Human pluripotent stem cell-derived kidney organoids for personalized congenital and idiopathic nephrotic syndrome modeling

التفاصيل البيبلوغرافية
العنوان:	Human pluripotent stem cell-derived kidney organoids for personalized congenital and idiopathic nephrotic syndrome modeling
المؤلفون:	Jansen, J., van den Berge, B. T., van den Broek, M., Maas, R. J., Daviran, D., Willemsen, B., Roverts, R., van der Kruit, M., Kuppe, C., Reimer, K. C., Giovanni, G. D., Mooren, F., Nlandu, Q., Mudde, H., Wetzels, R., den Braanker, D., Parr, N., Nagai, J. S., Drenic, V., Costa, I. G., Steenbergen, E., Nijenhuis, T., Dijkman, H., Endlich, N., van de Kar, N. C. A. J., Schneider, R. K., Wetzels, J. F. M., Akiva, A., van der Vlag, J., Kramann, R., Schreuder, M. F., Smeets, B.
المصدر:	Jansen , J , van den Berge , B T , van den Broek , M , Maas , R J , Daviran , D , Willemsen , B , Roverts , R , van der Kruit , M , Kuppe , C , Reimer , K C , Giovanni , G D , Mooren , F , Nlandu , Q , Mudde , H , Wetzels , R , den Braanker , D , Parr , N , Nagai , J S , Drenic , V , Costa , I G , Steenbergen , E , Nijenhuis , ....
سنة النشر:	2022
الوصف:	Nephrotic syndrome (NS) is characterized by severe proteinuria as a consequence of kidney glomerular injury due to podocyte damage. In vitro models mimicking in vivo podocyte characteristics are a prerequisite to resolve NS pathogenesis.
نوع الوثيقة:	article in journal/newspaper
وصف الملف:	application/pdf
اللغة:	English
DOI:	10.1242/dev.200198
الاتاحة:	https://pure.eur.nl/en/publications/338c3caf-c94c-4896-9c0f-aa159c09dd6b https://doi.org/10.1242/dev.200198 https://pure.eur.nl/ws/files/89906220/dev200198.pdf http://www.scopus.com/inward/record.url?scp=85129997517&partnerID=8YFLogxK https://www.scopus.com/inward/record.uri?eid=2-s2.0-85129997517&doi=10.1242%2fdev.200198&partnerID=40&md5=35638adc1cf871f0c7a314b604d5fa3b
Rights:	info:eu-repo/semantics/openAccess
رقم الانضمام:	edsbas.E1FC2996
قاعدة البيانات:	BASE

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الوصف
DOI:	10.1242/dev.200198