Zobrazeno 1 - 10
of 1 954
pro vyhledávání: '"Taylor Robert W"'
Autor:
Hilander, Taru, Awadhpersad, Ryan, Monteuuis, Geoffray, Broda, Krystyna L., Pohjanpelto, Max, Pyman, Elizabeth, Singh, Sachin Kumar, Nyman, Tuula A., Crevel, Isabelle, Taylor, Robert W., Saada, Ann, Balboa, Diego, Battersby, Brendan J., Jackson, Christopher B., Carroll, Christopher J.
Publikováno v:
In iScience 19 July 2024 27(7)
Autor:
Reda, Sherif M., Setti, Sharay E., Berthiaume, Andrée-Anne, Wu, Wei, Taylor, Robert W., Johnston, Jewel L., Stein, Liana R., Moebius, Hans J., Church, Kevin J.
Publikováno v:
In Neurotherapeutics July 2024 21(4)
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 14, Iss Suppl 1, p W12 (2012)
Externí odkaz:
https://doaj.org/article/d59fb1f0017940eeab4f1b2de4aeade9
Autor:
Brunet, Theresa, Zott, Benedikt, Lieftüchter, Victoria, Lenz, Dominic, Schmidt, Axel, Peters, Philipp, Kopajtich, Robert, Zaddach, Malin, Zimmermann, Hanna, Hüning, Irina, Ballhausen, Diana, Staufner, Christian, Bianzano, Alyssa, Hughes, Joanne, Taylor, Robert W., McFarland, Robert, Devlin, Anita, Mihaljević, Mihaela, Barišić, Nina, Rohlfs, Meino, Wilfling, Sibylle, Sondheimer, Neal, Hewson, Stacy, Marinakis, Nikolaos M., Kosma, Konstantina, Traeger-Synodinos, Joanne, Elbracht, Miriam, Begemann, Matthias, Trepels-Kottek, Sonja, Hasan, Dimah, Scala, Marcello, Capra, Valeria, Zara, Federico, van der Ven, Amelie T., Driemeyer, Joenna, Apitz, Christian, Krämer, Johannes, Strong, Alanna, Hakonarson, Hakon, Watson, Deborah, Mayr, Johannes A., Prokisch, Holger, Meitinger, Thomas, Borggraefe, Ingo, Spiegler, Juliane, Baric, Ivo, Paolini, Marco, Gerstl, Lucia, Wagner, Matias
Publikováno v:
In Genetics in Medicine February 2024 26(2)
Autor:
Chen, Wenqian, Rehsi, Preeya, Thompson, Kyle, Yeo, Mildrid, Stals, Karen, He, Langping, Schimmel, Paul, Chrzanowska-Lightowlers, Zofia M.A., Wakeling, Emma, Taylor, Robert W., Kuhle, Bernhard
Publikováno v:
In Molecular Genetics and Metabolism November 2023 140(3)
Autor:
Accogli, Andrea, Lin, Sheng-Jia, Severino, Mariasavina, Kim, Sung-Hoon, Huang, Kevin, Rocca, Clarissa, Landsverk, Megan, Zaki, Maha S., Al-Maawali, Almundher, Srinivasan, Varunvenkat M., Al-Thihli, Khalid, Schaefer, G. Bradly, Davis, Monica, Tonduti, Davide, Doneda, Chiara, Marten, Lara M., Mühlhausen, Chris, Gomez, Maria, Lamantea, Eleonora, Mena, Rafael, Nizon, Mathilde, Procaccio, Vincent, Begtrup, Amber, Telegrafi, Aida, Cui, Hong, Schulz, Heidi L., Mohr, Julia, Biskup, Saskia, Loos, Mariana Amina, Aráoz, Hilda Verónica, Salpietro, Vincenzo, Keppen, Laura Davis, Chitre, Manali, Petree, Cassidy, Raymond, Lucy, Vogt, Julie, Sawyer, Lindsey B., Basinger, Alice A., Pedersen, Signe Vandal, Pearson, Toni S., Grange, Dorothy K., Lingappa, Lokesh, McDunnah, Paige, Horvath, Rita, Cognè, Benjamin, Isidor, Bertrand, Hahn, Andreas, Gripp, Karen W., Jafarnejad, Seyed Mehdi, Østergaard, Elsebet, Prada, Carlos E., Ghezzi, Daniele, Gowda, Vykuntaraju K., Taylor, Robert W., Sonenberg, Nahum, Houlden, Henry, Sissler, Marie, Varshney, Gaurav K., Maroofian, Reza
Publikováno v:
In Genetics in Medicine November 2023 25(11)
Autor:
Blakely Emma L, Taylor Robert W, Price Gareth R, Zamzami Mazin A, Oancea Iulia, Bowling Francis, Duley John A
Publikováno v:
BMC Research Notes, Vol 4, Iss 1, p 426 (2011)
Abstract Background Developments in DNA resequencing microarrays include mitochondrial DNA (mtDNA) sequencing and mutation detection. Failure by the microarray to identify a base, compared to the reference sequence, is designated an 'N-call.' This st
Externí odkaz:
https://doaj.org/article/09cedaecce18407f84b208e1f916ae6c
Publikováno v:
Journal of Medical Case Reports, Vol 3, Iss 1, p 77 (2009)
Abstract Introduction There are currently 23 missense point mutations and one 4 basepair deletion spanning different mitochondrial genes associated with mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS). The spectrum of m
Externí odkaz:
https://doaj.org/article/d20c42097da44e37b44344e5efc1d2f4
Autor:
Vogel, Georg F., Mozer-Glassberg, Yael, Landau, Yuval E., Schlieben, Lea D., Prokisch, Holger, Feichtinger, René G., Mayr, Johannes A., Brennenstuhl, Heiko, Schröter, Julian, Pechlaner, Agnes, Alkuraya, Fowzan S., Baker, Joshua J., Barcia, Giulia, Baric, Ivo, Braverman, Nancy, Burnyte, Birute, Christodoulou, John, Ciara, Elzbieta, Coman, David, Das, Anibh M., Darin, Niklas, Della Marina, Adela, Distelmaier, Felix, Eklund, Erik A., Ersoy, Melike, Fang, Weiyan, Gaignard, Pauline, Ganetzky, Rebecca D., Gonzales, Emmanuel, Howard, Caoimhe, Hughes, Joanne, Konstantopoulou, Vassiliki, Kose, Melis, Kerr, Marina, Khan, Aneal, Lenz, Dominic, McFarland, Robert, Margolis, Merav Gil, Morrison, Kevin, Müller, Thomas, Murayama, Kei, Nicastro, Emanuele, Pennisi, Alessandra, Peters, Heidi, Piekutowska-Abramczuk, Dorota, Rötig, Agnès, Santer, René, Scaglia, Fernando, Schiff, Manuel, Shagrani, Mohmmad, Sharrard, Mark, Soler-Alfonso, Claudia, Staufner, Christian, Storey, Imogen, Stormon, Michael, Taylor, Robert W., Thorburn, David R., Teles, Elisa Leao, Wang, Jian-She, Weghuber, Daniel, Wortmann, Saskia
Publikováno v:
In Genetics in Medicine June 2023 25(6)
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