Citations for
1CHRND, CHRNG, NCAM1, RUNX1
Molecular analyses provide insight into mechanisms underlying sarcopenia and myofibre denervation in old skeletal muscles of mice.
Barns M, Gondro C, Tellam RL, Radley-Crabb HG, Grounds MD, Shavlakadze T.
Int J Biochem Cell Biol 53:174-85. doi: 10.1016/j.biocel.2014.04.025. Epub 2014 May 13. 2014
2CHRNG, MPTLT1
CHRNG genotype-phenotype correlations in the multiple pterygium syndromes.
Vogt J, Morgan NV, Rehal P, Faivre L, Brueton LA, Becker K, Fryns JP, Holder S, Islam L, Kivuva E, Lynch SA, Touraine R, Wilson LC, MacDonald F, Maher ER.
J Med Genet 49(1):21-6. doi: 10.1136/jmedgenet-2011-100378. 2012
3CHRNG
Alternatively spliced variants of gamma-subunit of muscle-type acetylcholine receptor in fetal and adult skeletal muscle of mouse.
Azim S, Banday AR, Sarwar T, Tabish M.
Cell Mol Neurobiol 32(6):957-63. doi: 10.1007/s10571-012-9838-y. Epub 2012 Apr 10. 2012
4CHRND, CHRNG
Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.
Saccone NL, Saccone SF, Hinrichs AL, Stitzel JA, Duan W, Pergadia ML, Agrawal A, Breslau N, Grucza RA, Hatsukami D, Johnson EO, Madden PA, Swan GE, Wang JC, Goate AM, Rice JP, Bierut LJ.
Am J Med Genet B Neuropsychiatr Genet 150B(4):453-66. doi: 10.1002/ajmg.b.30828. 2009
5CHRNG
Essential roles of the acetylcholine receptor gamma-subunit in neuromuscular synaptic patterning.
Liu Y, Padgett D, Takahashi M, Li H, Sayeed A, Teichert RW, Olivera BM, McArdle JJ, Green WN, Lin W.
Development 135(11):1957-67. doi: 10.1242/dev.018119. Epub 2008 Apr 23. 2008
6CHRNG, MPTLT1, MPTSE
Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome.
Morgan NV, Brueton LA, Cox P, Greally MT, Tolmie J, Pasha S, Aligianis IA, van Bokhoven H, Marton T, Al-Gazali L, Morton JE, Oley C, Johnson CA, Trembath RC, Brunner HG, Maher ER.
Am J Hum Genet 79(2):390-5. Epub 2006 Jun 20. 2006
7MPTSE, CHRNG
Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit.
Hoffmann K, Muller JS, Stricker S, Megarbane A, Rajab A, Lindner TH, Cohen M, Chouery E, Adaimy L, Ghanem I, Delague V, Boltshauser E, Talim B, Horvath R, Robinson PN, Lochmuller H, Hubner C, Mundlos S.
Am J Hum Genet 79(2):303-12. Epub 2006 Jun 20. 2006
8CHRNA1, 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
9CHRND, CHRNG
Linkage disequilibrium study of RFLPs detected ay the human muscle nicotinic acetylcholine receptor subunit genes.
Lobos EA, Rudnick CH, Watson MS, Isenberg KE.
Am J Hum Genet 44 : 522-533. 1989
10CHRNG
Localization of the acetylcholine receptor gamma subunit gene to human chromosome 2q32-qter.
Cohen-Haguenauer O, et al.
Cytogenet Cell Genet 52 : 124-127. 1989
11CHRNG, CHRND
Localisation of the human acetylcholine receptor gamma subunit gene to 2q32-qter.
Cohen-Haguenauer O, et al.
(HGM9) Cytogenet Cell Genet 46 : 595. 1987
12CHRNG
Cloning and sequence analysis of human genomic DNA encoding gamma subunit precursor of muscle acetylcholine receptor.
Shibahara S, et al.
Eur J Biochem 146 : 15-22. 1985