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We study the molecular mechanisms by which primary cilia assemble, disassemble, and function to coordinate diverse signaling pathways during development and tissue homeostasis. Furthermore, we study the molecular basis underlying diseases caused by defective cilia (ciliopathies). We primarily use mammalian cell cultures as model systems.
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论文共 105 篇作者统计合作学者相似作者
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Csenge Kata Rezi, Alina Frei, Fabiola Campestre, Christina Rahlff Berggreen, Julie Laplace, Aurelien Sicot, Geyi Li, Soren Lek Johansen, Julie K. T. Sorensen,Martin Werner Berchtold, Mohamed Chamlali,Soren Tvorup Christensen,
biorxiv(2024)
Csenge K. Rezi, Mariam G. Aslanyan,Gaurav D. Diwan,Tao Cheng, Mohamed Chamlali,Katrin Junger,Zeinab Anvarian,Esben Lorentzen, Kleo B. Pauly, Yasmin Afshar-Bahadori,Eduardo F. A. Fernandes,Feng Qian,
biorxiv(2024)
Methods in molecular biology (Clifton, N.J.) (2024): 147-166
Anne K. Nielsen, Maria Elena Steidl, Mariam Aslanyan,Sylvia E. van Beersum, Daniel Spies,Lotte B. Pedersen,Karsten Boldt,Ronald Roepman, Alessandra Boletta
Journal of the American Society of Nephrologyno. 11S (2023): 564-564
Reference Module in Life Sciencespp.164-188, (2022)
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