K_ATP channels and cardiovascular disease: Suddenly a syndrome

Keyphrases

• ABCC8 33%
• ABCC9 33%
• ATP-sensitive Potassium Channel 33%
• Atrial Fibrillation 33%
• Cantú Syndrome 33%
• Cardiomegaly 33%
• Cardiovascular Disease 100%
• Cardiovascular System 33%
• Channel Activity 33%
• Channel Gating 33%
• Channel Pore 33%
• Co-expression 33%
• Craniofacial Dysmorphology 33%
• Gain-of-function mutation 33%
• Gating Properties 33%
• Gene Family 33%
• Genetic mutation 33%
• Genomic Deletion 33%
• Heart Failure 33%
• Hypertrichosis 33%
• Inward Rectifier Potassium Channel 33%
• J Wave Syndrome 33%
• KATP Channel 100%
• KCNJ11 33%
• KCNJ8 33%
• Kir6.1 66%
• Kir6.2 33%
• Lymphedema 33%
• Multi-organ 33%
• Novel Therapeutics 33%
• Osteochondrodysplasias 33%
• Patent Ductus Arteriosus 33%
• Paucity 33%
• Pericardial Effusion 33%
• Pore Properties 33%
• Pore-forming 33%
• Protein Family 33%
• Reconstitution 33%
• SUR1 66%
• SUR2 100%
• Therapeutic Potential 33%

Medicine and Dentistry

• Adenosine Triphosphate 25%
• Adenosine Triphosphate Sensitive Potassium Channel 100%
• Atrial Fibrillation 25%
• Cardiomegaly 25%
• Cardiovascular Disease 100%
• Cardiovascular System 25%
• Channel Gating 25%
• Chondrodysplasia 25%
• Disease 25%
• Dysmorphology 25%
• Electrocardiogram 25%
• Gene Deletion 25%
• Gene Mutation 25%
• Heart Failure 25%
• Hypertrichosis 25%
• Inward-Rectifier Potassium Ion Channel 25%
• J Wave 25%
• KCNJ8 25%
• Kir6.2 25%
• Loss of Function Mutation 25%
• Lymphedema 25%
• Multigene Family 25%
• Patent Ductus Arteriosus 25%
• Pericardial Fluid 25%
• Protein Subfamily 25%
• Sulfonylurea Receptor 25%

Biochemistry, Genetics and Molecular Biology

• ABCC8 25%
• ABCC9 25%
• Adenosine Triphosphate 25%
• ATP-Sensitive Potassium Channel 100%
• Atrial Fibrillation 25%
• Channel Gating 25%
• Electrocardiogram 25%
• Gene Deletion 25%
• Gene Mutation 25%
• Inward-Rectifier Potassium Ion Channel 25%
• KCNJ8 25%
• Kir6.2 25%
• Loss of Function Mutation 25%
• Mouse 25%
• Multigene Family 25%
• Pericardial Effusion 25%
• Protein Subfamily 25%
• Sulfonylurea Receptor 25%