142 results on '"Aguib, Yasmine"'
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2. Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies.
3. Abstract 4144298: Structural Remodeling of Coronary Microvasculature in Hypertrophic Obstructive Cardiomyopathy
4. Abstract 4136813: Redox Serum Proteomics Of Left Ventricular Assist Device Unloaded Human Heart
5. Abstract 4124828: The Methylation Landscape Of Human Aortic And Mitral Valvular Interstitial Cells
6. The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings
7. Abstract 15077: Mitochondrial LonP1 Upregulation in End Stage Heart Failure
8. Potential long-term effects of SARS-CoV-2 infection on the pulmonary vasculature: a global perspective
9. Author Correction: Individualized interactomes for network-based precision medicine in hypertrophic cardiomyopathy with implications for other clinical pathophenotypes
10. Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
11. Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions
12. Cor Triatriatum Sinister (Divided Left Atrium): Histopathologic Features and Clinical Management
13. Abstract 14969: Transcriptome Signature of Cardiac Fibroblasts in HCM Patients Identifies Novel Drivers Of ECM Remodeling and Pro-Inflammatory Signaling
14. Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy
15. Individualized interactomes for network-based precision medicine in hypertrophic cardiomyopathy with implications for other clinical pathophenotypes
16. Thioredoxin‐1 and its mimetic peptide improve systolic cardiac function and remodeling after myocardial infarction
17. Aortic root dynamism, geometry, and function after the remodeling operation: Clinical relevance
18. New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic Cardiomyopathy
19. The Egyptian Collaborative Cardiac Genomics (ECCO-GEN) Project: defining a healthy volunteer cohort
20. Abstract P2036: Induced Pluripotent Stem Cell- Derived Cardiomyocytes Provide New Insights Of The Pathogenic Consequences Of The Novel Frameshift Variant (c.5769delG) In MYH7 Gene
21. Ethnicity, consanguinity, and genetic architecture of hypertrophic cardiomyopathy
22. Thioredoxin‐1 and its mimetic peptide improve systolic cardiac function and remodeling after myocardial infarction.
23. Structural and Functional Characterization of the Aorta in Hypertrophic Obstructive Cardiomyopathy
24. Generation of cardiomyocytes from human-induced pluripotent stem cells resembling atrial cells with ability to respond to adrenoceptor agonists
25. The penetrance of rare variants in cardiomyopathy-associated genes: a cross-sectional approach to estimate penetrance for secondary findings
26. Abstract P632: The Ballana Heart Study: Preliminary Results
27. Author Correction: Individualized interactomes for networkbased precision medicine in hypertrophic cardiomyopathy with implications for other clinical pathophenotypes.
28. Influence of ethnicity and consanguinity on the genetic architecture of Hypertrophic Cardiomyopathy: insights from an understudied population
29. Generation of cardiomyocytes from human induced pluripotent stem cells resembling atrial cells with ability to respond to adrenoceptor agonists
30. Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves
31. Potential long-term effects of SARS-CoV-2 infection on the pulmonary vasculature: a global perspective
32. Neuroendocrine cultured cells counteract persistent prion infection by down-regulation of PrP c
33. Autophagy, Prion Infection and their Mutual Interactions
34. Clinical, cellular, and molecular characterisation of cardiac rhabdomyoma in tuberous sclerosis
35. An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy
36. Profiling Genome-Wide DNA Methylation Patterns in Human Aortic and Mitral Valves
37. Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions
38. Analysis of HCM in an understudied population reveals a new mechanism of pathogenicity
39. Lithium induces clearance of protease resistant prion protein in prion-infected cells by induction of autophagy
40. Functional humanization of an anti-CD16 Fab fragment: obstacles of switching from murine λ to human λ or κ light chains
41. CpG and LPS can interfere negatively with prion clearance in macrophage and microglial cells
42. The genetic architecture of left ventricular non-compaction reveals both substantial overlap with other cardiomyopathies and a distinct aetiology in a subset of cases
43. Genomics of Egyptian Healthy Volunteers: The EHVol Study
44. CLINICAL AND MOLECULAR FEATURES OF ELEVEN EGYPTIAN FAMILIES WITH AUTOSOMAL RECESSIVE LONG QT SYNDROME
45. Advanced fluorescence microscopy techniques for the life sciences
46. Molecular mechanisms of cardiovascular benefits of exercise: Running for cover from heart disease
47. Pharmakologische und genetische Manipulation der Autophagie und ihre Auswirkungen in diversen Szenarien der Prion-Infektion
48. The Copenhagen City Heart Study (Østerbroundersøgelsen)
49. NaNog: A pluripotency homeobox (master) molecule
50. In search for molecular mechanisms of Post COVID-19 vascular damage
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