Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Xing Ming Shen"'
Publikováno v:
Neuromuscular Disorders. 15:753-759
We report a patient with a slow-channel congenital myasthenic syndrome who carries a novel slow-channel mutation in the epsilon subunit of the acetylcholine receptor and has tubulofilamentous inclusion bodies, in skeletal muscle of the type observed
Autor:
Joan M. Brengman, Kinji Ohno, P. Tonali, Xing Ming Shen, Hai Long Wang, Steven M. Sine, A. Tsujino, Anna Paola Batocchi, Andrew G. Engel, Margherita Milone
Publikováno v:
ResearcherID
By defining the functional defect in a congenital myasthenic syndrome (CMS), we show that the third transmembrane domain (M3) of the muscle acetylcholine receptor governs the speed and efficiency of gating of its channel. The clinical phenotype of th
Autor:
Jiri Vajsar, Steven M. Sine, Xing Ming Shen, Kinji Ohno, Hai Long Wang, A. Tsujino, Joan Brengmann, Andrew G. Engel, Nina Bren, Won Yong Lee
Publikováno v:
The Journal of General Physiology
By defining functional defects in a congenital myasthenic syndrome (CMS), we show that two mutant residues, located in a binding site region of the acetylcholine receptor (AChR) epsilon subunit, exert opposite effects on ACh binding and suppress chan
Autor:
D. Selcen, Margherita Milone, Kinji Ohno, Joan M. Brengman, C. Harper, Xing Ming Shen, Susan T. Iannaccone, Andrew G. Engel
Publikováno v:
Clinical Neurophysiology. 120:e106
Erratum: Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gating
Autor:
P. Tonali, Anna Paola Batocchi, Steven M. Sine, Joan M. Brengman, Hai Long Wang, Xing Ming Shen, A. Tsujino, Andrew G. Engel, Kinji Ohno, Margherita Milone
Publikováno v:
Nature Neuroscience. 2:485-485
Autor:
Sine, Steven M., Xing-Ming Shen, Hai-Long Wang, Kinji Ohno, Won-Yong Lee, Tsujino, Akira, Brengmann, Joan, Bren, Nina, Vajsar, Jiri, Engel, Andrew G.
Publikováno v:
Journal of General Physiology. Oct2002, Vol. 120 Issue 4, p483. 14p. 1 Color Photograph, 2 Diagrams, 3 Charts, 6 Graphs.