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Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 7/2006, Volume 63, Issue 14, pp. 1614 - 1631
The dystrophin glycoprotein complex (DGC) is a multimeric protein assembly associated with either the X-linked cytoskeletal protein dystrophin or its autosomal... 
Biochemistry, general | Dp71 | endothelial cell | dystrophin | epithelial cell | utrophin | targeted gene deletion | Biomedicine general | Cell Biology | choroid plexus | Life Sciences | homeostasis | kidney | Life Sciences, general | Blood-brain barrier | retina | transmembrane signaling | Choroid plexus | Endothelial cell | Targeted gene deletion | Utrophin | Homeostasis | Epithelial cell | Retina | Transmembrane signaling | Dystrophin | Kidney | blood-brain barrier | TEMPORAL-LOBE EPILEPSY | MULLER GLIAL-CELLS | NITRIC-OXIDE SYNTHASE | ACETYLCHOLINE-RECEPTOR AGGREGATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | WATER CHANNEL PROTEIN | BLOOD-BRAIN-BARRIER | CELL BIOLOGY | SYNTROPHIN PDZ DOMAIN | DUCHENNE MUSCULAR-DYSTROPHY | CENTRAL-NERVOUS-SYSTEM | ADULT SKELETAL-MUSCLE | Muscular Dystrophy, Animal - genetics | Dystroglycans - deficiency | Humans | Nerve Tissue Proteins - deficiency | Muscle, Skeletal - metabolism | Neuromuscular Junction - chemistry | Utrophin - deficiency | Kidney - metabolism | Mice, Inbred mdx | Muscle Proteins - physiology | Dystroglycans - physiology | Actin Cytoskeleton - metabolism | Sarcoglycans - metabolism | Mice, Knockout | Muscle Proteins - genetics | Utrophin - physiology | Models, Biological | Brain Chemistry | Dystrophin-Associated Protein Complex - physiology | Eye Proteins - physiology | Mice | Muscular Dystrophy, Duchenne - genetics | Blood-Brain Barrier | Neuromuscular Junction - physiology | Retina - metabolism | Dystrophin-Associated Protein Complex - chemistry | Utrophin - genetics | Choroid Plexus - metabolism | Muscle Proteins - deficiency | Neoplasm Proteins - metabolism | Dystrophin - physiology | Dystrophin-Associated Proteins - genetics | Dystrophin-Associated Proteins - metabolism | Dystrophin - deficiency | Muscular Dystrophy, Animal - metabolism | Membrane Proteins - metabolism | Eye Proteins - genetics | Nerve Tissue Proteins - physiology | Dystrophin-Associated Proteins - deficiency | Dystrophin - chemistry | Organ Specificity | Nerve Tissue Proteins - genetics | Protein Isoforms - physiology | Animals | Carrier Proteins - metabolism | Dystrophin - genetics | Protein Binding | Dystroglycans - genetics | Muscular Dystrophy, Duchenne - metabolism | Proteins | Cells
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/2017, Volume 292, Issue 24, pp. 10180 - 10196
We have previously shown that dysbindin is a potent inducer of cardiomyocyte hypertrophy via activation of Rho-dependent serum-response factor (SRF) signaling.... 
COACTIVATOR HTIF1 | SCHIZOPHRENIA-RELATED PROTEIN | NUCLEAR RECEPTORS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC-HYPERTROPHY | IN-VIVO | TRIPARTITE MOTIF | SERUM RESPONSE FACTOR | FAMILY PROTEINS | MUSCLE RING FINGER-1 | E3 UBIQUITIN LIGASE | Serum Response Factor - agonists | Serum Response Factor - genetics | Cardiomyopathy, Dilated - pathology | Rats, Wistar | Serum Response Factor - antagonists & inhibitors | Humans | Ubiquitin-Protein Ligases - antagonists & inhibitors | Recombinant Fusion Proteins - metabolism | Dystrophin-Associated Proteins - genetics | Dystrophin-Associated Proteins - metabolism | RNA Interference | Dystrophin-Associated Proteins - chemistry | Proteolysis | HEK293 Cells | Protein Stability | Peptide Fragments - genetics | Animals, Newborn | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Myocytes, Cardiac - cytology | Signal Transduction | Serum Response Factor - metabolism | Tripartite Motif Proteins - antagonists & inhibitors | Cardiomyopathy, Hypertrophic - metabolism | Carrier Proteins - antagonists & inhibitors | Cells, Cultured | Ubiquitin-Protein Ligases - metabolism | Rats | Recombinant Proteins - chemistry | Tripartite Motif Proteins - genetics | Transcription Factors - antagonists & inhibitors | Recombinant Fusion Proteins - chemistry | Transcription Factors - genetics | Cardiomyopathy, Dilated - metabolism | Transcription Factors - metabolism | Carrier Proteins - genetics | Myocytes, Cardiac - pathology | Peptide Fragments - chemistry | Animals | Carrier Proteins - metabolism | Myocytes, Cardiac - metabolism | Tripartite Motif Proteins - metabolism | Ubiquitin-Protein Ligases - genetics | Dysbindin | Apoptosis | Cardiomyopathy, Hypertrophic - pathology | Molecular Bases of Disease | cardiac signaling | cardiomyocyte | TRIM24 | apoptosis | SRF-signaling | cardiac hypertrophy | cardiomyopathy | dysbindin | TRIM32 | X-linked inhibitor of apoptosis protein (XIAP)
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 08/2005, Volume 280, Issue 32, pp. 28936 - 28943
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 07/2004, Volume 279, Issue 27, pp. 28393 - 28401
Journal Article
Biochemistry, ISSN 0006-2960, 10/2015, Volume 54, Issue 46, pp. 6931 - 6941
Macrophage ABCA1 effluxes lipid and has anti-inflammatory activity. The syntrophins, which are cytoplasmic PDZ protein scaffolding factors, can bind ABCA1 and... 
CAPACITY | CELLS | HEART-DISEASE | ABCA1-DEFICIENT MACROPHAGES | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHOLESTEROL EFFLUX | CASSETTE TRANSPORTER A1 | ATHEROSCLEROSIS | RECEPTOR | MICE | ASSOCIATION | Up-Regulation | Hydrocarbons, Fluorinated - pharmacology | Muscle Proteins - deficiency | RNA, Messenger - metabolism | ATP Binding Cassette Transporter 1 - metabolism | Membrane Proteins - deficiency | Multiprotein Complexes - metabolism | Biological Transport, Active | Dystrophin-Associated Proteins - genetics | Dystrophin-Associated Proteins - metabolism | Liver X Receptors | Muscle Proteins - metabolism | Mice, Inbred DBA | Membrane Proteins - metabolism | Protein Interaction Domains and Motifs | Protein Stability | Calcium-Binding Proteins - metabolism | Cell Line | Membrane Proteins - genetics | Mice, Inbred C57BL | Orphan Nuclear Receptors - agonists | RNA, Messenger - genetics | Calcium-Binding Proteins - deficiency | Dystrophin-Associated Proteins - deficiency | Lipid Metabolism | Apolipoprotein A-I - metabolism | Sulfonamides - pharmacology | Mice, Knockout | Muscle Proteins - genetics | Macrophages - metabolism | Multiprotein Complexes - chemistry | Animals | ATP Binding Cassette Transporter 1 - deficiency | Protein Binding | Macrophages - drug effects | Mice | ATP Binding Cassette Transporter 1 - genetics | Calcium-Binding Proteins - genetics | Macrophage colony stimulating factor | Research | Cholesterol | Agonists (Biochemistry)
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 01/2010, Volume 15, Issue 2, pp. 204 - 215
Previous studies have implicated DTNBP1 as a schizophrenia susceptibility gene and its encoded protein, dysbindin, as a potential regulator of synaptic vesicle... 
DTNBP1 | Pallidin | Schizophrenia | Synaptosomal-associated protein | Neurite extension | Biological plausibility | synaptosomal-associated protein | SCHIZOPHRENIA SUSCEPTIBILITY | PSYCHIATRY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CANDIDATE GENES | biological plausibility | schizophrenia | HIPPOCAMPAL-FORMATION | BINDING PROTEIN | NEUROSCIENCES | HERMANSKY-PUDLAK-SYNDROME | TUBULOVESICULAR RECYCLING ENDOSOMES | neurite extension | MOUSE MODEL | SUSCEPTIBILITY GENE | PSYCHIATRIC GENETICS | LYSOSOME-RELATED ORGANELLES | pallidin | Neurites - physiology | Embryo, Mammalian | SNARE Proteins - genetics | Neurons - cytology | Cattle | Hippocampus - growth & development | Gene Expression Regulation, Developmental - physiology | Animals, Newborn | Recombinant Proteins - metabolism | Hippocampus - embryology | Mice, Inbred C57BL | Cells, Cultured | Recombinant Proteins - genetics | Mice, Knockout | Protein Transport | Dystrophin-Associated Proteins | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Hippocampus - metabolism | Animals | Carrier Proteins - metabolism | Analysis of Variance | Qa-SNARE Proteins - metabolism | Protein Binding | Mice | Synaptosomal-Associated Protein 25 - metabolism | Mutation | Vesicle-Associated Membrane Protein 2 - metabolism | SNARE Proteins - metabolism | Dysbindin | Cellular proteins | Genetic susceptibility | Nerves | Genetic aspects | Inflammation | Research | Health aspects | Risk factors | primary cell culture | susceptibility gene | syntaxin
Journal Article
Autophagy, ISSN 1554-8627, 01/2015, Volume 11, Issue 1, pp. 113 - 130
P2RX7 is an ATP-gated ion channel, which can also exhibit an open state with a considerably wider permeation. However, the functional significance of the... 
mdx | EtBr, ethidium bromide | double-mutant mouse model | BzATP, 2′(3′)-O-(4-benzoylbenzoyl)adenosine 5′-triphosphate | C57BL/10ScSn-Dmd | LP, large pore, P2RX7-dependent | | J mouse model of DMD | LY, Lucifer Yellow | DMD | eATP, extracellular ATP | HSPA2/HSP70, heat shock protein 2 | LC3 | Wt, C57BL/10ScSn wild-type mouse | HSP90 | autophagy | HSP70 | cell death | ACTB, actin, β | PtdIns3K, phosphatidylinositol 3-kinase, class III | MAP1LC3B/LC3, microtubule-associated protein 1 light chain 3 β | LDH, lactate dehydrogenase | purinoceptors | P2RX7, purinergic receptor P2X, ligand-gated ion channel, 7 | BECN1, Beclin 1, autophagy-related | P2RX7 | HSP90, heat shock protein 90 | 3-MA, 3-methyladenine | DMD, Duchenne muscular dystrophy | CASP, caspase | DAPC, dystrophin associated protein complex | ATP | MAPK, mitogen-activated protein kinase | GA, geldanamycin | Cell death | Purinoceptors | Autophagy | EXTRACELLULAR ATP | ACTIVATION | PROTEIN | MEDIATED AUTOPHAGY | MUSCULAR-DYSTROPHY | CELL BIOLOGY | P2X7 RECEPTOR | SKELETAL-MUSCLE | P2X RECEPTORS | MOUSE MODEL | MOLECULAR-MECHANISMS | Calcium Channels - metabolism | Apoptosis - drug effects | Microtubule-Associated Proteins - metabolism | Male | Muscle, Skeletal - metabolism | Phosphoproteins - metabolism | Muscular Dystrophy, Animal - pathology | Autophagy - drug effects | Adenosine Triphosphate - pharmacology | Myoblasts - drug effects | Myoblasts - metabolism | Muscle, Skeletal - drug effects | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Female | Mice, Inbred C57BL | Enzyme Activation - drug effects | Myoblasts - pathology | HSP70 Heat-Shock Proteins - metabolism | Macrophages - metabolism | Animals | Signal Transduction - drug effects | Models, Biological | HSP90 Heat-Shock Proteins - metabolism | Receptors, Purinergic P2X7 - metabolism | Muscle, Skeletal - pathology | Proteome - metabolism
Journal Article
Journal Article
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 05/2004, Volume 279, Issue 21, pp. 22331 - 22346
Journal Article
15.