Resultats de la cerca - Helmut Fuchs

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  1. 1
    Effects of G-protein mutations on skin color

    Effects of G-protein mutations on skin color per Catherine D. Van Raamsdonk, Karen Fitch, Helmut Fuchs, Martin Hrabě de Angelis, Gregory S. Barsh

    Publicat 2004
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  2. 2
    The Notch ligand <i>Jagged1</i> is required for inner ear sensory development

    The Notch ligand <i>Jagged1</i> is required for inner ear sensory development per Amy E. Kiernan, Nadav Ahituv, Helmut Fuchs, Rudi Balling, Karen B. Avraham, Karen P. Steel, Martin Hrabě de Angelis

    Publicat 2001
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  3. 3
    Peroxidasin is essential for eye development in the mouse

    Peroxidasin is essential for eye development in the mouse per Xiaohe Yan, Sibylle Sabrautzki, Marion Horsch, Helmut Fuchs, Valérie Gailus‐Durner, Johannes Beckers, Martin Hrabě de Angelis, Jochen Graw

    Publicat 2014
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  4. 4
    A robust and reliable non-invasive test for stress responsivity in mice

    A robust and reliable non-invasive test for stress responsivity in mice per Annemarie Zimprich, Lillian Garrett, Jan M. Deussing, Carsten T. Wotjak, Helmut Fuchs, Valérie Gailus‐Durner, Martin Hrabě de Angelis, Wolfgang Wurst, Sabine M. Hölter

    Publicat 2014
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  5. 5
    Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation

    Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation per Amiel A. Dror, Yael Politi, Hashem Shahin, Danielle R. Lenz, Silvia Dossena, Charity Nofziger, Helmut Fuchs, Martin Hrabě de Angelis, Markus Paulmichl, Steve Weiner, Karen B. Avraham

    Publicat 2010
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  6. 6
    Genetics of dark skin in mice

    Genetics of dark skin in mice per Karen Fitch, Kelly A. McGowan, Catherine D. Van Raamsdonk, Helmut Fuchs, Daekee Lee, Anne Puech, Yann Hérault, David W. Threadgill, Martin Hrabé de Angelis, Gregory S. Barsh

    Publicat 2003
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  7. 7
    Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice

    Endogenous FGF21-signaling controls paradoxical obesity resistance of UCP1-deficient mice per Susanne Keipert, Dominik Lutter, Bjoern O. Schroeder, Daniel Brandt, Marcus Ståhlman, Thomas Schwarzmayr, Elisabeth Graf, Helmut Fuchs, Martin Hrabě de Angelis, Matthias H. Tschöp, Jan Rozman, Martin Jastroch

    Publicat 2020
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  8. 8
    Interplay between H1 and HMGN epigenetically regulates OLIG1&amp;2 expression and oligodendrocyte differentiation

    Interplay between H1 and HMGN epigenetically regulates OLIG1&amp;2 expression and oligodendrocyte differentiation per Tao Deng, Yuri V. Postnikov, Shaofei Zhang, Lillian Garrett, Lore Becker, Ildikó Rácz, Sabine M. Hölter, Wolfgang Wurst, Helmut Fuchs, Valérie Gailus‐Durner, Martin Hrabé de Angelis, Michael Bustin

    Publicat 2016
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  9. 9
    <scp>IL</scp>‐4 receptor α blockade prevents sensitization and alters acute and long‐lasting effects of allergen‐specific immunotherapy of murine allergic asthma

    <scp>IL</scp>‐4 receptor α blockade prevents sensitization and alters acute and long‐lasting effects of allergen‐specific immunotherapy of murine allergic asthma per Dennis Rußkamp, Juan Antonio Aguilar‐Pimentel, Francesca Alessandrini, Valérie Gailus‐Durner, Helmut Fuchs, Caspar Ohnmacht, Adam Chaker, Martin Hrabé de Angelis, Markus Ollert, Carsten B. Schmidt‐Weber, Simon Blank

    Publicat 2019
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  10. 10
    The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss

    The Novel Mouse Mutation Oblivion Inactivates the PMCA2 Pump and Causes Progressive Hearing Loss per Sarah L. Spiden, Mario Bortolozzi, Francesca Di Leva, Martin Hrabé de Angelis, Helmut Fuchs, Dmitry Lim, Saida Ortolano, Neil J. Ingham, Marisa Brini, Ernesto Carafoli, Fabio Mammano, Karen P. Steel

    Publicat 2008
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  11. 11
    Characterization of Phospholipase Cγ Enzymes with Gain-of-Function Mutations

    Characterization of Phospholipase Cγ Enzymes with Gain-of-Function Mutations per Katy L. Everett, Tom D. Bunney, Youngdae Yoon, Fernando Rodrigues‐Lima, Richard Harris, Paul C. Driscoll, Koichiro Abe, Helmut Fuchs, Martin Hrabé de Angelis, Philipp Yu, Wohnwa Cho, Matilda Katan

    Publicat 2009
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  12. 12
    ER Stress-Mediated Apoptosis in a New Mouse Model of Osteogenesis imperfecta

    ER Stress-Mediated Apoptosis in a New Mouse Model of Osteogenesis imperfecta per Thomas S. Lisse, Frank Thiele, Helmut Fuchs, Wolfgang Hans, Gerhard K. H. Przemeck, Koichiro Abe, Birgit Rathkolb, Leticia Quintanilla‐Martinez, Gabriele Hoelzlwimmer, Miep Helfrich, Eckhard Wolf, Stuart H. Ralston, Martin Hrabé de Angelis

    Publicat 2008
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  13. 13
    Opa1 processing is dispensable in mouse development but is protective in mitochondrial cardiomyopathy

    Opa1 processing is dispensable in mouse development but is protective in mitochondrial cardiomyopathy per Sofia Ahola, Lilli A. Pazurek, Fiona Carola Mayer, Philipp Lampe, Steffen Hermans, Lore Becker, Oana V. Amarie, Helmut Fuchs, Valerie Gailus-Durner, Martin Hrabé de Angelis, Dietmar Riedel, Hendrik Nolte, Thomas Langer

    Publicat 2024
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  14. 14
    Phenotypic comparison of common mouse strains developing high-fat diet-induced hepatosteatosis

    Phenotypic comparison of common mouse strains developing high-fat diet-induced hepatosteatosis per Melanie Kahle, Marion Horsch, Barbara Fridrich, Anett Seelig, Jürgen Schultheiß, Jörn Leonhardt, Martin Irmler, Johannes Beckers, Birgit Rathkolb, Eckhard Wolf, Nicole Franke, Valérie Gailus‐Durner, Helmut Fuchs, Martin Hrabě de Angelis, Susanne Neschen

    Publicat 2013
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  15. 15
    Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

    Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects per Kelly A. McGowan, Jun Z. Li, Christopher Y. Park, Veronica G. Beaudry, Holly K. Tabor, Amit J. Sabnis, Weibin Zhang, Helmut Fuchs, Martin Hrabě de Angelis, R Myers, Laura D. Attardi, Gregory S. Barsh

    Publicat 2008
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  16. 16
    Mechanisms Controlling Anaemia in Trypanosoma congolense Infected Mice

    Mechanisms Controlling Anaemia in Trypanosoma congolense Infected Mice per Harry Noyes, Mohammad Hossein Alimohammadian, Morris Agaba, Andy Brass, Helmut Fuchs, Valérie Gailus‐Durner, Helen Hulme, Fuad A. Iraqi, Stephen J. Kemp, Birgit Rathkolb, Eckhard Wolf, Martin Hrabé de Angelis, Delnaz Roshandel, Jan Naessens

    Publicat 2009
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  17. 17
    Alternative oxidase‐mediated respiration prevents lethal mitochondrial cardiomyopathy

    Alternative oxidase‐mediated respiration prevents lethal mitochondrial cardiomyopathy per Jayasimman Rajendran, Janne Purhonen, Saara Tegelberg, Olli‐Pekka Smolander, Matthias Mörgelin, Jan Rozman, Valérie Gailus‐Durner, Helmut Fuchs, Martin Hrabé de Angelis, Petri Auvinen, Eero Mervaala, Howard T. Jacobs, Marten Szibor, Vineta Fellman, Jukka Kallijärvi

    Publicat 2018
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  18. 18
    A Myo6 Mutation Destroys Coordination between the Myosin Heads, Revealing New Functions of Myosin VI in the Stereocilia of Mammalian Inner Ear Hair Cells

    A Myo6 Mutation Destroys Coordination between the Myosin Heads, Revealing New Functions of Myosin VI in the Stereocilia of Mammalian Inner Ear Hair Cells per Ronna Hertzano, Ella Shalit, Agnieszka Rzadzinska, Amiel A. Dror, Lin Song, Uri Ron, Joshua Tan, Alina Shitrit, Helmut Fuchs, Tama Hasson, Nir Ben‐Tal, H. Lee Sweeney, Martin Hrabé de Angelis, Karen P. Steel, Karen B. Avraham

    Publicat 2008
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  19. 19
    An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

    An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice per Morag A. Lewis, Elizabeth Quint, Anne M. Glazier, Helmut Fuchs, Martin Hrabě de Angelis, Cordelia Langford, Stijn van Dongen, Cei Abreu‐Goodger, Matias Piipari, Nick Redshaw, Tamás Dalmay, Miguel A. Moreno‐Pelayo, Anton J. Enright, Karen P. Steel

    Publicat 2009
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  20. 20
    Neuronal 3′,3,5-Triiodothyronine (T<sub>3</sub>) Uptake and Behavioral Phenotype of Mice Deficient in<i>Mct8</i>, the Neuronal T<sub>3</sub>Transporter Mutated in Allan–Herndon–Dudley Syndrome

    Neuronal 3′,3,5-Triiodothyronine (T<sub>3</sub>) Uptake and Behavioral Phenotype of Mice Deficient in<i>Mct8</i>, the Neuronal T<sub>3</sub>Transporter Mutated in Allan–Herndon–Dud... per Eva K. Wirth, Stephan Roth, Cristiane Blechschmidt, Sabine M. Hölter, Lore Becker, Ildikó Rácz, Andreas Zimmer, Thomas Klopstock, Valérie Gailus‐Durner, Helmut Fuchs, Wolfgang Wurst, T. Naumann, Anja U. Bräuer, Martin Hrabě de Angelis, Josef Köhrle, Annette Grüters, Ulrich Schweizer

    Publicat 2009
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