Acetylcholine receptor (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acetylcholine receptor" in English language version.

refsWebsite

Global rank English rank

8nih.gov

4^th place

7doi.org

2^nd place

5semanticscholar.org

11^th place

8^th place

2harvard.edu

18^th place

17^th place

2worldcat.org

5^th place

1slidesharecdn.com

low place

doi.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.
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. S2CID 18062185.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992-10-08). "Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic". Nature. 359 (6395): 500–505. Bibcode:1992Natur.359..500G. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829. S2CID 4266961.
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

ui.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.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992-10-08). "Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic". Nature. 359 (6395): 500–505. Bibcode:1992Natur.359..500G. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829. S2CID 4266961.

nih.gov

pubmed.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. S2CID 18062185.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992-10-08). "Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic". Nature. 359 (6395): 500–505. Bibcode:1992Natur.359..500G. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829. S2CID 4266961.
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.

ncbi.nlm.nih.gov

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.

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.
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. S2CID 18062185.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992-10-08). "Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic". Nature. 359 (6395): 500–505. Bibcode:1992Natur.359..500G. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829. S2CID 4266961.
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".

worldcat.org

search.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. S2CID 18062185.
Galzi, J. L.; Devillers-Thiéry, A.; Hussy, N.; Bertrand, S.; Changeux, J. P.; Bertrand, D. (1992-10-08). "Mutations in the channel domain of a neuronal nicotinic receptor convert ion selectivity from cationic to anionic". Nature. 359 (6395): 500–505. Bibcode:1992Natur.359..500G. doi:10.1038/359500a0. ISSN 0028-0836. PMID 1383829. S2CID 4266961.