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Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S, Baum MG, French CA, Nicod J, Coventry JA, Enard W, Fray M, Brown SD, Nolan PM, Pääbo S, Channon KM, Costa RM, Eilers J, Ehret G, Rawlins JN, Fisher SE. Groszer M, et al. Among authors: fisher se. Curr Biol. 2008 Mar 11;18(5):354-62. doi: 10.1016/j.cub.2008.01.060. Curr Biol. 2008. PMID: 18328704 Free PMC article.
On genes, speech, and language.
Fisher SE. Fisher SE. N Engl J Med. 2005 Oct 20;353(16):1655-7. doi: 10.1056/NEJMp058207. N Engl J Med. 2005. PMID: 16236736 No abstract available.
Generation of mice with a conditional Foxp2 null allele.
French CA, Groszer M, Preece C, Coupe AM, Rajewsky K, Fisher SE. French CA, et al. Among authors: fisher se. Genesis. 2007 Jul;45(7):440-6. doi: 10.1002/dvg.20305. Genesis. 2007. PMID: 17619227 Free PMC article.
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, Nicod J, Xiong L, Joober R, Enard W, Krinsky B, Nanba E, Richardson AJ, Riley BP, Martin NG, Strittmatter SM, Möller HJ, Rujescu D, St Clair D, Muglia P, Roos JL, Fisher SE, Wade-Martins R, Rouleau GA, Stein JF, Karayiorgou M, Geschwind DH, Ragoussis J, Kendler KS, Airaksinen MS, Oshimura M, DeLisi LE, Monaco AP. Francks C, et al. Among authors: fisher se. Mol Psychiatry. 2007 Dec;12(12):1129-39, 1057. doi: 10.1038/sj.mp.4002053. Epub 2007 Jul 31. Mol Psychiatry. 2007. PMID: 17667961 Free PMC article.
419 results