Výsledky vyhledávání - Annette F. Baas

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  1. 1
    Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRAD

    Activation of the tumour suppressor kinase LKB1 by the STE20-like pseudokinase STRAD Autor Annette F. Baas

    Vydáno 2003
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  2. 2
    Wnt Activates the Tak1/Nemo-like Kinase Pathway

    Wnt Activates the Tak1/Nemo-like Kinase Pathway Autor Linda Smit, Annette F. Baas, Jeroen Kuipers, Hendrik C. Korswagen, Marc van de Wetering, Hans Clevers

    Vydáno 2004
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  3. 3
    Truncating Titin ( TTN) Variants in Chemotherapy-Induced Cardiomyopathy

    Truncating Titin ( TTN) Variants in Chemotherapy-Induced Cardiomyopathy Autor Marijke Linschoten, Arco J. Teske, Annette F. Baas, Aryan Vink, Dennis Dooijes, Hubert F. Baars, Folkert W. Asselbergs

    Vydáno 2017
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  4. 4
    <i>Drosophila</i> Apc2 Is a Cytoskeletally-Associated Protein That Regulates Wingless Signaling in the Embryonic Epidermis

    <i>Drosophila</i> Apc2 Is a Cytoskeletally-Associated Protein That Regulates Wingless Signaling in the Embryonic Epidermis Autor Brooke M. McCartney, Herman A. Dierick, Catherine Kirkpatrick, Melissa M. Moline, Annette F. Baas, Mark Peifer, Amy Bejsovec

    Vydáno 1999
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  5. 5
    Complete Polarization of Single Intestinal Epithelial Cells upon Activation of LKB1 by STRAD

    Complete Polarization of Single Intestinal Epithelial Cells upon Activation of LKB1 by STRAD Autor Annette F. Baas, Jeroen Kuipers, Nicole N. van der Wel, Eduard Batlle, Henk K. Koerten, Peter J. Peters, Hans Clevers

    Vydáno 2004
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  6. 6
    MO25 / interact with STRAD / enhancing their ability to bind, activate and localize LKB1 in the cytoplasm

    MO25 / interact with STRAD / enhancing their ability to bind, activate and localize LKB1 in the cytoplasm Autor Jérôme Boudeau, Annette F. Baas, Mária Deák, Nick Morrice, Agnieszka Kieloch, Mike Schutkowski, Alan R. Prescott, Hans Clevers, Dario R. Alessi

    Vydáno 2003
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  7. 7
    Statin therapy is associated with improved survival after endovascular and open aneurysm repair

    Statin therapy is associated with improved survival after endovascular and open aneurysm repair Autor Jorg L. de Bruin, Annette F. Baas, Martijn W. Heymans, M.G. Buimer, Monique Prinssen, Diederick E. Grobbee, Jan D. Blankensteijn

    Vydáno 2013
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  8. 8
    Functional analysis of Peutz–Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity

    Functional analysis of Peutz–Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity Autor Christelle Forcet, Sandrine Etienne‐Manneville, Hélène Gaude, Laurence Fournier, Sébastien Debilly, Marko Salmi, Annette F. Baas, Sylviane Olschwang, Hans Clevers, Marc Billaud

    Vydáno 2005
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  9. 9
    A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle‐specific genes

    A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle‐specific genes Autor Magdaléna Harakaľová, Gijs J.M. Kummeling, Arjan Sammani, Marijke Linschoten, Annette F. Baas, Jasper van der Smagt, Pieter A. Doevendans, J. Peter van Tintelen, Dennis Dooijes, Michal Mokrý, Folkert W. Asselbergs

    Vydáno 2015
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  10. 10
    Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring

    Chromothripsis in Healthy Individuals Affects Multiple Protein-Coding Genes and Can Result in Severe Congenital Abnormalities in Offspring Autor Mirjam S. de Pagter, Markus J. van Roosmalen, Annette F. Baas, Ivo Renkens, Karen Duran, Ellen van Binsbergen, Masoumeh Tavakoli‐Yaraki, Ron Hochstenbach, Lars T. van der Veken, Edwin Cuppen, Wigard P. Kloosterman

    Vydáno 2015
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  11. 11
    Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience

    Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience Autor Maaike Brons, Steven A. Muller, Frans H. Rutten, Manon G. van der Meer, Alexander F. J. E. Vrancken, Monique C. Minnema, Annette F. Baas, Folkert W. Asselbergs, Marish I.F.J. Oerlemans

    Vydáno 2022
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  12. 12
    Long-Term Outcome of Open or Endovascular Repair of Abdominal Aortic Aneurysm

    Long-Term Outcome of Open or Endovascular Repair of Abdominal Aortic Aneurysm Autor Jorg L. de Bruin, Annette F. Baas, Jaap Buth, Monique Prinssen, Eric L.G. Verhoeven, Philippe W.M. Cuypers, Marc R.H.M. van Sambeek, Ron Balm, Diederick E. Grobbee, Jan D. Blankensteijn

    Vydáno 2010
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  13. 13
    UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking

    UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking Autor Arjan Sammani, M. Jansen, Marijke Linschoten, Ayoub Bagheri, Nicolaas de Jonge, Hans Kirkels, Linda W. van Laake, Aryan Vink, J. Peter van Tintelen, Dennis Dooijes, Anneline S.J.M. te Riele, Magdaléna Harakaľová, Annette F. Baas, Folkert W. Asselbergs

    Vydáno 2019
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  14. 14
    Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population

    Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population Autor Mimount Bourfiss, Marion van Vugt, Abdulrahman Alasiri, Bram Ruijsink, Jessica van Setten, Amand F. Schmidt, Dennis Dooijes, Esther Puyol‐Antón, Birgitta K. Velthuis, J. Peter van Tintelen, Anneline S.J.M. te Riele, Annette F. Baas, Folkert W. Asselbergs

    Vydáno 2022
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  15. 15
    Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome

    Agenesis of the corpus callosum and gray matter heterotopia in three patients with constitutional mismatch repair deficiency syndrome Autor Annette F. Baas, Michael T. Gabbett, Milan Rimac, Minttu Kansikas, Martine Raphaël, Rutger A. J. Nievelstein, Wayne Nicholls, Johan Offerhaus, Daniëlle Bodmer, Annekatrin Wernstedt, Birgit Krabichler, Ulrich Strasser, Minna Nyström, Johannes Zschocke, Stephen P. Robertson, Mieke M. van Haelst, Katharina Wimmer

    Vydáno 2012
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  16. 16
    Yield of family screening for dilated cardiomyopathy: 10-year experience at a multidisciplinary cardiogenetic outpatient clinic

    Yield of family screening for dilated cardiomyopathy: 10-year experience at a multidisciplinary cardiogenetic outpatient clinic Autor Isabelle Thierry, Steven A. Muller, Annette F. Baas, Dennis Dooijes, Rosa Laura E. van Loon, Angela E. Schoemaker, Pim van der Harst, Marish I.F.J. Oerlemans, Hubert F. Baars, Rutger J. Hassink, Folkert W. Asselbergs, J. Peter van Tintelen, Anneline S.J.M. te Riele

    Vydáno 2025
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  17. 17
    Pregnancy and Delivery Outcomes in Vascular Ehlers–Danlos Syndrome: A Retrospective Multicentre Cohort Study

    Pregnancy and Delivery Outcomes in Vascular Ehlers–Danlos Syndrome: A Retrospective Multicentre Cohort Study Autor Lisa M. van den Bersselaar, Ingrid M.B.H. van de Laar, Marieke J.H. Baars, Annette F. Baas, Eelco Dulfer, Apollonia T. J. M. Helderman‐van den Enden, Yvonne Hilhorst‐Hofstee, Robert M. Kauling, Marlies Kempers, Martijn A. Oudijk, Alessandra Maugeri, Hennie T. Brüggenwirth, Arjan C. Houweling, Serwet Demirdas

    Vydáno 2025
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  18. 18
    CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

    CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene Autor M.C.J. Jongmans, R.J.C. Admiraal, Kim P. van der Donk, Lisenka E.L.M. Vissers, Annette F. Baas, Livia Kapusta, Johanna M. van Hagen, D Donnai, Thomy de Ravel, Joris A. Veltman, Ad Geurts van Kessel, Bert B.A. de Vries, Han G. Brunner, Lies H. Hoefsloot, Conny M.A. van Ravenswaaij

    Vydáno 2005
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  19. 19
    Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy

    Individualized Family Screening for Arrhythmogenic Right Ventricular Cardiomyopathy Autor Steven A. Muller, Alessio Gasperetti, Laurens P. Bosman, Amand F. Schmidt, Annette F. Baas, Ahmad S. Amin, Arjan C. Houweling, Arthur A.M. Wilde, Paolo Compagnucci, Mattia Targetti, Michela Casella, Leonardo Calò, Claudio Tondo, Pim van der Harst, Folkert W. Asselbergs, J. Peter van Tintelen, Marish I.F.J. Oerlemans, Anneline S.J.M. te Riele

    Vydáno 2023
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  20. 20
    Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant

    Additional genetic variants in cardiomyopathy patients with the pathogenic PLN p.(Arg14del) founder variant Autor Esmée van Drie, Jan D.H. Jongbloed, Edgar T. Hoorntje, Paul A. van der Zwaag, Moniek G.P.J. Cox, Ronald H. Lekanne Deprez, Arjan C. Houweling, Virginnio Proost, A. A. M. Wilde, Dennis Dooijes, Annette F. Baas, Anneline S.J.M. te Riele, Karin Y. van Spaendonck‐Zwarts, Elisabeth M. Lodder, J. Peter van Tintelen

    Vydáno 2025
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