Estrous cycle dependent changes in expression and distribution of Fas, Fas ligand, Bcl-2, Bax, and pro- and active caspase-3 in the rat ovary
Slot, Karin A, Voorendt, Marsha, de Boer-Brouwer, Mieke, van Vugt, Harmke H, Teerds, Katja J
Published in Journal of endocrinology (01.02.2006)
Published in Journal of endocrinology (01.02.2006)
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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1
van Kessel, Ad Geurts, Hoenselaar, Eveline, Voorendt, Marsha, Kuiper, Roland P, Lee, Tracy Y H, Hendriks-Cornelissen, Sandra J B, Yuen, Siu Tsan, van Krieken, J Han J M, Leung, Suet Yi, Hoogerbrugge, Nicoline, Chan, Tsun Leung, Bodmer, Danielle, Ligtenberg, Marjolijn J L, Goossens, Monique, Hebeda, Konnie M, Tsui, Wai Yin, Brunner, Han G, Kong, Chi Kwan
Published in Nature genetics (01.01.2009)
Published in Nature genetics (01.01.2009)
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Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene
de Bot, Susanne T., Vermeer, Sascha, Buijsman, Wendy, Heister, Angelien, Voorendt, Marsha, Verrips, Aad, Scheffer, Hans, Kremer, Hubertus P. H., van de Warrenburg, Bart P. C., Kamsteeg, Erik-Jan
Published in Journal of neurology (01.07.2013)
Published in Journal of neurology (01.07.2013)
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Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients
Demirdas, Serwet, van den Bersselaar, Lisa M, Lechner, Rosan, Bos, Jessica, Alsters, Suzanne I M, Baars, Marieke J H, Baas, Annette F, Baysal, Özlem, van der Crabben, Saskia N, Dulfer, Eelco, Giesbertz, Noor A A, Helderman-van den Enden, Apollonia T J M, Hilhorst-Hofstee, Yvonne, Kempers, Marlies J E, Komdeur, Fenne L, Loeys, Bart, Majoor-Krakauer, Daniëlle, Ockeloen, Charlotte W, Overwater, Eline, van Tintelen, Peter J, Voorendt, Marsha, de Waard, Vivian, Maugeri, Alessandra, Brüggenwirth, Hennie T, van de Laar, Ingrid M B H, Houweling, Arjan C
Published in Circulation. Genomic and precision medicine (01.06.2024)
Published in Circulation. Genomic and precision medicine (01.06.2024)
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High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations
Out, Astrid A., van Minderhout, Ivonne J. H. M., van der Stoep, Nienke, van Bommel, Lysette S. R., Kluijt, Irma, Aalfs, Cora, Voorendt, Marsha, Vossen, Rolf H. A. M., Nielsen, Maartje, Vasen, Hans F. A., Morreau, Hans, Devilee, Peter, Tops, Carli M. J., Hes, Frederik J.
Published in Familial cancer (01.06.2015)
Published in Familial cancer (01.06.2015)
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