184 results on '"Chahine, Mohamed"'
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2. The angiotensin II type 1 receptor mediates the induction of oxidative stress, apoptosis, and autophagy in HUVECs induced by angiotensin II
3. Arrhythmias and ion channelopathies causing sudden cardiac death in Hispanic/Latino and Indigenous populations
4. Arrhythmias and Ion Channelopathies Causing Sudden Cardiac Death in Hispanic/Latino and Indigenous Populations
5. Channelopathies in epilepsy: an overview of clinical presentations, pathogenic mechanisms, and therapeutic insights
6. Cloning, functional expression, and pharmacological characterization of inwardly rectifying potassium channels (Kir) from Apis mellifera
7. Generation of three myotonic dystrophy type 1 patient iPSC lines (CBRCULi018-A, CBRCULi019-A, CBRCULi020-A) derived from lymphoblastoid cell lines for disease modelling and therapeutic research
8. Honeybee CaV4 has distinct permeation, inactivation, and pharmacology from homologous NaV channels
9. Generation of a patient-specific iPSC cell line with cardiac arrhythmias and dilated cardiomyopathy (CBRCULi016-A), an isogenic control (CBRCULi016-A-1), and a paternal control (CBRCULi017-A)
10. The impact of BMI on breast cancer – an updated systematic review and meta-analysis
11. Lymphoblastoid-derived human-induced pluripotent stem cells
12. Contributors
13. Biophysical properties of NaV1.5 channels from atrial-like and ventricular-like cardiomyocytes derived from human induced pluripotent stem cells
14. Generation of induced pluripotent stem cell lines from pediatric patients with congenital myotonic dystrophy (CBRCULi012-A and CBRCULi013-A) and age-matched controls (CBRCULi010-A and CBRCULi011-A)
15. Electrophysiological basis of cardiac arrhythmia in a mouse model of myotonic dystrophy type 1
16. Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels
17. Generation of control iPSC lines CBRCULi008-A and CBRCULi009-A derived from lymphoblastoid cell lines
18. Lymphoblastoid cell lines derived from iPSCs of a myotonic dystrophy type 1 patient carrying 700 CTG repeats (CBRCULi007-A) and a control (CBRCULi006-A)
19. Optical Mapping of Cardiomyocytes in Monolayer Derived from Induced Pluripotent Stem Cells
20. Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death
21. Role of Late Sodium Current During Repolarization and Its Pathophysiology
22. Pathophysiology of Cav1.3 L-type calcium channels in the heart
23. Generation of four myotonic dystrophy type 1 patient iPSC lines (CBRCULi002-A, CBRCULi003-A, CBRCULi004-A, CBRCULi005-A) and a control (CBRCULi001-A) derived from lymphoblastoids cell lines
24. The Effects of Ketogenic Diet on the Immune System: A Meta-Analysis
25. Combining Influenza and COVID-19 Booster Vaccination Strategy to Improve Vaccination Uptake Necessary for Managing the Health Pandemic: A Systematic Review and Meta-Analysis
26. Does Losing Weight Lower the Risk of Cancer: A Systematic Review and Meta-analysis
27. The impact of BMI on Ovarian Cancer- An Updated Systematic Review and Metanalysis
28. The impact of body mass index on prostate cancer: An updated systematic review and meta-analysis
29. Recent Progress and Challenges in the Development of Antisense Therapies for Myotonic Dystrophy Type 1
30. Combining NGN2 programming and dopaminergic patterning for a rapid and efficient generation of hiPSC-derived midbrain neurons
31. De novo Y1460C missense variant in NaV1.1 impedes the pore region and results in epileptic encephalopathy
32. Enhanced Delivery of Ligand-Conjugated Antisense Oligonucleotides (C16-HA-ASO) Targeting Dystrophia Myotonica Protein Kinase Transcripts for the Treatment of Myotonic Dystrophy Type 1
33. Regulation of Cardiac Voltage-Gated Sodium Channel by Kinases: Roles of Protein Kinases A and C
34. Editorial: Structure Related Druggability of Voltage-Gated Sodium and Calcium Ion-Channels to Treat Diseases
35. SCN2A-related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects
36. Review of: "Structure-guided unlocking of NaX reveals a non-selective tetrodotoxin-sensitive cation channel"
37. Racial Disparities in Ion Channelopathies and Inherited Cardiovascular Diseases Associated With Sudden Cardiac Death
38. NPRL2 Inhibition of mTORC1 Controls Sodium Channel Expression and Brain Amino Acid Homeostasis
39. Nav1.5 knockout in iPSCs: a novel approach to study Nav1.5 variants in a human cardiomyocyte environment
40. Biophysical characterization of SCN1A and SCN2A variants related to epilepsy
41. Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1
42. Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy
43. The Myocardial and Neuronal Infectivity of SARS-CoV-2 and Detrimental Outcomes
44. NaV1.5 knockout in iPSCs: a novel approach to study NaV1.5 variants in a human cardiomyocyte environment
45. B-PO05-022 CLINICAL AND FUNCTIONAL CHARACTERIZATION OF SCN5A VARIANTS LINKED TO ADRENERGIC VENTRICULAR ARRHYTHMIA: A MULTICENTER STUDY
46. Review of: "Disorganization of intercalated discs in dilated cardiomyopathy"
47. Performance Analysis of Vertical Handover using Predictable LGD Event based on IEEE 802.21
48. Regulation/Modulation of Sensory Neuron Sodium Channels
49. Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State
50. iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities
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