Showing results (41-50 of 165) with videos related to

Sort By:
Pageof 17
JIMD Reports|September 13, 2023
Development of tools to facilitate the diagnosis of hereditary fructose intoleranceBianca Panis, Lise E F Janssen, Dirk J Lefeber, et al.
Molecular Vision|April 24, 2023
Analysis of hemopexin plasma levels in patients with age-related macular degenerationSusette Lauwen, Bjorn Bakker, Eiko K de Jong, et al.
Infection and Immunity|November 26, 2003
Th1-directing adjuvants increase the immunogenicity of oligosaccharide-protein conjugate vaccines related to Streptococcus pneumoniae type 3Dirk J Lefeber, Barry Benaissa-Trouw, Johannes F G Vliegenthart, et al.
Developmental Medicine and Child Neurology|May 14, 2016
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancyCarmen Barba, Francesca Darra, Raffaella Cusmai, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 18, 2020
Cellular Fucosylation Inhibitors Based on Fluorinated Fucose-1-phosphates*Johan F A Pijnenborg, Eline A Visser, Marek Noga, et al.
Experimental Eye Research|October 25, 2021
Loss of the AMD-associated B3GLCT gene affects glycosylation of TSP1 without impairing secretion in retinal pigment epithelial cellsSusette Lauwen, Melissa Baerenfaenger, Sanne Ruigrok, et al.
Carbohydrate Research|May 9, 2002
Isolation of oligosaccharides from a partial-acid hydrolysate of pneumococcal type 3 polysaccharide for use in conjugate vaccinesDirk J Lefeber, Ricardo Gutiérrez Gallego, Christian H Grün, et al.
Human Molecular Genetics|January 2, 2015
Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acidMoniek Riemersma, Julia Sandrock, Thomas J Boltje, et al.
Pediatrics|July 2, 2014
Successful liver transplantation and long-term follow-up in a patient with MPI-CDGMirian C H Janssen, Ruben H de Kleine, Arie P van den Berg, et al.
European Journal of Human Genetics : EJHG|March 16, 2007
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermiaEva Morava, Renate Zeevaert, Eckhard Korsch, et al.
Pageof 17