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5. Contributors

7. Contributors

9. F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes

10. Investigating Genetic Diversity and Population Structure in Rice Breeding from Association Mapping of 116 Accessions Using 64 Polymorphic SSR Markers

11. Gene Dosage of F5 c.3481C>T Stop-Codon (p.R1161Ter) Switches the Clinical Phenotype from Severe Thrombosis to Recurrent Haemorrhage: Novel Hypotheses for Readthrough Strategy

12. Genetic variants associated with methotrexate-induced mucositis in cancer treatment: A systematic review and meta-analysis

13. circRNAs as Epigenetic Regulators of Integrity in Blood–Brain Barrier Architecture: Mechanisms and Therapeutic Strategies in Multiple Sclerosis.

17. In vitroand ex vivorescue of a nonsense mutation responsible for severe coagulation factor V deficiency

19. The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile

20. Host genetics impact on SARS-CoV-2 vaccine-induced immunoglobulin levels and dynamics: The role of TP53, ABO, APOE, ACE2, HLA-A, and CRP genes

21. Micropatterned Neurovascular Interface to Mimic the Blood–Brain Barrier’s Neurophysiology and Micromechanical Function: A BBB-on-CHIP Model

25. Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls

28. A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia

29. Sustainable Agriculture through Multidisciplinary Seed Nanopriming: Prospects of Opportunities and Challenges

30. Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis

31. Cis-Segregation of c.1171C>T Stop Codon (p.R391*) in SERPINC1 Gene and c.1691G>A Transition (p.R506Q) in F5 Gene and Selected GWAS Multilocus Approach in Inherited Thrombophilia

35. Genotype and PK Hemophilia B International Study (GePKHIS) - A progress Report

36. Hemostasis gene expression of the internal jugular and saphenous veins

38. Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes

39. Sex/Gender-Specific Imbalance in CVD: Could Physical Activity Help to Improve Clinical Outcome Targeting CVD Molecular Mechanisms in Women?

44. Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes

47. Recent Advances in Plant Nanobionics and Nanobiosensors for Toxicology Applications

49. “Bridging the Gap” Everything that Could Have Been Avoided If We Had Applied Gender Medicine, Pharmacogenetics and Personalized Medicine in the Gender-Omics and Sex-Omics Era

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