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1دورية أكاديمية
المؤلفون: Tobias Eisenberger, Christian Decker, Milan Hiersche, Ruben C Hamann, Eva Decker, Steffen Neuber, Valeska Frank, Hanno J Bolz, Henry Fehrenbach, Lars Pape, Burkhard Toenshoff, Christoph Mache, Kay Latta, Carsten Bergmann
المصدر: PLoS ONE, Vol 10, Iss 2, p e0116680 (2015)
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Milan Hiersche, Frank Rühle, Monika Stoll
المصدر: PLoS ONE, Vol 8, Iss 8, p e71775 (2013)
وصف الملف: electronic resource
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3
المؤلفون: Frank Rühle, Anika Witten, Andre Franke, Monika Stoll, Verena Limperger, Andrei Barysenka, Andreas Huge, Mona Riemenschneider, Rolf M. Mesters, Ulrike Nowak-Göttl, Astrid Arning, Anne Krümpel, Christine Heller, Wolfgang Lieb, Milan Hiersche
المساهمون: RS: FHML MaCSBio, RS: CARIM - R1.01 - Blood proteins & engineering, Biochemie
المصدر: Blood, 129(6), 783-790. The American Society of Hematology
مصطلحات موضوعية: Male, 0301 basic medicine, FAMILY-BASED TESTS, Genome-wide association study, 030204 cardiovascular system & hematology, Bioinformatics, medicine.disease_cause, Biochemistry, Cohort Studies, 0302 clinical medicine, Polymorphism (computer science), Glucuronosyltransferase, Child, RISK, Genetics, Mutation, GTPase-Activating Proteins, Chromosome Mapping, High-Throughput Nucleotide Sequencing, Venous Thromboembolism, Hematology, Child, Preschool, Chromosomes, Human, Pair 6, Female, Adolescent, Immunology, DNA-SEQUENCING DATA, Nerve Tissue Proteins, Single-nucleotide polymorphism, Biology, Thrombophilia, Polymorphism, Single Nucleotide, 03 medical and health sciences, GTP-Binding Proteins, LINKAGE, medicine, Humans, Genetic Predisposition to Disease, GENOME-WIDE ASSOCIATION, Nuclear family, METAANALYSIS, Genetic association, RELEASE, Siblings, Infant, Membrane Proteins, Cell Biology, medicine.disease, ARTERIAL ISCHEMIC-STROKE, 030104 developmental biology, Genetic Loci, THROMBOPHILIA, DISEQUILIBRIUM, Venous thromboembolism, Genome-Wide Association Study
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5852c888fd76966a7a3fc32126b86c81
https://doi.org/10.1182/blood-2016-07-728840 -
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المؤلفون: Carol Wicking, Milan Hiersche, Björn Hartleben, Walter Hunziker, Hao Lu, Peter Papathanasiou, Robert Tunningley, Shubha Vij, Friedhelm Hildebrandt, Valeska Frank, Heon Yung Gee, Graham D. Wright, Carsten Bergmann, Nadina Ortiz-Brüchle, Sudipto Roy, Klaus Zerres, Maria C. Rondón Galeano, Andrew C. Perkins, Nadescha Hilger, Melissa H. Little, Edgar A. Otto, Udo Vester, Daniel Epting, Elisabeth Ott, Elke Wühl, P. Jaya Kausalya, Vicki Metzis, Geraldine Kaeslin, Andrew D. Courtney, Belinda Whittle, Shang Yew Tay, Carina Kramer, Steffen Neuber
مصطلحات موضوعية: 0301 basic medicine, Male, Embryo, Nonmammalian, TRPP Cation Channels, Genetic Linkage, Medizin, Consanguinity, Biology, urologic and male genital diseases, Article, Pathogenesis, 03 medical and health sciences, Mice, 0302 clinical medicine, Genetics, Polycystic kidney disease, medicine, Basal body, Animals, Humans, Abnormalities, Multiple, Cilia, Zebrafish, Adaptor Proteins, Signal Transducing, Centrioles, Polycystic Kidney, Autosomal Recessive, Ciliary transition zone, Membrane Proteins, Zebrafish Proteins, medicine.disease, biology.organism_classification, female genital diseases and pregnancy complications, Autosomal Recessive Polycystic Kidney Disease, Transport protein, Pedigree, Mice, Inbred C57BL, Disease Models, Animal, Protein Transport, 030104 developmental biology, Gene Knockdown Techniques, Female, Chromosomes, Human, Pair 3, 030217 neurology & neurosurgery, Septins
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6dc29ffbf13e65bd4114bc34142261c
https://europepmc.org/articles/PMC5687889/ -
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المؤلفون: Anika Witten, Ulrike Nowak-Göttl, Monika Stoll, Gerhard Kurlemann, Milan Hiersche, Karin Kurnik, Astrid Arning, Daniela Manner
المصدر: Blood. 120:5231-5236
مصطلحات موضوعية: Adult, Male, Immunology, Genome-wide association study, Single-nucleotide polymorphism, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Biochemistry, medicine, Humans, Pediatric stroke, Gene Regulatory Networks, Genetic Predisposition to Disease, Age of Onset, Child, Stroke, Genetic association, Genetics, Systems Biology, ADAMTS, Infant, Cell Biology, Hematology, Transmission disequilibrium test, medicine.disease, ADAM Proteins, Child, Preschool, Female, Algorithms, Genome-Wide Association Study, SNP array
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::286b46019b28ca9924ed9bc34dc367f9
https://doi.org/10.1182/blood-2012-07-442038 -
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المؤلفون: Valeska Frank, Lars Pape, Kay Latta, Burkhard Toenshoff, Christoph J. Mache, Hanno J. Bolz, Milan Hiersche, Ruben C. Hamann, Tobias Eisenberger, Henry Fehrenbach, Eva Decker, Christian Decker, Steffen Neuber, Carsten Bergmann
المصدر: PLoS ONE, Vol 10, Iss 2, p e0116680 (2015)
PLoS ONEمصطلحات موضوعية: DNA Copy Number Variations, Autosomal dominant polycystic kidney disease, lcsh:Medicine, Protein Serine-Threonine Kinases, Biology, Kidney, urologic and male genital diseases, Bioinformatics, Gene Duplication, medicine, Polycystic kidney disease, Humans, Copy-number variation, lcsh:Science, False Negative Reactions, Genetic testing, Polycystic Kidney Diseases, Multidisciplinary, PKD1, medicine.diagnostic_test, Genetic heterogeneity, lcsh:R, High-Throughput Nucleotide Sequencing, Pyruvate Dehydrogenase Acetyl-Transferring Kinase, Kidney metabolism, medicine.disease, Molecular Diagnostic Techniques, Genetic Loci, lcsh:Q, Allelic heterogeneity, Pseudogenes, Research Article
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المؤلفون: Frank Rühle, Milan Hiersche, Monika Stoll
المصدر: PLoS ONE, Vol 8, Iss 8, p e71775 (2013)
PLoS ONEمصطلحات موضوعية: Clinical Research Design, Population Modeling, lcsh:Medicine, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Software, Genome Analysis Tools, Interaction network, Genetics, Genome-Wide Association Studies, Humans, Gene Regulatory Networks, Gene Networks, lcsh:Science, Multidisciplinary, Interpretation (logic), Population Biology, business.industry, Systems Biology, lcsh:R, Modeling, Computational Biology, High-Throughput Nucleotide Sequencing, Epistasis, Genetic, Molecular Sequence Annotation, Genomics, Data science, Visualization, Range (mathematics), Infectious Diseases, Workflow, Medicine, lcsh:Q, Infectious Disease Modeling, business, Sequence Analysis, Research Article, Genome-Wide Association Study, Network analysis
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المصدر: Blood. 118:3336-3336
مصطلحات موضوعية: Genetics, Immunology, Haplotype, Single-nucleotide polymorphism, Genome-wide association study, Cell Biology, Hematology, Transmission disequilibrium test, Biology, Bioinformatics, Biochemistry, Chromosome 15, Genotype, Multiple comparisons problem, SNP array
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::24b333fee34c1ef57a3598239c326b69
https://doi.org/10.1182/blood.v118.21.3336.3336