A Novel Dynein Light Intermediate Chain Colocalizes with the Retrograde Motor for Intraflagellar Transport at Sites of Axoneme Assembly in Chlamydomonas and Mammalian Cells

Por Perrone, Catherine A., Tritschler, Douglas, Taulman, Patrick, Bower, Raqual, Yoder, Bradley K., Porter, Mary E.
Publicado em 2003

Building Blocks of the Nexin-Dynein Regulatory Complex in Chlamydomonas Flagella

Por Lin, Jianfeng, Tritschler, Douglas, Song, Kangkang, Barber, Cynthia F., Cobb, Jennifer S., Porter, Mary E., Nicastro, Daniela
Publicado em 2011

In Situ Localization of N and C Termini of Subunits of the Flagellar Nexin-Dynein Regulatory Complex (N-DRC) Using SNAP Tag and Cryo-electron Tomography

Por Song, Kangkang, Awata, Junya, Tritschler, Douglas, Bower, Raqual, Witman, George B., Porter, Mary E., Nicastro, Daniela
Publicado no J Biol Chem (2015)

The N-DRC forms a conserved biochemical complex that maintains outer doublet alignment and limits microtubule sliding in motile axonemes

Por Bower, Raqual, Tritschler, Douglas, VanderWaal, Kristyn, Perrone, Catherine A., Mueller, Joshua, Fox, Laura, Sale, Winfield S., Porter, M. E.
Publicado em 2013

The role of the dynein light intermediate chain in retrograde IFT and flagellar function in Chlamydomonas

Por Reck, Jaimee, Schauer, Alexandria M., VanderWaal Mills, Kristyn, Bower, Raqual, Tritschler, Douglas, Perrone, Catherine A., Porter, Mary E.
Publicado no Mol Biol Cell (2016)

The nexin link and B-tubule glutamylation maintain the alignment of outer doublets in the ciliary axoneme

Por Alford, Lea M., Stoddard, Daniel, Li, Jennifer H., Hunter, Emily L., Tritschler, Douglas, Bower, Raqual, Nicastro, Daniela, Porter, Mary E., Sale, Winfield S.
Publicado no Cytoskeleton (Hoboken) (2016)

A differential cargo loading model of ciliary length regulation by IFT

Por Wren, Kathryne N., Craft, Julie M., Tritschler, Douglas, Schauer, Alexandria, Patel, Deep K., Smith, Elizabeth F., Porter, Mary E., Kner, Peter, Lechtreck, Karl F.
Publicado em 2013

The nexin-dynein regulatory complex subunit DRC 1 is essential for motile cilia function in algae and humans

Por Wirschell, Maureen, Olbrich, Heike, Werner, Claudius, Tritschler, Douglas, Bower, Raqual, Sale, Winfield, Loges, Niki T., Pennekamp, Petra, Lindberg, Sven, Stenram, Unne, Carlén, Birgitta, Horak, Elisabeth, Köhler, Gabriele, Nürnberg, Peter, Nürnberg, Gudrun, Porter, Mary E., Omran, Heymut
Publicado em 2013

Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease

Por Lewis, Wesley R., Malarkey, Erik B., Tritschler, Douglas, Bower, Raqual, Pasek, Raymond C., Porath, Jonathan D., Birket, Susan E., Saunier, Sophie, Antignac, Corinne, Knowles, Michael R., Leigh, Margaret W., Zariwala, Maimoona A., Challa, Anil K., Kesterson, Robert A., Rowe, Steven M., Drummond, Iain A., Parant, John M., Hildebrandt, Friedhelm, Porter, Mary E., Yoder, Bradley K., Berbari, Nicolas F.
Publicado no PLoS Genet (2016)

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