DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Dysbindin
Dysbindin
Ryanodine Receptors Are Part of the Myospryn Complex in Cardiac Muscle Received: 10 March 2017 Matthew A
Dystrophin Complex Functions As a Scaffold for Signalling Proteins☆
The Neurotransmitter Released at the Neuromuscular Junction Is
Genomics of Inherited Bone Marrow Failure and Myelodysplasia Michael
©Ferrata Storti Foundation
Α-Dystrobrevin-1 Recruits Α-Catulin to the Α1d- Adrenergic Receptor/Dystrophin-Associated Protein Complex Signalosome
2018 Mesh Headings by Subcategory
Pharmacological and Genetic Evidence of Dopamine Receptor 3-Mediated Vasoconstriction in Isolated Mouse Aorta
Cardiomyopathy-Associated 5) Is Associated with Left Ventricular Wall Thickness in Patients with Hypertension
The E3 Ligase TRIM32 Is an Effector of the RAS Family Gtpase RAP2
Dystroglycan in the Nervous System
The Growing Family of Limb-Girdle Muscular Dystrophies: Old and Newly Identified Members
Ryanodine Receptors Are Part of the Myospryn Complex in Cardiac Muscle
Sarcomeric Gene Variants and Their Role with Left Ventricular Dysfunction in Background of Coronary Artery Disease
Lola Regulates Glutamate Receptor Expression at the Drosophila Neuromuscular Junction
Ubiquitylation by Trim32 Causes Coupled Loss of Desmin, Z-Bands, and Thin Filaments in Muscle Atrophy
Gene Dosage in the Dysbindin Schizophrenia Susceptibility Network Differentially Affect Synaptic Function and Plasticity
The Dystrobrevin-Binding Protein 1 Gene
Top View
A Schizophrenia Associated CMYA5 Allele Displays Differential Binding with T Desmin ∗∗ ∗ Anting Hsiunga, Francisco J
TRIM32: a Multifunctional Protein Involved in Muscle Homeostasis, Glucose Metabolism, and Tumorigenesis
Schizophrenia Susceptibility Gene Dysbindin Regulates Glutamatergic and Dopaminergic Functions Via Distinctive Mechanisms in Drosophila
The Dysbindin-Containing Complex (BLOC-1) in Brain
Novel Genetic Defects in Titinopathies and Other Muscular Dystrophies
Essential Role for Insyn1 in Dystroglycan Complex Integrity And
Dysbindin Deficiency Alters Cardiac BLOC-1 Complex and Myozap
Notch3 Is Necessary for Blood Vessel Integrity in the Central Nervous System
A New Model for the Dystrophin Associated Protein Complex in Striated
Thin, a Trim32 Ortholog, Is Essential for Myo Fibril Stability and Is Required
The E3 Ligase Thin Controls Homeostatic Plasticity Through Neurotransmitter Release Repression
Human Dysbindin (DTNBP1) Gene Expression Innormal Brain and In
Dysbindin Links Presynaptic Proteasome Function to Homeostatic Recruitment of Low Release Probability Vesicles
Novel TRIM32 Mutation in Sarcotubular Myopathy
Type III Intermediate Filaments Desmin, Glial Fibrillary Acidic Protein (GFAP), Vimentin, and Peripherin
Lost in Transdifferentiation
Characterizing the Role of Hspb2 in Cardiac Metabolism and Muscle Structure Using Yeast and Mammalian Systems
Functional Study of Cmya5, a Candidate Gene for Schizophrenia
Regulation of Nicotinic Acetylcholine Receptor Stability at the Mouse Neuromuscular Junction By
Dysbindin-1 and Schizophrenia: from Genetics to Neuropathology
Investigation for Novel Schizophrenia Candidate
Misregulation of Autophagy and Protein Degradation Systems In
Dysbindin-1 Involvement in the Etiology of Schizophrenia
Schizophrenia Susceptibility Gene Dysbindin Regulates Glutamatergic and Dopaminergic Functions Via Distinctive Mechanisms in Drosophila
ANTIBODIES for NEUROSCIENCE 2 Antibodies for Neuroscience
Increased Dysbindin-1B Isoform Expression in Schizophrenia and Its Propensity in Aggresome Formation
The Ubiquitin Ligase Tripartite-Motif-Protein 32 Is Induced
Abnormal Dysbindin Expression in Cerebellar Mossy Fiber Synapses in the Mdx Mouse Model of Duchenne Muscular Dystrophy
The Role of Alpha-Dystrobrevin in Striated Muscle
TRIM32 Is an E3 Ubiquitin Ligase for Dysbindin