Visualizing the native cellular organization by coupling cryofixation with expansion microscopy (Cryo-ExM)

por Laporte, Marine H., Klena, Nikolai, Hamel, Virginie, Guichard, Paul
Publicado 2022

An In-depth Guide to the Ultrastructural Expansion Microscopy (U-ExM) of Chlamydomonas reinhardtii

por Klena, Nikolai, Maltinti, Giovanni, Batman, Umut, Pigino, Gaia, Guichard, Paul, Hamel, Virginie
Publicado 2023

Isolation and Fluorescence Imaging for Single-particle Reconstruction of Chlamydomonas Centrioles

por Klena, Nikolai, Gambarotto, Davide, Le Guennec, Maeva, Borgers, Susanne, Guichard, Paul, Hamel, Virginie
Publicado 2018

Kinesin-1 activity recorded in living cells with a precipitating dye

por Angerani, Simona, Lindberg, Eric, Klena, Nikolai, Bleck, Christopher K. E., Aumeier, Charlotte, Winssinger, Nicolas
Publicado 2021

Genetic link between renal birth defects and congenital heart disease

por 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.
Publicado 2016

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

por 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.
Publicado 2016

Architecture of the centriole cartwheel‐containing region revealed by cryo‐electron tomography

por Klena, Nikolai, Le Guennec, Maeva, Tassin, Anne‐Marie, van den Hoek, Hugo, Erdmann, Philipp S, Schaffer, Miroslava, Geimer, Stefan, Aeschlimann, Gabriel, Kovacik, Lubomir, Sadian, Yashar, Goldie, Kenneth N, Stahlberg, Henning, Engel, Benjamin D, Hamel, Virginie, Guichard, Paul
Publicado 2020

A helical inner scaffold provides a structural basis for centriole cohesion

por Le Guennec, Maeva, Klena, Nikolai, Gambarotto, Davide, Laporte, Marine H., Tassin, Anne-Marie, van den Hoek, Hugo, Erdmann, Philipp S., Schaffer, Miroslava, Kovacik, Lubomir, Borgers, Susanne, Goldie, Kenneth N., Stahlberg, Henning, Bornens, Michel, Azimzadeh, Juliette, Engel, Benjamin D., Hamel, Virginie, Guichard, Paul
Publicado 2020

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

por 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.
Publicado 2015

Biliary-Atresia-Associated Mannosidase-1-Alpha-2 Gene Regulates Biliary and Ciliary Morphogenesis and Laterality

por So, Juhoon, Ningappa, Mylarappa, Glessner, Joseph, Min, Jun, Ashokkumar, Chethan, Ranganathan, Sarangarajan, Higgs, Brandon W., Li, Dong, Sun, Qing, Schmitt, Lori, Biery, Amy C., Dobrowolski, Steven, Trautz, Christine, Fuhrman, Leah, Schwartz, Molly Christine, Klena, Nikolai Thomas, Fusco, Joseph, Prasadan, Krishna, Adenuga, Morayooluwa, Mohamed, Nada, Yan, Qi, Chen, Wei, Horne, William, Dhawan, Anil, Sharif, Khalid, Kelly, Deirdre, Squires, Robert H, Gittes, George K., Hakonarson, Hakon, Morell, Victor, Lo, Cecilia, Subramaniam, Shankar, Shin, Donghun, Sindhi, Rakesh
Publicado 2020

CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation

por Hjeij, Rim, Onoufriadis, Alexandros, Watson, Christopher M., Slagle, Christopher E., Klena, Nikolai T., Dougherty, Gerard W., Kurkowiak, Małgorzata, Loges, Niki T., Diggle, Christine P., Morante, Nicholas F.C., Gabriel, George C., Lemke, Kristi L., Li, You, Pennekamp, Petra, Menchen, Tabea, Konert, Franziska, Marthin, June Kehlet, Mans, Dorus A., Letteboer, Stef J.F., Werner, Claudius, Burgoyne, Thomas, Westermann, Cordula, Rutman, Andrew, Carr, Ian M., O’Callaghan, Christopher, Moya, Eduardo, Chung, Eddie M.K., Sheridan, Eamonn, Nielsen, Kim G., Roepman, Ronald, Bartscherer, Kerstin, Burdine, Rebecca D., Lo, Cecilia W., Omran, Heymut, Mitchison, Hannah M.
Publicado 2014

MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates

por Guimier, Anne, Gabriel, George C., Bajolle, Fanny, Tsang, Michael, Liu, Hui, Noll, Aaron, Schwartz, Molly, El Malti, Rajae, Smith, Laurie D., Klena, Nikolai T., Jimenez, Gina, Miller, Neil A., Oufadem, Myriam, Moreau de Bellaing, Anne, Yagi, Hisato, Saunders, Carol J., Baker, Candice N., Di Filippo, Sylvie, Peterson, Kevin A., Thiffault, Isabelle, Bole-Feysot, Christine, Cooley, Linda D., Farrow, Emily G., Masson, Cécile, Schoen, Patric, Deleuze, Jean-François, Nitschké, Patrick, Lyonnet, Stanislas, de Pontual, Loic, Murray, Stephen A., Bonnet, Damien, Kingsmore, Stephen F., Amiel, Jeanne, Bouvagnet, Patrice, Lo, Cecilia W., Gordon, Christopher T.
Publicado 2015

Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families

por 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.
Publicado 2015

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

por Prins, Bram P., Mead, Timothy J., Brody, Jennifer A., Sveinbjornsson, Gardar, Ntalla, Ioanna, Bihlmeyer, Nathan A., van den Berg, Marten, Bork-Jensen, Jette, Cappellani, Stefania, Van Duijvenboden, Stefan, Klena, Nikolai T., Gabriel, George C., Liu, Xiaoqin, Gulec, Cagri, Grarup, Niels, Haessler, Jeffrey, Hall, Leanne M., Iorio, Annamaria, Isaacs, Aaron, Li-Gao, Ruifang, Lin, Honghuang, Liu, Ching-Ti, Lyytikäinen, Leo-Pekka, Marten, Jonathan, Mei, Hao, Müller-Nurasyid, Martina, Orini, Michele, Padmanabhan, Sandosh, Radmanesh, Farid, Ramirez, Julia, Robino, Antonietta, Schwartz, Molly, van Setten, Jessica, Smith, Albert V., Verweij, Niek, Warren, Helen R., Weiss, Stefan, Alonso, Alvaro, Arnar, David O., Bots, Michiel L., de Boer, Rudolf A., Dominiczak, Anna F., Eijgelsheim, Mark, Ellinor, Patrick T., Guo, Xiuqing, Felix, Stephan B., Harris, Tamara B., Hayward, Caroline, Heckbert, Susan R., Huang, Paul L., Jukema, J. W., Kähönen, Mika, Kors, Jan A., Lambiase, Pier D., Launer, Lenore J., Li, Man, Linneberg, Allan, Nelson, Christopher P., Pedersen, Oluf, Perez, Marco, Peters, Annette, Polasek, Ozren, Psaty, Bruce M., Raitakari, Olli T., Rice, Kenneth M., Rotter, Jerome I., Sinner, Moritz F., Soliman, Elsayed Z., Spector, Tim D., Strauch, Konstantin, Thorsteinsdottir, Unnur, Tinker, Andrew, Trompet, Stella, Uitterlinden, André, Vaartjes, Ilonca, van der Meer, Peter, Völker, Uwe, Völzke, Henry, Waldenberger, Melanie, Wilson, James G., Xie, Zhijun, Asselbergs, Folkert W., Dörr, Marcus, van Duijn, Cornelia M., Gasparini, Paolo, Gudbjartsson, Daniel F., Gudnason, Vilmundur, Hansen, Torben, Kääb, Stefan, Kanters, Jørgen K., Kooperberg, Charles, Lehtimäki, Terho, Lin, Henry J., Lubitz, Steven A., Mook-Kanamori, Dennis O., Conti, Francesco J., Newton-Cheh, Christopher H., Rosand, Jonathan, Rudan, Igor, Samani, Nilesh J., Sinagra, Gianfranco, Smith, Blair H., Holm, Hilma, Stricker, Bruno H., Ulivi, Sheila, Sotoodehnia, Nona, Apte, Suneel S., van der Harst, Pim, Stefansson, Kari, Munroe, Patricia B., Arking, Dan E., Lo, Cecilia W., Jamshidi, Yalda
Publicado 2018