Time-lapse analysis of potential cellular responsiveness to Johrei, a Japanese healing technique

by Taft, Ryan, Moore, Dan, Yount, Garret
Published 2005

MicroRNAs in β-Cell Biology, Insulin Resistance, Diabetes and Its Complications

by Fernandez-Valverde, Selene L., Taft, Ryan J., Mattick, John S.
Published 2011

The relationship between transcription initiation RNAs and CCCTC-binding factor (CTCF) localization

by Taft, Ryan J, Hawkins, Peter G, Mattick, John S, Morris, Kevin V
Published 2011

Systematic interrogation of the Conus marmoreus venom duct transcriptome with ConoSorter reveals 158 novel conotoxins and 13 new gene superfamilies

by Lavergne, Vincent, Dutertre, Sébastien, Jin, Ai-hua, Lewis, Richard J, Taft, Ryan J, Alewood, Paul F
Published 2013

Information compression exploits patterns of genome composition to discriminate populations and highlight regions of evolutionary interest

by Hudson, Nicholas J, Porto-Neto, Laercio R, Kijas, James, McWilliam, Sean, Taft, Ryan J, Reverter, Antonio
Published 2014

Expression of Transposable Elements in Neural Tissues during Xenopus Development

by Faunes, Fernando, Sanchez, Natalia, Moreno, Mauricio, Olivares, Gonzalo H., Lee-Liu, Dasfne, Almonacid, Leonardo, Slater, Alex W., Norambuena, Tomas, Taft, Ryan J., Mattick, John S., Melo, Francisco, Larrain, Juan
Published 2011

Identification of nuclear-enriched miRNAs during mouse granulopoiesis

by Wong, Justin JL, Ritchie, William, Gao, Dadi, Lau, Katherine A, Gonzalez, Maria, Choudhary, Anupma, Taft, Ryan J, Rasko, John EJ, Holst, Jeff
Published 2014

Whole exome sequencing in family trios reveals de novo mutations in PURA as a cause of severe neurodevelopmental delay and learning disability

by Hunt, David, Leventer, Richard J, Simons, Cas, Taft, Ryan, Swoboda, Kathryn J, Gawne-Cain, Mary, Magee, Alex C, Turnpenny, Peter D, Baralle, Diana
Published 2014

Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient

by Miller, David K., Menezes, Minal J., Simons, Cas, Riley, Lisa G., Cooper, Sandra T., Grimmond, Sean M., Thorburn, David R., Christodoulou, John, Taft, Ryan J.
Published 2014

The Reality of Pervasive Transcription

by Clark, Michael B., Amaral, Paulo P., Schlesinger, Felix J., Dinger, Marcel E., Taft, Ryan J., Rinn, John L., Ponting, Chris P., Stadler, Peter F., Morris, Kevin V., Morillon, Antonin, Rozowsky, Joel S., Gerstein, Mark B., Wahlestedt, Claes, Hayashizaki, Yoshihide, Carninci, Piero, Gingeras, Thomas R., Mattick, John S.
Published 2011

A protocol for the identification and validation of novel genetic causes of kidney disease

by Mallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, I. Alexander, Stephen, Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, McCarthy, Hugh J., Hyland, Valentine, E. Hoy, Wendy, Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy, Helen, Little, Melissa
Published 2015

Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

by Thiffault, Isabelle, Wolf, Nicole I., Forget, Diane, Guerrero, Kether, Tran, Luan T., Choquet, Karine, Lavallée-Adam, Mathieu, Poitras, Christian, Brais, Bernard, Yoon, Grace, Sztriha, Laszlo, Webster, Richard I., Timmann, Dagmar, van de Warrenburg, Bart P., Seeger, Jürgen, Zimmermann, Alíz, Máté, Adrienn, Goizet, Cyril, Fung, Eva, van der Knaap, Marjo S., Fribourg, Sébastien, Vanderver, Adeline, Simons, Cas, Taft, Ryan J., Yates III, John R., Coulombe, Benoit, Bernard, Geneviève
Published 2015