DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» KCNJ10
KCNJ10
Aquaporin Channels in the Heart—Physiology and Pathophysiology
Kir4.1 May Represent a Novel Therapeutic Target for Diabetic Retinopathy (Review)
Ion Channels
The Role of Potassium Recirculation in Cochlear Amplification
Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery
Original Article Transcript Expression Profiles of Stria Vascularis in Mitf-M Knockout Mice
Comparative Transcriptome Profiling of the Human and Mouse Dorsal Root Ganglia: an RNA-Seq-Based Resource for Pain and Sensory Neuroscience Research
Dimethylation of Histone 3 Lysine 9 Is Sensitive to the Epileptic Activity
Pflugers Final
Supplementary Table 1. Only Kcnj9 Shows Differential Expression
Viewer [Data Initial flurothyl-Induced Gsts Are Consistent with Not Shown (Yang Et Al
Critical for Homeostasis and Neuron-Glia Signaling
Sodium Channel Mutations in Epilepsy and Other Neurological Disorders
Gene List of the Targeted NGS MCD and CCA Gene Panel AKT3,ALX1
Genetic Variations Associated with Pharmacoresistant Epilepsy (Review)
EGL Test Description
Genome-Wide Association Study for Hereditary Ataxia in the Parson
Regulatory Networks Specifying Cortical Interneurons from Human
Top View
Genome-Wide Gene Expression Profiling of Randall's Plaques In
Progress in the Neurobiology of Potassium Channels and Epilepsy
Genetic and Molecular Studies in Hyperinsulinemic Hypoglycemia and Congenital Polycystic Kidney Disease (HIPKD)
Integrin-Linked Kinase Controls Renal Branching Morphogenesis Via Dual Specificity Phosphatase 8
Channelopathy Pathogenesis in Autism Spectrum Disorders
Multidimensional Genetic Analysis of Repeated Seizures in the Hybrid Mouse Diversity Panel 10 Reveals a Novel Epileptogenesis Susceptibility Locus
Ion Channels in the P14 Rat Brain
KCNJ10 Gene Mutations Causing EAST Syndrome (Epilepsy, Ataxia, Sensorineural Deafness, and Tubulopathy) Disrupt Channel Function
Mapping Astrocyte Transcriptional Signatures in Response to Neuroactive Compounds
Ion Channels As Therapeutic Targets in High Grade Gliomas
Screen-Based Identification and Validation of Four New Ion Channels As Regulators of Renal Ciliogenesis Gisela G
Non-Coding Rnas in Hereditary Kidney Disorders
Original Article Functional Implication of KCNJ10 Gene Polymorphism in Childhood Epilepsy
An Update on Novel Mechanisms of Primary Aldosteronism
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
Novel KCNJ10 Mutation Identified in a Sesame Family Compromise Channel Function and Impairs Drosophila Locomotor Behavior
Mechanisms of Neurological Dysfunction in GOSR2 Progressive Myoclonus Epilepsy, a Golgi Snareopathy James E.C. Jepsona*, Roman
KCNJ15/Kir4.2 Couples with Polyamines to Sense Weak Extracellular Electric fields in Galvanotaxis