RAPSN (English Wikipedia)

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

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Buckel A, Beeson D, James M, Vincent A (August 1996). "Cloning of cDNA encoding human rapsyn and mapping of the RAPSN gene locus to chromosome 11p11.2-p11.1". Genomics. 35 (3): 613–616. doi:10.1006/geno.1996.0409. PMID 8812503.
Cossins J, Burke G, Maxwell S, Spearman H, Man S, Kuks J, et al. (October 2006). "Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations". Brain. 129 (Pt 10): 2773–2783. doi:10.1093/brain/awl219. PMID 16945936.
Müller JS, Baumeister SK, Rasic VM, Krause S, Todorovic S, Kugler K, et al. (October 2006). "Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations". Neurology. 67 (7): 1159–1164. doi:10.1212/01.wnl.0000233837.79459.40. PMID 16931511. S2CID 41593780.
Liao X, Wang Y, Lai X, Wang S (February 2023). "The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome". Biomolecules and Biomedicine. 23 (5): 772–784. doi:10.17305/bb.2022.8641. PMC 10494853. PMID 36815443. S2CID 257100080.
Fung ET, Lanahan A, Worley P, Huganir RL (October 1998). "Identification of a Torpedo homolog of Sam68 that interacts with the synapse organizing protein rapsyn". FEBS Letters. 437 (1–2): 29–33. doi:10.1016/S0014-5793(98)01151-X. PMID 9804166. S2CID 7842971.

Buckel A, Beeson D, James M, Vincent A (August 1996). "Cloning of cDNA encoding human rapsyn and mapping of the RAPSN gene locus to chromosome 11p11.2-p11.1". Genomics. 35 (3): 613–616. doi:10.1006/geno.1996.0409. PMID 8812503.
Cossins J, Burke G, Maxwell S, Spearman H, Man S, Kuks J, et al. (October 2006). "Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations". Brain. 129 (Pt 10): 2773–2783. doi:10.1093/brain/awl219. PMID 16945936.
Müller JS, Baumeister SK, Rasic VM, Krause S, Todorovic S, Kugler K, et al. (October 2006). "Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations". Neurology. 67 (7): 1159–1164. doi:10.1212/01.wnl.0000233837.79459.40. PMID 16931511. S2CID 41593780.
Liao X, Wang Y, Lai X, Wang S (February 2023). "The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome". Biomolecules and Biomedicine. 23 (5): 772–784. doi:10.17305/bb.2022.8641. PMC 10494853. PMID 36815443. S2CID 257100080.
Fung ET, Lanahan A, Worley P, Huganir RL (October 1998). "Identification of a Torpedo homolog of Sam68 that interacts with the synapse organizing protein rapsyn". FEBS Letters. 437 (1–2): 29–33. doi:10.1016/S0014-5793(98)01151-X. PMID 9804166. S2CID 7842971.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: RAPSN receptor-associated protein of the synapse".
Liao X, Wang Y, Lai X, Wang S (February 2023). "The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome". Biomolecules and Biomedicine. 23 (5): 772–784. doi:10.17305/bb.2022.8641. PMC 10494853. PMID 36815443. S2CID 257100080.

Müller JS, Baumeister SK, Rasic VM, Krause S, Todorovic S, Kugler K, et al. (October 2006). "Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations". Neurology. 67 (7): 1159–1164. doi:10.1212/01.wnl.0000233837.79459.40. PMID 16931511. S2CID 41593780.
Liao X, Wang Y, Lai X, Wang S (February 2023). "The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome". Biomolecules and Biomedicine. 23 (5): 772–784. doi:10.17305/bb.2022.8641. PMC 10494853. PMID 36815443. S2CID 257100080.
Fung ET, Lanahan A, Worley P, Huganir RL (October 1998). "Identification of a Torpedo homolog of Sam68 that interacts with the synapse organizing protein rapsyn". FEBS Letters. 437 (1–2): 29–33. doi:10.1016/S0014-5793(98)01151-X. PMID 9804166. S2CID 7842971.