scholarly article | Q13442814 |
P50 | author | Marco Crescenzi | Q43280564 |
Paola Torreri | Q47503166 | ||
Pompeo Macioce | Q55966260 | ||
P2093 | author name string | Gianfranco Macchia | |
Andrea Matteucci | |||
Anna Maria Salzano | |||
Federica Fratini | |||
Marina Ceccarini | |||
Tamara C. Petrucci | |||
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Biology of the striated muscle dystrophin-glycoprotein complex | Q37085050 | ||
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Molecular motors in neurons: transport mechanisms and roles in brain function, development, and disease. | Q37811131 | ||
alpha-Dystrobrevin isoforms differ in their colocalization with and stabilization of agrin-induced acetylcholine receptor clusters | Q43424007 | ||
Genomic organization and refined mapping of the mouse β-dystrobrevin gene | Q48011298 | ||
The 87K postsynaptic membrane protein from Torpedo is a protein-tyrosine kinase substrate homologous to dystrophin | Q48130360 | ||
beta-dystrobrevin, a kinesin-binding receptor, interacts with the extracellular matrix components pancortins | Q48292520 | ||
Biochemical evidence for association of dystrobrevin with the sarcoglycan-sarcospan complex as a basis for understanding sarcoglycanopathy | Q22253913 | ||
Desmuslin, an intermediate filament protein that interacts with alpha -dystrobrevin and desmin | Q24291234 | ||
DAMAGE, a Novel α-Dystrobrevin-associated MAGE Protein in Dystrophin Complexes | Q24299985 | ||
Cloning and characterization of the human homologue of a dystrophin related phosphoprotein found at the Torpedo electric organ post-synaptic membrane | Q24312463 | ||
Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene | Q24316279 | ||
FOXG1 is responsible for the congenital variant of Rett syndrome | Q24647431 | ||
Different dystrophin-like complexes are expressed in neurons and glia | Q24684826 | ||
Structure of a WW domain containing fragment of dystrophin in complex with beta-dystroglycan | Q27626122 | ||
Mass Spectrometric Sequencing of Proteins from Silver-Stained Polyacrylamide Gels | Q27860531 | ||
Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex | Q28143244 | ||
Beta-dystrobrevin interacts directly with kinesin heavy chain in brain | Q28182041 | ||
Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain | Q28505394 | ||
Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle | Q28511511 | ||
Dysbindin-containing complexes and their proposed functions in brain: from zero to (too) many in a decade. | Q30474256 | ||
Phosphoric acid as a matrix additive for MALDI MS analysis of phosphopeptides and phosphoproteins. | Q33206911 | ||
Association of dystrobrevin and regulatory subunit of protein kinase A: a new role for dystrobrevin as a scaffold for signaling proteins | Q33289941 | ||
The interaction with HMG20a/b proteins suggests a potential role for beta-dystrobrevin in neuronal differentiation. | Q33597444 | ||
Function and genetics of dystrophin and dystrophin-related proteins in muscle | Q34120764 | ||
Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein | Q34379805 | ||
Alpha-dystrobrevin-1 recruits alpha-catulin to the alpha1D-adrenergic receptor/dystrophin-associated protein complex signalosome. | Q34411579 | ||
Association of alpha-dystrobrevin with reorganizing tight junctions | Q34411963 | ||
The dystrophin–glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies | Q34464444 | ||
P433 | issue | 22 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | phosphorylation | Q242736 |
Dystrobrevin, beta | Q21496336 | ||
Kinesin family member 5A | Q21498974 | ||
P304 | page(s) | 4131–4144 | |
P577 | publication date | 2012-11-01 | |
P1433 | published in | FEBS Journal | Q1388041 |
P1476 | title | Phosphorylation on threonine 11 of β-dystrobrevin alters its interaction with kinesin heavy chain | |
P478 | volume | 279 |