Intraflagellar transport is essential for mammalian spermiogenesis but is absent in mature sperm

od San Agustin, Jovenal T., Pazour, Gregory J., Witman, George B.
izdano v Mol Biol Cell (2015)

Novel Role for a Sterol Response Element Binding Protein in Directing Spermatogenic Cell-Specific Gene Expression

od Wang, Hang, San Agustin, Jovenal T., Witman, George B., Kilpatrick, Daniel L.
Izdano 2004

Deletion of IFT20 in the mouse kidney causes misorientation of the mitotic spindle and cystic kidney disease

od Jonassen, Julie A., San Agustin, Jovenal, Follit, John A., Pazour, Gregory J.
Izdano 2008

Disruption of IFT Complex A Causes Cystic Kidneys without Mitotic Spindle Misorientation

od Jonassen, Julie A., SanAgustin, Jovenal, Baker, Stephen P., Pazour, Gregory J.
Izdano 2012

Distinct functions for IFT140 and IFT20 in opsin transport.

od Crouse, Jacquelin A., Lopes, Vanda S., SanAgustin, Jovenal T., Keady, Brian T., Williams, David S., Pazour, Gregory J.
Izdano 2014

Ift25 Is Not a Cystic Kidney Disease Gene but Is Required for Early Steps of Kidney Development

od Desai, Paurav B., San Agustin, Jovenal T., Stuck, Michael W., Jonassen, Julie A., Bates, Carlton M., Pazour, Gregory J.
izdano v Mech Dev (2018)

The Golgin GMAP210/TRIP11 Anchors IFT20 to the Golgi Complex

od Follit, John A., San Agustin, Jovenal T., Xu, Fenghui, Jonassen, Julie A., Samtani, Rajeev, Lo, Cecilia W., Pazour, Gregory J.
Izdano 2008

Arf4 Is Required for Mammalian Development but Dispensable for Ciliary Assembly

od Follit, John A., San Agustin, Jovenal T., Jonassen, Julie A., Huang, Tingting, Rivera-Perez, Jaime A., Tremblay, Kimberly D., Pazour, Gregory J.
Izdano 2014

IFT25 Links the Signal-Dependent Movement of Hedgehog Components to Intraflagellar Transport

od Keady, Brian T., Samtani, Rajeev, Tobita, Kimimasa, Tsuchya, Maiko, San Agustin, Jovenal T., Follit, John A., Jonassen, Julie A., Subramanian, Ramiah, Lo, Cecilia W., Pazour, Gregory J.
Izdano 2012

Genetic link between renal birth defects and congenital heart disease

od San Agustin, Jovenal T., Klena, Nikolai, Granath, Kristi, Panigrahy, Ashok, Stewart, Eileen, Devine, William, Strittmatter, Lara, Jonassen, Julie A., Liu, Xiaoqin, Lo, Cecilia W., Pazour, Gregory J.
izdano v Nat Commun (2016)

Erratum: Genetic link between renal birth defects and congenital heart disease

od San Agustin, Jovenal T., Klena, Nikolai, Granath, Kristi, Panigrahy, Ashok, Stewart, Eileen, Devine, William, Strittmatter, Lara, Jonassen, Julie A., Liu, Xiaoqin, Lo, Cecilia W., Pazour, Gregory J.
izdano v Nat Commun (2016)

Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome

od Cui, Cheng, Chatterjee, Bishwanath, Francis, Deanne, Yu, Qing, SanAgustin, Jovenal T., Francis, Richard, Tansey, Terry, Henry, Charisse, Wang, Baolin, Lemley, Bethan, Pazour, Gregory J., Lo, Cecilia W.
Izdano 2011

IFT27 Links the BBSome to IFT for Maintenance of the Ciliary Signaling Compartment

od Eguether, Thibaut, San Agustin, Jovenal T., Keady, Brian T., Jonassen, Julie A., Liang, Yinwen, Francis, Richard, Tobita, Kimimasa, Johnson, Colin A., Abdelhamed, Zakia A., Lo, Cecilia W., Pazour, Gregory J.
izdano v Dev Cell (2014)

Loss of Arf4 causes severe degeneration of the exocrine pancreas but not cystic kidney disease or retinal degeneration

od Pearring, Jillian N., San Agustin, Jovenal T., Lobanova, Ekaterina S., Gabriel, Christopher J., Lieu, Eric C., Monis, William J., Stuck, Michael W., Strittmatter, Lara, Jaber, Samer M., Arshavsky, Vadim Y., Pazour, Gregory J.
izdano v PLoS Genet (2017)

Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies

od Damerla, Rama Rao, Cui, Cheng, Gabriel, George C., Liu, Xiaoqin, Craige, Branch, Gibbs, Brian C., Francis, Richard, Li, You, Chatterjee, Bishwanath, San Agustin, Jovenal T., Eguether, Thibaut, Subramanian, Ramiah, Witman, George B., Michaud, Jacques L., Pazour, Gregory J., Lo, Cecilia W.
izdano v Hum Mol Genet (2015)

ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning

od Czarnecki, Peter G., Gabriel, George C., Manning, Danielle K., Sergeev, Mikhail, Lemke, Kristi, Klena, Nikolai T., Liu, Xiaoqin, Chen, Yu, Li, You, San Agustin, Jovenal T., Garnaas, Maija K., Francis, Richard J., Tobita, Kimimasa, Goessling, Wolfram, Pazour, Gregory J., Lo, Cecilia W., Beier, David R., Shah, Jagesh V.
izdano v Nat Commun (2015)

Wdpcp, a PCP Protein Required for Ciliogenesis, Regulates Directional Cell Migration and Cell Polarity by Direct Modulation of the Actin Cytoskeleton

od Cui, Cheng, Chatterjee, Bishwanath, Lozito, Thomas P., Zhang, Zhen, Francis, Richard J., Yagi, Hisato, Swanhart, Lisa M., Sanker, Subramaniam, Francis, Deanne, Yu, Qing, San Agustin, Jovenal T., Puligilla, Chandrakala, Chatterjee, Tania, Tansey, Terry, Liu, Xiaoqin, Kelley, Matthew W., Spiliotis, Elias T., Kwiatkowski, Adam V., Tuan, Rocky, Pazour, Gregory J., Hukriede, Neil A., Lo, Cecilia W.
Izdano 2013

Global genetic analysis in mice unveils central role for cilia in congenital heart disease

od Li, You, Klena, Nikolai T., Gabriel, George C, Liu, Xiaoqin, Kim, Andrew J., Lemke, Kristi, Chen, Yu, Chatterjee, Bishwanath, Devine, William, Damerla, Rama Rao, Chang, Chien-fu, Yagi, Hisato, San Agustin, Jovenal T., Thahir, Mohamed, Anderton, Shane, Lawhead, Caroline, Vescovi, Anita, Pratt, Herbert, Morgan, Judy, Haynes, Leslie, Smith, Cynthia L., Eppig, Janan T., Reinholdt, Laura, Francis, Richard, Leatherbury, Linda, Ganapathiraju, Madhavi K., Tobita, Kimimasa, Pazour, Gregory J., Lo, Cecilia W.
izdano v Nature (2015)