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IC138 defines a subdomain at the base of the I1 dynein that regulates microtubule sliding and flagellar motility. [electronic resource] by
- Bower, Raqual
- VanderWaal, Kristyn
- O'Toole, Eileen
- Fox, Laura
- Perrone, Catherine
- Mueller, Joshua
- Wirschell, Maureen
- Kamiya, R
- Sale, Winfield S
- Porter, Mary E
Producer: 20091027
In:
Molecular biology of the cell vol. 20
Availability: No items available.
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FAP57/WDR65 targets assembly of a subset of inner arm dyneins and connects to regulatory hubs in cilia. [electronic resource] by
- Lin, Jianfeng
- Le, Thuc Vy
- Augspurger, Katherine
- Tritschler, Douglas
- Bower, Raqual
- Fu, Gang
- Perrone, Catherine
- O'Toole, Eileen T
- Mills, Kristyn VanderWaal
- Dymek, Erin
- Smith, Elizabeth
- Nicastro, Daniela
- Porter, Mary E
Producer: 20200526
In:
Molecular biology of the cell vol. 30
Availability: No items available.
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The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans. [electronic resource] by
- Wirschell, Maureen
- Olbrich, Heike
- Werner, Claudius
- Tritschler, Douglas
- Bower, Raqual
- Sale, Winfield S
- Loges, Niki T
- Pennekamp, Petra
- Lindberg, Sven
- Stenram, Unne
- Carlén, Birgitta
- Horak, Elisabeth
- Köhler, Gabriele
- Nürnberg, Peter
- Nürnberg, Gudrun
- Porter, Mary E
- Omran, Heymut
Producer: 20130530
In:
Nature genetics vol. 45
Availability: No items available.
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Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease. [electronic resource] by
- 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
Producer: 20170322
In:
PLoS genetics vol. 12
Availability: No items available.
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Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia. [electronic resource] by
- 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
Producer: 20140219
In:
American journal of human genetics vol. 93
Availability: No items available.
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