共 76 条
[1]
Dietrich WF(1996)A comprehensive genetic map of the mouse genome Nature 380 149-152
[2]
Miller J(2004)Ribosomal protein L24 defect in belly spot and tail ( Development 131 3907-3920
[3]
Steen R(2011)), a mouse Minute J Biol Chem 286 3079-3093
[4]
Merchant MA(2001)Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse FEBS Lett 499 274-278
[5]
Damron-Boles D(2003)Homeodomain proteins Mox1 and Mox2 associate with Pax1 and Pax3 transcription factors Development 130 4655-4664
[6]
Husain Z(2009)The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites Dev Biol 332 383-395
[7]
Dredge R(2011)Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton Mol Cell Biol 31 1301-1308
[8]
Daly MJ(1984)Transient activation of Meox1 is an early component of the gene regulatory network downstream of Hoxa2 Molec Cell Biol 4 2239-2242
[9]
Ingalls KA(2013)Short direct repeats mediate spontaneous high-frequency deletions in DNA of minute virus of mice BMC Genet 14 95-161
[10]
O'Connor TJ(2013)Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype Am J Hum Genet 92 157-118