29 results on '"Orgil, Buyan‐Ochir"'
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2. Abstract 15846: Impaired Contraction and High Susceptibility to Arrhythmias in a Mouse Model of Desmoplakin-Mediated Arrhythmogenic Cardiomyopathy
3. Abstract 14573: Dissecting Genetic Determinants Underlying Cardioskeletal Phenotypes Induced by Myopalladin Mutation in Murine Genetic Reference Population of Hybrid BXD Strains
4. Myocardial Remodeling with Ventricular Assist Devices
5. Acetylation of Checkpoint suppressor 1 enhances its stability and promotes the progression of triple-negative breast cancer
6. Systems genetics analysis reveals the common genetic basis for pain sensitivity and cognitive function
7. Abstract 11608: Differences in Genetic Variants and Common Genetic Regulators between Arrhythmogenic Cardiomyopathy and Arrhythmogenic Dilated Cardiomyopathy Identified Using Systems Genetics Approaches
8. Left Ventricular Noncompaction Cardiomyopathy: From Clinical Features to Animal Modeling
9. Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach.
10. Expression Levels of the Tnni3k Gene in the Heart Are Highly Associated with Cardiac and Glucose Metabolism-Related Phenotypes and Functional Pathways
11. Abstract P1182: The Genetic Dissection Of Rpl3l As A Causal Gene For Neonatal Dilated Cardiomyopathy And Left Ventricular Noncompaction
12. Analysis of electrocardiography parameters in BXD strains and quantitative trait loci for arrhythmia disorders in the mouse BXD family
13. The TMEM43 S358L mutation affects cardiac, small intestine, and metabolic homeostasis in a knock-in mouse model
14. Cardiac copper content and its relationship with heart physiology: Insights based on quantitative genetic and functional analyses using BXD family mice
15. Echocardiography phenotyping in murine genetic reference population of BXD strains reveals significant QTLs associated with cardiac function and morphology
16. Analysis of cardiac function and morphology in genetic reference population of BXD strains reveals associated eQTLs and candidate causal and modifier genes
17. Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling
18. Combining whole exome sequencing with in silico analysis and clinical data to identify candidate variants in pediatric left ventricular noncompaction
19. Systems genetics analysis defines importance of TMEM43/LUMA for cardiac- and metabolic-related pathways
20. Ace2 and Tmprss2 Expressions Are Regulated by Dhx32 and Influence the Gastrointestinal Symptoms Caused by SARS-CoV-2
21. Abstract P414: Systems Genetics Analysis Reveals Significant Eqtls Associated With Echocardiography Parameters In Genetic Reference Population Of Bxd Strains.
22. Deficiency in nebulin repeats of sarcomeric nebulette is detrimental for cardiomyocyte tolerance to exercise and biomechanical stress
23. Systems genetics analysis defines importance of TMEM43/LUMA for cardiacand metabolic-related pathways.
24. The Tmem43-S358l Mutation Affects Cardiac and Small Intestine Homeostasis Contributing to Arvc5 Pathogenesis in Vivo
25. Left Ventricular Noncompaction Cardiomyopathy : From Clinical Features to Animal Modeling
26. Exploring the Regulation and Function of Rpl3l in the Development of Early-Onset Dilated Cardiomyopathy and Congestive Heart Failure Using Systems Genetics Approach.
27. The TMEM43 S358L mutation affects cardiac, small intestine, and metabolic homeostasis in a knock-in mouse model.
28. Systems genetics analysis defines importance of TMEM43/ LUMA for cardiac- and metabolic-related pathways.
29. Deficiency in nebulin repeats of sarcomeric nebulette is detrimental for cardiomyocyte tolerance to exercise and biomechanical stress.
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