Hakutulokset - Kathrin Saar

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  1. 1
    Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity

    Homozygosity Mapping in Families with Joubert Syndrome Identifies a Locus on Chromosome 9q34.3 and Evidence for Genetic Heterogeneity Tekijä Kathrin Saar, Lihadh Al‐Gazali, László Sztriha, Franz Rueschendorf, Mohammed Nur-E-Kamal, André Reis, Riad Bayoumi

    Julkaistu 1999
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  2. 2
    Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13

    Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13 Tekijä John C. Mulley, Kathrin Saar, Gerry Hewitt, Franz Rüschendorf, Hilary A. Phillips, Alison Colley, David Sillence, André Reis, Meredith Wilson

    Julkaistu 1998
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  3. 3
    PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption

    PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption Tekijä Eva L. Decker, Angelika Stellzig‐Eisenhauer, Britta Fiebig, Christiane Rau, Wolfram Kreß, Kathrin Saar, Franz Rüschendorf, Norbert Hübner, T. Grimm, Bernhard H. F. Weber

    Julkaistu 2008
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  4. 4
    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15 Tekijä Gerald Stöber, Kathrin Saar, Franz Rüschendorf, Jobst Meyer, Gudrun Nürnberg, Susanne Jatzke, Ernst Franzek, André Reis, Klaus‐Peter Lesch, Thomas F. Wienker, H. Beckmann

    Julkaistu 2000
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  5. 5
    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

    Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15 Tekijä Gerald Stöber, Kathrin Saar, Franz Rüschendorf, Jobst Meyer, Gudrun Nürnberg, Susanne Jatzke, Ernst Franzek, André Reis, Klaus‐Peter Lesch, Thomas F. Wienker, H. Beckmann

    Julkaistu 2000
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  6. 6
    Association of <i>AHSG</i> Gene Polymorphisms With Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study

    Association of <i>AHSG</i> Gene Polymorphisms With Fetuin-A Plasma Levels and Cardiovascular Diseases in the EPIC-Potsdam Study Tekijä Eva Fisher, Norbert Stefan, Kathrin Saar, Dagmar Drogan, Matthias B. Schulze, Andreas Fritsche, Hans‐Georg Joost, Hans‐Ulrich Häring, Norbert Hübner, Heiner Boeing, Cornelia Weikert

    Julkaistu 2009
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  7. 7
    WT1 controls antagonistic FGF and BMP-pSMAD pathways in early renal progenitors

    WT1 controls antagonistic FGF and BMP-pSMAD pathways in early renal progenitors Tekijä Fariba Jian Motamedi, Danielle A. Badro, Michael J. Clarkson, Maria Rita Lecca, Stephen Bradford, Fabian A. Buske, Kathrin Saar, Norbert Hübner, André W. Brändli, Andreas Schedl

    Julkaistu 2014
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  8. 8
    Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21

    Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21 Tekijä Katja Grohmann, Thomas F. Wienker, Kathrin Saar, Sabine Rudnik–Schöneborn, Gisela Stoltenburg‐Didinger, Rainer Rossi, Giuseppe Novelli, Gudrun Nürnberg, Arne Pfeufer, Brunhilde Wirth, André Reis, Klaus Zerres, Christoph Hübner

    Julkaistu 1999
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  9. 9
    A Genetic Basis for Mechanosensory Traits in Humans

    A Genetic Basis for Mechanosensory Traits in Humans Tekijä H Frenzel, Jörg Bohlender, Katrin Pinsker, B. Wohlleben, Jens Tank, Stefan G. Lechner, Daniela Schiska, Teresa Jaijo, Franz Rüschendorf, Kathrin Saar, Jens Jordan, José M. Millán, Manfred Gross, Gary R. Lewin

    Julkaistu 2012
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  10. 10
    Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

    Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene Tekijä Stefanie Weber, Katrin Hoffmann, Nikola Jeck, Kathrin Saar, Martin Boeswald, Eberhard Kuwertz-Broeking, Ivan IC Meij, Nine Knoers, Pierre Cochat, Tereza Šuláková, Klaus E. Bonzel, Marianne Soergel, Friedrich Manz, K Schaerer, Hannsjoerg W. Seyberth, André Reis, Martin Konrad

    Julkaistu 2000
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  11. 11
    Differential Gene Regulation under Altered Gravity Conditions in Follicular Thyroid Cancer Cells: Relationship between the Extracellular Matrix and the Cytoskeleton

    Differential Gene Regulation under Altered Gravity Conditions in Follicular Thyroid Cancer Cells: Relationship between the Extracellular Matrix and the Cytoskeleton Tekijä Claudia Ulbrich, Jessica Pietsch, Johannes Grosse, Markus Wehland, Herbert Schulz, Kathrin Saar, Norbert Hübner, Jens Hauslage, Ruth Hemmersbach, Markus Braun, Jack J. W. A. van Loon, Nicole Vagt, Marcel Egli, Peter Richter, Ralf Einspanier, Soroush Sharbati, Théo Baltz, Manfred Infanger, Xiao Ma, Daniela Grimm

    Julkaistu 2011
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  12. 12
    Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome

    Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome Tekijä Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis

    Julkaistu 1998
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  13. 13
    Inflammation-Induced Acute Phase Response in Skeletal Muscle and Critical Illness Myopathy

    Inflammation-Induced Acute Phase Response in Skeletal Muscle and Critical Illness Myopathy Tekijä Claudia Langhans, Steffen Weber‐Carstens, Franziska Schmidt, Jida Hamati, Melanie Kny, Xiaoxi Zhu, Tobias Wollersheim, Susanne Koch, Martin Krebs, Herbert Schulz, Doerte Lodka, Kathrin Saar, Siegfried Labeit, Claudia Spies, Norbert Hübner, Joachim Spranger, Simone Spuler, Michael Boschmann, Gunnar Dittmar, Gillian Butler‐Browne, Vincent Mouly, Jens Fielitz

    Julkaistu 2014
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  14. 14
    Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease

    Soluble epoxide hydrolase is a susceptibility factor for heart failure in a rat model of human disease Tekijä Jan Monti, Judith Fischer, Svetlana Paskaš, Matthias Heinig, Herbert Schulz, Claudia Gösele, Arnd Heuser, Robert Fischer, Cosima Schmidt, Alexander Schirdewan, Volkmar Groß, Oliver Hummel, Henrike Maatz, Giannino Patone, Kathrin Saar, Martin Vingron, Steven M. Weldon, Klaus Lindpaintner, Bruce D. Hammock, Klaus Rohde, Rainer Dietz, Stuart A. Cook, Wolf-Hagen Schunck, Friedrich C. Luft, Norbert Hübner

    Julkaistu 2008
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  15. 15
    Association and linkage of allelic variants of the dopamine transporter gene in ADHD

    Association and linkage of allelic variants of the dopamine transporter gene in ADHD Tekijä Susann Friedel, Kathrin Saar, Sascha Sauer, Astrid Dempfle, Susanne Walitza, Tobias Renner, Marcel Romanos, Christine M. Freitag, Christiane Seitz, Haukur Pálmason, André Scherag, Christine Windemuth-Kieselbach, Benno G. Schimmelmann, C. Wewetzer, Jobst Meyer, Andreas Warnke, Klaus‐Peter Lesch, Richard Reinhardt, Beate Herpertz‐Dahlmann, Mark W. Linder, Anke Hinney, Helmut Remschmidt, H. Schäfer, Kerstin Konrad, Norbert Hübner, Johannes Hebebrand

    Julkaistu 2002
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  16. 16
    The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance

    The genome sequence of the spontaneously hypertensive rat: Analysis and functional significance Tekijä Santosh S. Atanur, İnanç Birol, Victor Guryev, Martin Hirst, Oliver Hummel, Catherine Morrissey, Jacques Behmoaras, Xosé M. Fernández, Michelle D. Johnson, William McLaren, Giannino Patone, Enrico Petretto, Charles Plessy, Kathleen S. Rockland, Charles Rockland, Kathrin Saar, Yongjun Zhao, Piero Carninci, Paul Flicek, Ted Kurtz, Edwin Cuppen, Michal Pravenec, Norbert Hübner, Steven J.M. Jones, Ewan Birney, Timothy J. Aitman

    Julkaistu 2010
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  17. 17
    Self-sustaining IL-8 loops drive a prothrombotic neutrophil phenotype in severe COVID-19

    Self-sustaining IL-8 loops drive a prothrombotic neutrophil phenotype in severe COVID-19 Tekijä Rainer Kaiser, Alexander Leunig, Kami Pekayvaz, Oliver Popp, Markus Joppich, Vivien Polewka, Raphael Escaig, Afra Anjum, Marie‐Louise Hoffknecht, Christoph Gold, Sophia Brambs, Anouk Engel, Sven Stockhausen, Viktoria Knottenberg, Anna Titova, Mohamed Haji, Clemens Scherer, Maximilian Muenchhoff, Johannes C. Hellmuth, Kathrin Saar, Benjamin Schubert, Anne Hilgendorff, Christian Schulz, Stefan Kääb, Ralf Zimmer, Norbert Hübner, Steffen Maßberg, Philipp Mertins, Leo Nicolai, Konstantin Stark

    Julkaistu 2021
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  18. 18
    RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

    RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing Tekijä Wei Guo, Sebastian Schäfer, Marion L. Greaser, Michaël Radkë, Martin Liss, Thirupugal Govindarajan, Henrike Maatz, Herbert Schulz, Shijun Li, Amanda M. Parrish, Vita Dauksaite, Padmanabhan Vakeel, Sabine Klaassen, Brenda Gerull, Ludwig Thierfelder, Vera Regitz‐Zagrosek, Timothy A. Hacker, Kurt W. Saupe, G. William Dec, Patrick T. Ellinor, Calum A. MacRae, Bastian Spallek, Robert Fischer, Andreas Perrot, Cemil Özcelik, Kathrin Saar, Norbert Hübner, Michael Gotthardt

    Julkaistu 2012
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  19. 19
    Impaired endothelium-mediated cerebrovascular reactivity promotes anxiety and respiration disorders in mice

    Impaired endothelium-mediated cerebrovascular reactivity promotes anxiety and respiration disorders in mice Tekijä Jan Wenzel, Cathrin E. Hansen, Carla Bettoni, Miriam A. Vogt, Beate Lembrich, Rentsenkhand Natsagdorj, Gianna Huber, Josefine Brands, Kjestine Schmidt, Julian C. Assmann, Ines Stölting, Kathrin Saar, Jan Sedlacik, Jens Fiehler, Peter Ludewig, Michael Wegmann, Nina Feller, Marius Richter, Helge Müller‐Fielitz, Thomas Walther, Gabriele M. König, Evi Kostenis, Walter Raasch, Norbert Hübner, Peter Gass, Stefan Offermanns, Cor de Wit, Carsten A. Wagner, Markus Schwaninger

    Julkaistu 2020
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  20. 20
    Genome Sequencing Reveals Loci under Artificial Selection that Underlie Disease Phenotypes in the Laboratory Rat

    Genome Sequencing Reveals Loci under Artificial Selection that Underlie Disease Phenotypes in the Laboratory Rat Tekijä Santosh S. Atanur, Ana Garcia Diaz, Klio Maratou, Allison B. Sarkis, Maxime Rotival, Laurence Gamé, Michael Tschannen, Pamela J. Kaisaki, Georg Otto, Man Chun John, Thomas Keane, Oliver Hummel, Kathrin Saar, Wei Chen, Victor Guryev, Kathirvel Gopalakrishnan, Michael R. Garrett, Bina Joe, Lorena Citterio, Giuseppe Bianchi, Martin McBride, Anna F. Dominiczak, David J. Adams, Tadao Serikawa, Paul Flicek, Edwin Cuppen, Norbert Hübner, Enrico Petretto, Dominique Gauguier, Anne E. Kwitek, Howard J. Jacob, Timothy J. Aitman

    Julkaistu 2013
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