Citations for
1CHRNB1
Energetic contributions to channel gating of residues in the muscle nicotinic receptor β1 subunit.
Akk G, Eaton M, Li P, Zheng S, Lo J, Steinbach JH.
PLoS One 8(10):e78539. doi: 10.1371/journal.pone.0078539. eCollection 2013. 2013
2CHRNB1
Loss of heterozygosity (LOH) in tumour suppressor genes in benign and malignant mixed odontogenic tumours.
Galv„o CF, Gomes CC, Diniz MG, Vargas PA, de Paula AM, Mosqueda-Taylor A, Loyola AM, Gomez RS.
J Oral Pathol Med 41(5):389-93. doi: 10.1111/j.1600-0714.2011.01115.x. Epub 2011 Nov 15. 2012
3RAPSN, MPTLT2, CHRNA1, CHRNB1, CHRND
Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients.
Vogt J, Harrison BJ, Spearman H, Cossins J, Vermeer S, ten Cate LN, Morgan NV, Beeson D, Maher ER.
Am J Hum Genet 82(1):222-7. 2008
4CHRM1, CHRNB1
Gene-based analysis suggests association of the nicotinic acetylcholine receptor beta1 subunit (CHRNB1) and M1 muscarinic acetylcholine receptor (CHRM1) with vulnerability for nicotine dependence.
Lou XY, Ma JZ, Payne TJ, Beuten J, Crew KM, Li MD.
Hum Genet 120(3):381-9. Epub 2006 Jul 28. 2006
5CHAT, CHRNB1, CMS2B, CMS6
Congenital myasthenic syndromes.
Harper CM.
Semin Neurol 24(1):111-23. Review. 2004
6ALOX12, ATP1B2, CD68, CHD3, CHRNB1, EIF4A1, FGF11, FXR2, GUCY2D, KDM6B, NEUROD2, SHBG, TNFSF12, TNFSF13, TP53
Physical Map of 17p13 and the Genes Adjacent to p53.
Cousin P, Billotte J, Chaubert P, Shaw P.
Genomics 63(1):60-68. 2000
7CHRNB1, CMS2B
A beta-subunit mutation in the acetylcholine receptor channel gate causes severe Slow-Channel syndrome.
Gomez CM, et al.
Ann Neurol 39 : 712-723. 1996
8CHRNA1, CHRNB1, CHRND, CHRNE, CMS1A, CMS2B, CMS4A
New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.
Engel AG, Ohno K, Milone M, Wang HL, Nakano S, Bouzat C, Pruitt JN 2nd, Hutchinson DO, Brengman JM, Bren N, Sieb JP, Sine SM.
Hum Mol Genet 5 : 1217-1227. 1996
9CHRNB1, UBB
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p.
Guzzetta V, Franco B, Trask BJ, Zhang H, Saucedo-Cardenas O, Montes de Oca-Luna R, Greenberg F, Chinault AC, Lupski JR, Patel PI.
Genomics 13(3):551-9. 1992
10CHRNA1, CHRNB1, CHRND, CHRNG
Assignment of the human nicotinic acetylcholine receptor genes: the alpha and delta subunit genes to chromosome 2 and the beta subunit gene to chromosome 17.
Beeson D, Jeremiah S, West LF, Povey S, Newsom-Davis J.
Ann Hum Genet 54(Pt 3):199-208. 1990