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XB-GENEPAGE-6449529
Papers associated with chrnb1
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Former neuritic pathways containing endogenous neural agrin have high synaptogenic activity., Cohen MW, Moody-Corbett F, Godfrey EW., Dev Biol. February 1, 1995; 167 (2): 458-68. |
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Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome., Croxen R, Newland C, Beeson D, Oosterhuis H, Chauplannaz G, Vincent A, Newsom-Davis J., Hum Mol Genet. May 1, 1997; 6 (5): 767-74. |
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Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction., Gomez CM, Maselli R, Gundeck JE, Chao M, Day JW, Tamamizu S, Lasalde JA, McNamee M, Wollmann RL., J Neurosci. June 1, 1997; 17 (11): 4170-9. |
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Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome., Gomez CM, Maselli RA, Groshong J, Zayas R, Wollmann RL, Cens T, Charnet P., J Neurosci. August 1, 2002; 22 (15): 6447-57. |
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Genomic Takeover by Transposable Elements in the Strawberry Poison Frog., Rogers RL, Zhou L, Chu C, Márquez R, Corl A, Linderoth T, Freeborn L, MacManes MD, Xiong Z, Zheng J, Guo C, Xun X, Kronforst MR, Summers K, Wu Y, Yang H, Richards-Zawacki CL, Zhang G, Nielsen R., Mol Biol Evol. December 1, 2018; 35 (12): 2913-2927. |
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