Resultats de la cerca - B A Oostra

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  1. 1
    A fragile balance: FMR1 expression levels

    A fragile balance: FMR1 expression levels per B.A. Oostra, R. Willemsen

    Publicat 2003
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  2. 2
    Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation.

    Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation. per B. A. Oostra, Peter B. Jacky, W. Ted Brown, François Rousseau

    Publicat 1993
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  3. 3
    Trinucleotide repeat polymorphism in the androgen receptor gene (AR)

    Trinucleotide repeat polymorphism in the androgen receptor gene (AR) per H.F.B.M. SIeddens, B. A. Oostra, Brinkmann Ao, Jan Trapman

    Publicat 1992
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  4. 4
    In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome

    In Vitro Reactivation of the FMR1 Gene Involved in Fragile X Syndrome per Pietro Chiurazzi, Maria Grazia Pomponi, R. Willemsen, B.A. Oostra, Giovanni Neri

    Publicat 1998
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  5. 5
    Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients

    Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients per Esther de Graaff, Patricia Rouillard, Patrick J. Willems, Anne Smits, François Rousseau, B. A. Oostra

    Publicat 1995
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  6. 6
    Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex.

    Primary structure and processing of lysosomal alpha-glucosidase; homology with the intestinal sucrase-isomaltase complex. per L. H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Marian A. Kroos, J. Van Beeumen, Arnold Reuser, B. A. Oostra

    Publicat 1988
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  7. 7
    <i>ACE</i> Polymorphisms

    <i>ACE</i> Polymorphisms per Fakhredin A. Sayed‐Tabatabaei, B.A. Oostra, Aaron Isaacs, Cornelia M. van Duijn, J. C. M. Witteman

    Publicat 2006
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  8. 8
    Ectopic expression of CGG containing mRNA is neurotoxic in mammals

    Ectopic expression of CGG containing mRNA is neurotoxic in mammals per Vera I. Hashem, James N. Galloway, M. Mori, R. Willemsen, B.A. Oostra, Richard Paylor, David L. Nelson

    Publicat 2009
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  9. 9
    EVI5 is a risk gene for multiple sclerosis

    EVI5 is a risk gene for multiple sclerosis per Ilse A Hoppenbrouwers, Yurii S. Aulchenko, George C. Ebers, S. V. Ramagopalan, B. A. Oostra, Cornelia M. van Duijn, Rogier Q. Hintzen

    Publicat 2008
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  10. 10
    Normal phenotype in two brothers with a full FMR1 mutation

    Normal phenotype in two brothers with a full FMR1 mutation per H. J. M. Smeets, Anne Smits, Coleta Verheij, Joop Theelen, Rob Willemsen, I. van der Bürgt, A. T. Hoogeveen, JC Oosterwijk, B. A. Oostra

    Publicat 1995
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  11. 11
    Instability of a (CGG)98 repeat in the Fmr1 promoter

    Instability of a (CGG)98 repeat in the Fmr1 promoter per Carola Bontekoe, C.E. Bakker, Ingeborg M. Nieuwenhuizen, Herma van der Linde, Hannes Lans, Desiree De Lange, Mark C. Hirst, B. A. Oostra

    Publicat 2001
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  12. 12
    Sex-specific genetic effects influence variation in body composition

    Sex-specific genetic effects influence variation in body composition per M. Carola Zillikens, Mojgan Yazdanpanah, Luba M. Pardo, Fernando Rivadeneira, Yurii S. Aulchenko, B. A. Oostra, André G. Uitterlinden, Huibert A. P. Pols, Cornelia M. van Duijn

    Publicat 2008
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  13. 13
    Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique

    Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique per Rob Willemsen, Arie Smits, Serieta Mohkamsing, H. van Beerendonk, Anton de Haan, Bert de Vries, Ans van den Ouweland, Erik A. Sistermans, H. Galjaard, B. A. Oostra

    Publicat 1997
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  14. 14
    Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families

    Hereditary frontotemporal dementia is linked to chromosome 17q21—q22: A genetic and clinicopathological study of three dutch families per Peter Heutink, M Stevens, Patrizia Rizzu, Egbert Bakker, J. M. Kros, Aad Tibben, Martinus F. Niermeijer, Cornelia M. van Duijn, B. A. Oostra, John C. van Swieten

    Publicat 1997
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  15. 15
    Alternative splicing in the fragile X gene <i>FMR1</i>

    Alternative splicing in the fragile X gene <i>FMR1</i> per Annemieke J.M.H. Verkerk, Esther de Graaff, Kristel De Boulle, Evan E. Eichler, David Konecki, Edwin Reyniers, Antonella Manca, Annemarie Poustka, Patrick J. Willems, David L. Nelson, B. A. Oostra

    Publicat 1993
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  16. 16
    Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family.

    Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family. per Bert B de Vries, C. C. Jansen, Annelien Duits, Coleta Verheij, Rob Willemsen, J. O. Van Hemel, A M van den Ouweland, Martinus F. Niermeijer, B. A. Oostra, D. J. J. Halley

    Publicat 1996
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  17. 17
    Heritability of the Function and Structure of the Arterial Wall

    Heritability of the Function and Structure of the Arterial Wall per Fakhredin A. Sayed‐Tabatabaei, Marie Josee E. van Rijn, Anna FC Schut, Yurii S. Aulchenko, Esther Croes, M. Carola Zillikens, Huibert A. P. Pols, Jacqueline C.M. Witteman, B. A. Oostra, Cornelia M. van Duijn

    Publicat 2005
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  18. 18
    Genome-wide analyses of borderline personality features

    Genome-wide analyses of borderline personality features per Gitta H. Lubke, Charles Laurin, Najaf Amin, J-J Hottenga, Gonneke Willemsen, Gerard van Grootheest, Abdel Abdellaoui, Lennart C. Karssen, B. A. Oostra, Cornelia M. van Duijn, Brenda W.J.H. Penninx, Dorret I. Boomsma

    Publicat 2013
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  19. 19
    Shared genetic factors in migraine and depression

    Shared genetic factors in migraine and depression per A. H. Stam, Boukje de Vries, A. Cecile J.W. Janssens, Kaate R. J. Vanmolkot, Yurii S. Aulchenko, Peter Henneman, B. A. Oostra, Rune R. Frants, Arn M. J. M. van den Maagdenberg, Michel D. Ferrari, Cornelia M. van Duijn, Gisela M. Terwindt

    Publicat 2010
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  20. 20
    Genetic risk profiles for depression and anxiety in adult and elderly cohorts

    Genetic risk profiles for depression and anxiety in adult and elderly cohorts per Ayşe Demirkan, Brenda W.J.H. Penninx, Karin Hek, Naomi R. Wray, Najaf Amin, Yurii S. Aulchenko, Richard van Dyck, Eco J. C. de Geus, Roelande Hofman, André G. Uitterlinden, J-J Hottenga, W.A. Nolen, B. A. Oostra, Patrick F. Sullivan, Gonneke Willemsen, Frans G. Zitman, Henning Tiemeier, A. Cecile J.W. Janssens, Dorret I. Boomsma, Cornelia M. van Duijn, Christel M. Middeldorp

    Publicat 2010
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