Publications by: Richard Francis

Also publishes as (Richard J.B. Francis, Richard J. Francis)

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Number of items: 22.

Francis, Richard J.B., Agustin, Jovenal T.San, Rogers, Heather L.Szabo, Cui, Cheng, Jonassen, Julie A., Eguether, Thibaut, Follit, John A., Lo, Cecilia W., and Pazour, Gregory (2023) Autonomous and non-cell autonomous role of cilia in structural birth defects in mice. PLoS Biology, 21 (12). e3002425.

Francis, Richard (2023) The effects of acute hydrogen peroxide exposure on respiratory cilia motility and viability. PeerJ, 11. e14899.

Scopulovic, Luke, Francis, Deanne, Pandzic, Elvis, and Francis, Richard (2022) Quantifying cilia beat frequency using high-speed video microscopy: Assessing frame rate requirements when imaging different ciliated tissues. Physiological Reports, 10 (11). e15349.

Liang, Huazheng, Wang, Hongqin, Wang, Shaoshi, Francis, Richard, Paxinos, George, and Huang, Xufeng (2018) 3D imaging of PSD-95 in the mouse brain using the advanced CUBIC method. Molecular brain, 11. 50.

Solomon, George M., Francis, Richard, Chu, Kengyeh K., Birket, Susan E., Gabriel, George, Trombley, John E., Lemke, Kristi L., Klena, Nikolai, Turner, Brett, Tearney, Guillermo J., Lo, Cecilia W., and Rowe, Steven M. (2017) Assessment of ciliary phenotype in primary ciliary dyskinesia by micro-optical coherence tomography. JCI Insight, 2 (5). e91702.

Liang, Huazheng, Akladios, Bassem, Canales, Cesar P., Francis, Richard, Hardeman, Edna H., and Beverdam, Annemiek (2016) CUBIC protocol visualizes protein expression at single cell resolution in whole mount skin preparations. Journal of Visualized Experiments, 1 (114). e54401.

Li, You, Yagi, Hisato, Onuoha, Ezenwa Obi, Damerla, Rama Rao, Francis, Richard, Furutani, Yoshiyuki, Tariq, Muhammad, King, Stephen M., Hendricks, Gregory, Cui, Cheng, Saydmohammed, Manush, Lee, Dong Min, Zahid, Maliha, Sami, Iman, Leatherbury, Linda, Pazour, Gregory J., Ware, Stephanie M., Nakanishi, Toshio, Goldmuntz, Elizabeth, Tsang, Michael, and Lo, Cecilia W. (2016) DNAH6 and its interactions with PCD genes in heterotaxy and primary ciliary dyskinesia. PLoS Genetics, 12 (2). e1005821.

Czarnecki, Peter G., Gabriel, George C., Manning, Danielle K., Sergeev, Mikhail, Lemke, Kristi, Klena, Nikolai T., Liu, Xiaoqin, Chen, Yu, Li, You, Agustin, Jovenal T. San, Garnaas, Maija K., Francis, Richard J., Tobita, Kimimasa, Goessling, Wolfram, Pazour, Gregory J., Lo, Cecilia W., Beier, David R., and Shah, Jagesh V. (2015) ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterning. Nature Communications, 6. 6023.

Quinn, Shannon P., Zahid, Maliha J., Durkin, John R., Francis, Richard J., Lo, Cecilia W., and Chennubhotla, S. Chakra (2015) Automated identification of abnormal respiratory ciliary motion in nasal biopsies. Science Translational Medicine, 7 (299). 299ra124.

Kutten, Johannes C., McGovern, David, Hobson, Christopher M., Luffy, Sarah A., Nieponice, Alejandro, Tobita, Kimimasa, Francis, Richard J., Reynolds, Susan D., Isenberg, Jeffrey S., and Gilbert, Thomas W. (2015) Decellularized tracheal extracellular matrix supports epithelial migration, differentiation, and function. Tissue Engineering Part A: Tissue Engineering, 21 (1-2). pp. 75-84.

Welchering, Nils, Ochoa, Sebastian, Tian, Xin, Francis, Richard, Zahid, Maliha, Muñoz, Ricardo, and Lo, Cecilia W. (2015) Dexmedetomidine and fentanyl exhibit temperature dependent effects on human respiratory cilia. Frontiers in Pediatrics, 3. 7.

Akawi, Nadia, McRae, Jeremy, Ansari, Morad, Balasubramanian, Meena, Blyth, Moira, Brady, Angela F., Clayton, Stephen, Cole, Trevor, Deshpande, Charu, Fitzgerald, Tomas W., Foulds, Nicola, Francis, Richard, Gabriel, George, Gerety, Sebastian S., Goodship, Judith, Hobson, Emma, Jones, Wendy D., Joss, Shelagh, King, Daniel, Klena, Nikolai, Kumar, Ajith, Lees, Melissa, Lelliott, Chris, Lord, Jenny, McMullan, Dominic, O'Regan, Mary, Osio, Deborah, Piombo, Virginia, Prigmore, Elena, Rajan, Diana, Rosser, Elisabeth, Sifrim, Alejandro, Smith, Audrey, Swaminathan, Ganesh J., Turnpenny, Peter, Whitworth, James, Wright, Caroline F., Firth, Helen V., Barrett, Jeffrey C., Lo, Cecilia W., FitzPatrick, David R., Hurles, Matthew E., and for the DDD Study (2015) Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families. Nature Genetics, 47 (11). pp. 1363-1369.

Liang, Huazheng, Wang, Shaoshi, Francis, Richard, Whan, Renee, Watson, Charles, and Paxinos, George (2015) Distribution of raphespinal fibers in the mouse spinal cord. Molecular Pain, 11. 42.

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, Chienfu, 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., and Lo, Cecilia W. (2015) Global genetic analysis in mice unveils central role for cilia in congenital heart disease. Nature, 521 (7553). pp. 520-524.

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., and Lo, Cecilia W. (2015) Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies. Human Molecular Genetics, 24 (14). pp. 3994-4005.

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., and Pazour, Gregory J. (2014) IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment. Developmental Cell, 31 (3). pp. 279-290.

Harden, Brandon, Tian, Xin, Giese, Rachel, Nakhleh, Nader, Kureshi, Safina, Francis, Richard, Hanumanthaiah, Sridhar, Li, You, Swisher, Matthew, Kuehl, Karen, Sami, Iman, Olivier, Kenneth, Jonas, Richard, Lo, Cecilia W., and Leatherbury, Linda (2014) Increased postoperative respiratory complications in heterotaxy congenital heart disease patients with respiratory ciliary dysfunction. Journal of Thoracic and Cardiovascular Surgery, 147 (4). 1291-U287.

Liu, Xiaoqin, Francis, Richard, Kim, Andrew J., Ramirez, Ricardo, Chen, Guozhen, Subramanian, Ramiah, Anderton, Shane, Kim, Youngsil, Wong, Liyin, Morgan, Judy, Pratt, Herbert C., Reinholdt, Laura, Devine, William, Leatherbury, Linda, Tobita, Kimimasa, and Lo, Cecilia W. (2014) Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen. Circulation: Cardiovascular Imaging, 7 (1). pp. 31-42.

Damerla, Rama Rao, Chatterjee, Bishwanath, Li, You, Francis, Richard J.B., Fatakia, Sarosh N., and Lo, Cecilia W. (2014) Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis. Mammalian Genome, 25 (3-4). pp. 120-128.

Christopher, Adam B., Ochoa, Sebastian, Krushansky, Evonne, Francis, Richard, Tian, Xin, Zahid, Maliha, Munoz, Ricardo, and Lo, Cecilia W. (2014) The effects temperature and anesthetic agents on ciliary function in murine respiratory epithelia. Frontiers in Pediatrics, 2. 111.

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., and Lo, Cecilia W. (2013) Wdpcp, a PCP Protein Required for Ciliogenesis, Regulates Directional Cell Migration and Cell Polarity by Direct Modulation of the Actin Cytoskeleton. PLoS Biology, 11. e1001720.

Cui, Cheng, Chatterjee, Bishwanath, Francis, Deanne, Yu, Qing, SanAgustin, Jovenal T., Francis, Richard, Tansey, Terry, Henry, Charisse, Wang, Baolin, Lemley, Bethan, Pazour, Gregory J., and Lo, Cecilia W. (2011) Disruption of Mks1 localization to the mother centriole causes cilia defects and developmental malformations in Meckel-Gruber syndrome. Disease Models & Mechanisms, 4. pp. 43-56.

This list was generated on Wed Dec 25 04:40:10 2024 AEST.