نتائج البحث - Peter Propping

تنقيح النتائج
  1. 1
    A similarity-based method for genome-wide prediction of disease-relevant human genes

    A similarity-based method for genome-wide prediction of disease-relevant human genes حسب Johannes Freudenberg, Peter Propping

    منشور في 2002
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    Artigo
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  2. 2
    An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics

    An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics حسب Sigrid Weiland, Veit Witzemann, Alfredo Villarroel, Peter Propping, Ortrud K. Steinlein

    منشور في 1996
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    Artigo
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  3. 3
    Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome

    Hereditary Nonpolyposis Colorectal Cancer (HNPCC)/Lynch Syndrome حسب Verena Steinke, Christoph Engel, Reinhard Büttner, Hans Konrad Schackert, Wolff Schmiegel, Peter Propping

    منشور في 2013
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    Revisão
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  4. 4
    Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis

    Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis حسب Stefan Aretz, Siegfried Uhlhaas, Reiner Caspari, Elisabeth Mangold, Constanze Pagenstecher, Peter Propping, Waltraut Friedl

    منشور في 2003
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  5. 5
    Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in <i>MSH2</i> and <i>MLH1</i> genes

    Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in <i>MSH2</i> and <i>MLH1</i> genes حسب Yaping Wang, Waltraut Friedl, Christof Lamberti, Matthias Jungck, Micaela Mathiak, Constanze Pagenstecher, Peter Propping, Elisabeth Mangold

    منشور في 2002
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  6. 6
    Somatic<i>APC</i>mosaicism: a frequent cause of familial adenomatous polyposis (FAP)

    Somatic<i>APC</i>mosaicism: a frequent cause of familial adenomatous polyposis (FAP) حسب Stefan Aretz, Dietlinde Stienen, Nicolaus Friedrichs, Susanne Stemmler, Siegfried Uhlhaas, Nils Rahner, Peter Propping, Waltraut Friedl

    منشور في 2007
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  7. 7
    Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins

    Genetic Contribution to Variation in Cognitive Function: An fMRI Study in Twins حسب Jan Willem Koten, Guilherme Wood, Peter Hagoort, Rainer Goebel, Peter Propping, Klaus Willmes, Dorret I. Boomsma

    منشور في 2009
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  8. 8
    Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and Hyperplasias

    Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and Hyperplasias حسب Roland Kruse, Nadine Schweiger, Eva Jakob, Thomas Ruzicka, Arno Rütten, Micaela Mathiak, Peter Propping, Elisabeth Mangold, Michele Bisceglia

    منشور في 2003
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  9. 9
    Evidence for Linkage of Spelling Disability to Chromosome 15

    Evidence for Linkage of Spelling Disability to Chromosome 15 حسب Gerd Schulte‐Körne, T. Grimm, Markus M. Nöthen, Bertram Müller‐Myhsok, Sven Cichon, Ina R. Vogt, Peter Propping, Helmut Remschmidt

    منشور في 1998
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    Carta
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  10. 10
    Efficacy and Side-Effects of Clozapine: Testing for Association with Allelic Variation in the Dopamine D4 Receptor Gene

    Efficacy and Side-Effects of Clozapine: Testing for Association with Allelic Variation in the Dopamine D4 Receptor Gene حسب Marcella Rietschel, Dieter Naber, Heinrich Oberländer, Rüdiger Holzbach, Roulf Fimmers, Katja Eggermann, Hans‐Jürgen Möller, Peter Propping, Markus M. Nöthen

    منشور في 1996
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    Artigo
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  11. 11
    <i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

    <i>MUTYH</i>‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype حسب Stefan Aretz, Siegfried Uhlhaas, Heike Goergens, Kirsten Siberg, Matthias Vogel, Constanze Pagenstecher, Elisabeth Mangold, Reiner Caspari, Peter Propping, Waltraut Friedl

    منشور في 2006
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    Artigo
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  12. 12
    Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer

    Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with col... حسب C. Lamberti, Roland Kruse, Corina Ruelfs, Reiner Caspari, Y Wang, Matthias Jungck, Micaela Mathiak, Hamid Reza Hosseiny Malayeri, Waltraut Friedl, Tilman Sauerbruch, Peter Propping

    منشور في 1999
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  13. 13
    High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome

    High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome حسب Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, Steffan Loff, Walter Back, Constanze Pagenstecher, D. Ross McLeod, Gail E. Graham, Elisabeth Mangold, René Santer, Peter Propping, Waltraut Friedl

    منشور في 2005
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  14. 14
    Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease

    Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease حسب S Metzger, Rong Jiang, Huu Phuc Nguyen, Austin Cape, Jürgen Tomiuk, Anne S. Soehn, Peter Propping, Yun Freudenberg‐Hua, Jan Freudenberg, Liang Tong, S.-H. Li, Xing Li, O. Riess

    منشور في 2008
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  15. 15
    Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria

    Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria حسب Roland Kruse, Arno Rütten, Christof Lamberti, Hamid Reza Hosseiny–Malayeri, Yaping Wang, Corina Ruelfs, Matthias Jungck, Micaela Mathiak, Thomas Ruzicka, Wolfgang Hartschuh, Michele Bisceglia, Waltraut Friedl, Peter Propping

    منشور في 1998
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  16. 16
    Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis

    Expanded Extracolonic Tumor Spectrum in MUTYH-Associated Polyposis حسب Stefanie Vogt, Natalie B. Jones, Daria Christian, Christoph Engel, Maartje Nielsen, Astrid Kaufmann, Verena Steinke, Hans F. A. Vasen, Peter Propping, Julian R. Sampson, Frederik J. Hes, Stefan Aretz

    منشور في 2009
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  17. 17
    Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder

    Excess of High Activity Monoamine Oxidase A Gene Promoter Alleles in Female Patients with Panic Disorder حسب J. Deckert, Marco Catalano, Yana V. Syagailo, Monica Bosi, Olga Okladnova, Daniela Di Bella, Markus M. Nöthen, Pietro Maffei, Petra Franke, J. Fritze, W. Maier, Peter Propping, H. Beckmann, Laura Bellodi, Klaus‐Peter Lesch

    منشور في 1999
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  18. 18
    High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome

    High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome حسب Stefan Aretz, Dietlinde Stienen, Siegfried Uhlhaas, M. Stolte, Mark M. Entius, Steffan Loff, Walter Back, Astrid Kaufmann, KM Keller, Stefan Blaas, Reiner Siebert, Stefanie Vogt, S Spranger, Elke Holinski‐Feder, Lone Sunde, Peter Propping, W Friedl

    منشور في 2007
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  19. 19
    Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder

    Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder حسب Thomas G. Schulze, Sevilla D. Detera‐Wadleigh, Nirmala Akula, Ajay Gupta, Layla Kassem, J. Douglas Steele, Justin Pearl, Jana Strohmaier, René Breuer, Markus Schwarz, Peter Propping, Markus M. Nöthen, Sven Cichon, J Schumacher, Marcella Rietschel, Francis J. McMahon

    منشور في 2008
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  20. 20
    Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

    Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families حسب Markus M. Nöthen, Sven Cichon, H. Rohleder, Susanne Hemmer, Ernst Franzek, J. Fritze, Margot Albus, Margitta Borrmann-Hassenbach, R. Kreiner, Bettina Weigelt, Jürgen Minges, Dirk Lichtermann, W. Maier, Nick Craddock, Rolf Fimmers, Tobias Höller, Max P. Baur, Marcella Rietschel, Peter Propping

    منشور في 1999
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