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CACNA1H
The Mineralocorticoid Receptor Leads to Increased Expression of EGFR
Supplementary Table 1. Pain and PTSS Associated Genes (N = 604
Phenotypic Spectrum and Long-Term Outcome in Children with Genetic Causes of Early-Onset Epileptic Encephalopathy
An Advance About the Genetic Causes of Epilepsy
Transcriptomic Profiling of Ca Transport Systems During
Transcriptomic Uniqueness and Commonality of the Ion Channels and Transporters in the Four Heart Chambers Sanda Iacobas1, Bogdan Amuzescu2 & Dumitru A
Identification of Key Pathways and Genes in Dementia Via Integrated Bioinformatics Analysis
A Rare CACNA1H Variant Associated with Amyotrophic Lateral Sclerosis Causes Complete Loss of Cav3.2 T-Type Channel Activity Robin N
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
Co-Expression Network of Neural-Differentiation Genes Shows
1 1 2 3 Cell Type-Specific Transcriptomics of Hypothalamic
Graded Co-Expression of Ion Channel, Neurofilament, and Synaptic Genes in Fast- Spiking Vestibular Nucleus Neurons
Clinical, Molecular, and Immune Analysis of Dabrafenib-Trametinib
CLCN2 Clicks with Aldosterone-Producing Adenomas, Too!
Epilepsy Next-Generation Sequencing Guide
Genetic T-Type Calcium Channelopathies Norbert Weiss, 1 Gerald W Zamponi 2
A Meta-Analysis of the Effects of High-LET Ionizing Radiations in Human Gene Expression
Update on Genetics of Primary Aldosteronism
Top View
Repositioning Trimebutine Maleate As a Cancer Treatment Targeting Ovarian Cancer Stem Cells
Paralogue Annotation Identifies Novel Pathogenic Variants in Patients With
Ion Channels in the P14 Rat Brain
SUPPLEMENTARY DATA Supplementary Table 1. Characteristics of the Organ Donors and Human Islet Preparations Used for RNA-Seq
Investigations of Somatic and Germline Mutations in Primary Aldosteronism
Transcript Length Frequency 0 0 50 0 100 9 200 20 300 33 400 89 500
A Gain-Of-Function Mutation in the CLCN2 Chloride Channel Gene Causes Primary Aldosteronism
An Update on Novel Mechanisms of Primary Aldosteronism
Neurological Channelopathies T D Graves, M G Hanna
Ion Channel Expression in Human Melanoma Samples: in Silico Identification and Experimental Validation of Molecular Targets
A Somatic Mutation in CLCN2 Identified in a Sporadic Aldosterone-Producing Adenoma
A Common Haplotype Containing Functional CACNA1H Variants Is Frequently Coinherited with Increased TPSAB1 Copy Number
Plasma Membrane Protein Identifications from Human Bone Marrow Mesenchymal Stem Cells
Genbank Accession No. Gene Symbol Expression Ratio (Shm2/Shc9) Title
Mutations in Disordered Regions Cause Disease by Creating Endocytosis Motifs
Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
Of the Differential Expression of Cardiac Muscle Contraction (CMC)
List of Gene Panels Used for Epilepsy Diagnosis in Different Companies