The Pervasive Role of the miR-181 Family in Development, Neurodegeneration, and Cancer von Indrieri, Alessia, Carrella, Sabrina, Carotenuto, Pietro, Banfi, Sandro, Franco, Brunella

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Autophagy promotes primary ciliogenesis by removing OFD1 from centriolar satellites von Tang, Zaiming, Lin, Mary Grace, Stowe, Timothy Richard, Chen, She, Zhu, Muyuan, Stearns, Tim, Franco, Brunella, Zhong, Qing

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OFD Type I syndrome: lessons learned from a rare ciliopathy von Morleo, Manuela, Franco, Brunella

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Dopamine, Alpha-Synuclein, and Mitochondrial Dysfunctions in Parkinsonian Eyes von Indrieri, Alessia, Pizzarelli, Rocco, Franco, Brunella, De Leonibus, Elvira

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The Autophagy-Cilia Axis: An Intricate Relationship von Morleo, Manuela, Franco, Brunella

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Mutation-Independent Therapies for Retinal Diseases: Focus on Gene-Based Approaches von Carrella, Sabrina, Indrieri, Alessia, Franco, Brunella, Banfi, Sandro

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CiliaCarta: An integrated and validated compendium of ciliary genes von van Dam, Teunis J P, Kennedy, Julie, van der Lee, Robin, de Vrieze, Erik, Wunderlich, Kirsten A, Rix, Suzanne, Dougherty, Gerard W, Lambacher, Nils J, Li, Chunmei, Jensen, Victor L, Leroux, Michel R, Hjeij, Rim, Horn, Nicola, Texier, Yves, Wissinger, Yasmin, van Reeuwijk, Jeroen, Wheway, Gabrielle, Knapp, Barbara, Scheel, Jan F, Franco, Brunella, Mans, Dorus A, van Wijk, Erwin, Képès, François, Slaats, Gisela G, Toedt, Grischa, Kremer, Hannie, Omran, Heymut, Szymanska, Katarzyna, Koutroumpas, Konstantinos, Ueffing, Marius, Nguyen, Thanh-Minh T, Letteboer, Stef J F, Oud, Machteld M, van Beersum, Sylvia E C, Schmidts, Miriam, Beales, Philip L, Lu, Qianhao, Giles, Rachel H, Szklarczyk, Radek, Russell, Robert B, Gibson, Toby J, Johnson, Colin A, Blacque, Oliver E, Wolfrum, Uwe, Boldt, Karsten, Roepman, Ronald, Hernandez-Hernandez, Victor, Huynen, Martijn A

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The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery von Toriyama, Michinori, Lee, Chanjae, Taylor, S Paige, Duran, Ivan, Cohn, Daniel H, Bruel, Ange-Line, Tabler, Jacqueline M, Drew, Kevin, Kelly, Marcus R, Kim, Sukyoung, Park, Tae Joo, Braun, Daniela A, Pierquin, Ghislaine, Biver, Armand, Wagner, Kerstin, Malfroot, Anne, Panigrahi, Inusha, Franco, Brunella, Al-lami, Hadeel Adel, Yeung, Yvonne, Choi, Yeon Ja, Duffourd, Yannis, Faivre, Laurence, Rivière, Jean-Baptiste, Chen, Jiang, Liu, Karen J, Marcotte, Edward M, Hildebrandt, Friedhelm, Thauvin-Robinet, Christel, Krakow, Deborah, Jackson, Peter K, Wallingford, John B

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Synthetic long non-coding RNAs [SINEUPs] rescue defective gene expression in vivo von Indrieri, Alessia, Grimaldi, Claudia, Zucchelli, Silvia, Tammaro, Roberta, Gustincich, Stefano, Franco, Brunella

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The OFD1 protein is a novel player in selective autophagy: another tile to the cilia/autophagy puzzle von Morleo, Manuela, Franco, Brunella

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Cell-cell interaction determines cell fate of mesoderm-derived cell in tongue development through Hh signaling von Kawasaki, Maiko, Kawasaki, Katsushige, Sari, Finsa Tisna, Kudo, Takehisa, Nihara, Jun, Kitamura, Madoka, Nagai, Takahiro, Utama, Vanessa, Ishida, Yoko, Meguro, Fumiya, Kesuma, Alex, Fujita, Akira, Nishimura, Takayuki, Kogure, Yuan, Maruyama, Satoshi, Tanuma, Jun-Ichi, Kakihara, Yoshito, Maeda, Takeyasu, Ghafoor, Sarah, Khonsari, Roman H, Corre, Pierre, Sharpe, Paul T, Cobourne, Martyn, Franco, Brunella, Ohazama, Atsushi

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α-synuclein overexpression in the retina leads to vision impairment and degeneration of dopaminergic amacrine cells von Marrocco, Elena, Indrieri, Alessia, Esposito, Federica, Tarallo, Valeria, Carboncino, Anna, Alvino, Filomena Grazia, De Falco, Sandro, Franco, Brunella, De Risi, Maria, De Leonibus, Elvira

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The role of OFD1 in selective autophagy von Franco, Brunella, Morleo, Manuela

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miR‐181a/b downregulation exerts a protective action on mitochondrial disease models von Indrieri, Alessia, Carrella, Sabrina, Romano, Alessia, Spaziano, Alessandra, Marrocco, Elena, Fernandez‐Vizarra, Erika, Barbato, Sara, Pizzo, Mariateresa, Ezhova, Yulia, Golia, Francesca M, Ciampi, Ludovica, Tammaro, Roberta, Henao‐Mejia, Jorge, Williams, Adam, Flavell, Richard A, De Leonibus, Elvira, Zeviani, Massimo, Surace, Enrico M, Banfi, Sandro, Franco, Brunella

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Editorial: Regulation of proteostasis and cellular energy homeostasis at the primary cilium von Pfirrmann, Thorsten, Franco, Brunella, Kopinke, Daniel, Gerhardt, Christoph

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A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant von Mandato, Claudia, Siano, Maria Anna, Nazzaro, Lucia, Gelzo, Monica, Francalanci, Paola, Rizzo, Francesca, D'Agostino, Ylenia, Morleo, Manuela, Brillante, Simona, Weisz, Alessandro, Franco, Brunella, Vajro, Pietro

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Oral-facial-digital syndromes: Review and diagnostic guidelines von Gurrieri, Fiorella, Franco, Brunella, Toriello, Helga, Neri, Giovanni

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Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators von Liu, Yangfan P, Tsai, I-Chun, Morleo, Manuela, Oh, Edwin C, Leitch, Carmen C, Massa, Filomena, Lee, Byung-Hoon, Parker, David S, Finley, Daniel, Zaghloul, Norann A, Franco, Brunella, Katsanis, Nicholas

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Genetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie Syndrome von Ansari, Morad, Rainger, Jacqueline, Hanson, Isabel M, Williamson, Kathleen A, Sharkey, Freddie, Harewood, Louise, Sandilands, Angela, Clayton-Smith, Jill, Dollfus, Helene, Bitoun, Pierre, Meire, Francoise, Fantes, Judy, Franco, Brunella, Lorenz, Birgit, Taylor, David S, Stewart, Fiona, Willoughby, Colin E, McEntagart, Meriel, Khaw, Peng Tee, Clericuzio, Carol, Van Maldergem, Lionel, Williams, Denise, Newbury-Ecob, Ruth, Traboulsi, Elias I, Silva, Eduardo D, Madlom, Mukhlis M, Goudie, David R, Fleck, Brian W, Wieczorek, Dagmar, Kohlhase, Juergen, McTrusty, Alice D, Gardiner, Carol, Yale, Christopher, Moore, Anthony T, Russell-Eggitt, Isabelle, Islam, Lily, Lees, Melissa, Beales, Philip L, Tuft, Stephen J, Solano, Juan B, Splitt, Miranda, Hertz, Jens Michael, Prescott, Trine E, Shears, Deborah J, Nischal, Ken K, Doco-Fenzy, Martine, Prieur, Fabienne, Temple, I Karen, Lachlan, Katherine L, Damante, Giuseppe, Morrison, Danny A, van Heyningen, Veronica, FitzPatrick, David R

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miR‐181a/b downregulation: a mutation‐independent therapeutic approach for inherited retinal diseases von Carrella, Sabrina, Di Guida, Martina, Brillante, Simona, Piccolo, Davide, Ciampi, Ludovica, Guadagnino, Irene, Garcia Piqueras, Jorge, Pizzo, Mariateresa, Marrocco, Elena, Molinari, Marta, Petrogiannakis, Georgios, Barbato, Sara, Ezhova, Yulia, Auricchio, Alberto, Franco, Brunella, De Leonibus, Elvira, Surace, Enrico Maria, Indrieri, Alessia, Banfi, Sandro

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