아세틸콜린 수용체 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "아세틸콜린 수용체" in Korean language version.

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9nih.gov

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8doi.org

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3semanticscholar.org

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310^th place

2worldcat.org

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1springer.com

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1slidesharecdn.com

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1harvard.edu

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1archive.org

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archive.org

Shen, X. -M.; Brengman, J. M.; Edvardson, S.; Sine, S. M.; Engel, A. G. (2012). “Highly fatal fast-channel syndrome caused by AChR subunit mutation at the agonist binding site”. 《Neurology》 79 (5): 449–454. doi:10.1212/WNL.0b013e31825b5bda. PMC 3405251. PMID 22592360.

doi.org

dx.doi.org

R. C, Hogg; M. Raggenbass, D. Bertrand (2003년 4월 20일). “Nicotinic acetylcholine receptors: from structure to brain function”. 《Reviews of Physiology, Biochemistry and Pharmacology》 (Springer) 147: 1-46. doi:10.1007/s10254-003-0005-1. (구독 필요).
Doyle DA (2004). “Structural changes during ion channel gating”. 《Trends Neurosci.》 27 (6): 298–302. doi:10.1016/j.tins.2004.04.004. PMID 15165732. S2CID 36451231.
Miyazawa A, Fujiyoshi Y, Unwin N (2003). “Structure and gating mechanism of the acetylcholine receptor pore”. 《Nature》 423 (6943): 949–55. Bibcode:2003Natur.423..949M. doi:10.1038/nature01748. PMID 12827192. S2CID 205209809.
Ortells, M. O.; Lunt, G. G. (March 1995). “Evolutionary history of the ligand-gated ion-channel superfamily of receptors”. 《Trends in Neurosciences》 18 (3): 121–127. doi:10.1016/0166-2236(95)93887-4. ISSN 0166-2236. PMID 7754520.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992년 10월 8일). “Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic”. 《Nature》 359 (6395): 500–505. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829.
Cossins, J.; Burke, G.; Maxwell, S.; Spearman, H.; Man, S.; Kuks, J.; Vincent, A.; Palace, J.; Fuhrer, C.; Beeson, D. (2006). “Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations”. 《Brain》 129 (10): 2773–2783. doi:10.1093/brain/awl219. PMID 16945936.
Abicht, A.; Dusl, M.; Gallenmüller, C.; Guergueltcheva, V.; Schara, U.; Della Marina, A.; Wibbeler, E.; Almaras, S.; Mihaylova, V.; Von Der Hagen, M.; Huebner, A.; Chaouch, A.; Müller, J. S.; Lochmüller, H. (2012). “Congenital myasthenic syndromes: Achievements and limitations of phenotype-guided gene-after-gene sequencing in diagnostic practice: A study of 680 patients”. 《Human Mutation》 33 (10): 1474–1484. doi:10.1002/humu.22130. PMID 22678886. S2CID 30868022.
Shen, X. -M.; Brengman, J. M.; Edvardson, S.; Sine, S. M.; Engel, A. G. (2012). “Highly fatal fast-channel syndrome caused by AChR subunit mutation at the agonist binding site”. 《Neurology》 79 (5): 449–454. doi:10.1212/WNL.0b013e31825b5bda. PMC 3405251. PMID 22592360.

harvard.edu

adsabs.harvard.edu

Miyazawa A, Fujiyoshi Y, Unwin N (2003). “Structure and gating mechanism of the acetylcholine receptor pore”. 《Nature》 423 (6943): 949–55. Bibcode:2003Natur.423..949M. doi:10.1038/nature01748. PMID 12827192. S2CID 205209809.

nih.gov

ncbi.nlm.nih.gov

Doyle DA (2004). “Structural changes during ion channel gating”. 《Trends Neurosci.》 27 (6): 298–302. doi:10.1016/j.tins.2004.04.004. PMID 15165732. S2CID 36451231.
Miyazawa A, Fujiyoshi Y, Unwin N (2003). “Structure and gating mechanism of the acetylcholine receptor pore”. 《Nature》 423 (6943): 949–55. Bibcode:2003Natur.423..949M. doi:10.1038/nature01748. PMID 12827192. S2CID 205209809.
Ortells, M. O.; Lunt, G. G. (March 1995). “Evolutionary history of the ligand-gated ion-channel superfamily of receptors”. 《Trends in Neurosciences》 18 (3): 121–127. doi:10.1016/0166-2236(95)93887-4. ISSN 0166-2236. PMID 7754520.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992년 10월 8일). “Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic”. 《Nature》 359 (6395): 500–505. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829.
Cossins, J.; Burke, G.; Maxwell, S.; Spearman, H.; Man, S.; Kuks, J.; Vincent, A.; Palace, J.; Fuhrer, C.; Beeson, D. (2006). “Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations”. 《Brain》 129 (10): 2773–2783. doi:10.1093/brain/awl219. PMID 16945936.
Abicht, A.; Dusl, M.; Gallenmüller, C.; Guergueltcheva, V.; Schara, U.; Della Marina, A.; Wibbeler, E.; Almaras, S.; Mihaylova, V.; Von Der Hagen, M.; Huebner, A.; Chaouch, A.; Müller, J. S.; Lochmüller, H. (2012). “Congenital myasthenic syndromes: Achievements and limitations of phenotype-guided gene-after-gene sequencing in diagnostic practice: A study of 680 patients”. 《Human Mutation》 33 (10): 1474–1484. doi:10.1002/humu.22130. PMID 22678886. S2CID 30868022.
Shen, X. -M.; Brengman, J. M.; Edvardson, S.; Sine, S. M.; Engel, A. G. (2012). “Highly fatal fast-channel syndrome caused by AChR subunit mutation at the agonist binding site”. 《Neurology》 79 (5): 449–454. doi:10.1212/WNL.0b013e31825b5bda. PMC 3405251. PMID 22592360.

pubmed.ncbi.nlm.nih.gov

Ortells, M. O.; Lunt, G. G. (March 1995). “Evolutionary history of the ligand-gated ion-channel superfamily of receptors”. 《Trends in Neurosciences》 18 (3): 121–127. doi:10.1016/0166-2236(95)93887-4. ISSN 0166-2236. PMID 7754520.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992년 10월 8일). “Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic”. 《Nature》 359 (6395): 500–505. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829.

semanticscholar.org

api.semanticscholar.org

Doyle DA (2004). “Structural changes during ion channel gating”. 《Trends Neurosci.》 27 (6): 298–302. doi:10.1016/j.tins.2004.04.004. PMID 15165732. S2CID 36451231.
Miyazawa A, Fujiyoshi Y, Unwin N (2003). “Structure and gating mechanism of the acetylcholine receptor pore”. 《Nature》 423 (6943): 949–55. Bibcode:2003Natur.423..949M. doi:10.1038/nature01748. PMID 12827192. S2CID 205209809.
Abicht, A.; Dusl, M.; Gallenmüller, C.; Guergueltcheva, V.; Schara, U.; Della Marina, A.; Wibbeler, E.; Almaras, S.; Mihaylova, V.; Von Der Hagen, M.; Huebner, A.; Chaouch, A.; Müller, J. S.; Lochmüller, H. (2012). “Congenital myasthenic syndromes: Achievements and limitations of phenotype-guided gene-after-gene sequencing in diagnostic practice: A study of 680 patients”. 《Human Mutation》 33 (10): 1474–1484. doi:10.1002/humu.22130. PMID 22678886. S2CID 30868022.

slidesharecdn.com

image.slidesharecdn.com

“Reference at image.slidesharecdn.com”.

springer.com

link.springer.com

R. C, Hogg; M. Raggenbass, D. Bertrand (2003년 4월 20일). “Nicotinic acetylcholine receptors: from structure to brain function”. 《Reviews of Physiology, Biochemistry and Pharmacology》 (Springer) 147: 1-46. doi:10.1007/s10254-003-0005-1. (구독 필요).

worldcat.org

Ortells, M. O.; Lunt, G. G. (March 1995). “Evolutionary history of the ligand-gated ion-channel superfamily of receptors”. 《Trends in Neurosciences》 18 (3): 121–127. doi:10.1016/0166-2236(95)93887-4. ISSN 0166-2236. PMID 7754520.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992년 10월 8일). “Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic”. 《Nature》 359 (6395): 500–505. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829.