Torthaí cuardaigh - Niels Tommerup

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  1. 1
    Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders.

    Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disorders. de réir Niels Tommerup

    Foilsithe / Cruthaithe 1993
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  2. 2
    5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation.

    5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation. de réir Niels Tommerup, Hanne Poulsen, Karen Brøndum‐Nielsen

    Foilsithe / Cruthaithe 1981
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  3. 3
    Repression of transcriptional activity by heterologous KRAB domains present in zinc finger proteins

    Repression of transcriptional activity by heterologous KRAB domains present in zinc finger proteins de réir Henrik Vissing, Wolfram Meyer, Lissi Aagaard, Niels Tommerup, Hans‐Jürgen Thiesen

    Foilsithe / Cruthaithe 1995
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  4. 4
    Occurrence of cancer in women with Turner syndrome

    Occurrence of cancer in women with Turner syndrome de réir Henrik Hasle, Jørgen H. Olsen, Jørgen Nielsen, Jan Hansen, U Friedrich, Niels Tommerup

    Foilsithe / Cruthaithe 1996
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  5. 5
    Intrafamilial variation of the phenotype in Bardet-Biedl syndrome

    Intrafamilial variation of the phenotype in Bardet-Biedl syndrome de réir Ruth Riise, Sten Andréasson, M. Borgström, Alan F. Wright, Niels Tommerup, Thomas Rosenberg, Kristina Törnqvist

    Foilsithe / Cruthaithe 1997
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  6. 6
    The Human Intrinsic Factor-Vitamin B12 Receptor,Cubilin: Molecular Characterization and Chromosomal Mapping of the Gene to 10p Within the Autosomal Recessive Megaloblastic Anemia (MGA1) Region

    The Human Intrinsic Factor-Vitamin B12 Receptor,Cubilin: Molecular Characterization and Chromosomal Mapping of the Gene to 10p Within the Autosomal Recessive Megaloblastic Anemia (... de réir Renata Kozyraki, Mette Kristiansen, Asli Silahtaroglu, Claus Hansen, Christian Jacobsen, Niels Tommerup, P Verroust, Søren K. Moestrup

    Foilsithe / Cruthaithe 1998
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  7. 7
    MicroRNA expression in the adult mouse central nervous system

    MicroRNA expression in the adult mouse central nervous system de réir Mads Bak, Asli Silahtaroglu, Morten Møller, Mette Christensen, Martin F. Rath, Boris V. Skryabin, Niels Tommerup, Sakari Kauppinen

    Foilsithe / Cruthaithe 2008
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  8. 8
    REST–Mediated Recruitment of Polycomb Repressor Complexes in Mammalian Cells

    REST–Mediated Recruitment of Polycomb Repressor Complexes in Mammalian Cells de réir Nikolaj Dietrich, Mads Lerdrup, Eskild Landt, Shuchi Agrawal‐Singh, Mads Bak, Niels Tommerup, Juri Rappsilber, Erik Södersten, Klaus Hansen

    Foilsithe / Cruthaithe 2012
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  9. 9
    Jarid1b targets genes regulating development and is involved in neural differentiation

    Jarid1b targets genes regulating development and is involved in neural differentiation de réir Sandra U. Schmitz, Mareike Albert, Martina Malatesta, Lluís Morey, Jens Vilstrup Johansen, Mads Bak, Niels Tommerup, Iratxe Abarrategui, Kristian Helin

    Foilsithe / Cruthaithe 2011
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  10. 10
    Profiling microRNAs in lung tissue from pigs infected with Actinobacillus pleuropneumoniae

    Profiling microRNAs in lung tissue from pigs infected with Actinobacillus pleuropneumoniae de réir Agnieszka Podolska, Christian Anthon, Mads Bak, Niels Tommerup, Kerstin Skovgaard, Peter M. H. Heegaard, Jan Gorodkin, Susanna Cirera, Merete Fredholm

    Foilsithe / Cruthaithe 2012
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  11. 11
    Loss of the retinoblastoma protein-related p130 protein in small cell lung carcinoma

    Loss of the retinoblastoma protein-related p130 protein in small cell lung carcinoma de réir Kristian Helin, Karin Holm, Anita Niebuhr, Hans Eiberg, Niels Tommerup, Susanne Hougaard, Hans Skovgaard Poulsen, Mogens Spang‐Thomsen, Peter Nørgaard

    Foilsithe / Cruthaithe 1997
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  12. 12
    Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome

    Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome de réir J.M. Belloso, Iben Bache, Míriam Guitart, M.R. Caballı́n, Christina Halgren, Maria Kirchhoff, Hans‐Hilger Ropers, Niels Tommerup, Zeynep Tümer

    Foilsithe / Cruthaithe 2007
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  13. 13
    Heterogeneous Nuclear Ribonucleoproteins H, H′, and F Are Members of a Ubiquitously Expressed Subfamily of Related but Distinct Proteins Encoded by Genes Mapping to Different Chromosomes

    Heterogeneous Nuclear Ribonucleoproteins H, H′, and F Are Members of a Ubiquitously Expressed Subfamily of Related but Distinct Proteins Encoded by Genes Mapping to Different Chrom... de réir Bent Honoré, Hugo Hanne, Vorum Henrik, Dejgaard Kurt, Liu Xiangdang, Gromov Pavel, Peder Madsen, Gesser Borbala, Niels Tommerup, E. Celis Julio

    Foilsithe / Cruthaithe 1995
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  14. 14
    Comparative genomics beyond sequence-based alignments: RNA structures in the ENCODE regions

    Comparative genomics beyond sequence-based alignments: RNA structures in the ENCODE regions de réir Elfar Torarinsson, Zizhen Yao, Eric D. Wiklund, Jesper B. Bramsen, Claus Hansen, Jørgen Kjems, Niels Tommerup, Walter L. Ruzzo, Jan Gorodkin

    Foilsithe / Cruthaithe 2007
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  15. 15
    Molecular Characterization of a Novel Human Hybrid-type Receptor That Binds the α2-Macroglobulin Receptor-associated Protein

    Molecular Characterization of a Novel Human Hybrid-type Receptor That Binds the α2-Macroglobulin Receptor-associated Protein de réir Linda Jacobsen, Peder Madsen, Søren K. Moestrup, Anders H. Lund, Niels Tommerup, Anders Nykjær, Lars Sottrup‐Jensen, Jørgen Gliemann, Claus M. Petersen

    Foilsithe / Cruthaithe 1996
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  16. 16
    The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation

    The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation de réir Ana Carolina Fonseca, Adriano Bonaldi, Simone Aparecida Siqueira Fonseca, Paulo Alberto Otto, Fernando Kok, Mads Bak, Niels Tommerup, Angela Maria Vianna‐Morgante

    Foilsithe / Cruthaithe 2015
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  17. 17
    Genome-wide Analysis of CDX2 Binding in Intestinal Epithelial Cells (Caco-2)

    Genome-wide Analysis of CDX2 Binding in Intestinal Epithelial Cells (Caco-2) de réir Mette Boyd, Morten Hansen, Tine G.K. Jensen, Anna Perearnau, Anders Krüger Olsen, Lotte L. Bram, Mads Bak, Niels Tommerup, Jørgen Olsen, Jesper T. Troelsen

    Foilsithe / Cruthaithe 2010
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  18. 18
    A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies

    A Molecular Analysis of the Yemenite Deaf-Blind Hypopigmentation Syndrome: SOX10 Dysfunction Causes Different Neurocristopathies de réir Nadège Bondurand, Kirsten Kuhlbrodt, Véronique Pingault, Janna Enderich, M. Sajus, Niels Tommerup, Mette Warburg, Raoul C. M. Hennekam, Andrew Read, Michael Wegner, Michel Goossens

    Foilsithe / Cruthaithe 1999
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  19. 19
    A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation

    A Functional Link between the Histone Demethylase PHF8 and the Transcription Factor ZNF711 in X-Linked Mental Retardation de réir Daniela Kleine‐Kohlbrecher, Jesper Frank Christensen, Julien Vandamme, Iratxe Abarrategui, Mads Bak, Niels Tommerup, Xiaobing Shi, Or Gozani, Juri Rappsilber, Anna Elisabetta Salcini, Kristian Helin

    Foilsithe / Cruthaithe 2010
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  20. 20
    Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption?

    Mesomelia-synostoses syndrome: contiguous deletion syndrome, SULF1 haploinsufficiency or enhancer adoption? de réir Ingrid Bendas Feres Lima, Lúcia de Fátima Marques de Moraes, Carlos Roberto da Fonseca, Juan Clinton Llerena, Mana M. Mehrjouy, Niels Tommerup, Elenice Ferreira Bastos

    Foilsithe / Cruthaithe 2024
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