Wessels HJCT - Search Results

1

In Vitro Skeletal Muscle Model of PGM1 Deficiency Reveals Altered Energy Homeostasis.

Conte F, Ashikov A, Mijdam R, van de Ven EGP, van Scherpenzeel M, Veizaj R, Mahalleh-Yousefi SP, Post MA, Huijben K, Panneman DM, Rodenburg RJT, Voermans NC, Garanto A, Koopman WJH, Wessels HJCT, Noga MJ, Lefeber DJ. Conte F, et al. Int J Mol Sci. 2023 May 4;24(9):8247. doi: 10.3390/ijms24098247. Int J Mol Sci. 2023. PMID: 37175952 Free PMC article.

2

Automated measurement of permethylated serum N-glycans by MALDI-linear ion trap mass spectrometry.

Guillard M, Gloerich J, Wessels HJ, Morava E, Wevers RA, Lefeber DJ. Guillard M, et al. Carbohydr Res. 2009 Aug 17;344(12):1550-7. doi: 10.1016/j.carres.2009.06.010. Epub 2009 Jun 16. Carbohydr Res. 2009. PMID: 19577739

3

LC-MS/MS as an alternative for SDS-PAGE in blue native analysis of protein complexes.

Wessels HJ, Vogel RO, van den Heuvel L, Smeitink JA, Rodenburg RJ, Nijtmans LG, Farhoud MH. Wessels HJ, et al. Proteomics. 2009 Sep;9(17):4221-8. doi: 10.1002/pmic.200900157. Proteomics. 2009. PMID: 19688755

4

O-glycosylation disorders pave the road for understanding the complex human O-glycosylation machinery.

van Tol W, Wessels H, Lefeber DJ. van Tol W, et al. Curr Opin Struct Biol. 2019 Jun;56:107-118. doi: 10.1016/j.sbi.2018.12.006. Epub 2019 Jan 30. Curr Opin Struct Biol. 2019. PMID: 30708323 Free article. Review.

5

Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability.

Knapp KM, Luu R, Baerenfaenger M, Zijlstra F, Wessels HJCT, Jenkins D, Lefeber DJ, Neas K, Bicknell LS. Knapp KM, et al. J Hum Genet. 2020 Sep;65(9):743-750. doi: 10.1038/s10038-020-0764-4. Epub 2020 Apr 21. J Hum Genet. 2020. PMID: 32313197

6

Loss of the AMD-associated B3GLCT gene affects glycosylation of TSP1 without impairing secretion in retinal pigment epithelial cells.

Lauwen S, Baerenfaenger M, Ruigrok S, de Jong EK, Wessels HJCT, den Hollander AI, Lefeber DJ. Lauwen S, et al. Exp Eye Res. 2021 Dec;213:108798. doi: 10.1016/j.exer.2021.108798. Epub 2021 Oct 22. Exp Eye Res. 2021. PMID: 34695439 Free article.

7

MOGS-CDG: Quantitative analysis of the diagnostic Glc₃ Man tetrasaccharide and clinical spectrum of six new cases.

Post MA, de Wit I, Zijlstra FSM, Engelke UFH, van Rooij A, Christodoulou J, Tan TY, Le Fevre A, Jin D, Yaplito-Lee J, Lee BH, Low KJ, Mallick AA, Õunap K, Pitt J, Reardon W, Vals MA, Wortmann SB, Wessels HJCT, Bärenfänger M, van Karnebeek CDM, Lefeber DJ. Post MA, et al. J Inherit Metab Dis. 2023 Mar;46(2):313-325. doi: 10.1002/jimd.12588. Epub 2023 Feb 1. J Inherit Metab Dis. 2023. PMID: 36651519

8

Glycoproteomics in Cerebrospinal Fluid Reveals Brain-Specific Glycosylation Changes.

Baerenfaenger M, Post MA, Langerhorst P, Huijben K, Zijlstra F, Jacobs JFM, Verbeek MM, Wessels HJCT, Lefeber DJ. Baerenfaenger M, et al. Int J Mol Sci. 2023 Jan 18;24(3):1937. doi: 10.3390/ijms24031937. Int J Mol Sci. 2023. PMID: 36768261 Free PMC article.

9

The GlycoPaSER Prototype as a Real-Time N-Glycopeptide Identification Tool Based on the PaSER Parallel Computing Platform.

Armony G, Brehmer S, Srikumar T, Pfennig L, Zijlstra F, Trede D, Kruppa G, Lefeber DJ, van Gool AJ, Wessels HJCT. Armony G, et al. Int J Mol Sci. 2023 Apr 26;24(9):7869. doi: 10.3390/ijms24097869. Int J Mol Sci. 2023. PMID: 37175577 Free PMC article.

10

Plasma glycoproteomics delivers high-specificity disease biomarkers by detecting site-specific glycosylation abnormalities.

Wessels HJCT, Kulkarni P, van Dael M, Suppers A, Willems E, Zijlstra F, Kragt E, Gloerich J, Schmit PO, Pengelley S, Marx K, van Gool AJ, Lefeber DJ. Wessels HJCT, et al. J Adv Res. 2024 Jul;61:179-192. doi: 10.1016/j.jare.2023.09.002. Epub 2023 Sep 6. J Adv Res. 2024. PMID: 37683725 Free PMC article.

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