Risultati della ricerca - Jasper J. Saris

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  1. 1
    Prorenin Induces Intracellular Signaling in Cardiomyocytes Independently of Angiotensin II

    Prorenin Induces Intracellular Signaling in Cardiomyocytes Independently of Angiotensin II di Jasper J. Saris, Peter A.C. ‘t Hoen, Ingrid M. Garrelds, Dick H. W. Dekkers, Johan T. den Dunnen, Jos M. J. Lamers, A.H. Jan Danser

    Pubblicazione 2006
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  2. 2
    Prorenin-Induced Myocyte Proliferation

    Prorenin-Induced Myocyte Proliferation di Jasper J. Saris, Mark M. E. D. van den Eijnden, Jos M. J. Lamers, Pramod R. Saxena, Maarten A.D.H. Schalekamp, A.H. Jan Danser

    Pubblicazione 2002
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  3. 3
    Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).

    Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1). di M.H. Breuning, F.G.M. Snijdewint, HG Brunner, A. Verwest, Jacob W. IJdo, Jasper J. Saris, Johannes G. Dauwerse, Lau Blonden, Tim P. Keith, David F. Callen

    Pubblicazione 1990
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  4. 4
    High-affinity prorenin binding to cardiac man-6-P/IGF-II receptors precedes proteolytic activation to renin

    High-affinity prorenin binding to cardiac man-6-P/IGF-II receptors precedes proteolytic activation to renin di Jasper J. Saris, F. H. M. Derkx, René J.A. de Bruin, Dick H. W. Dekkers, Jos M. J. Lamers, Pramod R. Saxena, Maarten A.D.H. Schalekamp, A.H. Jan Danser

    Pubblicazione 2001
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  5. 5
    A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2)

    A Spectrum of Mutations in the Second Gene for Autosomal Dominant Polycystic Kidney Disease (PKD2) di Barbera Veldhuisen, Jasper J. Saris, Simone de Haij, Tomohito Hayashi, David M. Reynolds, Toshio Mochizuki, R Elles, Ragnheiður Fossdal, Nadja Bogdanova, Marjan A. van Dijk, Eliécer Coto, David Ravine, Søren Nørby, C. Verellen‐Dumoulin, M.H. Breuning, Stefan Somlo, Dorien J.M. Peters

    Pubblicazione 1997
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  6. 6
    Web-accessible application for identifying pathogenic transcripts with RNA-seq: Increased sensitivity in diagnosis of neurodevelopmental disorders

    Web-accessible application for identifying pathogenic transcripts with RNA-seq: Increased sensitivity in diagnosis of neurodevelopmental disorders di Jordy Dekker, Rachel Schot, Michiel Bongaerts, Walter G. de Valk, Monique M. van Veghel–Plandsoen, Kathryn Monfils, Hannie Douben, Peter Elfferich, Esmee Kasteleijn, Leontine van Unen, Geert Geeven, Jasper J. Saris, Yvette van Ierland, Frans W. Verheijen, Marianne L. T. van der Sterre, Farah Sadeghi Niaraki, Daphne J. Smits, Hidde H. Huidekoper, Monique Williams, Martina Wilke, Virginie J. M. Verhoeven, Marieke Joosten, Anneke J.A. Kievit, Ingrid M.B.H. van de Laar, Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Mark Nellist, Grazia M.S. Mancini, Tjakko J. van Ham

    Pubblicazione 2023
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  7. 7
    Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

    Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects di Terry Vrijenhoek, Ken Kraaijeveld, Martin Elferink, Joep de Ligt, Elcke Kranendonk, Gijs W.E. Santen, Isaäc J. Nijman, Derek Butler, Godelieve R.F. Claes, Adalberto Costessi, Wim Dorlijn, Winfried van Eyndhoven, Dicky Halley, Mirjam C. G. N. van den Hout, Steven van Hove, Lennart Johansson, Jan D.H. Jongbloed, Rick Kamps, Christel Kockx, Bart de Koning, Marjolein Kriek, Ronald Lekanne dit Deprez, Hans Lunstroo, Marcel M.A.M. Mannens, Olaf R.F. Mook, Marcel Nelen, M.C. Ploem, Marco Rijnen, Jasper J. Saris, Richard J. Sinke, Erik A. Sistermans, Marjon van Slegtenhorst, Frank Sleutels, Nienke van der Stoep, Marianne van Tienhoven, Martijn Vermaat, Maartje J. Vogel, Quinten Waisfisz, Janneke Weiss, Arthur van den Wijngaard, Wilbert van Workum, Helger Ijntema, Bert van der Zwaag, Wilfred F. J. van IJcken, Johan T. den Dunnen, Joris A. Veltman, Raoul C. M. Hennekam, Edwin Cuppen

    Pubblicazione 2015
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