Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tjessa Bondue"'
Autor:
Tjessa Bondue, Sante Princiero Berlingerio, Florian Siegerist, Elena Sendino-Garví, Maximilian Schindler, Hans Jacobus Baelde, Sara Cairoli, Bianca Maria Goffredo, Fanny Oliveira Arcolino, Jürgen Dieker, Manoe Jacoba Janssen, Nicole Endlich, Roland Brock, Rik Gijsbers, Lambertus van den Heuvel, Elena Levtchenko
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract Messenger RNA (mRNA) therapies are emerging in different disease areas, but have not yet reached the kidney field. Our aim was to study the feasibility to treat the genetic defect in cystinosis using synthetic mRNA in cell models and ctns
Externí odkaz:
https://doaj.org/article/e4841b6ebf164c40bbddf71bdbfa5308
Autor:
Koenraad Veys, Sante Princiero Berlingerio, Dries David, Tjessa Bondue, Katharina Held, Ahmed Reda, Martijn van den Broek, Koen Theunis, Mirian Janssen, Elisabeth Cornelissen, Joris Vriens, Francesca Diomedi-Camassei, Rik Gijsbers, Lambertus van den Heuvel, Fanny O. Arcolino, Elena Levtchenko
Publikováno v:
Cells, Vol 11, Iss 7, p 1245 (2022)
Nephropathic cystinosis is an inherited lysosomal storage disorder caused by pathogenic variants in the cystinosin (CTNS) gene and is characterized by the excessive shedding of proximal tubular epithelial cells (PTECs) and podocytes into urine, devel
Externí odkaz:
https://doaj.org/article/f9b949bccec54990b08489d83fa4c840
Autor:
Tjessa Bondue, Fanny O. Arcolino, Koenraad R. P. Veys, Oyindamola C. Adebayo, Elena Levtchenko, Lambertus P. van den Heuvel, Mohamed A. Elmonem
Publikováno v:
Cells, Vol 10, Iss 6, p 1413 (2021)
Epithelial cells exfoliated in human urine can include cells anywhere from the urinary tract and kidneys; however, podocytes and proximal tubular epithelial cells (PTECs) are by far the most relevant cell types for the study of genetic kidney disease
Externí odkaz:
https://doaj.org/article/64d226c3803f470f8fe7f6663acc37a8
Autor:
Tjessa Bondue, Sante P. Berlingerio, Florian Siegerist, Elena Sendino-Garví, Maximilian Schindler, Sara Cairoli, Bianca M. Goffredo, Fanny O. Arcolino, Jürgen Dieker, Manoe Janssen, Nicole Endlich, Roland Brock, Rik Gijsbers, Lambertus van den Heuvel, Elena Levtchenko
Messenger RNA (mRNA) therapies are emerging in different disease areas, but have not yet reached the kidney field. Our aim was to study the feasibility to correct the genetic defect in nephropathic cystinosis using synthetic mRNA. Cystinosis is a pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b23a4bb539cee4a217b1a036634bfe03
https://doi.org/10.1101/2023.04.28.538106
https://doi.org/10.1101/2023.04.28.538106
Publikováno v:
Pediatric Nephrology, 38, 2, pp. 327-344
Pediatric Nephrology, 38, 327-344
Pediatric Nephrology, 38, 327-344
Inherited kidney diseases (IKDs) are a large group of disorders affecting different nephron segments, many of which progress towards kidney failure due to the absence of curative therapies. With the current advances in genetic testing, the understand
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6d7ea0b25f0ab43e69de0579b33992
https://repository.ubn.ru.nl/handle/2066/287637
https://repository.ubn.ru.nl/handle/2066/287637
Autor:
Tjessa Bondue, Anas Kouraich, Sante Princiero Berlingerio, Koenraad Veys, Sandrine Marie, Khaled O. Alsaad, Essam Al-Sabban, Elena Levtchenko, Lambertus van den Heuvel
Publikováno v:
International Journal of Molecular Sciences, 24
International Journal of Molecular Sciences, 24, 2
International Journal of Molecular Sciences, 24, 2
Cystinosis is an autosomal recessive lysosomal storage disease, caused by mutations in the CTNS gene, resulting in multi-organ cystine accumulation. Three forms of cystinosis are distinguished: infantile and juvenile nephropathic cystinosis affecting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::363e5151229bb6fa9b70ac762137f8d1
https://doi.org/10.3390/ijms24021253
https://doi.org/10.3390/ijms24021253
Autor:
Lambertus P. van den Heuvel, Fanny Oliveira Arcolino, Mohamed A. Elmonem, Tjessa Bondue, Koenraad Veys, Elena Levtchenko, Oyindamola C Adebayo
Publikováno v:
Cells, 10, 6
Cells, 10
Cells
Cells, Vol 10, Iss 1413, p 1413 (2021)
Cells, 10
Cells
Cells, Vol 10, Iss 1413, p 1413 (2021)
Epithelial cells exfoliated in human urine can include cells anywhere from the urinary tract and kidneys; however, podocytes and proximal tubular epithelial cells (PTECs) are by far the most relevant cell types for the study of genetic kidney disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f7752f2347285f89367a4dc704f7c29
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