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2. A mammalian homolog of Drosophila tumorous imaginal discs, Tid1, mediates agrin signaling at the neuromuscular junction. Linnoila J; Wang Y; Yao Y; Wang ZZ Neuron; 2008 Nov; 60(4):625-41. PubMed ID: 19038220 [TBL] [Abstract][Full Text] [Related]
3. LRP4 third β-propeller domain mutations cause novel congenital myasthenia by compromising agrin-mediated MuSK signaling in a position-specific manner. Ohkawara B; Cabrera-Serrano M; Nakata T; Milone M; Asai N; Ito K; Ito M; Masuda A; Ito Y; Engel AG; Ohno K Hum Mol Genet; 2014 Apr; 23(7):1856-68. PubMed ID: 24234652 [TBL] [Abstract][Full Text] [Related]
4. A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. Ben Ammar A; Soltanzadeh P; Bauché S; Richard P; Goillot E; Herbst R; Gaudon K; Huzé C; Schaeffer L; Yamanashi Y; Higuchi O; Taly A; Koenig J; Leroy JP; Hentati F; Najmabadi H; Kahrizi K; Ilkhani M; Fardeau M; Eymard B; Hantaï D PLoS One; 2013; 8(1):e53826. PubMed ID: 23326516 [TBL] [Abstract][Full Text] [Related]
6. Dok-7/MuSK signaling and a congenital myasthenic syndrome. Yamanashi Y; Higuch O; Beeson D Acta Myol; 2008 Jul; 27(1):25-9. PubMed ID: 19108574 [TBL] [Abstract][Full Text] [Related]
7. Congenital myasthenic syndrome due to mutations in MUSK suggests that the level of MuSK phosphorylation is crucial for governing synaptic structure. Rodríguez Cruz PM; Cossins J; Cheung J; Maxwell S; Jayawant S; Herbst R; Waithe D; Kornev AP; Palace J; Beeson D Hum Mutat; 2020 Mar; 41(3):619-631. PubMed ID: 31765060 [TBL] [Abstract][Full Text] [Related]
8. [Pathophysiological characterization of congenital myasthenic syndromes: the example of mutations in the MUSK gene]. Chevessier F; Faraut B; Ravel-Chapuis A; Richard P; Gaudon K; Bauché S; Prioleau C; Herbst R; Goillot E; Ioos C; Azulay JP; Attarian S; Leroy JP; Fournier E; Legay C; Schaeffer L; Koenig J; Fardeau M; Eymard B; Pouget J; Hantaï D J Soc Biol; 2005; 199(1):61-77. PubMed ID: 16114265 [TBL] [Abstract][Full Text] [Related]
9. The MuSK activator agrin has a separate role essential for postnatal maintenance of neuromuscular synapses. Tezuka T; Inoue A; Hoshi T; Weatherbee SD; Burgess RW; Ueta R; Yamanashi Y Proc Natl Acad Sci U S A; 2014 Nov; 111(46):16556-61. PubMed ID: 25368159 [TBL] [Abstract][Full Text] [Related]
13. MuSk function during health and disease. Herbst R Neurosci Lett; 2020 Jan; 716():134676. PubMed ID: 31811897 [TBL] [Abstract][Full Text] [Related]
14. A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions. Chevessier F; Girard E; Molgó J; Bartling S; Koenig J; Hantaï D; Witzemann V Hum Mol Genet; 2008 Nov; 17(22):3577-95. PubMed ID: 18718936 [TBL] [Abstract][Full Text] [Related]
15. Collagen Q and anti-MuSK autoantibody competitively suppress agrin/LRP4/MuSK signaling. Otsuka K; Ito M; Ohkawara B; Masuda A; Kawakami Y; Sahashi K; Nishida H; Mabuchi N; Takano A; Engel AG; Ohno K Sci Rep; 2015 Sep; 5():13928. PubMed ID: 26355076 [TBL] [Abstract][Full Text] [Related]
16. Structure and activation of MuSK, a receptor tyrosine kinase central to neuromuscular junction formation. Hubbard SR; Gnanasambandan K Biochim Biophys Acta; 2013 Oct; 1834(10):2166-9. PubMed ID: 23467009 [TBL] [Abstract][Full Text] [Related]
18. The role of MuSK in synapse formation and neuromuscular disease. Burden SJ; Yumoto N; Zhang W Cold Spring Harb Perspect Biol; 2013 May; 5(5):a009167. PubMed ID: 23637281 [TBL] [Abstract][Full Text] [Related]
19. Distinct domains of MuSK mediate its abilities to induce and to associate with postsynaptic specializations. Zhou H; Glass DJ; Yancopoulos GD; Sanes JR J Cell Biol; 1999 Sep; 146(5):1133-46. PubMed ID: 10477765 [TBL] [Abstract][Full Text] [Related]
20. MuSK levels differ between adult skeletal muscles and influence postsynaptic plasticity. Punga AR; Maj M; Lin S; Meinen S; Rüegg MA Eur J Neurosci; 2011 Mar; 33(5):890-8. PubMed ID: 21255125 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]