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  1. Article

    Open Access

    Synaptotagmin-13 orchestrates pancreatic endocrine cell egression and islet morphogenesis

    During pancreas development endocrine cells leave the ductal epithelium to form the islets of Langerhans, but the morphogenetic mechanisms are incompletely understood. Here, we identify the Ca2+-independent atypi...

    Mostafa Bakhti, Aimée Bastidas-Ponce, Sophie Tritschler in Nature Communications (2022)

  2. Article

    Open Access

    Bardet-Biedl syndrome proteins modulate the release of bioactive extracellular vesicles

    Primary cilia are microtubule based sensory organelles important for receiving and processing cellular signals. Recent studies have shown that cilia also release extracellular vesicles (EVs). Because EVs have ...

    Ann-Kathrin Volz, Alina Frei, Viola Kretschmer in Nature Communications (2021)

  3. Article

    Open Access

    The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus

    Cilia are protrusions of the cell surface and composed of hundreds of proteins many of which are evolutionary and functionally well conserved. In cells assembling motile cilia the expression of numerous ciliar...

    Anja Beckers, Franziska Fuhl, Tim Ott, Karsten Boldt in Scientific Reports (2021)

  4. Article

    Open Access

    CFAP45 deficiency causes situs abnormalities and asthenospermia by disrupting an axonemal adenine nucleotide homeostasis module

    Axonemal dynein ATPases direct ciliary and flagellar beating via adenosine triphosphate (ATP) hydrolysis. The modulatory effect of adenosine monophosphate (AMP) and adenosine diphosphate (ADP) on flagellar bea...

    Gerard W. Dougherty, Katsutoshi Mizuno, Tabea Nöthe-Menchen in Nature Communications (2020)

  5. Article

    Open Access

    Extensive rewiring of the EGFR network in colorectal cancer cells expressing transforming levels of KRASG13D

    Protein-protein-interaction networks (PPINs) organize fundamental biological processes, but how oncogenic mutations impact these interactions and their functions at a network-level scale is poorly understood. ...

    Susan A. Kennedy, Mohamed-Ali Jarboui, Sriganesh Srihari in Nature Communications (2020)

  6. Article

    Open Access

    The evolutionary conserved FOXJ1 target gene Fam183b is essential for motile cilia in Xenopus but dispensable for ciliary function in mice

    The transcription factor FOXJ1 is essential for the formation of motile cilia throughout the animal kingdom. Target genes therefore likely constitute an important part of the motile cilia program. Here, we rep...

    Anja Beckers, Tim Ott, Karin Schuster-Gossler, Karsten Boldt in Scientific Reports (2018)

  7. Article

    Open Access

    A subset of RAB proteins modulates PP2A phosphatase activity

    Protein phosphatase 2A (PP2A) is one of the most abundant serine–threonine phosphatases in mammalian cells. PP2A is a hetero-trimeric holoenzyme participating in a variety of physiological processes whose dere...

    Francesca Sacco, Anna Mattioni, Karsten Boldt, Simona Panni in Scientific Reports (2016)

  8. Article

    Open Access

    An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

    Cellular organelles provide opportunities to relate biological mechanisms to disease. Here we use affinity proteomics, genetics and cell biology to interrogate cilia: poorly understood organelles, where defect...

    Karsten Boldt, Jeroen van Reeuwijk, Qianhao Lu in Nature Communications (2016)

  9. Article

    Open Access

    Correction: Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

    Nature Communications 6: Article number:7074 (2015); Published: 05 June 2015; Updated: 29 Marrch 2016 The financial support for this article was not fully acknowledged. The Acknowledgements should have include...

    Miriam Schmidts, Yuqing Hou, Claudio R. Cortés, Dorus A. Mans in Nature Communications (2016)

  10. Article

    Open Access

    TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

    The analysis of individuals with ciliary chondrodysplasias can shed light on sensitive mechanisms controlling ciliogenesis and cell signalling that are essential to embryonic development and survival. Here we ...

    Miriam Schmidts, Yuqing Hou, Claudio R. Cortés, Dorus A. Mans in Nature Communications (2015)