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au.\*:("STOLL, Monika")

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Results 1 to 25 of 39

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Angiotensin and its AT2 receptor : new insights into an old systemSTOLL, Monika; UNGER, Thomas.Regulatory peptides. 2001, Vol 99, Num 2-3, pp 175-182, issn 0167-0115Article

Advances in understanding stroke risk in children ― a geneticist's viewSTOLL, Monika; RÜHLE, Frank; NOWAK-GÖTTT, Ulrike et al.British journal of haematology. 2014, Vol 164, Num 5, pp 636-645, issn 0007-1048, 10 p.Article

Inherited Risk Factors for Thrombotic Diseases in Children: The Genome-Wide PerspectivePREUSS, Christoph; STOLL, Monika.Seminars in thrombosis and hemostasis. 2011, Vol 37, Num 7, pp 848-855, issn 0094-6176, 8 p.Article

Platelet reactivity and clopidogrel resistance are associated with the H2 haplotype of the P2Y12-ADP receptor geneSTARITZ, Peter; KURZ, Kerstin; STOLL, Monika et al.International journal of cardiology. 2009, Vol 133, Num 3, pp 341-345, issn 0167-5273, 5 p.Article

The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studiesBERGER, Klaus; STÖGBAUER, Florian; FUNKE, Harald et al.Human genetics. 2007, Vol 121, Num 2, pp 169-178, issn 0340-6717, 10 p.Article

Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populationsCROUCHER, Peter J. P; MASCHERETTI, Silvia; WON HO KIM et al.European journal of human genetics. 2003, Vol 11, Num 1, pp 6-16, issn 1018-4813, 11 p.Article

DNA methylation changes are a late event in acute promyelocytic leukemia and coincide with loss of transcription factor bindingSCHOOFS, Till; ROHDE, Christian; STOLL, Monika et al.Blood. 2013, Vol 121, Num 1, pp 178-187, issn 0006-4971, 10 p.Article

Inherited thrombophilia in children with venous thromboembolism and the familial risk of thromboembolism: an observational studyHOLZHAUER, Susanne; GOLDENBERG, Neil A; JUNKER, Ralf et al.Blood. 2012, Vol 120, Num 7, pp 1510-1515, issn 0006-4971, 6 p.Article

Extreme heterogeneity in CARD15 and DLG5 crohn disease-associated polymorphisms between German and Norwegian populationsMEDICI, Valentina; MASCHERETTI, Silvia; SCHREIBER, Stefan et al.European journal of human genetics. 2006, Vol 14, Num 4, pp 459-468, issn 1018-4813, 10 p.Article

Promotor polymorphisms of plasminogen activator inhibitor-1 and other thrombophilic genotypes in cerebral venous thrombosis: a case-control study in adultsRINGELSTEIN, Marius; JUNG, Alexander; BERGER, Klaus et al.Journal of neurology. 2012, Vol 259, Num 11, pp 2287-2292, issn 0340-5354, 6 p.Article

A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric strokeARNING, Astrid; HIERSCHE, Milan; WITTEN, Anika et al.Blood. 2012, Vol 120, Num 26, pp 5231-5236, issn 0006-4971, 6 p.Article

Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control StudiesASSIMES, Themistocles L; HOLM, Hilma; PATTERSON, Chris C et al.Journal of the American College of Cardiology. 2010, Vol 56, Num 19, pp 1552-1563, issn 0735-1097, 12 p.Article

A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczemaSCHULZ, Florian; MARENHOLZ, Ingo; STOLL, Monika et al.Journal of allergy and clinical immunology. 2007, Vol 120, Num 5, pp 1097-1102, issn 0091-6749, 6 p.Article

IBD5 is a general risk factor for inflammatory bowel disease: Replication of association with Crohn disease and identification of a novel association with ulcerative colitisGIALLOURAKIS, Cosmas; STOLL, Monika; MILLER, Katie et al.American journal of human genetics. 2003, Vol 73, Num 1, pp 205-211, issn 0002-9297, 7 p.Article

Differential regulation of thrombospondin-1 and fibronectin by angiotensin II receptor subtypes in cultured endothelial cellsFISCHER, Jens W; STOLL, Monika; HAHN, Alfred W. A et al.Cardiovascular research. 2001, Vol 51, Num 4, pp 784-791, issn 0008-6363Article

Genome-wide patterns of standing genetic variation in a marine population of three-spined sticklebacksFEULNER, Philine G. D; CHAIN, Frédéric J. J; REUSCH, Thorsten B. H et al.Molecular ecology. 2013, Vol 22, Num 3, pp 635-649, issn 0962-1083, 15 p.Article

Selective Loss of Noradrenaline Exacerbates Early Cognitive Dysfunction and Synaptic Deficits in APP/ PS1 MiceHAMMERSCHMIDT, Thea; KUMMER, Markus P; WEINSHENKER, David et al.Biological psychiatry (1969). 2013, Vol 73, Num 5, pp 454-463, issn 0006-3223, 10 p.Article

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation studyVOIGHT, Benjamin F; PELOSO, Gina M; SCHUNKERT, Heribert et al.Lancet (British edition). 2012, Vol 380, Num 9841, pp 572-580, issn 0140-6736, 9 p.Article

Osteopontin gene variation and cardio/cerebrovascular disease phenotypesSCHMIDT-PETERSEN, Klaus; BRAND, Eva; EVANS, Alun et al.Atherosclerosis. 2009, Vol 206, Num 1, pp 209-215, issn 0021-9150, 7 p.Article

Rat chromosome 19 transfer from SHR ameliorates hypertension, salt-sensitivity, cardiovascular and renal organ damage in salt-sensitive Dahl ratsWENDT, Norbert; SCHULZ, Angela; SIEGEL, Anja-Kristin et al.Journal of hypertension. 2007, Vol 25, Num 1, pp 95-102, issn 0263-6352, 8 p.Article

Regulation of transport of the angiotensin AT2 receptor by a novel membrane-associated golgi proteinWRUCK, Christoph J; FUNKE-KAISER, Heiko; PUFE, Thomas et al.Arteriosclerosis, thrombosis, and vascular biology. 2005, Vol 25, Num 1, pp 57-64, issn 1079-5642, 8 p.Article

A genomic-systems biology map for cardiovascular functionSTOLL, Monika; COWLEY, Allen W; TONELLATO, Peter J et al.Science (Washington, D.C.). 2001, Vol 294, Num 5547, pp 1723-1726, issn 0036-8075Article

DNA Methyltransferase Inhibition Reverses Epigenetically Embedded Phenotypes in Lung Cancer Preferentially Affecting Polycomb Target GenesHASCHER, Antje; HAASE, Ann-Kristin; OGAWA, Seishi et al.Clinical cancer research (Print). 2014, Vol 20, Num 4, pp 814-826, issn 1078-0432, 13 p.Article

Genetic variants implicated in telomere length associated with left ventricular function in patients with hypertension and cardiac organ damageHUBER, Matthias; TRESZL, Andras; VÖLLER, Heinz et al.Journal of molecular medicine (Berlin. Print). 2012, Vol 90, Num 9, pp 1059-1067, issn 0946-2716, 9 p.Article

The functional -374T/A polymorphism of the receptor for advanced glycation end products may modulate Crohn's diseaseDÄBRITZ, Jan; FRIEDRICHS, Frauke; FOELL, Dirk et al.American journal of physiology. Gastrointestinal and liver physiology. 2011, Vol 63, Num 5, issn 0193-1857, G823-G832Article

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