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NOA1 is an essential GTPase required for mitochondrial protein synthesis |
Authors: Kolanczyk, Mateusz; Pech, Markus; Zemojte, Tomasz; Yamamoto, Hiroshi; Mikula, Ivan; Calvaruso, Maria-Antonietta; van den Brand, Mariel; Richter, Ricarda; Fischer, Bjoern; Ritz, Anita; Kossler, Nadine; Thurisch, Boris; Spoerle, Ralf; Smeitink, Jan; Kornak, Uwe; Chan, Danny; Vingron, Martin; Martasek, Pavel; Lightowlers, Robert N.; Nijtmans, Leo; Schuelke, Markus; Nierhaus, Knud H.; Mundlos, Stefan | Date of Publication (YYYY-MM-DD): 2011-01-01 | Title of Journal: Molecular Biology of the Cell | Volume: 22 | Issue / Number: 1 | Start Page: 1 | End Page: 11 | Document Type: Article | ID: 538382.0 |
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Mutations in PYCR1 cause cutis laxa with progeroid features |
Authors: Reversade, Bruno; Escande-Beillard, Nathalie; Dimopoulou, Aikaterini; Fischer, Björn; Chng, Serene C.; Li, Yun; Shboul, Mohammad; Tham, Puay-Yoke; Kayserili, Hülya; Al-Gazali, Lihadh; Shahwan, Monzer; Brancati, Francesco; Lee, Hane; O'Connor, Brian D.; Schmidt-von Kegler, Mareen; Merriman, Barry; Nelson, Stanley F.; Masri, Amira; Alkazaleh, Fawaz; Guerra, Deanna; Ferrari, Paola; Nanda, Arti; Rajab, Anna; Markie, David; Gray, Mary; Nelson, John; Grix, Arthur; Sommer, Annemarie; Savarirayan, Ravi; Janecke, Andreas R.; Steichen, Elisabeth; Sillence, David; Haußer, Ingrid; Budde, Birgit; Nürnberg, Gudrun; Nürnberg, Peter; Seemann, Petra; Kunkel, Désirée; Zambruno, Giovanna; Dallapiccola, Bruno; Schuelke, Markus; Robertson, Stephen; Hamamy, Hanan; Wollnik, Bernd; Van Maldergem, Lionel; Mundlos, Stefan; Kornak, Uwe | Date of Publication (YYYY-MM-DD): 2009-09 | Title of Journal: Nature Genetics | Volume: 41 | Start Page: 1016 | End Page: 1021 | Document Type: Article | ID: 447542.0 |
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Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival |
Authors: Hucthagowder, Vishwanathan; Morava, Eva; Kornak, Uwe; Lefeber, Dirk J.; Fischer, Björn; Dimopoulou, Aikaterini; Aldinger, Annika; Choi, Jiwon; Davis, Elaine C.; Abuelo, Dianne N.; Adamowicz, Maciej; Al-Aama, Jumana; Basel-Vanagaite, Lina; Fernandez, Bridget; Greally, Marie T.; Gillessen-Kaesbach, Gabriele; Kayserili, Hulya; Lemyre, Emmanuelle; Tekin, Mustafa; Türkmen, Seval; Tuysuz, Beyhan; Yüksel-Konuk, Berrin; Mundlos, Stefan; Van Maldergem, Lionel; Wevers, Ron A.; Urban, Zsolt | Date of Publication (YYYY-MM-DD): 2009-06 | Title of Journal: Human Molecular Genetics | Volume: 18 | Issue / Number: 12 | Start Page: 2149 | End Page: 2165 | Document Type: Article | ID: 447495.0 |
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Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2 |
Authors: Kornak, Uwe; Reynders, Ellen; Dimopoulou, Aikaterini; van Reeuwijk, Jeroen; Fischer, Bjoern; Rajab, Anna; Budde, Birgit; Nürnberg, Peter; Foulquier, Francois; Lefeber, Dirk; Urban, Zsolt; Gruenewald, Stephanie; Annaert, Wim; Brunner, Han G; van Bokhoven, Hans; Wevers, Ron; Morava, Eva; Matthijs, Gert; Van Maldergem, Lionel; Mundlos, Stefan | Date of Publication (YYYY-MM-DD): 2008-01 | Title of Journal: Nature Genetics | Volume: 40 | Issue / Number: 1 | Start Page: 32 | End Page: 34 | Document Type: Article | ID: 411701.0 |
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