Resultats de la cerca - Hartmut Cuny

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  1. 1
    Novel Mechanism of Voltage-Gated N-type (Ca<sub>v</sub>2.2) Calcium Channel Inhibition Revealed through <i>α</i>-Conotoxin Vc1.1 Activation of the GABA<sub>B</sub> Receptor

    Novel Mechanism of Voltage-Gated N-type (Ca<sub>v</sub>2.2) Calcium Channel Inhibition Revealed through <i>α</i>-Conotoxin Vc1.1 Activation of the GABA<sub>B</sub> Receptor per Thuan G. Huynh, Hartmut Cuny, Paul A. Slesinger, David J. Adams

    Publicat 2014
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  2. 2
    Switching off calcium-dependent inactivation in <scp>l</scp> -type calcium channels by an autoinhibitory domain

    Switching off calcium-dependent inactivation in <scp>l</scp> -type calcium channels by an autoinhibitory domain per Christian Wahl‐Schott, Ludwig Baumann, Hartmut Cuny, Christian Eckert, Kristina Grießmeier, Martin Biel

    Publicat 2006
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  3. 3
    Differential Cav2.1 and Cav2.3 channel inhibition by baclofen and α-conotoxin Vc1.1 via GABAB receptor activation

    Differential Cav2.1 and Cav2.3 channel inhibition by baclofen and α-conotoxin Vc1.1 via GABAB receptor activation per Géza Berecki, Jeffrey R. McArthur, Hartmut Cuny, Richard J. Clark, David J. Adams

    Publicat 2014
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  4. 4
    γ-Aminobutyric Acid Type B (GABAB) Receptor Expression Is Needed for Inhibition of N-type (Cav2.2) Calcium Channels by Analgesic α-Conotoxins

    γ-Aminobutyric Acid Type B (GABAB) Receptor Expression Is Needed for Inhibition of N-type (Cav2.2) Calcium Channels by Analgesic α-Conotoxins per Hartmut Cuny, Andrew de Faoite, Thuan G. Huynh, Takahiro Yasuda, Géza Berecki, David J. Adams

    Publicat 2012
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  5. 5
    NAD deficiency due to environmental factors or gene–environment interactions causes congenital malformations and miscarriage in mice

    NAD deficiency due to environmental factors or gene–environment interactions causes congenital malformations and miscarriage in mice per Hartmut Cuny, Melissa Rapadas, Jessica Gereis, Ella MMA Martin, Rosemary B. Kirk, Hongjun Shi, Sally L. Dunwoodie

    Publicat 2020
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  6. 6
    The two-pore channel TPCN2 mediates NAADP-dependent Ca2+-release from lysosomal stores

    The two-pore channel TPCN2 mediates NAADP-dependent Ca2+-release from lysosomal stores per Xiangang Zong, Michael Schieder, Hartmut Cuny, Stefanie Fenske, Christian Grüner, Katrin Rötzer, Oliver Griesbeck, Hartmann Harz, Martin Biel, Christian Wahl‐Schott

    Publicat 2009
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  7. 7
    Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders

    Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders per Justin O. Szot, Carla Campagnolo, Ye Cao, Kavitha R. Iyer, Hartmut Cuny, Thomas A. Drysdale, Josue Flores-Daboub, Weimin Bi, Lauren Westerfield, Pengfei Liu, Tse Ngong Leung, Kwong Wai Choy, Gavin Chapman, Rui Xiao, Victoria Mok Siu, Sally L. Dunwoodie

    Publicat 2019
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  8. 8
    A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data

    A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data per Justin O. Szot, Hartmut Cuny, Gillian M. Blue, David T. Humphreys, Eddie Ip, Katrina Harrison, Gary F. Sholler, Eleni Giannoulatou, Paul Leo, Emma L. Duncan, Duncan B. Sparrow, Joshua W. K. Ho, Robert M. Graham, Nicholas Pachter, Gavin Chapman, David S. Winlaw, Sally L. Dunwoodie

    Publicat 2018
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  9. 9
    Identification of clinically actionable variants from genome sequencing of families with congenital heart disease

    Identification of clinically actionable variants from genome sequencing of families with congenital heart disease per Dimuthu Alankarage, Eddie Ip, Justin O. Szot, Jacob E. Munro, Gillian M. Blue, Katrina Harrison, Hartmut Cuny, Annabelle Enriquez, Michael Troup, David T. Humphreys, Meredith Wilson, Richard P. Harvey, Gary F. Sholler, Robert M. Graham, Joshua W. K. Ho, Edwin P. Kirk, Nicholas Pachter, Gavin Chapman, David S. Winlaw, Eleni Giannoulatou, Sally L. Dunwoodie

    Publicat 2018
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  10. 10
    High susceptibility to fatty liver disease in two-pore channel 2-deficient mice

    High susceptibility to fatty liver disease in two-pore channel 2-deficient mice per Christian Grimm, Lesca M. Holdt, Cheng‐Chang Chen, Sami Hassan, Christoph Müller, Simone Jörs, Hartmut Cuny, Sandra Kissing, Bernd Schröder, Elisabeth Butz, Bernd H. Northoff, Jan Castonguay, Christian A. Luber, Markus Moser, Saskia Spahn, Renate Lüllmann‐Rauch, Christina Fendel, Norbert Klugbauer, Oliver Griesbeck, Albert Haas, Matthias Mann, Franz Bracher, Daniel Teupser, Paul Säftig, Martin Biel, Christian Wahl‐Schott

    Publicat 2014
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  11. 11
    A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder

    A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder per Justin O. Szot, Hartmut Cuny, Ella MMA Martin, Delicia Z Sheng, Kavitha R. Iyer, Stephanie Portelli, Vivien Nguyen, Jessica Gereis, Dimuthu Alankarage, David Chitayat, Karen Chong, Ingrid M. Wentzensen, Catherine Vincent‐Delorme, Alban Lermine, Emma Burkitt‐Wright, Weizhen Ji, Lauren Jeffries, Lynn Pais, Tiong Yang Tan, James Pitt, C. Wise, Helen Wright, Israel D. Andrews, Brianna Pruniski, Theresa A. Grebe, Nicole Corsten‐Janssen, Katelijne Bouman, Cathryn Poulton, Supraja Prakash, Boris Keren, Natasha J. Brown, Matthew F. Hunter, Oliver Heath, Saquib A. Lakhani, John McDermott, David B. Ascher, Gavin Chapman, Kayleigh Bozon, Sally L. Dunwoodie

    Publicat 2024
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