Liu WW

References (8)

Title : Design, synthesis and biological evaluation of bakuchiol derivatives as multi-target agents for the treatment of Alzheimer's disease - Zhang_2024_Fitoterapia__105867
Author(s) : Zhang XQ , Xiang YN , Qin T , Zou JP , Guo QW , Han ST , Zhang ZY , Liu WW , Ding G , Dong JQ , Shi DH
Ref : Fitoterapia , :105867 , 2024
Abstract :
PubMedSearch : Zhang_2024_Fitoterapia__105867
PubMedID: 38382891

Title : Severe congenital myasthenic syndrome associated with novel biallelic mutation of the CHRND gene - Bonanno_2020_Neuromuscul.Disord__
Author(s) : Bonanno C , Rodolico C , Topf A , Foti FM , Liu WW , Beeson D , Toscano A , Lochmuller H
Ref : Neuromuscular Disorders , : , 2020
Abstract :
PubMedSearch : Bonanno_2020_Neuromuscul.Disord__
PubMedID: 32360402

Title : beta2-Adrenergic receptor agonists ameliorate the adverse effect of long-term pyridostigmine on neuromuscular junction structure - Vanhaesebrouck_2019_Brain_142_3713
Author(s) : Vanhaesebrouck AE , Webster R , Maxwell S , Rodriguez Cruz PM , Cossins J , Wickens J , Liu WW , Cetin H , Cheung J , Ramjattan H , Palace J , Beeson D
Ref : Brain , 142 :3713 , 2019
Abstract :
PubMedSearch : Vanhaesebrouck_2019_Brain_142_3713
PubMedID: 31633155

Title : Synthesis and bioactivity of novel C2-glycosyl oxadiazole derivatives as acetylcholinesterase inhibitors - Wang_2018_Heterocycl.Commun_24_333
Author(s) : Wang L , Wu YR , Ren ST , Yin L , Liu XJ , Cheng FC , Liu WW , Shi DH , Cao ZL , Sun HM
Ref : Heterocycl Commun , 24 :333 , 2018
Abstract :
PubMedSearch : Wang_2018_Heterocycl.Commun_24_333
PubMedID:

Title : A mouse model of the slow channel myasthenic syndrome: Neuromuscular physiology and effects of ephedrine treatment - Webster_2013_Exp.Neurol_248C_286
Author(s) : Webster RG , Cossins J , Lashley D , Maxwell S , Liu WW , Wickens JR , Martinez-Martinez P , de Baets M , Beeson D
Ref : Experimental Neurology , 248C :286 , 2013
Abstract :
PubMedSearch : Webster_2013_Exp.Neurol_248C_286
PubMedID: 23797154

Title : Congenital myasthenic syndromes due to mutations in ALG2 and ALG14 - Cossins_2013_Brain_136_944
Author(s) : Cossins J , Belaya K , Hicks D , Salih MA , Finlayson S , Carboni N , Liu WW , Maxwell S , Zoltowska K , Farsani GT , Laval S , Seidhamed MZ , Donnelly P , Bentley D , McGowan SJ , Muller J , Palace J , Lochmuller H , Beeson D
Ref : Brain , 136 :944 , 2013
Abstract :
PubMedSearch : Cossins_2013_Brain_136_944
PubMedID: 23404334

Title : Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates - Belaya_2012_Am.J.Hum.Genet_91_193
Author(s) : Belaya K , Finlayson S , Slater CR , Cossins J , Liu WW , Maxwell S , McGowan SJ , Maslau S , Twigg SR , Walls TJ , Pascual Pascual SI , Palace J , Beeson D
Ref : American Journal of Human Genetics , 91 :193 , 2012
Abstract :
PubMedSearch : Belaya_2012_Am.J.Hum.Genet_91_193
PubMedID: 22742743

Title : Identification of DPAGT1 as a new gene in which mutations cause a congenital myasthenic syndrome - Belaya_2012_Ann.N.Y.Acad.Sci_1275_29
Author(s) : Belaya K , Finlayson S , Cossins J , Liu WW , Maxwell S , Palace J , Beeson D
Ref : Annals of the New York Academy of Sciences , 1275 :29 , 2012
Abstract :
PubMedSearch : Belaya_2012_Ann.N.Y.Acad.Sci_1275_29
PubMedID: 23278575