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- Recurrent Copy Number Changes in Mentally Retarded Children Harbour Genes Involved in Cellular Localization and the Glutamate Receptor Complex
- Methods for Predicting Or Monitoring Whether a Patient Affected by a Cancer Is Responsive to a Treatment with a Molecule of the Taxoid Family
- KCNC3 (D-4): Sc-398047
- BK Channel Regulation of After-Potentials and Burst Firing in Cerebellar Purkinje Neurons
- Neuroscience
- Potassium Channels: Structures, Diseases, and Modulators
- Ion Channels in the P14 Rat Brain
- Mutations in Voltage-Gated Potassium Channel KCNC3 Cause Degenerative and Developmental Central Nervous System Phenotypes
- Upregulated Lncrna Pvt1 May Be Important for Cardiac Remodeling at the Infarct Border Zone
- Mechanism of Fibrosis in HNF1B-Related Autosomal Dominant Tubulointerstitial Kidney Disease
- Single-Cell Rnaseq Reveals Cell Adhesion Molecule Profiles
- Single-Cell Transcriptomic Profiling of Progenitors of the Oligodendrocyte Lineage Reveals Transcriptional Convergence During Development
- Functional Effects of Spinocerebellar Ataxia Type 13 Mutations Are
- Temporal Patterns of Gene Expression in the MNTB During Calyx of Held Development
- Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
- Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
- An Update on Novel Mechanisms of Primary Aldosteronism
- Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets