|1.||Götte, Martin: 2 articles (04/2008 - 07/2006)|
|2.||Yip, George W: 2 articles (04/2008 - 07/2006)|
|3.||Kiesel, Ludwig: 2 articles (04/2008 - 07/2006)|
|4.||Faiyaz-Ul-Haque, Muhammad: 2 articles (07/2006 - 07/2004)|
|5.||Rosmarin, David M: 1 article (06/2012)|
|6.||Carette, Jan E: 1 article (06/2012)|
|7.||Brummelkamp, Thijn R: 1 article (06/2012)|
|8.||Ploegh, Hidde L: 1 article (06/2012)|
|9.||Olive, Andrew J: 1 article (06/2012)|
|10.||Starnbach, Michael N: 1 article (06/2012)|
|1.||Ehlers-Danlos Syndrome (Syndrome, Ehlers-Danlos)
07/01/2004 - "A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type."
12/19/2002 - "Mutations of this gene were investigated in a case of Ehlers-Danlos syndrome (progeroid variant), since reduced activity of galactosyltransferase I had been reported in this disease by others. "
09/10/1999 - "Sequence analysis of beta4Gal-T7 from a fibroblast cell line of a patient with a progeroid syndrome and signs of the Ehlers-Danlos syndrome, previously shown to exhibit reduced galactosyltransferase I activity (Quentin, E., Gladen, A., Rodén, L., and Kresse, H. "
04/01/2008 - "Changes in heparan sulfate are associated with delayed wound repair, altered cell migration, adhesion and contractility in the galactosyltransferase I (beta4GalT-7) deficient form of Ehlers-Danlos syndrome."
07/01/2006 - "Defective glycosylation of decorin and biglycan, altered collagen structure, and abnormal phenotype of the skin fibroblasts of an Ehlers-Danlos syndrome patient carrying the novel Arg270Cys substitution in galactosyltransferase I (beta4GalT-7)."
|2.||Wounds and Injuries (Trauma)
|3.||Heparitin Sulfate (Heparan Sulfate)
|6.||UDP-galactose xylose galactosyltransferase