Rezultaty - Meyn, M. Stephen

Visualization and quantitative analysis of extrachromosomal telomere-repeat DNA in individual human cells by Halo-FISH od Komosa, Martin, Root, Heather, Meyn, M. Stephen

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Effects of arsenite on DNA repair in Escherichia coli od Rossman, Toby G., Meyn, M. Stephen, Troll, Walter

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Overexpression of a truncated human topoisomerase III partially corrects multiple aspects of the ataxia-telangiectasia phenotype od Fritz, Eberhard, Elsea, Sarah H., Patel, Pragna I., Meyn, M. Stephen

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The Yeast TEL1 Gene Partially Substitutes for Human ATM in Suppressing Hyperrecombination, Radiation-Induced Apoptosis and Telomere Shortening in A-T Cells od Fritz, Eberhard, Friedl, Anna A., Zwacka, Ralf M., Eckardt-Schupp, Friederike, Meyn, M. Stephen

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DNA damage-induced phosphorylation of the human telomere-associated protein TRF2 od Tanaka, Hiromi, Mendonca, Marc S., Bradshaw, Paul S., Hoelz, Derek J., Malkas, Linda H., Meyn, M. Stephen, Gilley, David

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Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice od Houghtaling, Scott, Timmers, Cynthia, Noll, Meenakshi, Finegold, Milton J., Jones, Stephen N., Meyn, M. Stephen, Grompe, Markus

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Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation od Demuth, Ilja, Bradshaw, Paul S., Lindner, Anika, Anders, Marco, Heinrich, Stefanie, Kallenbach, Julia, Schmelz, Karin, Digweed, Martin, Meyn, M. Stephen, Concannon, Patrick

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The cycle of genome-directed medicine od Buchanan, Janet A, Carson, Andrew R, Chitayat, David, Malkin, David, Meyn, M Stephen, Ray, Peter N, Shuman, Cheryl, Weksberg, Rosanna, Scherer, Stephen W

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Impaired telomere maintenance in Alazami syndrome patients with LARP7 deficiency od Holohan, Brody, Kim, Wanil, Lai, Tsung-Po, Hoshiyama, Hirotoshi, Zhang, Ning, Alazami, Anas M., Wright, Woodring E., Meyn, M. Stephen, Alkuraya, Fowzan S., Shay, Jerry W.

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Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study od Cohn, Iris, Paton, Tara A., Marshall, Christian R., Basran, Raveen, Stavropoulos, Dimitri J., Ray, Peter N., Monfared, Nasim, Hayeems, Robin Z., Meyn, M. Stephen, Bowdin, Sarah, Scherer, Stephen W., Cohn, Ronald D., Ito, Shinya

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Attenuated DNA damage responses and increased apoptosis characterize human hematopoietic stem cells exposed to irradiation od Biechonski, Shahar, Olender, Leonid, Zipin-Roitman, Adi, Yassin, Muhammad, Aqaqe, Nasma, Marcu-Malina, Victoria, Rall-Scharpf, Melanie, Trottier, Magan, Meyn, M. Stephen, Wiesmüller, Lisa, Beider, Katia, Raz, Yael, Grisaru, Dan, Nagler, Arnon, Milyavsky, Michael

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Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray od Hayeems, Robin Z., Bhawra, Jasmin, Tsiplova, Kate, Meyn, M. Stephen, Monfared, Nasim, Bowdin, Sarah, Stavropoulos, D. James, Marshall, Christian R., Basran, Raveen, Shuman, Cheryl, Ito, Shinya, Cohn, Iris, Hum, Courtney, Girdea, Marta, Brudno, Michael, Cohn, Ronald D., Scherer, Stephen W., Ungar, Wendy J.

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Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing od Costain, Gregory, Jobling, Rebekah, Walker, Susan, Reuter, Miriam S., Snell, Meaghan, Bowdin, Sarah, Cohn, Ronald D., Dupuis, Lucie, Hewson, Stacy, Mercimek-Andrews, Saadet, Shuman, Cheryl, Sondheimer, Neal, Weksberg, Rosanna, Yoon, Grace, Meyn, M. Stephen, Stavropoulos, Dimitri J., Scherer, Stephen W., Mendoza-Londono, Roberto, Marshall, Christian R.

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Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity od Costain, Gregory, Walker, Susan, Marano, Maria, Veenma, Danielle, Snell, Meaghan, Curtis, Meredith, Luca, Stephanie, Buera, Jason, Arje, Danielle, Reuter, Miriam S., Thiruvahindrapuram, Bhooma, Trost, Brett, Sung, Wilson W. L., Yuen, Ryan K. C., Chitayat, David, Mendoza-Londono, Roberto, Stavropoulos, D. James, Scherer, Stephen W., Marshall, Christian R., Cohn, Ronald D., Cohen, Eyal, Orkin, Julia, Meyn, M. Stephen, Hayeems, Robin Z.

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The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists od Boycott, Kym, Hartley, Taila, Adam, Shelin, Bernier, Francois, Chong, Karen, Fernandez, Bridget A, Friedman, Jan M, Geraghty, Michael T, Hume, Stacey, Knoppers, Bartha M, Laberge, Anne-Marie, Majewski, Jacek, Mendoza-Londono, Roberto, Meyn, M Stephen, Michaud, Jacques L, Nelson, Tanya N, Richer, Julie, Sadikovic, Bekim, Skidmore, David L, Stockley, Tracy, Taylor, Sherry, van Karnebeek, Clara, Zawati, Ma'n H, Lauzon, Julie, Armour, Christine M

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CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases od Kasak, Laura, Hunter, Jesse M., Udani, Rupa, Bakolitsa, Constantina, Hu, Zhiqiang, Adhikari, Aashish N., Babbi, Giulia, Casadio, Rita, Gough, Julian, Guerrero, Rafael F., Jiang, Yuxiang, Joseph, Thomas, Katsonis, Panagiotis, Kotte, Sujatha, Kundu, Kunal, Lichtarge, Olivier, Martelli, Pier Luigi, Mooney, Sean D., Moult, John, Pal, Lipika R., Poitras, Jennifer, Radivojac, Predrag, Rao, Aditya, Sivadasan, Naveen, Sunderam, Uma, VG, Saipradeep, Yin, Yizhou, Zaucha, Jan, Brenner, Steven E., Meyn, M. Stephen

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Recommendations for the Integration of Genomics into Clinical Practice od Bowdin, Sarah, Gilbert, Adel, Bedoukian, Emma, Carew, Christopher, Adam, Margaret P, Belmont, John, Bernhardt, Barbara, Biesecker, Leslie, Bjornsson, Hans T., Blitzer, Miriam, D’Alessandro, Lisa C. A., Deardorff, Matthew A., Demmer, Laurie, Elliott, Alison, Feldman, Gerald L., Glass, Ian A., Herman, Gail, Hindorff, Lucia, Hisama, Fuki, Hudgins, Louanne, Innes, A. Micheil, Jackson, Laird, Jarvik, Gail, Kim, Raymond, Korf, Bruce, Ledbetter, David H., Li, Mindy, Liston, Eriskay, Marshall, Christian, Medne, Livija, Meyn, M. Stephen, Monfared, Nasim, Morton, Cynthia, Mulvihill, John J., Plon, Sharon E., Rehm, Heidi, Roberts, Amy, Shuman, Cheryl, Spinner, Nancy B., Stavropoulos, D. James, Valverde, Kathleen, Waggoner, Darrel J., Wilkens, Alisha, Cohn, Ronald D., Krantz, Ian D.

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The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants od Reuter, Miriam S., Walker, Susan, Thiruvahindrapuram, Bhooma, Whitney, Joe, Cohn, Iris, Sondheimer, Neal, Yuen, Ryan K.C., Trost, Brett, Paton, Tara A., Pereira, Sergio L., Herbrick, Jo-Anne, Wintle, Richard F., Merico, Daniele, Howe, Jennifer, MacDonald, Jeffrey R., Lu, Chao, Nalpathamkalam, Thomas, Sung, Wilson W.L., Wang, Zhuozhi, Patel, Rohan V., Pellecchia, Giovanna, Wei, John, Strug, Lisa J., Bell, Sherilyn, Kellam, Barbara, Mahtani, Melanie M., Bassett, Anne S., Bombard, Yvonne, Weksberg, Rosanna, Shuman, Cheryl, Cohn, Ronald D., Stavropoulos, Dimitri J., Bowdin, Sarah, Hildebrandt, Matthew R., Wei, Wei, Romm, Asli, Pasceri, Peter, Ellis, James, Ray, Peter, Meyn, M. Stephen, Monfared, Nasim, Hosseini, S. Mohsen, Joseph-George, Ann M., Keeley, Fred W., Cook, Ryan A., Fiume, Marc, Lee, Hin C., Marshall, Christian R., Davies, Jill, Hazell, Allison, Buchanan, Janet A., Szego, Michael J., Scherer, Stephen W.

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Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test od Lionel, Anath C, Costain, Gregory, Monfared, Nasim, Walker, Susan, Reuter, Miriam S, Hosseini, S Mohsen, Thiruvahindrapuram, Bhooma, Merico, Daniele, Jobling, Rebekah, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Sung, Wilson W L, Wang, Zhuozhi, Bikangaga, Peter, Boelman, Cyrus, Carter, Melissa T, Cordeiro, Dawn, Cytrynbaum, Cheryl, Dell, Sharon D, Dhir, Priya, Dowling, James J, Heon, Elise, Hewson, Stacy, Hiraki, Linda, Inbar-Feigenberg, Michal, Klatt, Regan, Kronick, Jonathan, Laxer, Ronald M, Licht, Christoph, MacDonald, Heather, Mercimek-Andrews, Saadet, Mendoza-Londono, Roberto, Piscione, Tino, Schneider, Rayfel, Schulze, Andreas, Silverman, Earl, Siriwardena, Komudi, Snead, O Carter, Sondheimer, Neal, Sutherland, Joanne, Vincent, Ajoy, Wasserman, Jonathan D, Weksberg, Rosanna, Shuman, Cheryl, Carew, Chris, Szego, Michael J, Hayeems, Robin Z, Basran, Raveen, Stavropoulos, Dimitri J, Ray, Peter N, Bowdin, Sarah, Meyn, M Stephen, Cohn, Ronald D, Scherer, Stephen W, Marshall, Christian R

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Performance of the McGill Interactive Pediatric OncoGenetic Guidelines for Identifying Cancer Predisposition Syndromes od Goudie, Catherine, Witkowski, Leora, Cullinan, Noelle, Reichman, Lara, Schiller, Ian, Tachdjian, Melissa, Armstrong, Linlea, Blood, Katherine A., Brossard, Josée, Brunga, Ledia, Cacciotti, Chantel, Caswell, Kimberly, Cellot, Sonia, Clark, Mary Egan, Clinton, Catherine, Coltin, Hallie, Felton, Kathleen, Fernandez, Conrad V., Fleming, Adam J., Fuentes-Bolanos, Noemi, Gibson, Paul, Grant, Ronald, Hammad, Rawan, Harrison, Lynn W., Irwin, Meredith S., Johnston, Donna L., Kane, Sarah, Lafay-Cousin, Lucie, Lara-Corrales, Irene, Larouche, Valerie, Mathews, Natalie, Meyn, M. Stephen, Michaeli, Orli, Perrier, Renée, Pike, Meghan, Punnett, Angela, Ramaswamy, Vijay, Say, Jemma, Somers, Gino, Tabori, Uri, Thibodeau, My Linh, Toupin, Annie-Kim, Tucker, Katherine M., van Engelen, Kalene, Vairy, Stephanie, Waespe, Nicolas, Warby, Meera, Wasserman, Jonathan D., Whitlock, James A., Sinnett, Daniel, Jabado, Nada, Nathan, Paul C., Shlien, Adam, Kamihara, Junne, Deyell, Rebecca J., Ziegler, David S., Nichols, Kim E., Dendukuri, Nandini, Malkin, David, Villani, Anita, Foulkes, William D.

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