Onderzoeksoutput per jaar
Onderzoeksoutput per jaar
Onderzoeksoutput
- 34 resultaten
Zoekresultaten
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2024
A critical role for iron import through the transferrin receptor in developing ß-cells
Van Mulders, A., Staels, W., Willems, L., Coenen, S., Bourgeois, S., Ye, X., Tong, Y., Leuckx, G., Heremans, Y., De Koning, E., Carlotti, F., Scharfmann, R., Cnop, M. & De Leu, N., 16 nov. 2024, blz. 486. 487 blz.Onderzoeksoutput: Unpublished abstract
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ER stress relief drives ß-cell proliferation
Bourgeois, S., Staels, W., Van Mulders, A., Willems, L., Coenen, S., Degroote, L., Pierreux, J., Leuckx, G., Heremans, Y., De Leu, N., Heimberg, H., Cnop, M., Ye, X., Movahedi, K., Kancheva, D., Scheyltjens, I., de, K. E. & Carlotti, F., 16 nov. 2024, blz. 316. 317 blz.Onderzoeksoutput: Unpublished abstract
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Prevalence and hormonal correlates of arterial hypertension in overweight/obese children
Staels, W., Donckerwolcke, K. E., Vanbesien, J., Nauwynck, E., Anckaert, E., Mauel, R., De Schepper, J. & Gies, I., 16 nov. 2024, blz. 577. 578 blz.Onderzoeksoutput: Unpublished abstract
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Transient congenital hypothyroidism in a newborn with congenital goiter and compound heterozygosity for thyroglobulin
Nauwynck, E., Gheldof, A., Vanden Eynde, N. E. M., Vanbesien, J., Depoorter, S., Oosterlynck, C., Staels, W., Gies, I. & De Schepper, J., 16 nov. 2024, blz. 205. 205 blz.Onderzoeksoutput: Unpublished abstract
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Two unrelated cases of prenatal Shwachman-Diamond syndrome: a diagnosis complicated by a rare clinical presentation and a pseudogene
Vanden Eynde, N. E. M., Slegers, I., Vantroys, E., Symoens, S., Done, E., Leus, A., Brock, S., Keymolen, K., Hes, F. J., Dimitrov, B. & Van Berkel, K., 2024, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Unveiling HDR Syndrome in a 4-Year-Old Boy with Hypocalcemic Convulsions
De Wolf, A. C., Nauwynck, E., Vanden Eynde, N., Vantroys, E., de Ravel, T., Foulon, I., De Schepper, J. & Gies, I., 23 nov. 2024.Onderzoeksoutput: Unpublished abstract
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2022
Clinical characterization of 6 additional cases with a ARCN1 mutation: from severe fetal presentation to a recognizable craniofacial short stature syndrome
De Rademaeker, M., Van Berkel, K., De Schepper, J., Staels, W., France, A., Boecx, N., Mortier, G. R., Meuwissen, M., Wuyts, W., Brock, S., Keymolen, K., Vantroys, E., Slegers, I., Leus, A. & Dimitrov, B., sep. 2022, blz. 71. 1 blz.Onderzoeksoutput: Unpublished abstract
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Recurrent convulsions due to insulinoma-related hypoglycemia
van Weelden, M., Hoogwijs, I., van Berlaer, G., Vercauteren, C., Vanderlinden, K., Messaoudi, N., Kunda, R., Sys, M., Gies, I., Vanbesien, J., De Schepper, J. & Staels, W., mrt. 2022, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Serum 25-hydroxy vitamin D in Belgian obese children and adolescents : relationship with age, adiposity, puberty, ethnicity , season and insulin resistance.
Nauwynck, E. M., Lersberghe, J., Vanbesien, J., Staels, W., Verheyden, S., Rutteman, B., Anckaert, E., Weets, I., De Schepper, J. & Gies, I., 20 mei 2022, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Whole exome sequencing advances a genetic diagnosis in patients with differences of sex development and corroborates the role of RXFP2 in autosomal recessive bilateral cryptorchidism and infertility
Syryn, H., Verdin, H., Van de Velde, J., Peelman, F., Becker, M., Brachet, C., den Brinker, M., Depoorter, S., Fudvoye, J., Klink, D., Lysy, P. A., Massa, G., Reynaert, N., Rochtus, A., Staels, W., Van Loocke, M., Sinclair, A., ayers, K., Bathgate, R., Cools, M., & 1 anderen, 2022, (Unpublished).Onderzoeksoutput: Unpublished abstract
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2020
Trophectoderm specification: compaction, polarisation and inner and outer cells occur simultaneously in the human preimplantation embryo
Demtschenko, A., Essahib, W., Verheyen, G., Sermon, K., Tournaye, H. & Van De Velde, H., 2020. 1 blz.Onderzoeksoutput: Unpublished abstract
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Unraveling the molecular etiology of Pompe disease using RNA sequencing
Vo Ngoc, D. T. L., Franck, S., Seneca, S., Stouffs, K., De Dobbeleer, G., Jonckheere, A., Jansen, A., Regal, L., Sermon, K. & Gheldof, A., 6 mrt. 2020.Onderzoeksoutput: Unpublished abstract
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2019
CTG repeat instability and DMPK methylation in MSH2-deficient DM1 patient pluripotent stem cells
Franck, S., Sermon, K. & Barbé, L., 2019.Onderzoeksoutput: Unpublished abstract
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2018
MSH2 knock-out human pluripotent stem cells as model for CTG repeat instability in myotonic dystrophy type 1
Franck, S., Barbé, L. & Sermon, K., 20 okt. 2018.Onderzoeksoutput: Unpublished abstract
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MSH2 knock-out human pluripotent stem cells as model for CTG repeat instability in myotonic dystrophy type 1
Franck, S., Barbé, L. & Sermon, K., 25 apr. 2018, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Uncovering regulators of human embryonic stem cell differentiation bias towards definitive endoderm
Dziedzicka, D., Tewary, M., Tilleman, L., Keller, A. S., Östblom, J., Couvreu De Deckersberg, E., Markouli, C., Spits, C., Van Nieuwerburgh, F., Zandstra, P., Sermon, K. & Geens, M., 26 okt. 2018, (Unpublished).Onderzoeksoutput: Unpublished abstract
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2017
Complete spermatogenesis in intratesticular testis tissue xenografts from an immature non-human primate (Callithrix jacchus)
Ntemou, E., Mincheva, M., Kadam, P., Van Saen, D., Wistuba, J., Schlatt, S. & Goossens, E., 2017, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Fertility preservation procedures in Klinefelter syndrome during life span
Van Saen, D., Mateizel, I., Vloeberghs, V., De Schepper, J., Tournaye, H. & Goossens, E., 12 sep. 2017, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Gain of 20q11.21 negatively affects ectoderm differentiation potential in human embryonic stem cells
Markouli, C., Dziedzicka, D., Zambelli, F., Keller, A. S., De Kock, J., Marcelino Rodrigues, R., Sermon, K., Geens, M. & Spits, C., 24 nov. 2017, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Human embryonic stem cell differentiation bias during early lineage specification
Dziedzicka, D., Keller, A. S., Tilleman, L., Aribea, A., Markouli, C., Spits, C., Van Nieuwerburgh, F., Sermon, K. & Geens, M., 24 nov. 2017, (Unpublished).Onderzoeksoutput: Unpublished abstract
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MSH2 knock-out human pluripotent stem cells as model for CTG repeat instability in myotonic dystrophy type 1
Franck, S., Barbé, L. & Sermon, K., 5 sep. 2017, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Results of ESTEEM: an RCT to test preimplantation genetic testing for aneuploid oocytes
Sermon, K., Bosuyt, P., Goossens, V. & Geraedts, B. C. J. M., 2017.Onderzoeksoutput: Unpublished abstract
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2016
CpG methylation upstream of the CTG repeat in myotonic dystrophy type 1 affected human embryonic stem cell lines is correlated with maternal inheritance of the disease and a larger expansion size.
Barbé, L., Lopez Castel, A., Spits, C., Seneca, S. & Pearson, C., 22 jun. 2016.Onderzoeksoutput: Unpublished abstract
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Detection, isolation and characterization of differentiation resistant human embryonic stem cells
Keller, A. S., Dziedzicka, D., Sermon, K. & Geens, M., jul. 2016, (Unpublished) blz. i77.Onderzoeksoutput: Unpublished abstract
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Differentiation capacity of hESC lines carrying a 20q11.21 amplification
Markouli, C., Geens, M., Dziedzicka, D., De Kock, J., Sermon, K. & Spits, C., 2016, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Evaluation of the definitive endoderm differentiation bias between individual hESC lines by standardized methods
Dziedzicka, D., Keller, A. S., Markouli, C., Sermon, K. & Geens, M., 12 sep. 2016.Onderzoeksoutput: Unpublished abstract
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Fertility preservation in Klinefelter boys: an update after 6 years experience
Van Saen, D., 10 mrt. 2016.Onderzoeksoutput: Unpublished abstract
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Standardized approaches for evaluation of definitive endoderm differentiation bias between individual hESC lines
Dziedzicka, D., Markouli, C., Sermon, K. & Geens, M., 22 jun. 2016.Onderzoeksoutput: Unpublished abstract
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2015
MSH2 knock down triggers trinucleotide instability in myotonic dystrophy type I human embryonic stem cells
Barbé, L., Hilven, P., Spits, C. & Sermon, K., 2015.Onderzoeksoutput: Unpublished abstract
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MSH2 knock down triggers trinucleotide instability in myotonic dystrophy type I human embryonic stem cells
Barbé, L., Nguyen Thi, H., Hilven, P., Spits, C. & Sermon, K., jun. 2015, (Unpublished).Onderzoeksoutput: Unpublished abstract
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Open versus closed oocyte vitrification in an oocyte donation programme: a prospective randomized sibling oocyte study
De Munck, N., Santos-Ribeiro, S., Stoop, D., Van De Velde, H. & Verheyen, G., 2015.Onderzoeksoutput: Unpublished abstract
29 Citaten (Scopus) -
Optimization of embryoid body formation from single cell suspensions of human embryonic stem cells cultured on laminin-521
Dziedzicka, D., Markouli, C., Barbé, L., Spits, C., Sermon, K. & Geens, M., 24 jun. 2015.Onderzoeksoutput: Unpublished abstract
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The growth phase of the cells is a crucial factor for successful embryoid body formation from human pluripotent stem cells cultured on laminin-521
Dziedzicka, D., Markouli, C., Barbé, L., Spits, C., Sermon, K. & Geens, M., 20 apr. 2015.Onderzoeksoutput: Unpublished abstract
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2014
INHERITANCE OF MYOTONIC DYSTROPHY TYPE I IS CORRELATED WITH THE METHYLATION OF CPG SITES IN THE MYOTONIC DYSTROPHY LOCUS.
Barbé, L., Hilven, P., Spits, C. & Sermon, K., 2014.Onderzoeksoutput: Unpublished abstract