Cytoplasmic carboxypeptidase 5 regulates tubulin glutamylation and zebrafish cilia formation and function

Por Pathak, Narendra, Austin-Tse, Christina A., Liu, Yan, Vasilyev, Aleksandr, Drummond, Iain A.
Publicado em 2014

Assaying sensory ciliopathies using calcium biosensor expression in zebrafish ciliated olfactory neurons

Por Bergboer, Judith G. M., Wyatt, Cameron, Austin-Tse, Christina, Yaksi, Emre, Drummond, Iain A.
Publicado no Cilia (2018)

Evaluation of a point of care ultrasound curriculum for Indonesian physicians taught by first-year medical students

Por Lee, Jonathan B., Tse, Christina, Keown, Thomas, Louthan, Michael, Gabriel, Christopher, Anshus, Alexander, Hasjim, Bima, Lee, Katrina, Kim, Esther, Yu, Luke, Yu, Allen, Lahham, Shadi, Bunch, Steven, Alvarado, Maili, Gari, Abdulatif, Fox, John C.
Publicado no World J Emerg Med (2017)

Comparison of ultrasound-measured properties of the common carotid artery to tobacco smoke exposure in a cohort of Indonesian patients

Por Yu, Allen R., Hasjim, Bima, Yu, Luke E., Gabriel, Christopher, Anshus, Alexander, Lee, Jonathan B., Louthan, Michael J., Kim, Esther C., Lee, Katrina, Tse, Christina, Keown, Thomas, Lahham, Shadi, Alvarado, Maili, Bunch, Steven, Gari, Abdulatif, Fox, J. Christian
Publicado no World J Emerg Med (2017)

Mutation mapping and identification by whole-genome sequencing

Por Leshchiner, Ignaty, Alexa, Kristen, Kelsey, Peter, Adzhubei, Ivan, Austin-Tse, Christina A., Cooney, Jeffrey D., Anderson, Heidi, King, Matthew J., Stottmann, Rolf W., Garnaas, Maija K., Ha, Seungshin, Drummond, Iain A., Paw, Barry H., North, Trista E., Beier, David R., Goessling, Wolfram, Sunyaev, Shamil R.
Publicado em 2012

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms

Por Panizzi, Jennifer R., Becker-Heck, Anita, Castleman, Victoria H., Al-Mutairi, Dalal, Liu, Yan, Loges, Niki T., Pathak, Narendra, Austin-Tse, Christina, Sheridan, Eamonn, Schmidts, Miriam, Olbrich, Heike, Werner, Claudius, Häffner, Karsten, Hellman, Nathan, Chodhari, Rahul, Gupta, Amar, Kramer-Zucker, Albrecht, Olale, Felix, Burdine, Rebecca D., Schier, Alexander F., O’Callaghan, Christopher, Chung, Eddie MK, Reinhardt, Richard, Mitchison, Hannah M., King, Stephen M., Omran, Heymut, Drummond, Iain A.
Publicado em 2012

Electronic Health Record Phenotype in Subjects with Genetic Variants Associated with Arrhythmogenic Right Ventricular Cardiomyopathy: A Study in 30,716 Subjects with Exome Sequenci...

Por Haggerty, Christopher M., James, Cynthia A., Calkins, Hugh, Tichnell, Crystal, Leader, Joseph B., Hartzel, Dustin N., Nevius, Christopher D., Pendergrass, Sarah A., Person, Thomas N., Schwartz, Marci, Ritchie, Marylyn D., Carey, David J., Ledbetter, David H., Williams, Marc S., Dewey, Frederick E., Lopez, Alexander, Penn, John, Overton, John D., Reid, Jeffrey G., Lebo, Matthew, Mason-Suares, Heather, Austin-Tse, Christina, Rehm, Heidi L., Delisle, Brian P., Makowski, Daniel J., Mehra, Vishal C., Murray, Michael F., Fornwalt, Brandon K.
Publicado no Genet Med (2017)

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

Por Austin-Tse, Christina, Halbritter, Jan, Zariwala, Maimoona A., Gilberti, Renée M., Gee, Heon Yung, Hellman, Nathan, Pathak, Narendra, Liu, Yan, Panizzi, Jennifer R., Patel-King, Ramila S., Tritschler, Douglas, Bower, Raqual, O’Toole, Eileen, Porath, Jonathan D., Hurd, Toby W., Chaki, Moumita, Diaz, Katrina A., Kohl, Stefan, Lovric, Svjetlana, Hwang, Daw-Yang, Braun, Daniela A., Schueler, Markus, Airik, Rannar, Otto, Edgar A., Leigh, Margaret W., Noone, Peadar G., Carson, Johnny L., Davis, Stephanie D., Pittman, Jessica E., Ferkol, Thomas W., Atkinson, Jeffry J., Olivier, Kenneth N., Sagel, Scott D., Dell, Sharon D., Rosenfeld, Margaret, Milla, Carlos E., Loges, Niki T., Omran, Heymut, Porter, Mary E., King, Stephen M., Knowles, Michael R., Drummond, Iain A., Hildebrandt, Friedhelm
Publicado em 2013