Animal models of the neuromuscular junction, vitally informative for understanding function and the molecular mechanisms of congenital myasthenic syndromes

Animal models of the neuromuscular junction, vitally informative for understanding function and the molecular mechanisms of congenital myasthenic syndromes

The neuromuscular junction is the point of contact between motor nerve and skeletal muscle, its vital role in muscle function is reliant on the precise location and function of many proteins. Congenital myasthenic syndromes (CMS) are a heterogeneous group of disorders of neuromuscular transmission w...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριος συγγραφέας:	Webster, R
Μορφή:	Journal article
Έκδοση:	MDPI 2018

Παρόμοια τεκμήρια

Congenital myasthenic syndromes and the formation of the neuromuscular junction.
ανά: Beeson, D, κ.ά.
Έκδοση: (2008)

Congenital myasthenic syndromes and the formation of the neuromuscular junction
ανά: Beeson, D, κ.ά.
Έκδοση: (2008)

Congenital myasthenic syndromes and the neuromuscular junction.
ανά: Cruz, P, κ.ά.
Έκδοση: (2014)

Congenital myasthenic syndromes and the formation of the neuromuscular junction
ανά: Beeson, D
Έκδοση: (2008)

The neuromuscular junction and wide heterogeneity of congenital myasthenic syndromes
ανά: Rodríguez Cruz, P, κ.ά.
Έκδοση: (2018)

The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome
ανά: Xufeng Liao, κ.ά.
Έκδοση: (2023-09-01)

The spectrum of mutations that underlie the neuromuscular junction synaptopathy in DOK7 congenital myasthenic syndrome.
ανά: Cossins, J, κ.ά.
Έκδοση: (2012)

Effect of β2-adrenergic receptor agonists on neurotransmission and neuromuscular junction structure in congenital myasthenic syndromes
ανά: Vanhaesebrouck, A
Έκδοση: (2018)

Congenital myasthenic syndromes: Epidemiology, clinical phenotyping and aids to diagnosis in the neuromuscular clinic
ανά: Healy, E, κ.ά.
Έκδοση: (2014)

Autoregulation of Acetylcholine Release and Micro-Pharmacodynamic Mechanisms at Neuromuscular Junction: Selective Acetylcholinesterase Inhibitors for Therapy of Myasthenic Syndromes
ανά: Konstantin A. Petrov, κ.ά.
Έκδοση: (2018-07-01)

The congenital myasthenic syndromes.
ανά: Palace, J, κ.ά.
Έκδοση: (2008)

Congenital myasthenic syndromes.
ανά: Beeson, D, κ.ά.
Έκδοση: (1997)

Congenital Myasthenic Syndromes
ανά: J Gordon Millichap
Έκδοση: (1994-01-01)

Congenital Myasthenic Syndrome
ανά: WANG Wenqing, κ.ά.
Έκδοση: (2022-04-01)

Congenital myasthenic syndromes
ανά: Josef Finsterer
Έκδοση: (2019-02-01)

Congenital myasthenic syndromes: an update.
ανά: Finlayson, S, κ.ά.
Έκδοση: (2013)

Inheritance of Congenital Myasthenic Syndromes
ανά: J Gordon Millichap
Έκδοση: (2002-08-01)

Diagnosis of Congenital Myasthenic Syndromes
ανά: J Gordon Millichap
Έκδοση: (2004-02-01)

Presynaptic Congenital Myasthenic Syndrome
ανά: J Gordon Millichap
Έκδοση: (2001-08-01)

Calcium channel subtypes contributing to acetylcholine release from normal, 4-aminopyridine-treated and myasthenic syndrome auto-antibodies-affected neuromuscular junctions.
ανά: Giovannini, F, κ.ά.
Έκδοση: (2002)

Pathogenic mechanisms of RAPSN mutations in congenital myasthenic syndromes
ανά: Cheung, JY
Έκδοση: (2016)

Therapeutic strategies for congenital myasthenic syndromes
ανά: Lee, M, κ.ά.
Έκδοση: (2018)

Synaptic dysfunction in congenital myasthenic syndromes.
ανά: Beeson, D
Έκδοση: (2012)

DOK7 congenital myasthenic syndrome.
ανά: Palace, J
Έκδοση: (2012)

Congenital myasthenic syndromes: recent advances
ανά: Beeson, D
Έκδοση: (2016)

Congenital Myasthenic Syndrome with Agrin Mutations
ανά: J Gordon Millichap, κ.ά.
Έκδοση: (2014-10-01)

COLQ-Mutant Congenital Myasthenic Syndromes
ανά: J Gordon Millichap
Έκδοση: (2008-03-01)

AN UNUSUAL CASE OF CONGENITAL MYASTHENIC SYNDROME: THE MECHANISM FOR TREATMENT RESPONSE
ανά: Spillane, J, κ.ά.
Έκδοση: (2012)

The Electrophysiology of Presynaptic Congenital Myasthenic Syndromes With and Without Facilitation: From Electrodiagnostic Findings to Molecular Mechanisms
ανά: Stefan Nicolau, κ.ά.
Έκδοση: (2019-03-01)

Congenital myasthenic syndromes: Report of 7 Chile
ανά: Kleinsteuber, K, κ.ά.
Έκδοση: (2003)

Congenital myasthenic syndrome caused by mutations in DPAGT.
ανά: Klein, A, κ.ά.
Έκδοση: (2015)

The genetic diagnosis of congenital myasthenic syndromes (CMS)
ανά: Man, S, κ.ά.
Έκδοση: (2005)

Congenital Myasthenic Syndrome and AChR Mutation
ανά: J Gordon Millichap
Έκδοση: (2000-09-01)

DOK7 Mutations in Congenital Myasthenic Syndromes
ανά: J Gordon Millichap
Έκδοση: (2007-06-01)

Clinical and genetic basis of congenital myasthenic syndromes
ανά: Paulo Victor Sgobbi de Souza, κ.ά.

Repouso da junção neuromuscular no tratamento de crises miastênicas e colinérgicas Management of the myasthenic and cholinergic crisis by neuromuscular junction rest
ανά: J. Lamartine de Assis, κ.ά.
Έκδοση: (1968-06-01)

A mouse model of the slow channel myasthenic syndrome: Neuromuscular physiology and effects of ephedrine treatment.
ανά: Webster, R, κ.ά.
Έκδοση: (2013)

Neuromuscular Active Zone Structure and Function in Healthy and Lambert-Eaton Myasthenic Syndrome States
ανά: Scott P. Ginebaugh, κ.ά.
Έκδοση: (2022-05-01)

Congenital myasthenic syndrome patients due to AChR epsilon subunit mutations
ανά: Bonifati, D, κ.ά.
Έκδοση: (2004)

Slow channel congenital myasthenic syndrome responsive to a combination of fluoxetine and salbutamol.
ανά: Finlayson, S, κ.ά.
Έκδοση: (2013)