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Neurology|November 9, 2014
Mutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disabilityXin-Ming Shen, Duygu Selcen, Joan Brengman, et al.
Naunyn-Schmiedeberg'S Archives of Pharmacology|January 1, 1986
Identity of inhibitory presynaptic 5-hydroxytryptamine (5-HT) autoreceptors in the rat brain cortex with 5-HT1B binding sitesG Engel, M Göthert, D Hoyer, et al.
Medwave|June 22, 2019
Congenital myasthenic syndrome due to rapsyn deficiency: A case report with a new mutation and compound heterozygosityIvan O Espinoza, Carolina Reynoso, Giulliana Chávez, et al.
Neuroreport|July 17, 1998
Quinidine normalizes the open duration of slow-channel mutants of the acetylcholine receptorT Fukudome, K Ohno, J M Brengman, et al.
Physical Review. E|February 17, 2024
Spin-orbit-coupled fractional oscillators and trapped Bose-Einstein condensatesV A Stephanovich, E V Kirichenko, G Engel, et al.
British Journal of Clinical Pharmacology|February 12, 1998
The involvement of CYP1A2 and CYP3A4 in the metabolism of clozapineB Eiermann, G Engel, I Johansson, et al.
Journal of Neuropathology and Experimental Neurology|March 1, 1980
Ultrastructural localization of the terminal and lytic ninth complement component (C9) at the motor end-plate in myasthenia gravisK Sahashi, A G Engel, E H Lambert, et al.
The Journal of Biological Chemistry|January 2, 2004
C-terminal and heparin-binding domains of collagenic tail subunit are both essential for anchoring acetylcholinesterase at the synapseLewis M Kimbell, Kinji Ohno, Andrew G Engel, et al.
Blood|June 1, 1994
Isolation and characterization of the human interleukin-9 receptor geneM S Chang, G Engel, C Benedict, et al.
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