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CHRNE
Protein Identities in Evs Isolated from U87-MG GBM Cells As Determined by NG LC-MS/MS
Research Article Microarray-Based Comparisons of Ion Channel Expression Patterns: Human Keratinocytes to Reprogrammed Hipscs To
Stem Cells and Ion Channels
Ion Channels
Replicated Risk Nicotinic Cholinergic Receptor Genes for Nicotine Dependence
Congenital Myasthenic Syndrome Due to Mutation in CHRNE Gene
Pathscore: a Web Tool for Identifying Altered Pathways in Cancer Data Stephen G
Naturally Occurring Variants of Human A9 Nicotinic Receptor Differentially Affect Bronchial Cell Proliferation and Transformation
Altered Expression of Genes Encoding Neurotransmitter Receptors in Gnrh Neurons of Proestrous Mice
ION CHANNEL RECEPTORS TÁMOP-4.1.2-08/1/A-2009-0011 Ion Channel Receptors
Ion Channels in the P14 Rat Brain
Congenital Myasthenic Syndrome Treatment Heterogeneity Makes Diagnosis and Treatment Challenging
Identification of Differentially Expressed Genes in Pathways of Cerebral Neurotransmission of Anovulatory Mice
Escobar Syndrome; Pterygium Syndrome; Multiple Pterygium Syndrome, Non- Lethal Type; Familial Pterygium Syndrome; Pterygium Colli Syndrome; Pterygium Universale
Transcriptional Landscapes of Emerging Autoimmunity
Molecular Neurobiology and Genetics: Review Investigation of Neural Function and Dysfunction
Microarray-Based Comparisons of Ion Channel Expression Patterns: Human Keratinocytes to Reprogrammed Hipscs to Differentiated Neuronal and Cardiac Progeny
Viewed from the Extracellular Space Appear Tetraploidization [17] After It Diverged from Sarcopterygii Clockwise in the Order Α-Δ-Β-Α-Ε
Top View
Congenital Myasthenic Syndromes Genereview – Achr Subunit Genes Authors: Abicht A, Müller J, Lochmüller H Updated: July 2016
Genetic Neurological Channelopathies: Molecular Genetics and Clinical Phenotypes J Spillane,1,2 D M Kullmann,2,3 M G Hanna2,3
Nicotinic Acetylcholine Receptor-Mediated Signaling Pathways in Pluripotent Stem Cells
Animal Models of the Neuromuscular Junction, Vitally Informative for Understanding Function and the Molecular Mechanisms of Congenital Myasthenic Syndromes
Ligand-Gated Ion Channels
Congenital Myasthenic Syndromes Josef Finsterer
Disruption of Retinal Pigment Epithelial Cell Properties Under the Exposure
Nutritional Contingency Reduces Alcohol Drinking by Altering Central Neurotransmitter Receptor Gene Expression in Rats
Sex Difference in Expression of Autism Candidate Gene Gabrb3 in Mouse Amygdala
Ion Channels Product Listing | Edition 1
Distinct Evolutionary Trajectories of Neuronal and Hair Cell Nicotinic Acetylcholine Receptors
CHRNG Gene Cholinergic Receptor Nicotinic Gamma Subunit
Gut Acellular Matrix for the in Vitro Study of Enteric Nervous System Cells
Human Ligand Gated Ion Channels Primer Library
Ethnically Unique Mutations in Muscle Nicotinic Acetylcholine Receptor Subunits
Endogenous Cholinergic Neurotransmission Contributes to Behavioral Sensitization to Morphine
Transcriptomic Profiling of Ca2+ Transport Systems During the Formation of the Cerebral Cortex in Mice Alexandre Bouron
CHRNE Gene Cholinergic Receptor Nicotinic Epsilon Subunit