Publications by authors named "G Matthijs"

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ATP6AP2-Related Disease Caused by Splicing Defects: Abnormal Glycosylation and the First Affected Female.
Alexandre Raynor, Jean-Madeleine de Sainte-Agathe, Merel A Post, Magalie Barth, Fokje Zijlstra, Gert Matthijs

J Inherit Metab Dis· November 2025

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Genetic Modulators of Diversity in the Biological Expression of Sickle Cell Anemia in Patients from Democratic Republic of Congo: Role of βs-globin Haplotypes.
Mamy Ngole, Gloire Mbayabo, Paul Lumbala, Valerie Race, Nono Mvuama, Gert Matthijs

Mediterr J Hematol Infect Dis· January 2025

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Absence of the dolichol synthesis gene DHRSX leads to N-glycosylation defects in Lec5 and Lec9 Chinese hamster ovary cells.
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Gert Matthijs

J Biol Chem· December 2024

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A pseudoautosomal glycosylation disorder prompts the revision of dolichol biosynthesis.
Matthew P Wilson, Takfarinas Kentache, Charlotte R Althoff, Céline Schulz, Geoffroy de Bettignies, Gert Matthijs

Cell· July 2024

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The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene.
Takfarinas Kentache, Charlotte R Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Gert Matthijs

bioRxiv· June 2024

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