Fragile X Mental Retardation Protein: Nucleocytoplasmic Shuttling and Association with Somatodendritic Ribosomes
Tóm tắt
Từ khóa
Tài liệu tham khảo
Bonfa, 1989, Antiribosomal S10 antibodies in humans and MRL/lpr mice with systemic lupus erythematosus., Arthritis Rheum, 32, 1252, 10.1002/anr.1780321010
Frey, 1991, Long-term potentiation induced changes in protein synthesis of hippocampal subfields of freely moving rats: time-course., Biomed Biochim Acta, 50, 1231
Krajewski, 1993, Investigation of the subcellular distribution of the bcl-2 oncoprotein: residence in the nuclear envelope, endoplasmic reticulum, and outer mitochondrial membranes., Cancer Res, 53, 4701
Rousseau, 1995, Prevalence of carriers of premutation-size alleles of the FMRI gene and implications for the population genetics of the fragile X syndrome., Am J Hum Genet, 57, 1006
Siomi, 1995, FXR1, an autosomal homolog of the fragile X mental retardation gene., EMBO J, 14, 2401, 10.1002/j.1460-2075.1995.tb07237.x
Thompson, 1989, Inhibition of in vivo and in vitro transcription by monoclonal antibodies prepared against wheat germ RNA polymerase II that react with the heptapeptide repeat of eukaryotic RNA polymerase II., J Biol Chem, 264, 11511, 10.1016/S0021-9258(18)60493-4