Hasil Pencarian - Ingo Kurth

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  1. 1
    Isolation and Primary Cell Culture of Mouse Dorsal Root Ganglion Neurons

    Isolation and Primary Cell Culture of Mouse Dorsal Root Ganglion Neurons oleh Theresa Heinrich, Christian Hübner, Ingo Kurth

    Diterbitkan 2016-04-01
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  2. 2
    No cure, no care? Diagnostic and therapeutic challenges in rare neuropathic pain syndromes

    No cure, no care? Diagnostic and therapeutic challenges in rare neuropathic pain syndromes oleh Maike F. Dohrn, Christina Dumke, Ingo Kurth, Stephan Züchner

    Diterbitkan 2023-04-01
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  3. 3
    No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria

    No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria oleh Kathrin Olschok, Udo Vester, Sven Lahme, Ingo Kurth, Thomas Eggermann

    Diterbitkan 2018-10-01
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  4. 4
    Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

    Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation oleh Florian Kraft, Katharina Wesseler, Matthias Begemann, Ingo Kurth, Miriam Elbracht, Thomas Eggermann

    Diterbitkan 2019-02-01
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  5. 5
    MiR-145 expression and rare NOTCH1 variants in bicuspid aortic valve-associated aortopathy.

    MiR-145 expression and rare NOTCH1 variants in bicuspid aortic valve-associated aortopathy. oleh Evaldas Girdauskas, Johannes Petersen, Niklas Neumann, Martin Ungelenk, Ingo Kurth, Hermann Reichenspurner, Tanja Zeller

    Diterbitkan 2018-01-01
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  6. 6
    Variant of the catalytic cysteine of UFSP2 leads to spondyloepimetaphyseal dysplasia type Di Rocco

    Variant of the catalytic cysteine of UFSP2 leads to spondyloepimetaphyseal dysplasia type Di Rocco oleh Larissa Mattern, Matthias Begemann, Heide Delbrück, Petra Holschbach, Silvia Schröder, Sabine M. Schacht, Ingo Kurth, Miriam Elbracht

    Diterbitkan 2023-06-01
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  7. 7
    Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neuropathy

    Generation of two induced pluripotent stem cell lines from skin fibroblasts of sisters carrying a c.1094C>A variation in the SCN10A gene potentially associated with small fiber neu... oleh Thomas Klein, Katharina Klug, Lisa Henkel, Chee Keong Kwok, Frank Edenhofer, Eva Klopocki, Ingo Kurth, Nurcan Üçeyler

    Diterbitkan 2019-03-01
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  8. 8
    DDX41 germline variants causing donor cell leukemia indicate a need for further genetic workup in the context of hematopoietic stem cell transplantation

    DDX41 germline variants causing donor cell leukemia indicate a need for further genetic workup in the context of hematopoietic stem cell transplantation oleh Benjamin Rolles, Robert Meyer, Matthias Begemann, Miriam Elbracht, Edgar Jost, Matthias Stelljes, Ingo Kurth, Tim H. Brümmendorf, Gerda Silling

    Diterbitkan 2023-05-01
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  9. 9
    Isolation and transfection of myenteric neurons from mice for patch-clamp applications

    Isolation and transfection of myenteric neurons from mice for patch-clamp applications oleh Samuel Kuehs, Laura Teege, Ann-Katrin Hellberg, Christina Stanke, Natja Haag, Natja Haag, Ingo Kurth, Robert Blum, Carla Nau, Enrico Leipold

    Diterbitkan 2022-12-01
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  10. 10
    Sepsis induces long-lasting impairments in CD4+ T-cell responses despite rapid numerical recovery of T-lymphocyte populations.

    Sepsis induces long-lasting impairments in CD4+ T-cell responses despite rapid numerical recovery of T-lymphocyte populations. oleh Christoph Ammer-Herrmenau, Upasana Kulkarni, Nico Andreas, Martin Ungelenk, Sarina Ravens, Christian Hübner, Angela Kather, Ingo Kurth, Michael Bauer, Thomas Kamradt

    Diterbitkan 2019-01-01
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  11. 11
    Gain-of-function mutation in SCN11A causes itch and affects neurogenic inflammation and muscle function in Scn11a+/L799P mice.

    Gain-of-function mutation in SCN11A causes itch and affects neurogenic inflammation and muscle function in Scn11a+/L799P mice. oleh Matthias Ebbinghaus, Lorena Tuchscherr, Gisela Segond von Banchet, Lutz Liebmann, Volker Adams, Mieczyslaw Gajda, Christian A Hübner, Ingo Kurth, Hans-Georg Schaible

    Diterbitkan 2020-01-01
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  12. 12
    Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling

    Novel homozygous nonsense mutation in the P5′N‐1 coding gene as an alternative cause for hereditary anemia with basophilic stippling oleh Martin Kirschner, Inga Rebecca Heinen, Steffen Koschmieder, Licinio Manco, Celeste Bento, Thomas Eggermann, Ingo Kurth, Edgar Jost, Tim H. Brümmendorf, Roland Fuchs

    Diterbitkan 2022-03-01
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  13. 13
    Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives

    Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives oleh Danielle Christine Maria van der Kaay, Anne Rochtus, Gerhard Binder, Ingo Kurth, Dirk Prawitt, Irène Netchine, Gudmundur Johannsson, Anita C S Hokken-Koelega, Miriam Elbracht, Thomas Eggermann

    Diterbitkan 2022-10-01
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  14. 14
    Novel Pathogenic Variants in a Cassette Exon of CCM2 in Patients With Cerebral Cavernous Malformations

    Novel Pathogenic Variants in a Cassette Exon of CCM2 in Patients With Cerebral Cavernous Malformations oleh Christiane D. Much, Konrad Schwefel, Dariush Skowronek, Loay Shoubash, Felix von Podewils, Miriam Elbracht, Stefanie Spiegler, Ingo Kurth, Agnes Flöel, Henry W. S. Schroeder, Ute Felbor, Matthias Rath

    Diterbitkan 2019-11-01
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  15. 15
    Diagnosing small fiber neuropathy in clinical practice: a deep phenotyping study

    Diagnosing small fiber neuropathy in clinical practice: a deep phenotyping study oleh Nadine Egenolf, Caren Meyer zu Altenschildesche, Luisa Kreß, Katja Eggermann, Barbara Namer, Franziska Gross, Alexander Klitsch, Tobias Malzacher, Daniel Kampik, Rayaz A. Malik, Ingo Kurth, Claudia Sommer, Nurcan Üçeyler

    Diterbitkan 2021-03-01
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  16. 16
    Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception.

    Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception. oleh Deborah Chiabrando, Marco Castori, Maja di Rocco, Martin Ungelenk, Sebastian Gießelmann, Matteo Di Capua, Annalisa Madeo, Paola Grammatico, Sophie Bartsch, Christian A Hübner, Fiorella Altruda, Lorenzo Silengo, Emanuela Tolosano, Ingo Kurth

    Diterbitkan 2016-12-01
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  17. 17
    Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach

    Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach oleh Larissa Bilo, Eguzkine Ochoa, Sunwoo Lee, Daniela Dey, Ingo Kurth, Florian Kraft, Fay Rodger, France Docquier, Ana Toribio, Leonardo Bottolo, Gerhard Binder, György Fekete, Miriam Elbracht, Eamonn R. Maher, Matthias Begemann, Thomas Eggermann

    Diterbitkan 2023-03-01
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  18. 18
    The difficulty to model Huntington’s disease in vitro using striatal medium spiny neurons differentiated from human induced pluripotent stem cells

    The difficulty to model Huntington’s disease in vitro using striatal medium spiny neurons differentiated from human induced pluripotent stem cells oleh Kim Le Cann, Alec Foerster, Corinna Rösseler, Andelain Erickson, Petra Hautvast, Sebastian Giesselmann, Daniel Pensold, Ingo Kurth, Markus Rothermel, Virginia B. Mattis, Geraldine Zimmer-Bensch, Stephan von Hörsten, Bernd Denecke, Tim Clarner, Jannis Meents, Angelika Lampert

    Diterbitkan 2021-03-01
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  19. 19
    Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN)

    Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) oleh Thomas Eggermann, Miriam Elbracht, Ingo Kurth, Anders Juul, Trine Holm Johannsen, Irène Netchine, George Mastorakos, Gudmundur Johannsson, Thomas J. Musholt, Martin Zenker, Dirk Prawitt, Alberto M. Pereira, Olaf Hiort, on behalf of the European Reference Network on Rare Endocrine Conditions (ENDO-ERN

    Diterbitkan 2020-06-01
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  20. 20
    Genetic Variants in the Promoter Region of the Macrophage Migration Inhibitory Factor are Associated with the Severity of Hepatitis C Virus-Induced Liver Fibrosis

    Genetic Variants in the Promoter Region of the Macrophage Migration Inhibitory Factor are Associated with the Severity of Hepatitis C Virus-Induced Liver Fibrosis oleh Theresa Hildegard Wirtz, Petra Fischer, Christina Backhaus, Irina Bergmann, Elisa Fabiana Brandt, Daniel Heinrichs, Maria Teresa Koenen, Kai Markus Schneider, Thomas Eggermann, Ingo Kurth, Christian Stoppe, Jürgen Bernhagen, Tony Bruns, Janett Fischer, Thomas Berg, Christian Trautwein, Marie-Luise Berres

    Diterbitkan 2019-07-01
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