Items where Author is "Martens, Pernille"
Number of items: 2. 2021Gonçalves, André Brás and Hasselbalch, Sarah Kirstine and Joensen, Beinta Biskopstø and Patzke, Sebastian and Martens, Pernille and Ohlsen, Signe Krogh and Quinodoz, Mathieu and Nikopoulos, Konstantinos and Suleiman, Reem and Damsø Jeppesen, Magnus Per and Weiss, Catja and Christensen, Søren Tvorup and Rivolta, Carlo and Andersen, Jens S. and Farinelli, Pietro and Pedersen, Lotte Bang. (2021) CEP78 functions downstream of CEP350 to control biogenesis of primary cilia by negatively regulating CP110 levels. eLife, 10. e63731. 2020Ascari, Giulia and Peelman, Frank and Farinelli, Pietro and Rosseel, Toon and Lambrechts, Nina and Wunderlich, Kirsten A. and Wagner, Matias and Nikopoulos, Konstantinos and Martens, Pernille and Balikova, Irina and Derycke, Lara and Holtappels, Gabriële and Krysko, Olga and Van Laethem, Thalia and De Jaegere, Sarah and Guillemyn, Brecht and De Rycke, Riet and De Bleecker, Jan and Creytens, David and Van Dorpe, Jo and Gerris, Jan and Bachert, Claus and Neuhofer, Christiane and Walraedt, Sophie and Bischoff, Almut and Pedersen, Lotte B. and Klopstock, Thomas and Rivolta, Carlo and Leroy, Bart P. and De Baere, Elfride and Coppieters, Frauke. (2020) Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility. Human mutation, 41 (5). pp. 998-1011. |
