J Ouwendijk
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Explore the profile of J Ouwendijk including associated specialties, affiliations and a list of published articles.
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8
Citations
279
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Recent Articles
1.
Fava E, Dehghany J, Ouwendijk J, Muller A, Niederlein A, Verkade P, et al.
Diabetologia
. 2012 Jan;
55(4):1013-23.
PMID: 22252472
Aims/hypothesis: Knowledge of number, size and content of insulin secretory granules is pivotal for understanding the physiology of pancreatic beta cells. Here we re-evaluated key structural features of rat beta...
2.
Lanoix J, Ouwendijk J, Stark A, Szafer E, Cassel D, Dejgaard K, et al.
J Cell Biol
. 2001 Dec;
155(7):1199-212.
PMID: 11748249
We present evidence for two subpopulations of coatomer protein I vesicles, both containing high amounts of Golgi resident proteins but only minor amounts of anterograde cargo. Early Golgi proteins p24alpha2,...
3.
Axelsson M, Karlsson N, Steel D, Ouwendijk J, Nilsson T, Hansson G
Glycobiology
. 2001 Aug;
11(8):633-44.
PMID: 11479274
Addition of the weak base ammonium chloride (NH4Cl) or the proton pump inhibitor bafilomycin A1 to cultured HeLa and LS 174T cells effectively neutralized the pH gradient of the secretory...
4.
Lanoix J, Ouwendijk J, Lin C, Stark A, Love H, Ostermann J, et al.
EMBO J
. 1999 Sep;
18(18):4935-48.
PMID: 10487746
Upon addition of GTPgammaS to in vitro budding reactions, COP I vesicles form but retain their coat, making them easy to isolate and analyze. We have developed an in vitro...
5.
Ouwendijk J, Peters W, te Morsche R, van de Vorstenbosch R, Ginsel L, Naim H, et al.
Biochim Biophys Acta
. 1998 Jun;
1406(3):299-306.
PMID: 9630686
A glutamine for proline substitution at position 1098 was previously shown to result in accumulation of brush-border sucrase-isomaltase in the Golgi apparatus. The substitution is present in a highly homologous...
6.
Ouwendijk J, Peters W, van de Vorstenbosch R, Ginsel L, Naim H, Fransen J
J Biol Chem
. 1998 Apr;
273(12):6650-5.
PMID: 9506961
Human lactase-phlorizin hydrolase (LPH) is a digestive enzyme that is expressed in the small intestinal brush-border membrane. After terminal glycosylation in the Golgi apparatus, the 230-kDa pro-LPH is cleaved into...
7.
Moolenaar C, Ouwendijk J, Wittpoth M, Wisselaar H, Hauri H, Ginsel L, et al.
J Cell Sci
. 1997 Mar;
110 ( Pt 5):557-67.
PMID: 9092938
A point mutation in the cDNA of human intestinal sucrase-isomaltase has been recently identified in phenotype II of congenital sucrase-isomaltase deficiency. The mutation results in a substitution of glutamine by...
8.
Ouwendijk J, Moolenaar C, Peters W, Hollenberg C, Ginsel L, Fransen J, et al.
J Clin Invest
. 1996 Feb;
97(3):633-41.
PMID: 8609217
Congenital sucrase-isomaltase deficiency is an example of a disease in which mutant phenotypes generate transport-incompetent molecules. Here, we analyze at the molecular level a phenotype of congenital sucrase-isomaltase deficiency in...