يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"Roman Tremmel"', وقت الاستعلام: 0.78s تنقيح النتائج
  1. 1
    Praxisrelevante pharmakogenetische Diagnostik zur Verbesserung der Arzneimitteltherapie

    المؤلفون: Roman Tremmel, Elke Schaeffeler, Severin Schricker, Simon Jäger, Matthias Schwab

    المصدر: DMW - Deutsche Medizinische Wochenschrift. 146:23-29

    مصطلحات موضوعية: medicine.medical_specialty, medicine.diagnostic_test, business.industry, MEDLINE, General Medicine, medicine.disease, 030226 pharmacology & pharmacy, Clinical Practice, 03 medical and health sciences, 0302 clinical medicine, 030220 oncology & carcinogenesis, Pharmacogenomics, medicine, Personalized medicine, Drug reaction, business, Intensive care medicine, Adverse drug reaction, Genetic testing

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::bd9af0f14fe3fa79c222d1c51b20df8f
    https://doi.org/10.1055/a-1109-0814

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  2. 2
    The impact of CYP3A4*22 on tacrolimus pharmacokinetics and outcome in clinical practice at a single kidney transplant center

    المؤلفون: Emaad Abdel-Kahaar, Stefan Winter, Roman Tremmel, Elke Schaeffeler, Christoph J. Olbricht, Eberhard Wieland, Matthias Schwab, Maria Shipkova, Simon U. Jaeger

    المصدر: Frontiers in Genetics, Vol 10 (2019)
    Frontiers in Genetics

    مصطلحات موضوعية: 0301 basic medicine, CYP3A5, ACUTE REJECTION, Gastroenterology, Pharmakogenetik, 0302 clinical medicine, Medicine, Cytochrome P-450 CYP3A, tacrolimus, VARIANT ALLELE, Genetics (clinical), pharmacogenetics, medicine.diagnostic_test, Area under the curve, ABCB1, renal transplantation, Drug monitoring, 3. Good health, 030220 oncology & carcinogenesis, Molecular Medicine, Risk, medicine.medical_specialty, lcsh:QH426-470, therapeutic drug monitoring, Renal function, Delayed Graft Function, DONOR, Tacrolimus, 03 medical and health sciences, Pharmacokinetics, Internal medicine, ddc:570, Genetic model, Genetics, CYP3A4*22, POLYMORPHISMS, business.industry, DOSE REQUIREMENTS, Kidney Transplantation, Polymorphismus, Transplantation, lcsh:Genetics, RECIPIENTS, 030104 developmental biology, Therapeutic drug monitoring, Pharmacogenetics, business, CYP3A5 GENOTYPE

    وصف الملف: application/pdf; image/tiff; application/vnd.openxmlformats-officedocument.wordprocessingml.document

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2086b9ac28cbcd0211889092a69f8bf5

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  3. 3
    Identification of Cardiomyopathy-Associated Circulating miRNA Biomarkers in Muscular Dystrophy Female Carriers Using a Complementary Cardiac Imaging and Plasma Profiling Approach

    المؤلفون: Anca Florian, Alexandru Patrascu, Roman Tremmel, Sabine Rösch, Udo Sechtem, Matthias Schwab, Elke Schaeffeler, Ali Yilmaz

    المصدر: Frontiers in Physiology, Vol 9 (2018)
    Frontiers in Physiology

    مصطلحات موضوعية: muscular dystrophy, medicine.medical_specialty, Physiology, Cardiomyopathy, 030204 cardiovascular system & hematology, lcsh:Physiology, 03 medical and health sciences, cardiovascular magnetic resonance, 0302 clinical medicine, Physiology (medical), Internal medicine, medicine, Muscular dystrophy, Myopathy, Original Research, medicine.diagnostic_test, biology, microRNA, lcsh:QP1-981, business.industry, Skeletal muscle, Magnetic resonance imaging, medicine.disease, female carriers, Circulating MicroRNA, medicine.anatomical_structure, Cardiology, biology.protein, Creatine kinase, medicine.symptom, business, cardiomyopathy, 030217 neurology & neurosurgery, Blood drawing

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e188f9d3b35541945db771ec0e2c2e
    https://www.frontiersin.org/article/10.3389/fphys.2018.01770/full

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  4. 4
    Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies

    المؤلفون: Kathrin Klein, Matthias Schwab, Richard M. Weinshilboum, Reedik Mägi, Richard S. Houlston, Martin Schrappe, Irena Mlinarič Raščan, Elke Schaeffeler, Stefan Winter, Martin Stanulla, Evelin Mihailov, Lili Milani, Roman Tremmel, Andres Metspalu, Anja Möricke, Alenka Šmid, Riin Tamm

    المصدر: Clinical Pharmacology & Therapeutics

    مصطلحات موضوعية: 0301 basic medicine, Estonia, Genome-wide association study, Biology, Article, 03 medical and health sciences, Genetic variation, Genotype, medicine, Humans, Pharmacology (medical), Allele, Alleles, Genetic testing, Pharmacology, Genetics, Polymorphism, Genetic, medicine.diagnostic_test, Thiopurine methyltransferase, Methyltransferases, Mercaptopurine, 3. Good health, 030104 developmental biology, Phenotype, biology.protein, Pharmacogenetics, medicine.drug, Genome-Wide Association Study

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f59942c7e46d99dc0b5ba8cd1dd35b8
    https://pubmed.ncbi.nlm.nih.gov/27770449

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