Congenital myasthenic syndrome comprises a heterogeneous group of inherited disorders of neuromuscular transmission. Acetylcholine receptor (AChR) deficiency is the most common form of congenital myasthenic syndrome and in most cases results from mutations within the coding region of the AChR subuni
Rapsyn-mediated clustering of acetylcholine receptor subunits requires the major cytoplasmic loop of the receptor subunits
✍ Scribed by Huebsch, Kimberly A. ;Maimone, Margaret M.
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 354 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0022-3034
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Idiopathic generalized epilepsy (IGE) refers to a common group of epilepsies, and genetic factors play an important role in the pathogenesis of these disorders. Mutations in __CHRNA4__ and __CHRNB2__ are associated with some cases of familial epilepsies classified as autosomal‐dominant
solution revealed that they regenerated the halted activity. ### 3.3 Zoosporicides The methanol extract of unripe fruits of Ginkgo biloba L showed lytic activity toward the zoospores and the bioassay-guided fractionation resulted in isolation of a mixture of anacardic acid homologues (11) as an ac
## Abstract Nicotinic acetylcholine receptors (nAChR) are widely distributed in the central nervous system, where they exert a modulatory influence on synaptic transmission. For the striatum, pharmacological evidence supports the presence of presynaptic α3β2\* and α4β2\* nAChR that modulate dopamin
Standard two-electrode voltage-clamp techniques were used to investigate some of the pharmacological and functional properties of two types of rat neuronal nicotinic acetylcholine receptors expressed in Xenopus oocytes after pairwise injection of e3/74 or c~3/72 mRNAs. Currents of several gA amplitu