1              Observation in vivo showed that extrajunctional AChR aggregates were associated with PSC

2 strate a functional role for upregulation of extrajunctional AChRs.

3 g mutant synapses and dramatically increased extrajunctional DLG.

4  in adult muscle, denervation results in its extrajunctional expression, although a discernible conce

5 lcholine escapes from endplates and binds to extrajunctional fetal-type AChRs only during large, evok

6 he nanodisc-embedded protein may be like the extrajunctional form, existing in a disordered lipid env

7                                       On the extrajunctional membrane, INa and AP thresholds and rate

8 es; the latter two were also examined on the extrajunctional membrane.

9 enes encoding for ubiquitously expressed and extrajunctional molecules has changed our previous view

10                                              Extrajunctional MuSK is first apparent 3 days after dene

11 engage in constant diffusional exchange with extrajunctional pools.

12                  Intracellular recordings of extrajunctional potentials (EJPs) evoked in these muscle

13 of Golgi complex and related proteins in the extrajunctional region of muscle fibers.

14 lopmental event that rids receptors from the extrajunctional region of the developing muscle fiber.

15                                       In the extrajunctional region the safety factor estimated from

16 y for low epsilon subunit gene expression in extrajunctional regions of the muscle fiber.

17 hosphorylated, is the predominant isoform in extrajunctional regions, and is also present at NMJs and

18                                           In extrajunctional regions, fast pattern stimulation preser

19  junction assembly and has been localized at extrajunctional sites in association with actin filament