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KCNJ16
The Mineralocorticoid Receptor Leads to Increased Expression of EGFR
The Chondrocyte Channelome: a Novel Ion Channel Candidate in the Pathogenesis of Pectus Deformities
Ion Channels
Altered Physiological Functions and Ion Currents in Atrial Fibroblasts From
Dimethylation of Histone 3 Lysine 9 Is Sensitive to the Epileptic Activity
Pflugers Final
Caveolin-1 Deficiency Inhibits the Basolateral K Channels in The
Renal Phenotype in Mice Lacking the Kir5.1 (Kcnj16) K Channel Subunit
Disease Associated Mutations in KIR Proteins Linked to Aberrant Inward Rectifier Channel Trafficking
RT² Profiler PCR Array (96-Well Format and 384-Well [4 X 96] Format)
Inwardly Rectifying Potassium Channel
Genome-Wide Analysis of Differential Gene Expression and Splicing in Excitatory Neurons and Interneuron Subtypes
Rare Independent Mutations in Renal Salt Handling Genes Contribute to Blood Pressure Variation
Recurrent Copy Number Changes in Mentally Retarded Children Harbour Genes Involved in Cellular Localization and the Glutamate Receptor Complex
Viewed Papers: Yin K, Baillie GJ and Vetter I
RT² Profiler PCR Array (Rotor-Gene® Format) Mouse Neuronal Ion Channels
Transcriptomes of Major Renal Collecting Duct Cell Types In
The Effect of Calcineurin Inhibition on the Expression and Activation of Renal Electrolyte Transporters
Top View
Integrin-Linked Kinase Controls Renal Branching Morphogenesis Via Dual Specificity Phosphatase 8
Ion Channels Expression and Function Are Strongly Modified in Solid Tumors and Vascular Malformations
Biallelic Loss-Of-Function Variants in KCNJ16 Presenting with Hypokalemic Metabolic Acidosis
Potassium Channels: Structures, Diseases, and Modulators
Ion Channels in the P14 Rat Brain
KCNJ10 Gene Mutations Causing EAST Syndrome (Epilepsy, Ataxia, Sensorineural Deafness, and Tubulopathy) Disrupt Channel Function
SUPPLEMENTARY DATA Supplementary Table 1. Characteristics of the Organ Donors and Human Islet Preparations Used for RNA-Seq
Potassium Channels in Prostate and Colonic Cancer
Single-Cell Transcriptomic Profiling of Progenitors of the Oligodendrocyte Lineage Reveals Transcriptional Convergence During Development
Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia
Ion Channel Pharmacology
An Update on Novel Mechanisms of Primary Aldosteronism
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Supplemental Table S18. Cellular Process Enrichment Analysis Output
Plasma Membrane Protein Identifications from Human Bone Marrow Mesenchymal Stem Cells
Supplementary Table 1. Genes Screened in the Present Study
The Intratumoral Balance Between Metabolic and Immunologic Gene
Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa