يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"Roman Tremmel"', وقت الاستعلام: 0.80s تنقيح النتائج
  1. 1
    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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  2. 2
    Copy number variation profiling in pharmacogenes using panel-based exome resequencing and correlation to human liver expression

    المؤلفون: Roman Tremmel, Kathrin Klein, Saskia Biskup, Tim Scheurenbrand, Elke Schaeffeler, Ulrich M. Zanger, S. Fehr, Stefan Winter, Matthias Schwab, Florian Battke

    المصدر: Human Genetics

    مصطلحات موضوعية: Genetic Markers, congenital, hereditary, and neonatal diseases and abnormalities, endocrine system diseases, DNA Copy Number Variations, Computational biology, Biology, Correlation, 03 medical and health sciences, Exon, mental disorders, Exome Sequencing, Genetics, Humans, Copy-number variation, Exome, Gene, Genetics (clinical), 030304 developmental biology, Retrospective Studies, 0303 health sciences, 030305 genetics & heredity, Computational Biology, High-Throughput Nucleotide Sequencing, Human genetics, 3. Good health, Liver, Genetic marker, Pharmacogenetics, Pharmacogenomics

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb48b313c29c11ca18404cbeb9224fa4
    https://pubmed.ncbi.nlm.nih.gov/31786673

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest
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  3. 3
    A New Panel-Based Next-Generation Sequencing Method for ADME Genes Reveals Novel Associations of Common and Rare Variants With Expression in a Human Liver Cohort

    المؤلفون: Kathrin Klein, Roman Tremmel, Stefan Winter, Sarah Fehr, Florian Battke, Tim Scheurenbrand, Elke Schaeffeler, Saskia Biskup, Matthias Schwab, Ulrich M. Zanger

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

    مصطلحات موضوعية: lcsh:QH426-470, Biology, DNA sequencing, 03 medical and health sciences, 0302 clinical medicine, Genotype, Genetics, Coding region, Indel, Gene, Genetics (clinical), 030304 developmental biology, Original Research, next generation sequencing, pharmacogenomics, 0303 health sciences, Intron, rare variants, 3. Good health, Minor allele frequency, lcsh:Genetics, genomic DNA, ADME, eQTL analysis, 030220 oncology & carcinogenesis, Molecular Medicine

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86568e793f6c4b9717e85eadc291864e
    http://europepmc.org/articles/PMC6365429

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  4. 4
    Genetic variation in human drug-related genes

    المؤلفون: Debora S. Marks, Charlotta P I Schärfe, Roman Tremmel, Matthias Schwab, Oliver Kohlbacher

    المصدر: Genome Medicine
    Genome Medicine, Vol 9, Iss 1, Pp 1-15 (2017)

    مصطلحات موضوعية: 0301 basic medicine, Drug, Exome sequence analysis, Drug-Related Side Effects and Adverse Reactions, Pharmacogenomic Variants, lcsh:QH426-470, media_common.quotation_subject, Population, lcsh:Medicine, Biology, Bioinformatics, Efficacy, 03 medical and health sciences, 0302 clinical medicine, Bioinformatics analysis, Mutation Rate, Pharmacokinetics, Genetic variation, Genetics, Humans, Quantitative Biology - Genomics, Genetic variability, Adverse effect, education, Gene, Molecular Biology, Genetics (clinical), Exome sequencing, 030304 developmental biology, media_common, Genomics (q-bio.GN), 0303 health sciences, education.field_of_study, Genome, Human, Research, lcsh:R, Human genetics, 3. Good health, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, FOS: Biological sciences, Pharmacogenomics, Molecular Medicine

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::babef81becda05909090c789729097ad

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest
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