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Human Mutation|April 14, 2025
Biochemical and Genetic Testing of GAA in Over 30.000 Symptomatic Patients Suspected to Be Affected With Pompe DiseaseSukirthini Balendran-Braun, Ursula Vinatzer, Sandra Liebmann-Reindl, et al.Acta Crystallographica. Section D, Biological Crystallography|March 3, 2004
Crystallization and preliminary X-ray diffraction study of fructan 1-exohydrolase IIa from Cichorium intybusMaureen Verhaest, Wim Van den Ende, Midori Yoshida, et al.Biochemical and Biophysical Research Communications|August 9, 2005
Molecular identification of wheat endoxylanase inhibitor TAXI-II and the determinants of its inhibition specificityGert Raedschelders, Katleen Fierens, Stefaan Sansen, et al.Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|March 3, 2006
Crystallization and preliminary X-ray diffraction study of a cell-wall invertase from Arabidopsis thalianaMaureen Verhaest, Katrien Le Roy, Stefaan Sansen, et al.Biochimica Et Biophysica Acta|February 12, 2004
Properties of TAXI-type endoxylanase inhibitorsKurt Gebruers, Kristof Brijs, Christophe M Courtin, et al.Journal of Biotechnology|April 21, 2007
Targeted molecular engineering of a family 11 endoxylanase to decrease its sensitivity towards Triticum aestivum endoxylanase inhibitor typesTine M Bourgois, Dung V Nguyen, Stefaan Sansen, et al.The FEBS Journal|November 11, 2005
His374 of wheat endoxylanase inhibitor TAXI-I stabilizes complex formation with glycoside hydrolase family 11 endoxylanasesKatleen Fierens, Ann Gils, Stefaan Sansen, et al.Orphanet Journal of Rare Diseases|May 15, 2025
TREAT: systematic and inclusive selection process of genes for genomic newborn screening as part of the Screen4Care projectChristina Saier, Stefaan Sansen, Joanne Berghout, et al.Orphanet Journal of Rare Diseases|September 28, 2024
Leaving no patient behind! Expert recommendation in the use of innovative technologies for diagnosing rare diseasesClara D M van Karnebeek, Anne O'Donnell-Luria, Gareth Baynam, et al.BMJ Open|April 20, 2024
Patient preferences in genetic newborn screening for rare diseases: study protocolSylvia Martin, Emanuele Angolini, Jennifer Audi, et al.Pageof 3