3 results for author:"Lemmers R.J.L.F." in Literature citations
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| FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients. Rijkers T., Deidda G., van Koningsbruggen S., van Geel M., Lemmers R.J.L.F., van Deutekom J.C.T., Figlewicz D., Hewitt J.E., Padberg G.W., Frants R.R. et al. J. Med. Genet. 41:826-836(2004) · UniProtKB (3) |
| Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter. Leegwater P.A.J., Vermeulen G., Koenst A.A.M., Naidu S., Mulders J., Visser A., Kersbergen P., Mobach D., Fonds D., van Berkel C.G.M. et al. |
| Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. van Deutekom J.C.T., Lemmers R.J.L.F., Grewal P.K., van Geel M., Romberg S., Dauwerse H.G., Wright T.J., Padberg G.W., Hofker M.H., Hewitt J.E. et al. Hum. Mol. Genet. 5:581-590(1996) · UniProtKB (1) |