| P50 | author | Satoru Nagatoishi | Q61829200 |
| P2093 | author name string | Tohru Tezuka | |
| | Kouhei Tsumoto | |
| | Yuji Yamanashi | |
| | Ryo Ueta | |
| | Sadanori Miyoshi | |
| | Yosuke Izawa | |
| P2860 | cites work | Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes | Q48199451 |
| | Epigenetics: H3K27 methylation in transgenerational epigenetic memory. | Q50775201 |
| | Molecular characterisation of congenital myasthenic syndromes in Southern Brazil | Q57390073 |
| | The cytoplasmic adaptor protein Dok7 activates the receptor tyrosine kinase MuSK via dimerization | Q24337679 |
| | To build a synapse: signaling pathways in neuromuscular junction assembly | Q24631081 |
| | Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment | Q28082722 |
| | Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting | Q28085606 |
| | Distinct roles of nerve and muscle in postsynaptic differentiation of the neuromuscular synapse | Q28185780 |
| | The muscle protein Dok-7 is essential for neuromuscular synaptogenesis | Q28247970 |
| | The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo | Q28280767 |
| | Clinical features of the DOK7 neuromuscular junction synaptopathy | Q28298999 |
| | Lrp4 is a receptor for Agrin and forms a complex with MuSK | Q28505665 |
| | Lrp4 is a retrograde signal for presynaptic differentiation at neuromuscular synapses | Q28507936 |
| | LRP4 serves as a coreceptor of agrin | Q28508023 |
| | Patterning of muscle acetylcholine receptor gene expression in the absence of motor innervation | Q28511900 |
| | The in vitro and in vivo phosphotyrosine map of activated MuSK. | Q30862651 |
| | The juxtamembrane region of MuSK has a critical role in agrin-mediated signaling | Q33179395 |
| | Diversity in protein recognition by PTB domains | Q33801830 |
| | Induction of multiple signaling loops by MuSK during neuromuscular synapse formation | Q33952121 |
| | Dok-7 regulates neuromuscular synapse formation by recruiting Crk and Crk-L | Q34244283 |
| | Development of the neuromuscular junction | Q34544510 |
| | The MuSK activator agrin has a separate role essential for postnatal maintenance of neuromuscular synapses | Q34581104 |
| | Antibodies in myasthenia gravis and related disorders | Q35573393 |
| | Structural and evolutionary division of phosphotyrosine binding (PTB) domains. | Q35965222 |
| | Distinct roles of muscle and motoneuron LRP4 in neuromuscular junction formation | Q36173668 |
| | Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients | Q36942782 |
| | The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome | Q39337788 |
| | Dok-7 activates the muscle receptor kinase MuSK and shapes synapse formation | Q39879618 |
| | Mutations causing DOK7 congenital myasthenia ablate functional motifs in Dok-7. | Q40029298 |
| | Dok-7 mutations underlie a neuromuscular junction synaptopathy | Q40242364 |
| | Postnatal knockdown of dok-7 gene expression in mice causes structural defects in neuromuscular synapses and myasthenic pathology | Q40793178 |
| | MuSK controls where motor axons grow and form synapses | Q41788843 |
| | Neuromuscular disease. DOK7 gene therapy benefits mouse models of diseases characterized by defects in the neuromuscular junction | Q42186779 |
| | Pre- and post-synaptic abnormalities associated with impaired neuromuscular transmission in a group of patients with 'limb-girdle myasthenia'. | Q42498797 |
| P433 | issue | 3 | |
| P304 | page(s) | 269-277 | |
| P577 | publication date | 2017-03-01 | |
| P1433 | published in | Journal of Biochemistry | Q6294839 |
| P1476 | title | The carboxyl-terminal region of Dok-7 plays a key, but not essential, role in activation of muscle-specific receptor kinase MuSK and neuromuscular synapse formation | |
| P478 | volume | 161 | |