski, Jacek; Morgan, Kenneth; Kmoch, Stanislav; Pshezhetsky, Alexey V. 分享 收藏
Common polymorphisms in the promoter of the visfatin gene (PBEF1) influence plasma insulin levels in a French-Canadian population Bailey, Swneke D.; Loredo-Osti, J. C.; Lepage, Pierre; Faith, Janet; Fontaine, Joelle; Desbiens, Katia M.; Hudson, Thomas J.; Bouchard, Claude; Gaudet, Daniel; Perusse, Louis; Vohl, Marie-Claude; Engert, James C. 分享 收藏
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type (vol 38, pg 93, 2006) Lerner-Ellis, Jordan P.; Tirone, Jamie C.; Pawelek, Peter D.; Dore, Carole; Atkinson, Janet L.; Watkins, David; Morel, Chantal F.; Fujiwara, T. Mary; Moras, Emily; Hosack, Angela R.; Dunbar, Gail V.; Antonicka, Hana; Forgetta, Vince; Dobson, C. Melissa; Leclerc, Daniel; Gravel, Roy A.; Shoubridge, Eric A.; Coulton, James W.; Lepage, Pierre; Rommens, Johanna M.; Morgan, Kenneth; Rosenblatt, David S. 分享 收藏
Mutation and biochemical analysis of patients belonging to the cb1B complementation class of vitamin B12-dependent methylmalonic aciduria Lerner-Ellis, JP; Gradinger, AB; Watkins, D; Tirone, JC; Villeneuve, A; Dobson, CM; Montpetit, A; Lepage, P; Gravel, RA; Rosenblatt, DS 分享 收藏
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type Lerner-Ellis, JP; Tirone, JC; Pawelek, PD; Doré, C; Atkinson, JL; Watkins, D; Morel, CF; Fujiwara, TM; Moras, E; Hosack, AR; Dunbar, GV; Antonicka, H; Forgetta, V; Dobson, CM; Leclerc, D; Gravel, RA; Shoubridge, EA; Coulton, JW; Lepage, P; Rommens, JM; Morgan, K; Rosenblatt, DS 分享 收藏
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