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1. Hubbard and Heisenberg models on hyperbolic lattices -- Metal-insulator transitions, global antiferromagnetism and enhanced boundary fluctuations

2. Flat band projections: Sign problem mapping for frustrated spin systems

3. Phases and Exotic Phase Transitions of a Two-Dimensional Su-Schrieffer-Heeger Model

4. Valence-bond solid to antiferromagnet transition in the two-dimensional Su-Schrieffer-Heeger model by Langevin dynamics

6. Codebase release 2.0 for ALF (Algorithms for Lattice Fermions)

8. Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction

11. Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population

12. Repeated Replication and a Prospective Meta-Analysis of the Association Between Chromosome 9p21.3 and Coronary Artery Disease

13. Lack of Association Between the MEF2A Gene and Myocardial Infarction

14. Abstract 3452: The Common Variant Rs9939609 In The FTO Gene Is Associated With Myocardial Infarction In Two Large German Populations (German Family MI Study And KORA-B)

15. Association between arterial pressure and coronary artery calcification

16. Ultrafine mapping of Dyscalc1 to an 80-kb chromosomal segment on chromosome 7 in mice susceptible for dystrophic calcification

17. Association of a functional polymorphism in the CYP4A11 gene with systolic blood pressure in survivors of myocardial infarction

18. Association of angiotensin-converting enzyme 2 (ACE2) gene polymorphisms with parameters of left ventricular hypertrophy in men

19. Association of the T8590C Polymorphism of CYP4A11 With Hypertension in the MONICA Augsburg Echocardiographic Substudy

20. Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.

21. Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease--A Mendelian Randomisation Study.

22. Association of a functional polymorphism in the CYP4A11gene with systolic blood pressure in survivors of myocardial infarction

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