Výsledky vyhledávání - "Nicole van Koetsveld"

Akademický článek

Generation of Trophoblast Organoids from Chorionic Villus Sampling

Autor: Bas van Rijn, Diane Van Opstal, Nicole van Koetsveld, Maarten Knapen, Joost Gribnau, Olivier Schäffers

Publikováno v: Organoids, Vol 3, Iss 1, Pp 54-66 (2024)

Studying human placental development and function presents significant challenges due to the inherent difficulties in obtaining and maintaining placental tissue throughout the course of an ongoing pregnancy. Here, we provide a detailed protocol for g

Externí odkaz: https://doaj.org/article/915fd07a61854dfd85647d755452748e

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Noninvasive prenatal testing as compared to chorionic villus sampling is more sensitive for the detection of confined placental mosaicism involving the cytotrophoblast

Autor: Geerke M. Eggenhuizen, Karin E. M. Diderich, Nicole van Koetsveld, Attie T.J.I. Go, Malgorzata I. Srebniak, Femke A. T. de Vries, Wai Yee Cheung, Diane Van Opstal, Lutgarde C.P. Govaerts, Walter G. de Valk, Robert-Jan H. Galjaard, Stefanie van Veen, Lies H. Hoefsloot, Maarten F. C. M. Knapen, Marieke Joosten, Marjan Boter, Fernanda Sarquis Jehee, Iris H.I.M. Hollink

Publikováno v: Prenatal Diagnosis
Prenatal Diagnosis, 40(10), 1338-1342. John Wiley & Sons Ltd.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0ce0680b84a6d40bf6fbf7f74cc62b5
https://doi.org/10.1002/pd.5766

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Placental studies elucidate discrepancies between NIPT showing a structural chromosome aberration and a differently abnormal fetal karyotype

Autor: Diane Van Opstal, Dimitri N.M. Papatsonis, Joke Polak, Lies H. Hoefsloot, Malgorzata I. Srebniak, Karin E. M. Diderich, Krista A. K. E. Prinsen, Marjan Boter, Stefanie van Veen, Nicole van Koetsveld, Marieke Joosten, Lutgarde C.P. Govaerts, Attie T.J.I. Go

Publikováno v: Prenatal Diagnosis. John Wiley & Sons Ltd.
Prenatal Diagnosis

Objective Placental cytogenetic studies may reveal the origin of discordant noninvasive prenatal testing (NIPT). We performed placental studies to elucidate discordances between NIPT showing a structural chromosome aberration and the fetus having a d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ae3011dae9a8bc4e0a198cb6237728f
https://doi.org/10.1002/pd.5531

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