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Molecular basis for the progeroid variant of Ehlers-Danlos syndrome. Identification and characterization of two mutations in galactosyltransferase I gene.
Okajima T, Fukumoto S, Furukawa K, Urano T. Okajima T, et al. J Biol Chem. 1999 Oct 8;274(41):28841-4. doi: 10.1074/jbc.274.41.28841. J Biol Chem. 1999. PMID: 10506123 Free article.
Recently, we isolated cDNA of the galactosyltransferase I (XGalT-1) (Okajima, T., Yoshida, K., Kondo, T., and Furukawa, K. (1999) J. Biol. ...Therefore, we analyzed mutations in this gene of a patient with progeroid type E-D syndrome by reverse transcription …
Recently, we isolated cDNA of the galactosyltransferase I (XGalT-1) (Okajima, T., Yoshida, K., Kondo, T., and Furukawa, …
b-series Ganglioside deficiency exhibits no definite changes in the neurogenesis and the sensitivity to Fas-mediated apoptosis but impairs regeneration of the lesioned hypoglossal nerve.
Okada M, Itoh Mi M, Haraguchi M, Okajima T, Inoue M, Oishi H, Matsuda Y, Iwamoto T, Kawano T, Fukumoto S, Miyazaki H, Furukawa K, Aizawa S, Furukawa K. Okada M, et al. Among authors: okajima t. J Biol Chem. 2002 Jan 18;277(3):1633-6. doi: 10.1074/jbc.C100395200. Epub 2001 Oct 26. J Biol Chem. 2002. PMID: 11682464 Free article.
462 results