Resultados da busca - Monika Stoll
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Long Non-Coding RNA Databases in Cardiovascular Research por Frank Rühle, Monika Stoll
Publicado em 2016Revisão -
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IBD5 is a General Risk Factor for Inflammatory Bowel Disease: Replication of Association with Crohn Disease and Identification of a Novel Association with Ulcerative Colitis por Cosmas Giallourakis, Monika Stoll, Katie Miller, Jochen Hampe, Eric S. Lander, Mark J. Daly, Stefan Schreiber, John D. Rioux
Publicado em 2003Artigo -
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Cardiac Myocyte De Novo DNA Methyltransferases 3a/3b Are Dispensable for Cardiac Function and Remodeling after Chronic Pressure Overload in Mice por Thomas Nührenberg, N. Hammann, Tilman Schnick, Sebastian Preißl, Anika Witten, Monika Stoll, Ralf Gilsbach, Franz‐Josef Neumann, Lutz Hein
Publicado em 2015Artigo -
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Regulation of Transport of the Angiotensin AT2 Receptor by a Novel Membrane-Associated Golgi Protein por Christoph Jan Wruck, Heiko Funke‐Kaiser, Thomas Pufe, Heike Kusserow, Mario Menk, Jan H. Schefe, Marie L. Kruse, Monika Stoll, Thomas Unger
Publicado em 2004Artigo -
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Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational study por Susanne Holzhauer, Neil A. Goldenberg, Ralf Junker, Christine Heller, Monika Stoll, Daniela Manner, Rolf M. Mesters, Anne Krümpel, Michael Stach, Ulrike Nowak‐Göttl
Publicado em 2012Artigo -
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New Target Regions for Human Hypertension via Comparative Genomics por Monika Stoll, Anne E. Kwitek, Allen W. Cowley, Eugenie L. Harris, Stephen Harrap, José Eduardo Krieger, Morton P. Printz, Abraham P. Provoost, J Sassard, Howard J. Jacob
Publicado em 2000Artigo -
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Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations por Peter J.P. Croucher, Silvia Mascheretti, Jochen Hampe, Klaus Huse, H Frenzel, Monika Stoll, Tim Lu, Susanna Nikolaus, Suk‐Kyun Yang, Michael Krawczak, Won Ho Kim, Stefan Schreiber
Publicado em 2003Artigo -
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Ear2 Deletion Causes Early Memory and Learning Deficits in APP/PS1 Mice por Markus P. Kummer, Thomas Hammerschmidt, Alfredo Martı́nez, Dick Terwel, Gregor Eichele, Anika Witten, S. Figura, Monika Stoll, Stephanie Schwartz, Hans‐Christian Pape, Joachim L. Schultze, David Weinshenker, Michael T. Heneka
Publicado em 2014Artigo -
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Increased afterload induces pathological cardiac hypertrophy: a new in vitro model por Marc N. Hirt, Nils A. Sörensen, Lena M. Bartholdt, Jasper Boeddinghaus, Sebastian Schaaf, Alexandra Eder, Ingra Vollert, Andrea Stöhr, Thomas G. Schulze, Anika Witten, Monika Stoll, Arne Hansen, Thomas Eschenhagen
Publicado em 2012Artigo -
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Selective Loss of Noradrenaline Exacerbates Early Cognitive Dysfunction and Synaptic Deficits in APP/PS1 Mice por Thea Hammerschmidt, Markus P. Kummer, Dick Terwel, Ana Maria Blanco Martinez, Ali Gorji, Hans‐Christian Pape, Karen S. Rommelfanger, Jason P. Schroeder, Monika Stoll, Joachim L. Schultze, David Weinshenker, Michael T. Heneka
Publicado em 2012Artigo -
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Extensive Copy-Number Variation of Young Genes across Stickleback Populations por Frédéric J. J. Chain, Philine G. D. Feulner, Mahesh Panchal, Christophe Eizaguirre, Irene E. Samonte, Martin Kalbe, Tobias L. Lenz, Monika Stoll, Erich Bornberg‐Bauer, Manfred Milinski, Thorsten B. H. Reusch
Publicado em 2014Artigo -
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Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study por Gili Kenet, Fenella J. Kirkham, Thomas Niederstadt, Achim Heinecke, Dawn E. Saunders, Monika Stoll, Benjamin Brenner, Christoph Bidlingmaier, Christine Heller, Ralf Knöfler, R. Schobeß, Barbara Zieger, Guillaume Sébire, Ulrike Nowak‐Göttl
Publicado em 2007Artigo -
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Genomics of Divergence along a Continuum of Parapatric Population Differentiation por Philine G. D. Feulner, Frédéric J. J. Chain, Mahesh Panchal, Yun Huang, Christophe Eizaguirre, Martin Kalbe, Tobias L. Lenz, Irene E. Samonte, Monika Stoll, Erich Bornberg‐Bauer, Thorsten B. H. Reusch, Manfred Milinski
Publicado em 2015Artigo -
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Genome‐wide patterns of standing genetic variation in a marine population of three‐spined sticklebacks por Philine G. D. Feulner, Frédéric J. J. Chain, Mahesh Panchal, Christophe Eizaguirre, Martin Kalbe, Tobias L. Lenz, Marvin Mundry, Irene E. Samonte, Monika Stoll, Manfred Milinski, Thorsten B. H. Reusch, Erich Bornberg‐Bauer
Publicado em 2012Artigo
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Assuntos relacionados
Biology
Medicine
Gene
Genetics
Internal medicine
Genotype
Disease
Single-nucleotide polymorphism
Biochemistry
Cardiology
Cell biology
Population
Genome-wide association study
Allele
Chemistry
Endocrinology
Gene expression
Immunology
Receptor
Locus (genetics)
Environmental health
Genetic association
Genome
Haplotype
Heart failure
Linkage disequilibrium
Neuroscience
Phenotype
Atrial fibrillation
Bioinformatics