Search Results - Rost, Simone

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  1. 1
    Confirmation of warfarin resistance of naturally occurring VKORC1 variants by coexpression with coagulation factor IX and in silico protein modelling

    Confirmation of warfarin resistance of naturally occurring VKORC1 variants by coexpression with coagulation factor IX and in silico protein modelling by Müller, Elisabeth, Keller, Alexander, Fregin, Andreas, Müller, Clemens R, Rost, Simone

    Published 2014
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  2. 2
    Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype

    Identification of variants in MBNL1 in patients with a myotonic dystrophy-like phenotype by Larsen, Mirjam, Kress, Wolfram, Schoser, Benedikt, Hehr, Ute, Müller, Clemens R, Rost, Simone

    Published 2016
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  3. 3
    Distribution and Structure of DM2 Repeat Tract Alleles in the German Population

    Distribution and Structure of DM2 Repeat Tract Alleles in the German Population by Mahyera, Alexis S., Schneider, Tamara, Halliger-Keller, Birgit, Schrooten, Katja, Hörner, Eva-Maria, Rost, Simone, Kress, Wolfram

    Published 2018
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  4. 4
    New Insights on Genetic Diagnostics in Cardiomyopathy and Arrhythmia Patients Gained by Stepwise Exome Data Analysis

    New Insights on Genetic Diagnostics in Cardiomyopathy and Arrhythmia Patients Gained by Stepwise Exome Data Analysis by Kolokotronis, Konstantinos, Pluta, Natalie, Klopocki, Eva, Kunstmann, Erdmute, Messroghli, Daniel, Maack, Christoph, Tejman-Yarden, Shai, Arad, Michael, Rost, Simone, Gerull, Brenda

    Published 2020
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  5. 5
    Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin?

    Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin? by Rost, Simone, Pelz, Hans-Joachim, Menzel, Sandra, MacNicoll, Alan D, León, Vanina, Song, Ki-Joon, Jäkel, Thomas, Oldenburg, Johannes, Müller, Clemens R

    Published 2009
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  6. 6
    Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1

    Diagnostic approach for FSHD revisited: SMCHD1 mutations cause FSHD2 and act as modifiers of disease severity in FSHD1 by Larsen, Mirjam, Rost, Simone, El Hajj, Nady, Ferbert, Andreas, Deschauer, Marcus, Walter, Maggie C, Schoser, Benedikt, Tacik, Pawel, Kress, Wolfram, Müller, Clemens R

    Published 2015
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  7. 7
    Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation‐negative early‐onset and high‐risk breast cancer patients

    Single CpG hypermethylation, allele methylation errors, and decreased expression of multiple tumor suppressor genes in normal body cells of mutation‐negative early‐onset and high‐r... by Böck, Julia, Appenzeller, Silke, Haertle, Larissa, Schneider, Tamara, Gehrig, Andrea, Schröder, Jörg, Rost, Simone, Wolf, Beat, Bartram, Claus R., Sutter, Christian, Haaf, Thomas

    Published 2018
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  8. 8
    Paternal age effects on sperm FOXK1 and KCNA7 methylation and transmission into the next generation

    Paternal age effects on sperm FOXK1 and KCNA7 methylation and transmission into the next generation by Atsem, Stefanie, Reichenbach, Juliane, Potabattula, Ramya, Dittrich, Marcus, Nava, Caroline, Depienne, Christel, Böhm, Lena, Rost, Simone, Hahn, Thomas, Schorsch, Martin, Haaf, Thomas, El Hajj, Nady

    Published 2016
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  9. 9
    Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6

    Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6 by Rost, Simone, Bach, Elisa, Neuner, Cordula, Nanda, Indrajit, Dysek, Sandra, Bittner, Reginald E, Keller, Alexander, Bartsch, Oliver, Mlynski, Robert, Haaf, Thomas, Müller, Clemens R, Kunstmann, Erdmute

    Published 2014
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  10. 10
    Targeted Gene Expression Profile Reveals CDK4 as Therapeutic Target for Selected Patients With Adrenocortical Carcinoma

    Targeted Gene Expression Profile Reveals CDK4 as Therapeutic Target for Selected Patients With Adrenocortical Carcinoma by Liang, Raimunde, Weigand, Isabel, Lippert, Juliane, Kircher, Stefan, Altieri, Barbara, Steinhauer, Sonja, Hantel, Constanze, Rost, Simone, Rosenwald, Andreas, Kroiss, Matthias, Fassnacht, Martin, Sbiera, Silviu, Ronchi, Cristina L.

    Published 2020
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  11. 11
    The Genetic Basis of Resistance to Anticoagulants in Rodents

    The Genetic Basis of Resistance to Anticoagulants in Rodents by Pelz, Hans-Joachim, Rost, Simone, Hünerberg, Mirja, Fregin, Andreas, Heiberg, Ann-Charlotte, Baert, Kristof, MacNicoll, Alan D., Prescott, Colin V., Walker, Anne-Sophie, Oldenburg, Johannes, Müller, Clemens R.

    Published 2005
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  12. 12
    Early and lethal neurodegeneration with myasthenic and myopathic features: A new ALG14-CDG

    Early and lethal neurodegeneration with myasthenic and myopathic features: A new ALG14-CDG by Schorling, David C., Rost, Simone, Lefeber, Dirk J., Brady, Lauren, Müller, Clemens R., Korinthenberg, Rudolf, Tarnopolsky, Mark, Bönnemann, Carsten G., Rodenburg, Richard J., Bugiani, Marianna, Beytia, Maria, Krüger, Marcus, van der Knaap, Marjo, Kirschner, Jan

    Published 2017
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  13. 13
    Exon-4 Mutations in KRAS Affect MEK/ERK and PI3K/AKT Signaling in Human Multiple Myeloma Cell Lines

    Exon-4 Mutations in KRAS Affect MEK/ERK and PI3K/AKT Signaling in Human Multiple Myeloma Cell Lines by Weißbach, Susann, Heredia-Guerrero, Sofia Catalina, Barnsteiner, Stefanie, Großhans, Lukas, Bodem, Jochen, Starz, Hanna, Langer, Christian, Appenzeller, Silke, Knop, Stefan, Steinbrunn, Torsten, Rost, Simone, Einsele, Hermann, Bargou, Ralf Christian, Rosenwald, Andreas, Stühmer, Thorsten, Leich, Ellen

    Published 2020
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