Resultados de búsqueda - Martijn H. Breuning

Limitar resultados
  1. 1
    Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2)

    Genes homologous to the autosomal dominant polycystic kidney disease genes (PKD1 and PKD2) por Barbera Veldhuisen, Lia Spruit, Hans G. Dauwerse, Martijn H. Breuning, Dorien J.M. Peters

    Publicado 1999
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  2. 2
    Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses

    Two-color multiplex ligation-dependent probe amplification: Detecting genomic rearrangements in hereditary multiple exostoses por Stefan J. White, Geraldine R. Vink, Marjolein Kriek, Wim Wuyts, Jan Schouten, Egbert Bakker, Martijn H. Breuning, Johan T. den Dunnen

    Publicado 2004
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  3. 3
    Comparison between siblings and twins supports a role for modifier genes in ADPKD

    Comparison between siblings and twins supports a role for modifier genes in ADPKD por Alexandre Persu, M. Duyme, Yves Pirson, Xosé M. Lens, T. Messiaen, Martijn H. Breuning, Dominique Chauveau, Micheline Lévy, Jean‐Pierre Grünfeld, Olivier Devuyst

    Publicado 2004
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  4. 4
    Scattered Deletion of PKD1 in Kidneys Causes a Cystic Snowball Effect and Recapitulates Polycystic Kidney Disease

    Scattered Deletion of PKD1 in Kidneys Causes a Cystic Snowball Effect and Recapitulates Polycystic Kidney Disease por Wouter N. Leonhard, Malu Zandbergen, Kimberley Veraar, Susan Berg, Louise van der Weerd, Martijn H. Breuning, Emile de Heer, Dorien J.M. Peters

    Publicado 2014
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  5. 5
    Diagnosis of genetic abnormalities in developmentally delayed patients: A new strategy combining MLPA and array‐CGH

    Diagnosis of genetic abnormalities in developmentally delayed patients: A new strategy combining MLPA and array‐CGH por Marjolein Kriek, Jeroen Knijnenburg, Stefan J. White, Carla Rosenberg, Johan T. den Dunnen, Gert‐Jan B. van Ommen, Hans J. Tanke, Martijn H. Breuning, Károly Szuhai

    Publicado 2007
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  6. 6
    Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase

    Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase por Saskia A.J. Lesnik Oberstein, Marjolein Kriek, Stefan J. White, M.E. Kalf, Károly Szuhai, Johan T. den Dunnen, Martijn H. Breuning, Raoul C. M. Hennekam

    Publicado 2006
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  7. 7
    Dose-Dependent Effects of Sirolimus on mTOR Signaling and Polycystic Kidney Disease

    Dose-Dependent Effects of Sirolimus on mTOR Signaling and Polycystic Kidney Disease por Zlata Novalić, Annemieke M. van der Wal, Wouter N. Leonhard, Gudrun E. Koehl, Martijn H. Breuning, Edward K. Geissler, Emile de Heer, Dorien J.M. Peters

    Publicado 2012
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  8. 8
    Pathogenic Sequence for Dissecting Aneurysm Formation in a Hypomorphic Polycystic Kidney Disease 1 Mouse Model

    Pathogenic Sequence for Dissecting Aneurysm Formation in a Hypomorphic Polycystic Kidney Disease 1 Mouse Model por Sabrine Hassane, Nanna Claij, Irma S Lantinga‐van Leeuwen, J. Conny van Munsteren, Natascha van Lent, Roeland Hanemaaijer, Martijn H. Breuning, Dorien J.M. Peters, Marco C. DeRuiter

    Publicado 2007
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  9. 9
    Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization

    Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization por Stefan J. White, M.E. Kalf, Qiang Liu, Michel P Villerius, Dieuwke Engelsma, Marjolein Kriek, Ellen Vollebregt, Egbert Bakker, Gert‐Jan B. van Ommen, Martijn H. Breuning, Johan T. den Dunnen

    Publicado 2002
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  10. 10
    Conventional and Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair in Hereditary Colorectal Tumors

    Conventional and Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair in Hereditary Colorectal Tumors por Yvonne Hendriks, Patrick Franken, Jan Willem F Dierssen, Wiljo de Leeuw, Juul Wijnen, Enno Dreef, Carli Tops, Martijn H. Breuning, Annette Bröcker‐Vriends, Hans F. A. Vasen, Riccardo Fodde, Hans Morreau

    Publicado 2003
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  11. 11
    Elevated TGFβ–Smad signalling in experimental <i>Pkd1</i> models and human patients with polycystic kidney disease

    Elevated TGFβ–Smad signalling in experimental <i>Pkd1</i> models and human patients with polycystic kidney disease por Sabrine Hassane, Wouter N. Leonhard, Annemieke van der Wal, Lukas J.A.C. Hawinkels, Irma S Lantinga‐van Leeuwen, Peter ten Dijke, Martijn H. Breuning, Emile de Heer, Dorien J.M. Peters

    Publicado 2010
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  12. 12
    Spectrum of Mutations in the Batten Disease Gene, CLN3

    Spectrum of Mutations in the Batten Disease Gene, CLN3 por Patricia B. Munroe, Hannah M. Mitchison, Angela O'Rawe, John W. Anderson, Rose-Mary Boustany, Terry J. Lerner, Peter E.M. Taschner, Nanneke de Vos, Martijn H. Breuning, R. Mark Gardiner, Sara Mole

    Publicado 1997
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  13. 13
    A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first

    A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first por Antoinet C.J. Gijsbers, Janet YK Lew, Cathy A.J. Bosch, Janneke Schuurs-Hoeijmakers, Arie van Haeringen, Nicolette S. den Hollander, Sarina G. Kant, Emilia K. Bijlsma, Martijn H. Breuning, Egbert Bakker, Claudia Ruivenkamp

    Publicado 2009
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  14. 14
    Lacunar Infarcts Are the Main Correlate With Cognitive Dysfunction in CADASIL

    Lacunar Infarcts Are the Main Correlate With Cognitive Dysfunction in CADASIL por Michael Liem, Jeroen van der Grond, Joost Haan, Rivka van den Boom, Michel D. Ferrari, Yvette M. Knaap, Martijn H. Breuning, Mark A. van Buchem, Huub A. M. Middelkoop, Saskia A.J. Lesnik Oberstein

    Publicado 2007
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  15. 15
    The clinical spectrum of complete FBN1 allele deletions

    The clinical spectrum of complete FBN1 allele deletions por Yvonne Hilhorst‐Hofstee, Ben C.J. Hamel, Joanne Verheij, M Rijlaarsdam, Grazia M.S. Mancini, Jan M. Cobben, Cindy Giroth, Claudia AL Ruivenkamp, Kerstin Hansson, Janneke Timmermans, Henriëtte A. Moll, Martijn H. Breuning, Gerard Pals

    Publicado 2010
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  16. 16
    Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease

    Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease por Alex Odermatt, Peter E.M. Taschner, Stephen W. Scherer, Barbara Beatty, Vijay K. Khanna, David R. Cornblath, Vinay Chaudhry, Won-Chee Yee, Bertold Schrank, George Karpati, Martijn H. Breuning, Nine Knoers, David H. MacLennan

    Publicado 1997
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  17. 17
    Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease

    Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease por Jeroen Roelfsema, Stefan J. White, Yavuz Ariyürek, Deborah Bartholdi, Dunja Niedrist, Francesco Papadia, Carlos A. Bacino, Johan T. den Dunnen, Gert‐Jan B. van Ommen, Martijn H. Breuning, Raoul C. M. Hennekam, Dorien J.M. Peters

    Publicado 2005
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  18. 18
    Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease

    Lowering of Pkd1 expression is sufficient to cause polycystic kidney disease por Irma S Lantinga‐van Leeuwen, Johannes G. Dauwerse, Hans J. Baelde, Wouter N. Leonhard, Annemieke van de Wal, Christopher J. Ward, Sjef Verbeek, Marco C. DeRuiter, Martijn H. Breuning, Emile de Heer, Dorien J.M. Peters

    Publicado 2004
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  19. 19
    Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene

    Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene por Yu Sun, Rowida Almomani, Emmelien Aten, Jacopo Celli, Jaap van der Heijden, Hanka Venselaar, Stephen P. Robertson, Anna Baroncini, Brunella Franco, Lina Basel‐Vanagaite, Emiko Horii, Ricardo Drut, Yavuz Ariyürek, Johan T. den Dunnen, Martijn H. Breuning

    Publicado 2010
    Enlace del recurso Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:
  20. 20
    Unified Criteria for Ultrasonographic Diagnosis of ADPKD

    Unified Criteria for Ultrasonographic Diagnosis of ADPKD por York Pei, James Obaji, Annie Dupuis, Andrew D. Paterson, Riccardo Magistroni, Elizabeth Dicks, Patrick S. Parfrey, B. Cramer, Eliécer Coto, Roser Torrá, José L. San Millán, Robert N. Gibson, Martijn H. Breuning, Dorien J.M. Peters, David Ravine

    Publicado 2008
    Enlace del recurso
    Artigo
    Agregar a favoritos
    Guardado en:

Herramientas de búsqueda: