| 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 : |
| PubMedSearch : Shen_2003_J.Clin.Invest_111_497 |
| PubMedID: 12588888 |
| 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 : |
| 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 : |
| PubMedSearch : Shapira_2002_Neurology_58_603 |
| PubMedID: 11865139 |
| 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 : |
| PubMedSearch : Wang_1999_Nat.Neurosci_2_226 |
| PubMedID: 10195214 |
| 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 : |
| PubMedSearch : Ohno_1998_Proc.Natl.Acad.Sci.U.S.A_95_9654 |
| PubMedID: 9689136 |