The NIMA-family kinase, Nek1 affects the stability of centrosomes and ciliogenesis

Por White, Mark C, Quarmby, Lynne M
Publicado em 2008

Cilia and the cell cycle?

Por Quarmby, Lynne M., Parker, Jeremy D.K.
Publicado em 2005

A NIMA-related Kinase, Fa2p, Localizes to a Novel Site in the Proximal Cilia of Chlamydomonas and Mouse Kidney Cells

Por Mahjoub, Moe R., Qasim Rasi, M., Quarmby, Lynne M.
Publicado em 2004

A Role for Katanin-mediated Axonemal Severing during Chlamydomonas Deflagellation

Por Lohret, Timothy A., McNally, Francis J., Quarmby, Lynne M.
Publicado em 1998

Phylogenetic Analysis of the Neks Reveals Early Diversification of Ciliary-Cell Cycle Kinases

Por Parker, Jeremy D. K., Bradley, Brian A., Mooers, Arne O., Quarmby, Lynne M.
Publicado em 2007

NEK8 Mutations Affect Ciliary and Centrosomal Localization and May Cause Nephronophthisis

Por Otto, Edgar A., Trapp, Melissa L., Schultheiss, Ulla T., Helou, Juliana, Quarmby, Lynne M., Hildebrandt, Friedhelm
Publicado em 2008

Katanin Knockdown Supports a Role for Microtubule Severing in Release of Basal Bodies before Mitosis in Chlamydomonas

Por Rasi, M. Qasim, Parker, Jeremy D.K., Feldman, Jessica L., Marshall, Wallace F., Quarmby, Lynne M.
Publicado em 2009

Separation and Characterization of Inositol Phospholipids from the Pulvini of Samanea saman

Por Coté, Gary G., DePass, Anthony L., Quarmby, Lynne M., Tate, Bonnie F., Morse, M. J., Satter, Ruth L., Crain, Richard C.
Publicado em 1989

Centrioles are freed from cilia by severing prior to mitosis

Por Parker, Jeremy D.K., Hilton, Laura K., Diener, Dennis R., Rasi, M. Qasim, Mahjoub, Moe R., Rosenbaum, Joel L., Quarmby, Lynne M.
Publicado em 2010

A Forward Genetic Screen and Whole Genome Sequencing Identify Deflagellation Defective Mutants in Chlamydomonas, Including Assignment of ADF1 as a TRP Channel

Por Hilton, Laura K., Meili, Fabian, Buckoll, Paul D., Rodriguez-Pike, Julie C., Choutka, Courtney P., Kirschner, Jaime A., Warner, Freda, Lethan, Mette, Garces, Fabian A., Qi, Jingnan, Quarmby, Lynne M.
Publicado no G3 (Bethesda) (2016)

Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins

Por Bialas, Nathan J., Inglis, Peter N., Li, Chunmei, Robinson, Jon F., Parker, Jeremy D. K., Healey, Michael P., Davis, Erica E., Inglis, Chrystal D., Toivonen, Tiina, Cottell, David C., Blacque, Oliver E., Quarmby, Lynne M., Katsanis, Nicholas, Leroux, Michel R.
Publicado em 2009

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport

Por Blacque, Oliver E., Reardon, Michael J., Li, Chunmei, McCarthy, Jonathan, Mahjoub, Moe R., Ansley, Stephen J., Badano, Jose L., Mah, Allan K., Beales, Philip L., Davidson, William S., Johnsen, Robert C., Audeh, Mark, Plasterk, Ronald H.A., Baillie, David L., Katsanis, Nicholas, Quarmby, Lynne M., Wicks, Stephen R., Leroux, Michel R.
Publicado em 2004

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

Por O’Toole, John F., Liu, Yangjian, Davis, Erica E., Westlake, Christopher J., Attanasio, Massimo, Otto, Edgar A., Seelow, Dominik, Nurnberg, Gudrun, Becker, Christian, Nuutinen, Matti, Kärppä, Mikko, Ignatius, Jaakko, Uusimaa, Johanna, Pakanen, Salla, Jaakkola, Elisa, van den Heuvel, Lambertus P., Fehrenbach, Henry, Wiggins, Roger, Goyal, Meera, Zhou, Weibin, Wolf, Matthias T.F., Wise, Eric, Helou, Juliana, Allen, Susan J., Murga-Zamalloa, Carlos A., Ashraf, Shazia, Chaki, Moumita, Heeringa, Saskia, Chernin, Gil, Hoskins, Bethan E., Chaib, Hassan, Gleeson, Joseph, Kusakabe, Takehiro, Suzuki, Takako, Isaac, R. Elwyn, Quarmby, Lynne M., Tennant, Bryan, Fujioka, Hisashi, Tuominen, Hannu, Hassinen, Ilmo, Lohi, Hellevi, van Houten, Judith L., Rotig, Agnes, Sayer, John A., Rolinski, Boris, Freisinger, Peter, Madhavan, Sethu M., Herzer, Martina, Madignier, Florence, Prokisch, Holger, Nurnberg, Peter, Jackson, Peter K., Khanna, Hemant, Katsanis, Nicholas, Hildebrandt, Friedhelm
Publicado em 2010

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy

Por O’Toole, John F., Liu, Yangjian, Davis, Erica E., Westlake, Christopher J., Attanasio, Massimo, Otto, Edgar A., Seelow, Dominik, Nurnberg, Gudrun, Becker, Christian, Nuutinen, Matti, Kärppä, Mikko, Ignatius, Jaakko, Uusimaa, Johanna, Pakanen, Salla, Jaakkola, Elisa, van den Heuvel, Lambertus P., Fehrenbach, Henry, Wiggins, Roger, Goyal, Meera, Zhou, Weibin, Wolf, Matthias T.F., Wise, Eric, Helou, Juliana, Allen, Susan J., Murga-Zamalloa, Carlos A., Ashraf, Shazia, Chaki, Moumita, Heeringa, Saskia, Chernin, Gil, Hoskins, Bethan E., Chaib, Hassan, Gleeson, Joseph, Kusakabe, Takehiro, Suzuki, Takako, Isaac, R. Elwyn, Quarmby, Lynne M., Tennant, Bryan, Fujioka, Hisashi, Tuominen, Hannu, Hassinen, Ilmo, Lohi, Hellevi, van Houten, Judith L., Rotig, Agnes, Sayer, John A., Rolinski, Boris, Freisinger, Peter, Madhavan, Sethu M., Herzer, Martina, Madignier, Florence, Prokisch, Holger, Nurnberg, Peter, Jackson, Peter, Khanna, Hemant, Katsanis, Nicholas, Hildebrandt, Friedhelm
Publicado em 2010