Report for Ohno K

General

Full name : Ohno Kinji

First name : Kinji

Mail : Nagoya University Graduate School of Medicine\; Neurogenetics\; 65 Tsurumai\; Showa-ku\; Nagoya\; 4668550

Zip Code :

City :

Country : Japan

Email : ohnok@med.nagoya-u.ac.jp

Phone : +81527442446

Fax :

Website : \/\/profs.provost.nagoya-u.ac.jp\/view\/html\/100001410_en.html

Directory :

References (59)

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 : Expression of alcohol acyltransferase is a potential determinant of fruit volatile ester variations in Capsicum - Koeda_2023_Plant.Cell.Rep__
Author(s) : Koeda S , Noda T , Hachisu S , Kubo A , Tanaka Y , Yamamoto H , Ozaki S , Kinoshita M , Ohno K , Tomi K , Kamiyoshihara Y
Ref : Plant Cell Rep , : , 2023
Abstract : Koeda_2023_Plant.Cell.Rep__
ESTHER : Koeda_2023_Plant.Cell.Rep__
PubMedSearch : Koeda_2023_Plant.Cell.Rep__
PubMedID: 37642676

Title : Gene Expression Profile at the Motor Endplate of the Neuromuscular Junction of Fast-Twitch Muscle - Huang_2020_Front.Mol.Neurosci_13_154
Author(s) : Huang K , Li J , Ito M , Takeda JI , Ohkawara B , Ogi T , Masuda A , Ohno K
Ref : Front Mol Neurosci , 13 :154 , 2020
Abstract : Huang_2020_Front.Mol.Neurosci_13_154
ESTHER : Huang_2020_Front.Mol.Neurosci_13_154
PubMedSearch : Huang_2020_Front.Mol.Neurosci_13_154
PubMedID: 33117128

Title : Protein-anchoring therapy to target extracellular matrix proteins to their physiological destinations - Ito_2018_Matrix.Biol_68-69_628
Author(s) : Ito M , Ohno K
Ref : Matrix Biol , 68-69 :628 , 2018
Abstract : Ito_2018_Matrix.Biol_68-69_628
ESTHER : Ito_2018_Matrix.Biol_68-69_628
PubMedSearch : Ito_2018_Matrix.Biol_68-69_628
PubMedID: 29475025

Title : [Studies on therapeutic strategies for congenital myasthenic syndromes.] - Ohno_2017_Clin.Calcium_27_421
Author(s) : Ohno K
Ref : Clin Calcium , 27 :421 , 2017
Abstract : Ohno_2017_Clin.Calcium_27_421
ESTHER : Ohno_2017_Clin.Calcium_27_421
PubMedSearch : Ohno_2017_Clin.Calcium_27_421
PubMedID: 28232657

Title : Agrin-LRP4-MuSK signaling as a therapeutic target for myasthenia gravis and other neuromuscular disorders - Ohno_2017_Expert.Opin.Ther.Targets_21_949
Author(s) : Ohno K , Ohkawara B , Ito M
Ref : Expert Opin Ther Targets , 21 :949 , 2017
Abstract : Ohno_2017_Expert.Opin.Ther.Targets_21_949
ESTHER : Ohno_2017_Expert.Opin.Ther.Targets_21_949
PubMedSearch : Ohno_2017_Expert.Opin.Ther.Targets_21_949
PubMedID: 28825343

Title : Splicing regulation and dysregulation of cholinergic genes expressed at the neuromuscular junction - Ohno_2017_J.Neurochem_142 Suppl 2_64
Author(s) : Ohno K , Rahman MA , Nazim M , Nasrin F , Lin Y , Takeda JI , Masuda A
Ref : Journal of Neurochemistry , 142 Suppl 2 :64 , 2017
Abstract : Ohno_2017_J.Neurochem_142 Suppl 2_64
ESTHER : Ohno_2017_J.Neurochem_142 Suppl 2_64
PubMedSearch : Ohno_2017_J.Neurochem_142 Suppl 2_64
PubMedID: 28072465

Title : Competitive regulation of alternative splicing and alternative polyadenylation by hnRNP H and CstF64 determines acetylcholinesterase isoforms -
Author(s) : Nazim M , Masuda A , Rahman MA , Nasrin F , Takeda JI , Ohe K , Ohkawara B , Ito M , Ohno K
Ref : Nucleic Acids Research , 45 :1455 , 2017
PubMedID: 28180311

Title : Effects of donepezil and serotonin reuptake inhibitor on acute regression during adolescence in Down syndrome - Tamasaki_2016_Brain.Dev_38_113
Author(s) : Tamasaki A , Saito Y , Ueda R , Ohno K , Yokoyama K , Satake T , Sakuma H , Takahashi Y , Kondoh T , Maegaki Y
Ref : Brain Dev , 38 :113 , 2016
Abstract : Tamasaki_2016_Brain.Dev_38_113
ESTHER : Tamasaki_2016_Brain.Dev_38_113
PubMedSearch : Tamasaki_2016_Brain.Dev_38_113
PubMedID: 26143664

Title : Roles of collagen Q in MuSK antibody-positive myasthenia gravis - Ohno_2016_Chem.Biol.Interact_259_266
Author(s) : Ohno K , Otsuka K , Ito M
Ref : Chemico-Biological Interactions , 259 :266 , 2016
Abstract : Ohno_2016_Chem.Biol.Interact_259_266
ESTHER : Ohno_2016_Chem.Biol.Interact_259_266
PubMedSearch : Ohno_2016_Chem.Biol.Interact_259_266
PubMedID: 27119269

Title : Collagen Q and anti-MuSK autoantibody competitively suppress agrin\/LRP4\/MuSK signaling - Otsuka_2015_Sci.Rep_5_13928
Author(s) : Otsuka K , Ito M , Ohkawara B , Masuda A , Kawakami Y , Sahashi K , Nishida H , Mabuchi N , Takano A , Engel AG , Ohno K
Ref : Sci Rep , 5 :13928 , 2015
Abstract : Otsuka_2015_Sci.Rep_5_13928
ESTHER : Otsuka_2015_Sci.Rep_5_13928
PubMedSearch : Otsuka_2015_Sci.Rep_5_13928
PubMedID: 26355076

Title : SRSF1 and hnRNP H antagonistically regulate splicing of COLQ exon 16 in a congenital myasthenic syndrome - Rahman_2015_Sci.Rep_5_13208
Author(s) : Rahman MA , Azuma Y , Nasrin F , Takeda J , Nazim M , Ahsan KB , Masuda A , Engel AG , Ohno K
Ref : Sci Rep , 5 :13208 , 2015
Abstract : Rahman_2015_Sci.Rep_5_13208
ESTHER : Rahman_2015_Sci.Rep_5_13208
PubMedSearch : Rahman_2015_Sci.Rep_5_13208
PubMedID: 26282582

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 : Collagen Q is a Key Player for Developing Rational Therapy for Congenital Myasthenia and for Dissecting the Mechanisms of Anti-MuSK Myasthenia Gravis - Ohno_2014_J.Mol.Neurosci_53_359
Author(s) : Ohno K , Ito M , Kawakami Y , Ohtsuka K
Ref : Journal of Molecular Neuroscience , 53 :359 , 2014
Abstract : Ohno_2014_J.Mol.Neurosci_53_359
ESTHER : Ohno_2014_J.Mol.Neurosci_53_359
PubMedSearch : Ohno_2014_J.Mol.Neurosci_53_359
PubMedID: 24234034

Title : Specific binding of collagen Q to the neuromuscular junction is exploited to cure congenital myasthenia and to explore bases of myasthenia gravis - Ohno_2013_Chem.Biol.Interact_203_335
Author(s) : Ohno K , Ito M , Kawakami Y , Krejci E , Engel AG
Ref : Chemico-Biological Interactions , 203 :335 , 2013
Abstract : Ohno_2013_Chem.Biol.Interact_203_335
ESTHER : Ohno_2013_Chem.Biol.Interact_203_335
PubMedSearch : Ohno_2013_Chem.Biol.Interact_203_335
PubMedID: 22981737

Title : Protein-anchoring strategy for delivering acetylcholinesterase to the neuromuscular junction - Ito_2012_Mol.Ther_20_1384
Author(s) : Ito M , Suzuki Y , Okada T , Fukudome T , Yoshimura T , Masuda A , Takeda S , Krejci E , Ohno K
Ref : Mol Ther , 20 :1384 , 2012
Abstract : Ito_2012_Mol.Ther_20_1384
ESTHER : Ito_2012_Mol.Ther_20_1384
PubMedSearch : Ito_2012_Mol.Ther_20_1384
PubMedID: 22371845

Title : Congenital myasthenic syndromes - Ohno_2012_Rinsho.Shinkeigaku_52_1159
Author(s) : Ohno K
Ref : Rinsho Shinkeigaku , 52 :1159 , 2012
Abstract : Ohno_2012_Rinsho.Shinkeigaku_52_1159
ESTHER : Ohno_2012_Rinsho.Shinkeigaku_52_1159
PubMedSearch : Ohno_2012_Rinsho.Shinkeigaku_52_1159
PubMedID: 23196549

Title : Anti-MuSK antibodies in myasthenia gravis block binding of collagen Q to MuSK - Ohno_2012_Rinsho.Shinkeigaku_52_1306
Author(s) : Ohno K
Ref : Rinsho Shinkeigaku , 52 :1306 , 2012
Abstract : Ohno_2012_Rinsho.Shinkeigaku_52_1306
ESTHER : Ohno_2012_Rinsho.Shinkeigaku_52_1306
PubMedSearch : Ohno_2012_Rinsho.Shinkeigaku_52_1306
PubMedID: 23196600

Title : Structural bases of Wolman disease and cholesteryl ester storage disease - Saito_2012_Mol.Genet.Metab_105_244
Author(s) : Saito S , Ohno K , Suzuki T , Sakuraba H
Ref : Mol Genet Metab , 105 :244 , 2012
Abstract : Saito_2012_Mol.Genet.Metab_105_244
ESTHER : Saito_2012_Mol.Genet.Metab_105_244
PubMedSearch : Saito_2012_Mol.Genet.Metab_105_244
PubMedID: 22138108
Gene_locus related to this paper: human-LIPA

Title : Anti-MuSK autoantibodies block binding of collagen Q to MuSK - Kawakami_2011_Neurology_77_1819
Author(s) : Kawakami Y , Ito M , Hirayama M , Sahashi K , Ohkawara B , Masuda A , Nishida H , Mabuchi N , Engel AG , Ohno K
Ref : Neurology , 77 :1819 , 2011
Abstract : Kawakami_2011_Neurology_77_1819
ESTHER : Kawakami_2011_Neurology_77_1819
PubMedSearch : Kawakami_2011_Neurology_77_1819
PubMedID: 22013178

Title : [Genetic defects and disorders at the neuromuscular junction] - Ohno_2011_Brain.Nerve_63_669
Author(s) : Ohno K
Ref : Brain Nerve , 63 :669 , 2011
Abstract : Ohno_2011_Brain.Nerve_63_669
ESTHER : Ohno_2011_Brain.Nerve_63_669
PubMedSearch : Ohno_2011_Brain.Nerve_63_669
PubMedID: 21747136

Title : Structural basis of neuronal ceroid lipofuscinosis 1 - Ohno_2010_Brain.Dev_32_524
Author(s) : Ohno K , Saito S , Sugawara K , Suzuki T , Togawa T , Sakuraba H
Ref : Brain Dev , 32 :524 , 2010
Abstract : Ohno_2010_Brain.Dev_32_524
ESTHER : Ohno_2010_Brain.Dev_32_524
PubMedSearch : Ohno_2010_Brain.Dev_32_524
PubMedID: 19793631
Gene_locus related to this paper: human-PPT1

Title : [Molecular bases and therapeutic strategies in defective neuromuscular transmissions: lessons learned from a prototypical synapse] - Ohno_2009_Nihon.Shinkei.Seishin.Yakurigaku.Zasshi_29_145
Author(s) : Ohno K , Ito M , Masuda A
Ref : Nihon Shinkei Seishin Yakurigaku Zasshi , 29 :145 , 2009
Abstract : Ohno_2009_Nihon.Shinkei.Seishin.Yakurigaku.Zasshi_29_145
ESTHER : Ohno_2009_Nihon.Shinkei.Seishin.Yakurigaku.Zasshi_29_145
PubMedSearch : Ohno_2009_Nihon.Shinkei.Seishin.Yakurigaku.Zasshi_29_145
PubMedID: 19764481

Title : Viral vector-mediated [corrected] expression of human collagen Q in cultured cells - Ito_2008_Chem.Biol.Interact_175_346
Author(s) : Ito M , Masuda A , Jinno S , Katagiri T , Krejci E , Ohno K
Ref : Chemico-Biological Interactions , 175 :346 , 2008
Abstract : Ito_2008_Chem.Biol.Interact_175_346
ESTHER : Ito_2008_Chem.Biol.Interact_175_346
PubMedSearch : Ito_2008_Chem.Biol.Interact_175_346
PubMedID: 18374322

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 : Synaptic scaffolding molecule (S-SCAM) membrane-associated guanylate kinase with inverted organization (MAGI)-2 is associated with cell adhesion molecules at inhibitory synapses in rat hippocampal neurons - Sumita_2007_J.Neurochem_100_154
Author(s) : Sumita K , Sato Y , Iida J , Kawata A , Hamano M , Hirabayashi S , Ohno K , Peles E , Hata Y
Ref : Journal of Neurochemistry , 100 :154 , 2007
Abstract : Sumita_2007_J.Neurochem_100_154
ESTHER : Sumita_2007_J.Neurochem_100_154
PubMedSearch : Sumita_2007_J.Neurochem_100_154
PubMedID: 17059560

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 : Poster (88) Analysis of human collagenic tailed acetylcholinesterase binding to the frog neuromuscular junction and to perlecan -
Author(s) : Kimbell L , Ohno K , Engel AG , Rotundo RL
Ref : In: Cholinesterases in the Second Millennium: Biomolecular and Pathological Aspects , (Inestrosa NC, Campos EO) P. Universidad Catolica de Chile-FONDAP Biomedicina :367 , 2004
PubMedID:

Title : Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine - Banwell_2004_Neuromuscul.Disord_14_202
Author(s) : Banwell BL , Ohno K , Sieb JP , Engel AG
Ref : Neuromuscular Disorders , 14 :202 , 2004
Abstract : Banwell_2004_Neuromuscul.Disord_14_202
ESTHER : Banwell_2004_Neuromuscul.Disord_14_202
PubMedSearch : Banwell_2004_Neuromuscul.Disord_14_202
PubMedID: 15036330

Title : Congenital myasthenic syndromes. -
Author(s) : Engel AG , Ohno K , Sine MS
Ref : Cholinergic Mechanisms, CRC Press :213 , 2004
PubMedID:

Title : C-terminal and heparin-binding domains of collagenic tail subunit are both essential for anchoring acetylcholinesterase at the synapse - Kimbell_2004_J.Biol.Chem_279_10997
Author(s) : Kimbell LM , Ohno K , Engel AG , Rotundo RL
Ref : Journal of Biological Chemistry , 279 :10997 , 2004
Abstract : Kimbell_2004_J.Biol.Chem_279_10997
ESTHER : Kimbell_2004_J.Biol.Chem_279_10997
PubMedSearch : Kimbell_2004_J.Biol.Chem_279_10997
PubMedID: 14702351

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 : Congenital myasthenic syndromes: A diverse array of molecular targets - Engel_2003_J.Neurocytol_32_1017
Author(s) : Engel AG , Ohno K , Sine SM
Ref : Journal of Neurocytology , 32 :1017 , 2003
Abstract : Engel_2003_J.Neurocytol_32_1017
ESTHER : Engel_2003_J.Neurocytol_32_1017
PubMedSearch : Engel_2003_J.Neurocytol_32_1017
PubMedID: 15034283

Title : Congenital myasthenic syndromes: progress over the past decade - Engel_2003_Muscle.Nerve_27_4
Author(s) : Engel AG , Ohno K , Sine SM
Ref : Muscle & Nerve , 27 :4 , 2003
Abstract : Engel_2003_Muscle.Nerve_27_4
ESTHER : Engel_2003_Muscle.Nerve_27_4
PubMedSearch : Engel_2003_Muscle.Nerve_27_4
PubMedID: 12508290

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 : Sleuthing molecular targets for neurological diseases at the neuromuscular junction -
Author(s) : Engel AG , Ohno K , Sine SM
Ref : Nat Rev Neurosci , 4 :339 , 2003
PubMedID: 12728262

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 : Congenital myasthenic syndromes: genetic defects of the neuromuscular junction - Ohno_2002_Curr.Neurol.Neurosci.Rep_2_78
Author(s) : Ohno K , Engel AG
Ref : Curr Neurol Neurosci Rep , 2 :78 , 2002
Abstract : Ohno_2002_Curr.Neurol.Neurosci.Rep_2_78
ESTHER : Ohno_2002_Curr.Neurol.Neurosci.Rep_2_78
PubMedSearch : Ohno_2002_Curr.Neurol.Neurosci.Rep_2_78
PubMedID: 11898587

Title : The spectrum of congenital myasthenic syndromes - Engel_2002_Mol.Neurobiol_26_347
Author(s) : Engel AG , Ohno K , Sine SM
Ref : Molecular Neurobiology , 26 :347 , 2002
Abstract : Engel_2002_Mol.Neurobiol_26_347
ESTHER : Engel_2002_Mol.Neurobiol_26_347
PubMedSearch : Engel_2002_Mol.Neurobiol_26_347
PubMedID: 12428764

Title : Fundamental gating mechanism of nicotinic receptor channel revealed by mutation causing a congenital myasthenic syndrome - Wang_2000_J.Gen.Physiol_116_449
Author(s) : Wang HL , Ohno K , Milone M , Brengman JM , Evoli A , Batocchi AP , Middleton LT , Christodoulou K , Engel AG , Sine SM
Ref : Journal of General Physiology , 116 :449 , 2000
Abstract : Wang_2000_J.Gen.Physiol_116_449
ESTHER : Wang_2000_J.Gen.Physiol_116_449
PubMedSearch : Wang_2000_J.Gen.Physiol_116_449
PubMedID: 10962020

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 : Congenital End-Plate Acetylcholinesterase Deficiency Caused by a Nonsense Mutation and an A-->G Splice-Donor-Site Mutation at Position +3 of the Collagenlike-Tail-Subunit Gene (COLQ): How Does G at Position +3 Result in Aberrant Splicing? - Ohno_1999_Am.J.Hum.Genet_65_635
Author(s) : Ohno K , Brengman JM , Felice KJ , Cornblath DR , Engel AG
Ref : American Journal of Human Genetics , 65 :635 , 1999
Abstract : Ohno_1999_Am.J.Hum.Genet_65_635
ESTHER : Ohno_1999_Am.J.Hum.Genet_65_635
PubMedSearch : Ohno_1999_Am.J.Hum.Genet_65_635
PubMedID: 10441569

Title : Mutation causing congenital myasthenia reveals acetylcholine receptor beta\/delta subunit interaction essential for assembly - Quiram_1999_J.Clin.Invest_104_1403
Author(s) : Quiram PA , Ohno K , Milone M , Patterson MC , Pruitt NJ , Brengman JM , Sine SM , Engel AG
Ref : J Clinical Investigation , 104 :1403 , 1999
Abstract : Quiram_1999_J.Clin.Invest_104_1403
ESTHER : Quiram_1999_J.Clin.Invest_104_1403
PubMedSearch : Quiram_1999_J.Clin.Invest_104_1403
PubMedID: 10562302

Title : Congenital myasthenic syndromes: recent advances - Engel_1999_Arch.Neurol_56_163
Author(s) : Engel AG , Ohno K , Sine SM
Ref : Archives of Neurology , 56 :163 , 1999
Abstract : Engel_1999_Arch.Neurol_56_163
ESTHER : Engel_1999_Arch.Neurol_56_163
PubMedSearch : Engel_1999_Arch.Neurol_56_163
PubMedID: 10025421

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 : Congenital myasthenic syndromes. New insights from molecular genetic and patch-clamp studies -
Author(s) : Engel AG , Ohno K , Milone M , Sine SM
Ref : Annals of the New York Academy of Sciences , 841 :140 , 1998
PubMedID: 9668233

Title : Congenital myasthenic syndromes: experiments of nature - Engel_1998_J.Physiol.Paris_92_113
Author(s) : Engel AG , Ohno K , Sine SM
Ref : Journal de Physiologie (Paris) , 92 :113 , 1998
Abstract : Engel_1998_J.Physiol.Paris_92_113
ESTHER : Engel_1998_J.Physiol.Paris_92_113
PubMedSearch : Engel_1998_J.Physiol.Paris_92_113
PubMedID: 9782453

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

Title : Human endplate acetylcholinesterase deficiency caused by mutations in the collagen-like tail subunit (ColQ) of the asymmetric enzyme - Ohno_1998_Proc.Natl.Acad.Sci.U.S.A_95_9654
Author(s) : Ohno K , Brengman J , Tsujino A , Engel AG
Ref : Proceedings of the National Academy of Sciences of the United States of America , 95 :9654 , 1998
Abstract : Ohno_1998_Proc.Natl.Acad.Sci.U.S.A_95_9654
ESTHER : Ohno_1998_Proc.Natl.Acad.Sci.U.S.A_95_9654
PubMedSearch : Ohno_1998_Proc.Natl.Acad.Sci.U.S.A_95_9654
PubMedID: 9689136

Title : Congenital myasthenic syndromes due to heteroallelic nonsense\/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations - Ohno_1997_Hum.Mol.Genet_6_753
Author(s) : Ohno K , Quiram PA , Milone M , Wang HL , Harper MC , Pruitt JN, 2nd , Brengman JM , Pao L , Fischbeck KH , Crawford TO , Sine SM , Engel AG
Ref : Hum Mol Genet , 6 :753 , 1997
Abstract : Ohno_1997_Hum.Mol.Genet_6_753
ESTHER : Ohno_1997_Hum.Mol.Genet_6_753
PubMedSearch : Ohno_1997_Hum.Mol.Genet_6_753
PubMedID: 9158150

Title : Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases the rate of agonist dissociation - Wang_1997_J.Gen.Physiol_109_757
Author(s) : Wang HL , Auerbach A , Bren N , Ohno K , Engel AG , Sine SM
Ref : Journal of General Physiology , 109 :757 , 1997
Abstract : Wang_1997_J.Gen.Physiol_109_757
ESTHER : Wang_1997_J.Gen.Physiol_109_757
PubMedSearch : Wang_1997_J.Gen.Physiol_109_757
PubMedID: 9222901

Title : Slow-channel myasthenic syndrome caused by enhanced activation, desensitization, and agonist binding affinity attributable to mutation in the M2 domain of the acetylcholine receptor alpha subunit - Milone_1997_J.Neurosci_17_5651
Author(s) : Milone M , Wang HL , Ohno K , Fukudome T , Pruitt JN , Bren N , Sine SM , Engel AG
Ref : Journal of Neuroscience , 17 :5651 , 1997
Abstract : Milone_1997_J.Neurosci_17_5651
ESTHER : Milone_1997_J.Neurosci_17_5651
PubMedSearch : Milone_1997_J.Neurosci_17_5651
PubMedID: 9221765

Title : End-plate acetylcholine receptor deficiency due to nonsense mutations in the epsilon subunit - Engel_1996_Ann.Neurol_40_810
Author(s) : Engel AG , Ohno K , Bouzat C , Sine SM , Griggs RC
Ref : Annals of Neurology , 40 :810 , 1996
Abstract : Engel_1996_Ann.Neurol_40_810
ESTHER : Engel_1996_Ann.Neurol_40_810
PubMedSearch : Engel_1996_Ann.Neurol_40_810
PubMedID: 8957026

Title : New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome - Engel_1996_Hum.Mol.Genet_5_1217
Author(s) : Engel AG , Ohno K , Milone M , Wang HL , Nakano S , Bouzat C , Pruitt JN, 2nd , Hutchinson DO , Brengman JM , Bren N , Sieb JP , Sine SM
Ref : Hum Mol Genet , 5 :1217 , 1996
Abstract : Engel_1996_Hum.Mol.Genet_5_1217
ESTHER : Engel_1996_Hum.Mol.Genet_5_1217
PubMedSearch : Engel_1996_Hum.Mol.Genet_5_1217
PubMedID: 8872460

Title : Congenital myasthenic syndrome caused by decreased agonist binding affinity due to a mutation in the acetylcholine receptor epsilon subunit - Ohno_1996_Neuron_17_157
Author(s) : Ohno K , Wang HL , Milone M , Bren N , Brengman JM , Nakano S , Quiram P , Pruitt JN , Sine SM , Engel AG
Ref : Neuron , 17 :157 , 1996
Abstract : Ohno_1996_Neuron_17_157
ESTHER : Ohno_1996_Neuron_17_157
PubMedSearch : Ohno_1996_Neuron_17_157
PubMedID: 8755487

Title : Congenital myasthenic syndrome caused by prolonged acetylcholine receptor channel openings due to a mutation in the M2 domain of the epsilon subunit - Ohno_1995_Proc.Natl.Acad.Sci.U.S.A_92_758
Author(s) : Ohno K , Hutchinson DO , Milone M , Brengman JM , Bouzat C , Sine SM , Engel AG
Ref : Proc Natl Acad Sci U S A , 92 :758 , 1995
Abstract : Ohno_1995_Proc.Natl.Acad.Sci.U.S.A_92_758
ESTHER : Ohno_1995_Proc.Natl.Acad.Sci.U.S.A_92_758
PubMedSearch : Ohno_1995_Proc.Natl.Acad.Sci.U.S.A_92_758
PubMedID: 7531341

Title : Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinity - Sine_1995_Neuron_15_229
Author(s) : Sine SM , Ohno K , Bouzat C , Auerbach A , Milone M , Pruitt JN , Engel AG
Ref : Neuron , 15 :229 , 1995
Abstract : Sine_1995_Neuron_15_229
ESTHER : Sine_1995_Neuron_15_229
PubMedSearch : Sine_1995_Neuron_15_229
PubMedID: 7619526