Full name : Shen Xin-Ming
First name : Xin-Ming
Mail : Department of Neurology, Mayo Clinic, Rochester, MN
Zip Code :
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Country : USA
Email : shen.xinming@mayo.edu
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| Title : Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review - Ohno_2023_Int.J.Mol.Sci_24_ |
| Author(s) : Ohno K , Ohkawara B , Shen XM , Selcen D , Engel AG |
| Ref : Int J Mol Sci , 24 : , 2023 |
| Abstract : Ohno_2023_Int.J.Mol.Sci_24_ |
| ESTHER : Ohno_2023_Int.J.Mol.Sci_24_ |
| PubMedSearch : Ohno_2023_Int.J.Mol.Sci_24_ |
| PubMedID: 36835142 |
| Gene_locus related to this paper: human-PREPL |
| Title : The unfolding landscape of the congenital myasthenic syndromes - Engel_2018_Ann.N.Y.Acad.Sci_1413_25 |
| Author(s) : Engel AG , Shen XM , Selcen D |
| Ref : Annals of the New York Academy of Sciences , 1413 :25 , 2018 |
| Abstract : Engel_2018_Ann.N.Y.Acad.Sci_1413_25 |
| ESTHER : Engel_2018_Ann.N.Y.Acad.Sci_1413_25 |
| PubMedSearch : Engel_2018_Ann.N.Y.Acad.Sci_1413_25 |
| PubMedID: 29355968 |
| Title : Involvement of Three Esterase Genes from Panonychus citri (McGregor) in Fenpropathrin Resistance - Shen_2016_Int.J.Mol.Sci_17_ |
| Author(s) : Shen XM , Liao CY , Lu XP , Wang Z , Wang JJ , Dou W |
| Ref : Int J Mol Sci , 17 : , 2016 |
| Abstract : Shen_2016_Int.J.Mol.Sci_17_ |
| ESTHER : Shen_2016_Int.J.Mol.Sci_17_ |
| PubMedSearch : Shen_2016_Int.J.Mol.Sci_17_ |
| PubMedID: 27548163 |
| Title : Impaired Synaptic Development, Maintenance, and Neuromuscular Transmission in LRP4-Related Myasthenia - Selcen_2015_JAMA.Neurol_72_889 |
| Author(s) : Selcen D , Ohkawara B , Shen XM , McEvoy K , Ohno K , Engel AG |
| Ref : JAMA Neurol , 72 :889 , 2015 |
| Abstract : Selcen_2015_JAMA.Neurol_72_889 |
| ESTHER : Selcen_2015_JAMA.Neurol_72_889 |
| PubMedSearch : Selcen_2015_JAMA.Neurol_72_889 |
| PubMedID: 26052878 |
| Title : PREPL deficiency with or without cystinuria causes a novel myasthenic syndrome - Regal_2014_Neurology_82_1254 |
| Author(s) : Regal L , Shen XM , Selcen D , Verhille C , Meulemans S , Creemers JW , Engel AG |
| Ref : Neurology , 82 :1254 , 2014 |
| Abstract : Regal_2014_Neurology_82_1254 |
| ESTHER : Regal_2014_Neurology_82_1254 |
| PubMedSearch : Regal_2014_Neurology_82_1254 |
| PubMedID: 24610330 |
| Gene_locus related to this paper: human-PREPL |
| Title : Highly fatal fast-channel syndrome caused by AChR epsilon subunit mutation at the agonist binding site - Shen_2012_Neurology_79_449 |
| Author(s) : Shen XM , Brengman JM , Edvardson S , Sine SM , Engel AG |
| Ref : Neurology , 79 :449 , 2012 |
| Abstract : Shen_2012_Neurology_79_449 |
| ESTHER : Shen_2012_Neurology_79_449 |
| PubMedSearch : Shen_2012_Neurology_79_449 |
| PubMedID: 22592360 |
| Title : Myasthenic syndrome AChRalpha C-loop mutant disrupts initiation of channel gating - Shen_2012_J.Clin.Invest_122_2613 |
| Author(s) : Shen XM , Brengman JM , Sine SM , Engel AG |
| Ref : J Clinical Investigation , 122 :2613 , 2012 |
| Abstract : Shen_2012_J.Clin.Invest_122_2613 |
| ESTHER : Shen_2012_J.Clin.Invest_122_2613 |
| PubMedSearch : Shen_2012_J.Clin.Invest_122_2613 |
| PubMedID: 22728938 |
| Title : Beneficial effect of albuterol in congenital myasthenic syndrome with epsilon-subunit mutations - Sadeh_2011_Muscle.Nerve_44_289 |
| Author(s) : Sadeh M , Shen XM , Engel AG |
| Ref : Muscle & Nerve , 44 :289 , 2011 |
| Abstract : Sadeh_2011_Muscle.Nerve_44_289 |
| ESTHER : Sadeh_2011_Muscle.Nerve_44_289 |
| PubMedSearch : Sadeh_2011_Muscle.Nerve_44_289 |
| PubMedID: 21721016 |
| Title : What have we learned from the congenital myasthenic syndromes - Engel_2010_J.Mol.Neurosci_40_143 |
| Author(s) : Engel AG , Shen XM , Selcen D , Sine SM |
| Ref : Journal of Molecular Neuroscience , 40 :143 , 2010 |
| Abstract : Engel_2010_J.Mol.Neurosci_40_143 |
| ESTHER : Engel_2010_J.Mol.Neurosci_40_143 |
| PubMedSearch : Engel_2010_J.Mol.Neurosci_40_143 |
| PubMedID: 19688192 |
| Title : Further observations in congenital myasthenic syndromes - Engel_2008_Ann.N.Y.Acad.Sci_1132_104 |
| Author(s) : Engel AG , Shen XM , Selcen D , Sine SM |
| Ref : Annals of the New York Academy of Sciences , 1132 :104 , 2008 |
| Abstract : Engel_2008_Ann.N.Y.Acad.Sci_1132_104 |
| ESTHER : Engel_2008_Ann.N.Y.Acad.Sci_1132_104 |
| PubMedSearch : Engel_2008_Ann.N.Y.Acad.Sci_1132_104 |
| PubMedID: 18567859 |
| Title : Congenital myasthenia-related AChR delta subunit mutation interferes with intersubunit communication essential for channel gating - Shen_2008_J.Clin.Invest_118_1867 |
| Author(s) : Shen XM , Fukuda T , Ohno K , Sine SM , Engel AG |
| Ref : J Clinical Investigation , 118 :1867 , 2008 |
| Abstract : Shen_2008_J.Clin.Invest_118_1867 |
| ESTHER : Shen_2008_J.Clin.Invest_118_1867 |
| PubMedSearch : Shen_2008_J.Clin.Invest_118_1867 |
| PubMedID: 18398509 |
| Title : Slow-channel mutation in acetylcholine receptor alphaM4 domain and its efficient knockdown - Shen_2006_Ann.Neurol_60_128 |
| Author(s) : Shen XM , Deymeer F , Sine SM , Engel AG |
| Ref : Annals of Neurology , 60 :128 , 2006 |
| Abstract : Shen_2006_Ann.Neurol_60_128 |
| ESTHER : Shen_2006_Ann.Neurol_60_128 |
| PubMedSearch : Shen_2006_Ann.Neurol_60_128 |
| PubMedID: 16685696 |
| Title : Subunit-specific contribution to agonist binding and channel gating revealed by inherited mutation in muscle acetylcholine receptor M3-M4 linker - Shen_2005_Brain_128_345 |
| Author(s) : Shen XM , Ohno K , Sine SM , Engel AG |
| Ref : Brain , 128 :345 , 2005 |
| Abstract : Shen_2005_Brain_128_345 |
| ESTHER : Shen_2005_Brain_128_345 |
| PubMedSearch : Shen_2005_Brain_128_345 |
| PubMedID: 15615813 |
| Title : Are MuSK antibodies the primary cause of myasthenic symptoms? - Selcen_2004_Neurology_62_1945 |
| Author(s) : Selcen D , Fukuda T , Shen XM , Engel AG |
| Ref : Neurology , 62 :1945 , 2004 |
| Abstract : Selcen_2004_Neurology_62_1945 |
| ESTHER : Selcen_2004_Neurology_62_1945 |
| PubMedSearch : Selcen_2004_Neurology_62_1945 |
| PubMedID: 15184594 |
| Title : Congenital myasthenic syndromes: multiple molecular targets at the neuromuscular junction - Engel_2003_Ann.N.Y.Acad.Sci_998_138 |
| Author(s) : Engel AG , Ohno K , Shen XM , Sine SM |
| Ref : Annals of the New York Academy of Sciences , 998 :138 , 2003 |
| Abstract : Engel_2003_Ann.N.Y.Acad.Sci_998_138 |
| ESTHER : Engel_2003_Ann.N.Y.Acad.Sci_998_138 |
| PubMedSearch : Engel_2003_Ann.N.Y.Acad.Sci_998_138 |
| PubMedID: 14592871 |
| Title : Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating - Shen_2003_J.Clin.Invest_111_497 |
| Author(s) : Shen XM , Ohno K , Tsujino A , Brengman JM , Gingold M , Sine SM , Engel AG |
| Ref : J Clinical Investigation , 111 :497 , 2003 |
| Abstract : Shen_2003_J.Clin.Invest_111_497 |
| ESTHER : Shen_2003_J.Clin.Invest_111_497 |
| PubMedSearch : Shen_2003_J.Clin.Invest_111_497 |
| PubMedID: 12588888 |
| Title : Mechanistic diversity underlying fast channel congenital myasthenic syndromes - Sine_2003_Ann.N.Y.Acad.Sci_998_128 |
| Author(s) : Sine SM , Wang HL , Ohno K , Shen XM , Lee WY , Engel AG |
| Ref : Annals of the New York Academy of Sciences , 998 :128 , 2003 |
| Abstract : Sine_2003_Ann.N.Y.Acad.Sci_998_128 |
| ESTHER : Sine_2003_Ann.N.Y.Acad.Sci_998_128 |
| PubMedSearch : Sine_2003_Ann.N.Y.Acad.Sci_998_128 |
| PubMedID: 14592870 |
| Title : Naturally occurring mutations at the acetylcholine receptor binding site independently alter ACh binding and channel gating - Sine_2002_J.Gen.Physiol_120_483 |
| Author(s) : Sine SM , Shen XM , Wang HL , Ohno K , Lee WY , Tsujino A , Brengmann J , Bren N , Vajsar J , Engel AG |
| Ref : Journal of General Physiology , 120 :483 , 2002 |
| Abstract : Sine_2002_J.Gen.Physiol_120_483 |
| ESTHER : Sine_2002_J.Gen.Physiol_120_483 |
| PubMedSearch : Sine_2002_J.Gen.Physiol_120_483 |
| PubMedID: 12356851 |
| Title : Three novel COLQ mutations and variation of phenotypic expressivity due to G240X - Shapira_2002_Neurology_58_603 |
| Author(s) : Shapira YA , Sadeh ME , Bergtraum MP , Tsujino A , Ohno K , Shen XM , Brengman J , Edwardson S , Matoth I , Engel AG |
| Ref : Neurology , 58 :603 , 2002 |
| Abstract : Shapira_2002_Neurology_58_603 |
| ESTHER : Shapira_2002_Neurology_58_603 |
| PubMedSearch : Shapira_2002_Neurology_58_603 |
| PubMedID: 11865139 |
| Title : The spectrum of mutations causing end-plate acetylcholinesterase deficiency - Ohno_2000_Ann.Neurol_47_162 |
| Author(s) : Ohno K , Engel AG , Brengman JM , Shen XM , Heidenreich F , Vincent A , Milone M , Tan E , Demirci M , Walsh P , Nakano S , Akiguchi I |
| Ref : Annals of Neurology , 47 :162 , 2000 |
| Abstract : Ohno_2000_Ann.Neurol_47_162 |
| ESTHER : Ohno_2000_Ann.Neurol_47_162 |
| PubMedSearch : Ohno_2000_Ann.Neurol_47_162 |
| PubMedID: 10665486 |
| Title : Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gating - Wang_1999_Nat.Neurosci_2_226 |
| Author(s) : Wang HL , Milone M , Ohno K , Shen XM , Tsujino A , Batocchi AP , Tonali P , Brengman J , Engel AG , Sine SM |
| Ref : Nat Neurosci , 2 :226 , 1999 |
| Abstract : Wang_1999_Nat.Neurosci_2_226 |
| ESTHER : Wang_1999_Nat.Neurosci_2_226 |
| PubMedSearch : Wang_1999_Nat.Neurosci_2_226 |
| PubMedID: 10195214 |
| Title : Mode switching kinetics produced by a naturally occurring mutation in the cytoplasmic loop of the human acetylcholine receptor epsilon subunit - Milone_1998_Neuron_20_575 |
| Author(s) : Milone M , Wang HL , Ohno K , Prince R , Fukudome T , Shen XM , Brengman JM , Griggs RC , Sine SM , Engel AG |
| Ref : Neuron , 20 :575 , 1998 |
| Abstract : Milone_1998_Neuron_20_575 |
| ESTHER : Milone_1998_Neuron_20_575 |
| PubMedSearch : Milone_1998_Neuron_20_575 |
| PubMedID: 9539130 |